AU2003204611B2 - Alpha-olefins and olefin polymers and processes therefor - Google Patents

Description

P/00/011 Regulation 3.2

AUSTRALIA

Patents Act 1990 COMPLETE SPECIFICATION FOR A DIVISIONAL PATENT

ORIGINAL

TO BE COMPLETED BY APPLICANT Name of Applicant: Actual Inventor(s): Address for Service: Invention Title: E.I. DU PONT DE NEMOURS AND COMPANY and UNIVERSITY OF NORTH CAROLINA CHAPEL HILL Lynda Kaye JOHNSON, Maurice S. BROOKHART, Daniel Joseph TEMPEL, Anju PARTHASARATHY, Steven Dale ITTEL, Edward Bryan, COUGHLIN, Margaret Anne BENNETT, Stephan James McLAIN, Kristina Ann KREUTZER, Elizabeth McCORD, Jerald FELDMAN, Samuel David ARTHUR, and Christopher Moore KILLIAN.

CALLINAN LAWRIE, 711 High Street, Kew, Victoria 3101, Australia a-OLEFINS AND OLEFIN POLYMERS AND PROCESSES THEREFOR The following statement is a full description of this invention, including the best method of performing it known to us:- 02/06/03.swl331 ]spa, I

TITLE

ct-OLEFINS AND OLEFIN POLYMERS AND PROCESSES THEREFOR This application is a divisional application of Australian Patent Application No. 71835/00, which was a divisional of Australian Patent Application No. 50208/96, the entire disclosures of AU 71835/00 and AU 50208/96 are incorporated herein by reference.

FIELD OF THE INVENTION The invention concerns novel homo- and copolymers of ethylene and/or one or more acyclic olefins, and/or selected cyclic olefins, and optionally selected ester, carboxylic acid, or other functional group containing olefins as comonomers; selected transition metal containing polymerization catalysts; and processes for making such polymers, intermediates for such catalysts, and new processes for making such catalysts.

Also disclosed herein is a process for the production of linear alpha-olefins by contacting ethylene with a nickel compound of the formula [DAB]NiX 2 wherein DAB is a selected adiimine and X is chlorine, bromine, iodine or alkyl, and a selected Lewis or Bronsted acid, or by contacting ethylene with other selected a-diimine nickel complexes.

BACKGROUND OF THE INVENTION Homo- and copolymers of ethylene and/or one or more acyclic olefins, and/or cyclic olefins, and/or substituted olefins, and optionally selected olefinic esters or carboxylic acids, and other types of monomers, are useful materials, being used a plastics for packaging materials, molded items, films, etc., and as elastomers for molded goods, belts of various types, in tires, adhesives, and for other uses. It is well known in the art that the structure of these various polymers, and hence their properties and uses, are highly dependent on the catalyst and specific conditions used during their synthesis. In addition to these factors, processes in which these types of polymers can be made at reduced cost are also important. Therefore, improved processes for making such (new) polymers are of interest. Also disclosed herein are uses for the novel polymers.

la- -Oo6/03,sw1331 Ispa.l a-Olefins are commercial materials being particularly useful as monomers and as chemical intermediates. For a review of a-olefins, including their uses and preparation, see B. Elvers, et al., Ed., Ullmann's Encyclopedia of Industrial Chemistry, 5 th Ed., Vol. A13, VCH Verlagsgesellschaft mbH, Weinheim, 1989, p.

238-251. They are useful as chemical intermediates and they are often made by the oligomerization of ethylene using various types of catalysts. Therefore catalysts which are capable or forming a-olefins from ethylene are constantly sought.

SUMMARY OF THE INVENTION This invention concerns a process for the polymerization of olefins, comprising, contacting, at a temperature of-100 0 C to 200 0 C, a transition metal complex of a bidentate ligand selected from the group consisting of: R2

R

3

I

R4 N R2(CR 3 2

R

29

R

4

N=CR

4

(XXX)

(VIII)

(xxl) (XXXII) with an olefin wherein: said olefin is selected from the group consisting of ethylene, an olefin of 17 17 the formula R CH=CH 2 or R CH=CHR 7 cyclobutene, cyclopentene, norbornene, or a substituted norbornene; 10/01/06,ck1331 1janl0.spc,2 said transition metal is selected from the group consisting of Ti, Zr, Sc, V, Cr, a rare earth metal, Fe, Co, Ni or Pd;

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring;

R

44 is hydrocarbyl or substituted hydrocarbyl, and R 2 8 is hydrogen, hydrocarbyl or substituted hydrocarbyl or R 4 4 and R 28 taken together form a ring;

R

45 is hydrocarbyl or substituted hydrocarbyl, and R 29 is hydrogen, substituted hydrocarbyl or hydrocarbyl, or R 45 and R 29 taken together form a ring; each R 30 is independently hydrogen, substituted hydrocarbyl or hydrocarbyl, or two of R 3 0 taken together form a ring;

R

20 and R 23 are independently hydrocarbyl or substituted hydrocarbyl;

R

2 1 and R 22 are each in independently hydrogen, hydrocarbyl or substituted hydrocarbyl; each R 1 7 is independently hydrocarbyl or substituted hydrocarbyl provided that any olefinic bond in said olefin is separated from any other olefinic bond or aromatic ring by a quaternary carbon atom or at least two saturated carbon atoms; and provided that: when said bidentate ligand is (XXX) M is not Pd; when M is Pd a diene is not present; and said transition metal also has bonded to it a ligand that may be displaced by said olefin or add to said olefin; when norbornene or substituted norbornene is used no other olefin is present 31/01/06,atl331 .specipg,2 -3- Preferably the transition metal is in a positive oxidation state and has a d 8 electronic configuration.

Preferably the transition metal is nickel, cobalt, iron or palladium, more preferably nickel or palladium, even more preferably nickel.

Preferably the transition metal has further bonded to it a group Q, a group S or both, in an amount equal to the oxidation state of the transition metal, wherein Q and S are independently an alkyl, chloride, iodide or bromide In a preferred embodiment the catalyst used in the process further comprises a compound W, which is a neutral Lewis acid capable of abstracting either Q or S- to form WQ- or WS-, provided that the anion formed is a weakly coordinating anion; or a cationic Lewis or Bronsted acid whose counterion is a weakly coordinating anion.

In a further preferred embodiment the transition metal has an oxidation state of 2.

Preferably the compound W is further capable of transferring a hydride or alkyl group to the transition metal.

In a further preferred embodiment the catalyst used in the invention further comprises an alkyl aluminum compound.

In another preferred embodiment the transition metal has bonded to it another ligand that may be displaced by said olefin or add to said olefin, or both.

In yet another preferred embodiment the catalyst used is characterized in that the bidentate ligand is an oa-diimine.

In another preferred aspect the transition metal complex of the catalyst composition is of the formula R2 R3

I

-N .Q)Y

M

R

4 'N )z

R

5

(XI)

wherein: M is Ti, Zr, Sc, V, Cr, a rare earth metal, Co, Fe, Ni or Pd in the m oxidation state; y+z=m 10/01/06,ck1331 lljan0O.spc,2 3a-

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring; each Q is independently alkyl, hydride, chloride, iodide, or bromide; and each S is independently alkyl, hydride, chloride, iodide, or bromide.

Preferably: M is Ni and m is 2; M is Pd and m is 2; M is Fe and m is 2; M is Co and m is 2; M is Zr and m is 4; M is Sc and m is 3; M is Cr and m is 2 or 3; or M is V and m is 3.

10/01/06,ckl331 IjanlO.spc,2 3b- Even more preferably: M is Ti(IV), Q and S are chloride, and y and z are both 2; M is Zr(IV), Q and S are chloride, and y and z are both 2; M is Sc(III), Q and S are chloride, y is I and z is 2; M is Cr(III), Q and S are chloride, y is 1 and z is 2; M is Cr(II), Q and S are chloride, y is 1 and z is 1; or M is V(III), Q and S are chloride, y is 1 and z is 2.

Even more preferably M is Ni(II), or M is Pd(II).

In another preferred embodiment the transition metal complex is of the formula R52 R3 I

I

R53s

(XXXVI)

wherein:

R

5 2 is substituted phenyl; and

R

53 is phenyl or substituted phenyl; and groups in the 2 and 6 positions of R 5 2 have a difference in E3 of 0.15 or more.

Preferably the groups in the 2 and 6 positions of R 53 have a difference in Es of 0.15 or more.

In yet another preferred embodiment the transition metal complex is of the formula

(XXXXI)

R2 4\ Pd R4

(XXXXI)

wherein:

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl; and -4 0206/03.sw33 11spa,4 Me is methyl.

In another preferred embodiment the transition metal complex is of the formula (II) or (III) R2 Pd

T

R N

Z

R

5

X"

(II)

R2 R3 I \N \p Ni R4 N

Z

R

5

X

(III)

wherein: R2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring; T' is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, R' or Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound is less than about 6; X is a weakly coordinating anion; and

R

15 is hydrocarbyl not containing olefinic or acetylenic bonds; provided that in (II) when R 3 and R 4 taken together are hydrocarbylene to form a carbocyclic ring, Z is not an organic nitrile.

Preferably R 3 and R 4 are each independently phenyl or substituted phenyl.

Preferably the transition metal complex is of the formula (III); R 3 and R 4 are each independently hydrogen or hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene to form a ring; T' is methyl; and Z is R 6 2 0, wherein each R 6 is independently alkyl.

02/06/03,sw 3311 spa Preferably X is BAF, SbF 6

PF

6 or BE 4 Preferably the transition metal complex is of the formula and each of R RN

R

4

R

5 Z, and X are as follows: R 2 R 3 Rt 4 R jZ X 2,6-i-PrPh 2,6-i-PrPh 2,6-MePh 2,6-MePh 2,6-i-PrPh 2,6-i-PrPh 2,6-i-PrPh 2,6-i-PrPh 2,4,6-MePh 2,6-i-PrPh 2,6-i-P rPh Ph 2,6-EtPh 2,6-EtPh 2-t-BuPh 1-Np Ph 2

CH

2-PhPh Ph Ph Ph Ph 2

CH

Ph 2

CH

2,6-i-PrPh 2,6-i-PrPh 2,6-MePh 2,6-MePh 2,6-i-PrPh 2,6-i-PrPb 2,6-i-PrPh 2,6-i-PrPh 2,4,6-MePh 2,6-i-PrPh 2,6-i-PrPh Ph 2,6-EtPh 2,6-EtPh 2-t-BuPh 1 -Np Ph 2

CH

2-PhPh Ph Ph Ph Ph 2

CH

Ph 2

CH

OEt 2 Ot 2 Ot 2 ORt 2 GEt 2 OEt 2 Ot 2 OPt 2 OEt 2 Ot 2 NCMe NCMe NCMe NCMe NCMe NCMe NCMe NCMe NCMe NCMe -NCMe NCMe

SMC

2

BAF

BAP

RAP

BAF

SbF 6

BF

4

PF

6 SbF 6 SbF 6 SbF 6 SbF 6 SbF 6

BAF

SbE 6 ShE 6 SbF 6 SbF 6 SbF 6

BAF

ShE 6

BAF

S bE 6 SbF 6 a CMe 2

CH

2 CMe 2 In another preferred embodiment the transition metal complex is of the formnula 02/06/03,sw1331 I spa,6

(IV)

wherein:

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; M is Ni(II) or Pd(II); each R 16 is independently hydrogen or alkyl containing 1 to 10 carbon atoms; n is 1, 2, or 3; X- is a weakly coordinating anion; and

R

8 is hydrocarbyl.

Preferably R 3 and R 4 are each independently hydrogen or hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene to form a ring; and X is BAF, SbF 6

PF

6 or BF 4 In yet another preferred aspect the present invention provides the transition metal complex is of the formula R2 R 2

R

3

R

3 N\ /T /N R /Pd -E-Pd R< -S v R4) N 1

N,

115 R4 R X

(V)

wherein:

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; 02/06/03,sa1331 spa,7 E is halogen or -OR 1 8

R

18 is hydrocarbyl not containing olefinic or acetylenic bonds; T is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, R 5C

O)-

or R"OC

R

1 5 is hydrocarbyl not containing olefinic or acetylenic bonds; and X- is a weakly coordinating anion.

In yet another preferred aspect the invention provides a transition metal complex is of the formula R2

R

3 1 N, PT 3 M CHR 11 R4)-"N ,11, R4 I R HC X-

(VI)

wherein: M is Ni(II) or Pd(II);

R

2 and R 5 are hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; each is independently hydrogen, alkyl or -(CH 2 )mCO 2

R'

T

3 is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, or -CH2

CH

2

CH

2

CO

2 Rg; P is a divalent group containing one or more repeat units derived from the polymerization of one or more of ethylene, an olefin of the formula R t 7CH=CH 2 or

R'

7

CH=CHR'

7 cyclobutene, cyclopentene, substituted norbornene, or norborene and, when M is Pd(II), optionally one or more of: a compound of the formula CH2=CH(CH 2 )mCO 2 CO, or a vinyl ketone; R is hydrocarbyl; m is 0 or an integer from 1 to 16; R' is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to 10 carbon atoms; and X- is a weakly coordinating anion.

-8- 037/6/03,sw13311 spa, In yet another preferred aspect the invention provides a the transition metal complex of the formula R2 R3 t Pd\

R

4 ~N

X

R

5

(VII)

wherein:

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring;

T

2 is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, hydrocarbyl substituted with keto or ester groups but not containing olefinic or acetylenic bonds, R' 5 or R1OC(=O)-;

R

1 5 is hydrocarbyl not containing olefinic or acetylenic bonds; and X is a weakly coordinating anion.

In even another preferred aspect the invention provides a transition metal complex of the formula k 2 N\ H

R

(XVI) (X)a wherein: M is Zr, Ti, Sc, V, Cr, a rare earth metal, Fe, Co, Ni or Pd of oxidation state m;

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, 02//03.sw 133 11sps, 9 or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; each R" is independently hydrogen, or alkyl, or both of R" taken together are hydrocarbylene to form a carbocyclic ring;

T

3 is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, or

CH

2

CH

2

CH

2

CO

2 R8; P is a divalent group containing one or more repeat units derived from the polymerization of one or more monomers selected from the group consisting of ethylene, an olefin of the formula R" 7

CH

C H 2 or R"CH=CHR 7, cyclopentene, cyclobutene, substituted norborene, and norbornene, and optionally, when M is Pd(II), one or more of: a compound of the formula CH 2

=CH(CH

2 )mCO2R', CO, or a vinyl ketone; Q is a monovalent anion;

R

8 is hydrocarbyl; a is 1 or 2; y+a+ =m; each R' 7 is independently hydrocarbyl or substituted hydrocarbyl provided that any olefinic bond in said olefin is separated from any other olefinic bond or aromatic ring by a quaternary carbon atom or at least two saturated carbon atoms; R' is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to 10 carbon atoms; m is 0 or an integer of 1 to 16; and X is a weakly coordinating anion.

In yet another preferred aspect the invention provides a transition metal complex of the formula R2 R3

I

CHR"'

R

4 R'HC X- R 5

(IX)

wherein: M is Ni(II) or Pd(II);

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; 02/06/03,swl331

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; each R' 4 is independently hydrogen, alkyl or -(CH 2 )mCO 2

R';

R' is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to 10 carbon atoms;

T

4 is alkyl, -R 60

C(O)OR

8 or RSOC(=O)-;

R'

5 is hydrocarbyl not containing olefinic or acetylenic bonds;

R

60 is alkylene not containing olefinic or acetylenic bonds; R8 is hydrocarbyl; and X is a weakly coordinating anion; provided that when R 1 4 is -(CH 2 )mCO 2 or T 4 is not alkyl, M is Pd(II).

In yet another preferred aspect the transition metal complex is of the formula

R

2

R'

N"/ A R* s X"

XXXVII

wherein: M is Ni(II) or Pd(II); A is a n-allyl or t-benzyl group;

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; each R 1 7 is independently hydrocarbyl or substituted hydrocarbyl provided that any olefinic bond in said olefin is separated from any other olefinic bond or aromatic ring by a quaternary carbon atom or at least two saturated carbon atoms; R' is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to 10 carbon atoms; and X is a weakly coordinating anion.

11 02/06/03,sw133 I spa, I In yet another preferred aspect the transition metal complex is of the formula (XVIll) wherein:

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or

R

3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring;

R

5 4 is hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; each R 55 is independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or a functional group; W is alkylene or substituted alkylene containing 2 or more carbon atoms; Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur, or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound (measured in water) is less than about 6, or an olefin of the formula R17CH=CHR17; each R 17 is independently hydrogen, saturated hydrocarbyl or substituted saturated hydrocarbyl; and X is a weakly coordinating anion; provided that when M is Ni, W is alkylene and each R 17 is independently hydrogen or saturated hydrocarbyl.

In another preferred aspect the transition metal complex is of the formula

R

2 R Ni 0 R OMe (XXXXm) wherein: 12- 02/06/03,sw1331 Isp.l12

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; and

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring.

Preferably the transition metal complex is of the formula

R

28 (CR30 2 )n R 29 I =N N=CR 4 (S)z

(XVII)

wherein: M is Ti, Zr, V, Cr, a rare earth metal, Co, Fe, Sc, Pd, or Ni, of oxidation state m;

R

44 is hydrocarbyl or substituted hydrocarbyl, and R 28 is hydrogen, substituted hydrocarbyl or hydrocarbyl, or R 44 and R 28 taken together form a ring;

R

45 is hydrocarbyl or substituted hydrocarbyl, and R 29 is hydrogen, substituted hydrocarbyl or hydrocarbyl, or R 45 and R 29 taken together form'a ring; each R 3 0 is independently hydrogen, substituted hydrocarbyl or hydrocarbyl, or two of R 30 taken together form a ring; n is 2 or 3; y and z are positive integers; y+z=m Q is alkyl, hydride, chloride, iodide, or bromide; and S is alkyl, hydride, chloride, iodide, or bromide.

Preferably the catalyst composition is supported on a heterogenous support.

Preferably the catalyst composition is adapted for the polymerization of ethylene.

Preferably X is part of a heterogeneous support.

The present invention further concerns a process for preparing a compound of the formula (II) as set forth above, comprising the step of contacting, at a temperature of about -400C to about +60 0 C, a compound of the formula [(r 4 -1,5-COD)PdT'Z]+X' and a diimine of the formula 13- 02/0603.sw331 Ispl.13 R2

R

3

\,N

R4/

N

R

s

(VIII)

wherein: COD is Z is R'iCN; and

R

I is hydrocarbyl not containing olefinic or acetylenic bonds.

Preferably the process is carried out in a solvent of the formula R"°CN, wherein R 1 is hydrocarbyl not containing olefinic or acetylenic bonds.

In yet another aspect the invention concerns a process for the production of a compound of the formula (XXXVIII) as set forth above, comprising the step of heating a compound of the formula R3 z X" R4 1"

(XXXIX)

at a temperature of about -30°C to about +100°C for a sufficient time to produce (XXXVIII), and wherein:

R

56 is alkyl containing 2 to 30 carbon atoms; and

T

5 is alkyl.

In a further aspect the invention concerns a process for preparing a compound of the formula (XXXXI) as set forth above, comprising the step of contacting, at a temperature of about -80 0 C to about +20 0 C, a compound of the formula (rI 4 PdMe 2 and a diimine of the formula R2 R3 R4 R

(VIII)

14- 02/06/03,sw133 I1spa. 14 wherein COD is The invention also concerns a compound of the formula [(r4-1 ,5-COD)PdT'Z]+ X-, wherein: T' is hydrocarbyl not containing olefinic or acetylenic bonds; X- is a weakly coordinating anion; COD is Z is RiCN; and R' is hydrocarbyl not containing olefinic or acetylenic bonds.

Preferably T' is methyl.

Preferably Z is methyl and X is BAF, SbF 6

PF

6 or BF 4 The invention further concerns a compound of the formula (VIII) R3

I

N

R4):N R51

(VIII)

wherein: is substituted phenyl;

R

51 is phenyl or substituted phenyl;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; and provided that groups in the 2 and 6 positions of R 5 0 have a difference in E, of about 0.15 or more.

Preferably groups in the 2 and 6 of R 5 have a difference in Es of about 0.60 or more.

The invention also concerns a homopolymer of cyclopentene, characterized in that said homopolymer has a degree of polymerization of about 50 or more and an end of melting point of about 100'C to about 320 0 C, provided that said homopolymer has less than 5 mole percent of enchained linear olefin containing pentylene units.

Preferably the homopolymer is characterized in that an X-ray powder diffraction pattern thereof has reflections at approximately 17.30, 19.30, 21.2', 24.2°, and 40.7° The invention also concerns a homopolymer of cyclopentene, characterized in that said homopolymer has an X-ray diffraction pattern with reflections at approximately 17.3°, 19.30, 21.20, 24.2°, and 40.70 2 0.

15 0 2 /06/3,sw13311 Preferably the homopolymer has a monoclinic unit cell of the approximate dimensions: a=0.561 nm; b=0.607 nm; c=7.37 nm; and g=123.2°.

Preferably the homopolymer is characterized in that at least 90 percent of repeat units are 1,3-cyclopentylene repeat units.

Preferably the homopolymer has at least 95 percent of repeat units are cis-1,3cyclopentylene repeat units.

Preferably the homopolymer has at least 95 percent of repeat units are cis-1,3cyclopentylene repeat units.

The invention further concerns a copolymer of cyclopentene and ethylene, characterized in that at least 75 mole percent of enchained cyclopentylene units are 1,3cyclopentylene units.

Preferably the copolymer has at least 50 mole percent of the repeat units are derived from cyclopentene.

Preferably there are at least 20 branches per 1000 methylene carbon atoms in the above defined copolymer.

The invention also concerns a copolymer of cyclopentene and ethylene, characterized in that there are at least 20 branches per 1000 methylene carbon atoms, and said copolymer consists essentially of repeat units derived from ethylene and cyclopentene.

Preferably the copolymer has at least 50 mole percent of the repeat units are derived from ethylene.

The invention further concerns a copolymer of cyclopentene and ethylene, characterized in that at least 50 mole percent of the repeat units are derived from cyclopentene, and at least 90 mole percent of the units derived from cyclopentene are 1,3cyclopentylene units.

The invention also concerns a copolymer comprising repeat units of cyclopentene and an ac-olefin, characterized in that at least 90 mole percent of repeat units derived from cyclopentene are cis-1,3-cyclopentylene units.

Preferably repeat units derived from ethylene are also present in the complex.

The invention further concerns a copolymer of an olefin of the formula

R

7

CH=CHR'

7 and a fluorinated olefin of the formula H 2 C=CH(CH2)aRfR 42 wherein: each R 1 7 is independently hydrogen or saturated hydrocarbyl; a is an integer of 2 to 20; Rf is perfluoroalkylene optionally containing one or more ether groups; and

R

42 is a functional group other than fluorine.

02/06/03,sw13311spal16 Preferably the copolymer is characterized in that R 42 is ester, sulfonic acid, or sulfonyl halide.

Preferably the copolymer is characterized in that Rf is -(CF 2 wherein b is 2 to or -(CF 2 )dOCF 2

CF

2 wherein d is 2 to Preferably the copolymer is characterized in that said olefin is ethylene or wherein said olefin is R 7

CH=CH

2 wherein R 17 is n-alkyl.

Preferably the copolymer is characterized in that said fluorinated olefin is about 1 to 20 mole percent of repeat units in said copolymer.

The invention concerns a process for the formation of linear a-olefins, comprising o0 the step of contacting, at a temperature of about -100 0 C to about +200, ethylene with a catalyst composition adapted for the oligomerization of ethylene to one or more a-olefins, characterized in that the catalyst composition comprises a transition metal complex of the formula (XXXI) R2 R3

I

R4:N

R

(XXXI)

wherein:

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl;

R

3 and R 4 are each independently hydrogen, substituted hydrocarbyl, hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; and Q and S are each independently chlorine, bromine, iodine or alkyl; and the catalyst composition further comprises a compound W, which is a neutral Lewis acid capable of abstracting X" to form WX-, provided that the anion formed is a weakly coordinating anion, or a cationic Lewis or Bronsted acid whose counterion is a weakly coordinating anion; wherein an c-olefin containing 4 to 40 carbon atoms is produced.

Preferably said compound W is an alkyl aluminum compound.

Preferably said compound W is R93AI, R 9 2 AICI, R 9 AIC12, R 9 AIO or R93A2CI3, wherein R 9 is alkyl containing 1 to 25 carbon atoms.

Preferably R 9 contains 1 to 4 carbon atoms.

17- 02/06/03,wl331 Ispa,17 The invention also concerns a process for the formation of linear a-olefins, comprising the step of contacting, at a temperature of about -100 0 C to about +200, ethylene with a catalyst composition adapted for the oligomerization of ethylene to one or more a-olefins, characterized in that the catalyst composition comprises a transition metal complex of the formula (III) or (XXXIV) R2 R3 1

R

4 N Z

X

I0 wherein:

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl; R? and R are each independently hydrogen, substituted hydrocarbyl, hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; R4 N

(XXXIV)

wherein:

R

2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl;

R

3 and R 4 are each independently hydrogen, substituted hydrocarbyl, hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; T1 is hydrogen or n-alkyl containing up to 38 carbon atoms; Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur, or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound (measured in water) is less than about 6; U is n-alkyl containing up to 38 carbon atoms; and X is a noncoordinating anion; and wherein an a-olefin containing 4 to 40 carbon atoms is produced.

The invention concerns a process for the formation of linear a-olefins, comprising the step of contacting, at a temperature of about -100 0 C to about +200 0 C, ethylene with a catalyst composition adapted for the oligomerization of ethylene to one or more ca-olefins, 18- 02/0603,sw1331 lspa.IS characterized in that the catalyst composition comprises a Ni{II} complex of a ligand of the formula (VIII) R2 R3

I

N

R4

N

(VIII)

wherein:

R

2 and R' are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it;

R

3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or

R

3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring; and wherein an a-olefin containing 4 to 40 carbon atoms is produced.

Preferably R 3 and R 4 are hydrogen, methyl or 1,8-naphthylylene.

Preferably R 2 and R 5 are phenyl.

Preferably a partial pressure of said ethylene is about atmospheric pressure to about 275 MPa.

DETAILS OF THE INVENTION Herein certain terms are used to define certain chemical groups or compounds.

These terms are defined below A "hydrocarbyl group" is a univalent group containing only carbon and hydrogen. If not otherwise stated, it is preferred that hydrocarbyl groups herein contain 1 to about 30 carbon atoms.

By "not containing olefinic or acetylenic bonds" is meant the grouping does not contain olefinic carbon-carbon double bonds (but aromatic rings are not excluded) and carbon-carbon triple bonds.

19- 0 2 /06/03,osw331 spa,19 By "substituted hydrocarbyl" herein is meant a hydrocarbyl group which contains one or more substituent groups which are inert under the process conditions to which the compound containing these groups is subjected. The substituent groups also do not substantially interfere with the process. If not otherwise stated, it is preferred that substituted hydrocarbyl groups herein contain 1 to about 30 carbon atoms. Included in the meaning of "substituted" are heteroaromatic rings.

By an alkyl aluminum compound is meant a compound in which at least one alkyl group is bound to an aluminum atom. Other groups such as alkoxide, 02/06/03.sw1331I stazed, it is preferred that saturated hydrccarmyl groups herein contain 1 to about 30 carbon atoms.

By "neutral Lewis base" is meant a compound, which is not an ion, which can act as a Lewis base.

Examples of such compounds include ethers, amines, sulfides, and organic nitriles.

By "cationic Lewis acid" is meant a cation which can act as a Lewis acid. Examples of such cations are sodium and silver cations.

By "a-olefin" is meant a compound of the formula CiH=CHR 9 wherein R 9 is n-alkyl or branched alkyl, preferably n-alkyl.

By "linear a-olefin" is meant a compound of the formula CH 2

=CHR

19 wherein R 19 is n-alkyl. It is preferred that the linear a-olefin have 4 to 40 carbon atoms.

By a "saturated carbon atom" is meant a carbon atom which is bonded to other atoms by single bonds only. Not included in saturated carbon atoms are carbon atoms which are part of aromatic rings.

By a quaternary carbon atom is meant a saturated carbon atom which is not bound to any hydrogen atoms. A preferred quaternary carbon atom is bound to four other carbon atoms.

By an olefinic bond is meant a carbon-carbon double bond, but does not include bonds in aromatic rings.

By a rare earth metal is meant one of lanthanum, cerium, praeseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium or lutetium.

This invention concerns processes for making polymers, comprising, contacting one or more selected olefins or cycloolefins, and optionally an ester or carboxylic acid of the formula CH2=CH(CH 2 )mCO 2 and other selected monomers,.with a transition metal containing catalyst (and possibly bther catalyst -21- 0 2 106/03,sw331 spa,21 components), Such catalysts are, for instance, various complexes of a diimine with these metals. By a "polymerization process herein (and the polymers made therein)" is meant a process which produces a polymer Swith a degree of polymerization (DP) of about 20 or more, preferably about 40 or more (except where otherwise noted, as in P in compound By "DP" is meant the average number of repeat (monomer) units in the polymer.

One of these catalysts may generally be written as R2 R3

I

M

R

4

S

(I)

wherein: M is Ni(II), Co(II), Fe(-II) or Pd(II); R 2 and R are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R 4 taken together are.hydrocarbylene or substituted nydrocarbylene to form a ring; 0 is alkyl, hydride, chloride, iodide, or bromide; and S is alkyl, hydride, chloride, iodide, or bromide. Preferably M is Ni(I;) or Pd(II).

In a preferred form of R' and R 4 are each independently hydrogen or hydrocarbyl. If Q and/or S is alkyl, it is preferred that the alkyl contains I to 4 carbon atoms, and more preferably is methyl.

Another useful catalyst is 0 2 /06/ 0 3 ,sw13311 pa,22 R2 R3 R :Pd R4 N

Z

X"

(II)

wherein:

R

2 and R s are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; T 1 is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, R 5 or R' 5

Z

is a neutral Lewis base wherein the donating atom is nitrogen, sulfur or oxygen, provided that, if the donating atom is nitrogen, then the pKa of the conjugate acid of that compound is less than about 6; X is a weakly coordinating anion; and R"5 is hydrocarbyl not containing olefinic or acetylenic bonds.

In one preferred form of

R

3 and R' are each independently hydrogen or hydrocarbyl. In a more preferred form of

T

1 is alkyl, and T' is especially preferably methyl. It is preferred that Z is R'0 or R CN, wherein each R' is independently hydrocarbyl and R7 is hydrocarbyl. It is preferred that

R

6 and R: are alkyl, and it is more preferred that they are methyl or ethyl. It is preferred that X is BAF, SbF 6 PFs or BF 4 Another useful catalyst is -23- 02/06/03.sw13311 sp,23 R2

R

3 r N T Ni Z

R

4 -N

Z

R

5

X

(III)

wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, or substituted hydrocarbylene, or R 3 and R' taken together are hydrocarbylene or substituted hydrocarbylene zo form a ring; T' is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, R1 5 or

Z

is a neutral Lewis base wherein the donating atom is nitrogen, sulfur or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound is less than about 6; X is a weakly coordinating anion; and R 15 is hydrocarbyl not containing olefinic or acetylenic bonds.

In one preferred form of (III), R 3 and R' are each independently hydrogen, hydrocarbyl. In a more preferred form of (III) T 1 is alkyl,, and T: is especially preferably methyl. It is preferred that Z is R,O or R'CN, wherein each R 6 is independen:ly hydrocarbyl and R7 is hydrocarbyl. It is preferred that R 6 and R are alkyl, and it is especially preferred that they are methyl or ethyl. It is preferred that X is BAF', SbF,-, PF 6 or BF-.

Relatively weakly coordinating anions are known to the artisan. Such anions are often bulky anions, particularly those that may delocalize their negative charge. Suitable weakly coordinating anions in this Application include (Ph phenyl), (herein 24 0 2 /063,sw133Hsp&.24 abbreviated BAF), PF 3F4 SbF trifluoromethanesulfonate, p-toluenesulfonate, (RfS0 2 2 and (C 6 Fs) Preferred weakly coordinating anions include BAF PF7, BF4 and SbFg Also useful as a polymerization catalyst is a compound of the formula R2 OR 8

R

3 I

I

N O=C

M

R4. N '(CHRl 6 )n

X

(IV)

wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R and R are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; M is Ni(II) or Pd(II); each R" is.independently hydrogen or alkyl containing 1 to 10 carbon atoms; n is 1, 2, or 3; X is a weakly coordinating anion; and Re is hydrocarbyl.

It is preferred that n is 3, and all of R" are hydrogen. It is also preferred that R 8 is alkyl or substituted alkyl, especially preferred that it is alkyl, and more preferred that R e is methyl.

Another useful catalyst is R2

R

2

R

3 I I R 3 T ,N Pd-E-Pd R4 1 N T

N

R X"

(V)

25 02/06/03.swl331 wherein:

R

2 and R 5 are hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R' are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R' taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; T is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, RS 5 or R"OC(=O)- R' is hydrocarbyl not containing olefinic or acetylenic bonds; E is halogen or -OR 8

R

8 is hydrocarbyl not containing olefinic or acetylenic bonds; and X is a weakly coordinating anion. It is preferred that T' is alkyl containing 1 to 4 carbon atoms, and more preferred that it is methyl. In other preferred compounds

R

3 and R 4 are methyl or hydrogen and R 2 and R s are 2 ,6-diisopropylphenyl and X is BAF. It is also preferred that E is chlorine.

Another useful catalyst is a compound of the formula R2

R

3

I

N T Pd

R

4 "N

X

(VII)

wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R' and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a 26 02/06/03,swl331 spa,26 ring; T' is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, hydrocarbyl substituted with keto or ester groups but not containing olefinic or acetylenic bonds, R 1 or R1 5 R" is hydrocarbyl not containing olefinic or acetylenic bonds; and X is a weakly coordinating anion. In a more preferred form of (VII), T 2 is alkyl containing 1 to 4 carbon atoms and T 2 is especially preferably methyl.

It is preferred that X is perfluoroalkylsulfonate, especially trifluoromethanesulfonate (triflate). If X is an extremely weakly coordinating anion such as BAF, (VII) may not form. Thus it may be said that (VII) forms usually with weakly, but perhaps not extremely weakly, coordinating anions.

In all compounds, intermediates, catalysts, processes, etc. in which they appear it is preferred that R and R5 are each independently hydrocarbyl, and in one form it is especially preferred that R 2 and R are both 2,6-diisopropylphenyl, particularly when R 3 and R 4 are each independently hydrogen or methyl. It is also preferred that R 3 and R 4 are each independently hydrogen, hydrocarbyl or taken together hydrocarbylene to form a carbocyclic ring.

Compounds of the formula wherein M is Pd, Q is alkvl and S is halogen may be made by the reac:tin of the corresponding 1,5-cyclooctadiene (COD) Pd complex with the appropriate diimine. When M is Ni, can be made by the displacement of a another ligand, such as a dialkylether or a polyether such as 1,2dimethoxyethane, by an appropriate diimine.

Catalysts of formula wherein X' is BAF', may be made by reacting a compound of formula wherein Q is alkyl and S is halogen, with about one equivalent of an alkali metal salt, particularly the sodium salt, of HBAF, in the presence of a coordinating ligand, particularly a nitrile such as acetonitrile. When X is an anion such as BAF', SbF 6 or BF 4 the same -27- 02/0603,sw 131 Ispa27 starting palladium compound can be reacted with the silver salt AgX.

However, sometimes the reaction of a diimine with a 1,5-COD Pd complex as described above to make compounds of formula (II) may be slow and/or give poor conversions, thereby rendering it difficult to make the starting material for (II) using the method described in the preceding paragraph. For instance when:

R

2 =R =PhCH- and R3=R 4 R'=RS=Ph- and R 3

=R

4 =Ph; R2=Rs=2t-butylphenyl and R =R 4

=CH

3

R

2 =R =a-naphthyl and R =R =CH 3 and R2=R =2-phenylphenyl and R =R =CH, difficulty may be encountered in making a compound of formula (II).

In these instances it has been found more convenient to prepare (II) by reacting COD)PdT'Z]'X-, wherein T 1 and X are as defined above and Z is an organic nitrile ligand, preferably in an organic nitrile solvent, with a diimine of the formula R2 R3

I

N

R

4

N

RS

(VIII)

By a "nitrile solvent" is meant a solvent that is at least 20 volume percent nitrile compound. The product of this reaction is in which the Z ligand is the nitrile used in the synthesis. In a preferred synthesis, T' is methyl and the nitrile used is the same as in the starting palladium compound, and is more preferably acetonitrile. The process is carried out in solution, preferably when the nitrile is substantially all of the solvent, at a temperature of about -400C to about +60CC, preferably about 0°C to about 30 0 C. It is 28 o02 0 603.sw1331 Isp2 preferred that the reactants be used in substantially equimolar quantities.

The compound [(r'-1,5-COD)PdTZ] wherein T' is alkyl, Z is an organic nitrile and X is a weakly coordinating anion may be made by the reaction of wherein A is Cl, Br or I and T' is alkyl with the silver salt of AgX, or if X is BAF with an alkali metal salt of HBAF, in the presence of an organic nitrile, which of course will become the ligand In a preferred process A is Cl, T 1 is alkyl, more preferably methyl, and the organic nitrile is an alkyl nitrile, more preferably acetonitrile. The starting materials are preferably present in approximately equimolar amounts, except for the nitrile which is present preferably in excess. The solvent is preferably a non-coordinating solvent such as a halocarbon. Methylene chloride is useful as such a solvent. The process preferably is carried out at a temperature of about -40°C to about +50°C. It is preferred to exclude water and other hydroxyl containing compounds from the prqcess, and this may be done by purification of the ingredients and keeping the process mass under an inert gas such as nitrogen.

Compounds of formula (II) [or (III) when the metal is nickel] can also be made by the reaction of R2

R

3 I T 1 R4,AN

'T'

(X)

with a source of the conjugate acid of the anion X, the acid MX or its equivalent (such as a trityl salt) in the presence of a solvent which is a weakly coordinating ligand such as a dialkyl ether or an alkyl 02/06/03,sw13311 sp,29 nitrile. It is preferred to carry out this reaction at about -80 0 C to about 30 0

C.

Compounds of formula (XXXXI) can be made by a process, comprising, contacting, at a temperature of about -80 0 C to about +20

C

C, a compound of the formula q 4 -1,5-COD)PdMe 2 and a diimine of the formula R2 R3

I

N

(VIII)

wherein: COD is 1,5-cyclooctadiene;

R

2 and R are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; and R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring. .It is preferred that the temperature is about -50 0 C to about +10 0 C. It is also preferred that the two starting materials be used in approximately-equimolar quantities, and/or that the reaction be carried out in solution. It is preferred that R 2 and R 5 are both 2-t-butylphenyl or butylphenyl and that R 3 and R 4 taken together are An, or R and R' are both hydrogen or methyl.

Compounds of formula (IV) can be made by several routes. In one method a compound of formula (II) is reacted with an acrylate ester of the formula

CH

2 =CHCOR wherein R' is as defined above. This reaction is carried out in a non-coordinating solvent such as methylene chloride, preferably using a greater than 1 to 50 fold excess of the acrylate ester. In a 02o/603,swl331 preferred reaction, Q is methyl, and R- is alkyi containing 1 to 4 carbon atoms, more preferably methyl.

The process is carried out at a temperature of about 100 0 C to about +100C, preferably about 0°C to about 50C. It is preferred to exclude water and other hydroxyl containing compounds from the process, and this may be done by purification of the ingredients and keeping the process mass under an inert gas such as nitrogen Alternatively, (IV) may be prepared by reacting wherein Q is alkyl and S is Cl, Br or I with a source of an appropriate weakly coordinating anion such as AgX or an alkali metal salt of BAF and an acrylate ester (formula as immediately above) in a single step..

Approximately equimolar quantities of and the weakly coordinating anion source are preferred, but the acrylate ester may be present in greater than 1 to fold excess. In a preferred reaction, Q is methyl, and R' is alkyl containing 1 to 4 carbon atoms, more preferably methyl. The process is preferably carried out at a temperature of about -100°C to about +100 0

C,

preferably about 0°C to about 50 0 C. It is preferred to exclude water and other hydroxyl containing compounds from the process, and this may be done by purification of the ingredients and keeping the process mass under an inert gas such as nitrogen.

In another variation of the preparation of (IV) from the source of the weakly coordinating anion is a compound which itself does not contain an anion, but which can combine with S [of to form such a weakly coordinating anion. Thus in this type of process by "source of weakly coordinating anion" is meant a compound which itself contains the anion which will become or a compound which during the process can combine with other process ingredients to form such an anion.

Catalysts of formula wherein X" is BAF', may be made by reacting a compound of formula wherein Q -31 02/0603.sw 13311 ]pa.31 is alkyl and S is halogen, with about one-ha_- or an equivalent of an alkali metal salt, particularly the sodium salt, of HBAF. Alternatively, containing other anions may be prepared by reacting wherein Q is alkyl and S is Cl, Br or I with one-half equivalent of a source of an appropriate weakly coordinating anion such as AgX.

Some of the nickel and palladium compounds described above are useful in processes for polymerizing various olefins, and optionally also copolymerizing olefinic esters, carboxylic acids, or other functional olefins, with these olefins. When (I) is used as a catalyst, a neutral Lewis acid or a cationic Lewis or Bronsted acid whose counterion is a weakly coordinating anion is also present as part of the catalyst system (sometimes called a "first compound" in the claims). By a "neutral Lewis acid" is meant a compound which is a Lewis acid capable for abstracting Q' or S_ from to form a weakly coordination anion. The neutral Lewis acid is originally uncharged not ionic). Suitable neutral Lewis acids include SbFs, Ar 3 B (wherein Ar is aryl), and BF,. By a cationic Lewis acid is meant a cation with a positive charge such as Ag H ,.and Na'.

In those instances in which (and similar catalysts which require the presence'of a neutral Lewis acid or a cationic Lewis or Bronsted acid), does not contain an alkyl or hydride group already bonded to the metal neither Q or S is alkyl or hydride), the neutral Lewis acid or a cationic Lewis or Bronsted acid also alkylates or adds a hydride to the metal, i.e., causes an alkyl group or hydride to become bonded to the metal atom.

A preferred neutral Lewis acid, which can alkylate the metal, is a selected alkyl aluminum compound, such as RtAl, R'.AlC1, R'AICl 2 and "R9AlO" (alkylaluminoxanes), wherein R 9 is alkyl containing 1 to 25 carbcn atoms, preferably 1 to 4 carbon atoms.

-32 O0206S/036,sw !33tspa32 Suitable alkyl aluminum compounds include methylaluminoxane (which is an oligomer with the general formula (MeAlO]n), (C2Hs) 2 ACl, CH s AlCI 2 and

S(CH

3 CHCH) 3 A1.

Metal hydrides such as NaBH, may be used to bond hydride groups to the metal M.

The first compound and are contacted, usually in the liquid phase, and in the presence of the olefin, and/or 4-vinylcyclohexene, cyclopentene, cyclobutene, substituted norbornene, or norbornene. The liquid phase may include a compound added just as a solvent and/or may include the monomer(s) itself. The molar ratio of first compound:nickel or palladium complex is about 5 to about 1000, preferably about 10 to about 100. The temperature at which the polymerization is carried out is about -1000C to about +200 0 C, preferably about -200C to about +80 0 C. The pressure at which the polymerization is carried out is not critical, atmospheric pressure to about 275 MPa, or more, being a suitable range. The pressure may affect the microstructure of the polyolefin produced (see below).

When using as a catalyst, it is preferred that f 3 and R 4 are hydrogen, methyl, or taken together are (An) It is also preferred that both R 2 and R 5 are 2,6diisopropylphenyl, 2,6-dimethylphenyl, 2,6diethylphenyl, 4-methylphenyl, phenyl, 2,4,6trimethylphenyl, and 2-t-butylphenyl. When M is Ni(II), it is preferred that Q and S are each independently chloride or bromide, while when M is Pd(II) it is preferred that Q is methyl, chloride, or bromide, and S is chloride, bromide or methyl. In 02/0603.sw 13311 spa33 addition, the specific combinations of groups' in 'the catalysts listed in Table I are especially preferred.

Table I R R R5 R 5 Q S M 2,6-i-PrPh 2,6-i-PrPh 2,6-i-PrPh 2,6-MePh 4-MePh 4-MePh 2,6-i-PrPh 2,6-i-PrPh 2,6-MePh 2,6-i-PrPh 2,6-i-PrPh 2,6-MePh Ph 2,6-EtPh 2,4,6-MePh 2,6-MePh 2,6-i-PrPh 2, -MePh 2-t-BuPh 2-i-Pr-6-MePh 2-i-Pr-6-MePh 2,6-t-BuPh 2,6-t-BuPh 2,6-t-BuPh 2-t-BuPh Note In

H

Me An

H

H

Me Me

H

H

H

Me

H

Me Me Me Me An An An An An Me

H

Me An Me

H

Me An

H

H

Me Me

H

H

H

Me

H

Me Me Me Me An An An An An Me

H

Me An Me 2,6-i-PrPh 2,6-i-PrPh 2,6-i-PrPh 2,6-MePh 4-MePh 4-MePh 2,6-i-PrPh 2,6-i-PrPh 2,6-MePh 2,6-i-PrPh 2,6-i-PrPh 2,6-MePh Ph 2,6-EtPh 2,4,6-MePh 2,6-MePh 2,6-i-PrPh 2,6-MePh 2-t-BuPh 2,5-t-BuPh 2-i-Pr-6-MePh 2-i-Pr-6-MePh 2,6-t-BuPh 2,6-t-BuPh 2,6-t-BuPh 2-t-BuPh Me Me Me Me Me Me Me Me Me Br Br Br Me Me Me Br Br Br Br Br Br Br Br Br Br Br Cl Cl C1 Cl Cl Cl Me Me Me Br Br Br Cl Cl Cl Br Br Br Br Br Br Br Br Br Br Br Pd Pd Pd Pd Pd Pd Pd Pd Pd Ni Ni Ni Pd Pd Pd Ni Ni Ni Ni Ni Ni Ni Ni Ni Ni Ni Tables I and II, and elsewhere herein, the following convention and abbreviations are used.

For R 2 and R 5 when a substituted phenyl ring is present, the amount of substitution is indicated by the number of numbers indicating positions on the phenyl 34- 02W003,sw1331 spa,34 ring, so that, for example, 2,6-i-PrPh is 2,6diisopropylphenyl. The following abbreviations are used: i-Pr isopropyl; Me methyl; Et ethyl; t-Bu t-butyl; Ph phenyl; Np naphthyl; An 1,8naphthylylene (a divalent radical used for both R 3 and

R

4 wherein R 3 and R 4 taken together form a ring, which is part of an acenaphthylene group); OTf triflate; and BAF bis(trifluoromethyl)phenyl)borate.

Preferred olefins in the polymerization are one or more of ethylene, propylene, 1-butene, 2-butene, 1hexene 1-octene, 1-pentene, 1-tetradecene, norbornene, and cyclopentene, with ethylene, propylene and cyclopentene being more preferred. Ethylene (alone as a homopolymer) is especially preferred.

The polymerizations with may be run in the presence of various liquids, particularly aprotic organic liquids. The catalyst system, monomer(s), and polymer may be soluble or insoluble in these liquids, but obviously these liquids should not prevent the polymerization from occurring. Suitable liquids include alkanes, cycloalkanes, selected halogenated hydrocarbons, and aromatic hydrocarbons. Specific useful solvents include hexane, toluene and benzene.

Whether such a liquid is used, and which and how much liquid is used, may affect the product obtained.

It may affect the yield, microstructure, molecular weight, etc., of the polymer obtained.

Compounds of formulas (XIII), (XV) and (XIX) may also be used as catalysts for the polymerization of the same monomers as compounds of formula The polymerization conditions are the same for (XI), (XIII), (XV) and (XIX) as for and the same Lewis and Bronsted acids are used as co-catalysts. Preferred groupings R 2

R

3

R

4 and R 5 (when present) in (XI) and (XIII) are the same as in both in a polymerization process and as compounds in their own right.

02/06103.sw13311 Preferred (XI) compounds have the metals Sc(III) Zr(IV), Ni(II), Ni(I), Pd(II), Fe(II), and Co(II).

When M is Zr, Ti, Fe, and Sc it is preferred that all of Q and S are chlorine or bromine more preferably chlorine. When M is Ni or Co it is preferred that all of Q and S are chlorine, bromine or iodine, more preferably bromine.

In (XVII) preferred metals are Ni(II) and Ti{IV} It is preferred that all of Q and S are halogen. It is also preferred that all of R 28

R

9 and R" are hydrogen, and/or that both R 44 and R" 4 are 2,4,6trimethyiphenyl or 9-anthracenyl.

In (XV) it is preferred that both of R 3 are hydrogen.

In (XIII), (XXIII) and (XXXII) (as polymerization catalysts and as novel compounds) it is preferred that all of R 2

R

2

R

22 and R 23 are methyl. It is also preferred that T 1 and T 2 are methyl. For (XIII), when M is Ni(I) or it is preferred that both Q and S are bromine, while when M is Pd it is preferred that Q is methyl and S is chlorine.

Compounds (IV) or (VII) will each also cause the polymerization of one or more of an olefin, and/or a selected cyclic olefin such as cyclobutene, cyclopentene or norbornene, and, when it is a Pd(II) complex, optionally copolymerize an:ester or carboxylic acid of the formula CH 2

=CH(CH

2 )mCO 2

R

1 wherein m is 0 or an integer of 1 to 16 and R1 is hydrogen or hydrocarbyl or substituted hydrocarbyl, by themselves (without cocatalysts). However, (III) often cannot be used when the ester is present. When norbornene or substituted norbornene is present no other monomer should be present.

Other monomers which may be used with compounds (IV) or (VII) (when it is a Pd(II) complex) to form copolymers with olefins and selected cycloolefins are carbon monoxide and vinyl ketones of the general formula HC=CHC(O)R 5 wherein R 2 is alkyl -36- 02/06/03,sw] 331 spa,36 containing 1 to 20 carbon atoms, and it is preferred that R 2S is methyl. In the case of the vinyl ketones, the same compositional limits on the polymers produced apply as for the carboxylic acids and-esters described as comonomers in the immediately preceding paragraph.

CO forms alternating copolymers with the various' olefins and cycloolefins which may be polymerized with compounds (IV) or (VII). The polymerization to form the alternating copolymers is done with both CO and the olefin simultaneously in the process mixture, and available to the catalyst. It is also possible to form block copolymers containing the alternating CO/(cyclo)olefin copolymers and other blocks containing just that olefin or other olefins or mixtures thereof.

This may be done simply by sequentially exposing compounds (IV) or (VII), and their subsequent living polymers, to the appropriate monomer or mixture of monomers to form the desired blocks. Copolymers of CO, a (cyclo)olefin and a saturated carboxylic acid or ester of the formula CH,=CH(CH2)mCO 2 R, wherein m is 0 or an integer of 1 to 16 and R 1 is hydrogen or hydrocarbyl or substituted hydrocarbyl, may also be made by simultaneously exposing the polymerization catalyst or living polymer to these 3 types of monomers.

The polymerizations may be carried out with (II), (III), (IV) or (VII), and other catalyst molecules or combinations, initially in the solid state [assuming (III) (IV) or (VII) is a solid] or in solution.

The olefin and/or cycloolefin may be in the gas or liquid state (including gas dissolved in a solvent). A liquid, which may or may not be a solvent for any or all of the reactants and/or products may also be.

present. Suitable liquids include alkanes, cycloalkanes, halogenated alkanes and cycloalkanes, ethers, water, and alcohols, except that when (III) is used, hydrocarbons should preferably be used as solvents. Specific useful solvents include methylene -37 0-2/0603,sw 1331 Ispa.37 chloride, hexane, C0 2 chloroform, perfluor6'(nbutyltetrahydrofuran) (herein sometimes called toluene, dichlorobenzene, 2-ethylhexanol, and benzene.

It is particularly noteworthy that one of the liquids which can be used in this polymerization process with (III), (IV) or (VII) is water, see for instance Examples 213-216. Not only can water be present but the polymerization "medium" may be largely water, and various types of surfactants may be employed so that an emulsion polymerization may be done, along with a suspension polymerization when surfactants are not employed.

Preferred olefins and cycloolefins in the polymerization using (III) or (IV) are one or more of ethylene, propylene, l-butene, l-hexene, 1octene, l-butene, cyclopentene, 1-tetradecene, and norbornene; and ethylene, propylene and cyclopentene are more preferred. Ethylene alone is especially preferred.

Olefinic esters or carboxylic acids of the formula

CH,=CH(CH

2 )mCO 2

R

1 wherein R is hydrogen, hydrocarbyl, or substituted hydrocarbyl, and m is 0 or an integer of 1 to 16. It is preferred if R1 hydrocarbyl or substituted hydrocarbyl and it is more preferred if it is alkyl containing 1 to 10 carbon atoms, or glycidyl.

It is also preferred if m is 0 and/dr R' is alkyl containing 1 to 10 carbon atoms. It is preferred to make copolymers containing up to about 60 mole percent, preferably up to about 20 mole percent of repeat units derived from the olefinic ester or carboxylic acid.

Total repeat unit units in the polymer herein refer not only to those in the main chain from each monomer unit, but those in branches or side chains as well.

When using (III), (IV) or (VII) as a catalyst it is preferred that R 3 and R 4 are hydrogen, methyl, or taken together are 38- 02/06/03.sil33 spa,38

C--A

(An) It is also preferred that both R 2 and R 5 are 2,6diisopropylphenyl, 2,6-dimethylphenyl, 4-methylphenyl, phenyl, 2,6-diethylphenyl, 2,4,6-trimethylphenyl and 2t-butylphenyl. When (II) is used, it is preferred that T' is methyl, R' is methyl or ethyl and R7 is methyl.

When (III) is used it is preferred that T' is methyl and said Lewis base is R 20, wherein R' is methyl or ethyl. When (IV) is used it is preferred that R 6 is methyl, n is 3 and R" is hydrogen. In addition in Table II are listed all particularly preferred combinations as catalysts for (III), (IV) and

(VII).

39- 02/06103,sw1331 Ispa.39 Table I i Corn- R R 3 R5 r/T 2 z M x pound

R

Type I1T 2, 6 -1- Pr Ph (I 1) 2, 6-i- PrPh Pr6-h PrPh (III) 2,6-i MePh (I 1) 2,6- Me Ph (I1) 2,6- 2,6-i- PrPh (ii) 2,6-i- Pr Ph (ii) 2,6-1- PrPh (II7 2,6-i- PrPh (11) 2,6-i- P rPh (Ii" (IE) Ph (II) 2,6- E tPh (ii) 2-t- BuPh Me Me H H Me Me H H H H Me Me Me Me Me Me Me Me H H Me Me An An Me Me Me Me Me Me Me Me 2, 6-i- PrPh 2,6-i- PrPh 2,6G-i- Pr Ph 2, 6-i- PrPh 2, 6-Me Ph 2, 6-MePh 2,6-i- PrPh 2, 6-i- PrPh 2, 6-i- PrPh 2, 6-i- PrPh 2,4,6- MePh 2, 6-i- PrPh 2, 6-i- PrPh Ph 2, 6-EtPh 2, 6 EtPh OEt, Pd BAP OEt Pd BAF DEt 2 N i DAF DELI N i BAF

DEL

1 P_ d BAF

DEL

2 Pd BAF

DEL

2 Pd SbE 6 DEL 2 Pd BHF, CEc- Pd PP 6

DEL

2 P d SbF 6 OEt~ P d SbFE DEt. Pd SbFE NCMe Pd SbF 6 NCMe Pd SbF 6 NCMe Pd HAP NCMe Pd SbF 6 Me Me 2-t-BuPh 40 Me WCMe Pd SbF 6 02/06f03,swi3i I (II) 1-Np Me Me i-Np Me NCMe Pd SbFc (II) Ph 2

CH

(II) 2-PhPh (II) Ph (IV) 2,6-i- PrPh (IV) 2,6-i- PrPh (IV: 2,6-i- PrPh (IV) 2,6-i- PrPh H H Ph 2

CH

Me Me 2-PhPh a a Ph Me Me 2,6-i- PrPh Me Me 2,6-i- PrPh H H 2,6-i- PrPh Me Me 2,6-i- PrPh NCMe NCMe NCMe b SbF 6 SbF,

BAF

SbF Me b Pd BAF b Pd SbF 6 b Pd B(C 6

F

s 3 C

(II)

(VII)

(II)

(II)

Ph 2,6-i- PrPh Ph Ph 2

CH

Ph 2,6-i- PrPh Ph Ph 2

CH

NCMe Pd Pd SbF, OTf Me NCMe Me NCMe Pd BAF Pd SbF, aThis group is -CMe 2

CH

2 CMe 2 b This group is -(CH 2 3 CO2Me When using (III), (IV) or (VII) the temperature at which the polymerization is carried out is about -100°C to about +200 0 C, preferably about 0 C to about 150 0 C, more preferably about 25 0 C to about 100CC.

The pressure at which the polymerization is carried out is not critical, atmospheric pressure to about.275 MPa being a suitable range. The pressure can affect the microstructure of the polyolefin produced (see below).

Catalysts of the formulas (III), (IV) and (VII) may also be supported on a solid catalyst (as opposed to just being added as a solid or in solution), for instance on silica gel (see Example 98). By supported is meant that the catalyst may simply be carried physically on the surface of the solid support, may be adsorbed, or carried by the support by other means.

02/06/03,swI331 spa,41 When using (XXX) as a ligand or in any process or reaction herein it is preferred that n is 2, all of

R

3 R2 6 and R 29 are hydrogen, and both of R" and R 45 are 9-anthracenyl.

Another polymerization process comprises contacting a compound of the formula [Pd(R"CN)4]X, or a combination of Pd[OC(O)R 4 and HX, with a compound of the formula R2 R3

N

R

4

N

I R5

(VIII)

and one or more monomers selected from the group consisting of ethylene, an olefin of the formula RCH=CH or R"CH=CHR" 1 cyclopentene, cyclobutene, substituted norbornene and norbornene, wherein: R 2 and R are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R' are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R and R' taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring; each R- is independently hydrocarbyl or substituted hydrocarbyl provided that R 17 contains no olefinic bonds; R 40 is hydrocarbyl or substituted hydrocarbyl; and X is a weakly coordinating anion; provided that when norbornene or substituted norbornene is present no other monomer is present.

It is believed that in this process a catalyst similar to (II) may be initially generated, and this then causes the polymerization. Therefore, all of the conditions, monomers (including olefinic esters and '2 02/06/03,sw1331 spa,42 carboxylic acids), etc., which are applicable to the process using (II) as a polymerization catalyst are applicable to this process. All preferred items are also the same, including appropriate groups such as R 2 R R 4

R

5 and combinations thereof. This process however should be run so that all of the ingredients can contact each other, preferably in a single phase.

Initially at least, it is preferred that this is done in solution. The molar ratio of (VIII) to palladium compound used is not critical, but for most economical use of the compounds, a moderate excess, about 25 to 100% excess, of (VIII) is preferably used.

As mentioned above, it is believed that in the polymerization using (VIII) and [Pd(R CN) 4 or a Pd[II) carboxylate a catalyst similar to (II) is formed. Other combinations of starting materials that can combine into catalysts similar to (III), (IV) and (VII) often also cause similar polymerizations, see for instance Examples 238 and 239.

Also combinations of a-diimines or other diimino ligands described herein with: a nickel or nickel compound, oxygen, an alkyl aluminum compound and an olefin; a nickel or nickel compound, an acid such as HX and an olefin; or an a-diimine Ni[0] or nickel complex, oxygen, an alkyl aluminum compound and an olefin. Thus active catalysts'from a-diimines and other bidentate imino compounds can be formed beforehand or in the same "pot" (in situ) in which the polymerization takes place. In all of the polymerizations in which the catalysts are formed in situ, preferred groups on the a-diimines are the same as for the preformed catalysts.

In general Ni[0), Ni[I]- or Ni(II) compounds may be used as precursors to active catalyst species. They must have ligands which can be displaced by the appropriate bidentate nitrogen ligand, or must already contain such a bidentate ligand already bound to the nickel atom. Ligands which may be displaced include 43 and tris(o-tolyl)phosphite, which may be present in Ni[l) compounds, or dibenzylideneacetone, as in the useful Pd[0] precursor tris(dibenzylideneacetone)dipalladium(0l. These lower valence nickel compounds are believed to be converted into active Ni[II] catalytic species. As such they must also be contacted (react with) with an oxidizing agent and a source of a weakly coordinating anion Oxidizing agents include oxygen, HX (wherein X is a weakly coordinating anion), and other well known oxidizing agents. Sources of X" include HX, alkylaluminum compounds, alkali metal and silver salts of X As can be seen above, some compounds such as HX may act as both an oxidizing agent and a source of X'.

Compounds containing other lower valent metals may be converted into active catalyst species by similar methods.

When contacted with an alkyl aluminum compound or HX useful Nil0] compounds include

R

3

COD

R

4

R

RR

5

'OM

(XXXIII)I (XX III) o (XXXxiXV or (XXXXV) N N (XXXXTV) or (XXXXV) Various types of Ni[0] compounds are known in the literature. Below are listed references for the types shown immediately above.

-44- 02/06/03,sw13311 sp, 4 4 (XXXIII) G. van Koten, et al., Adr.

Organometal. Chem., vol. 21, p. 151-239 (1982).

(XXXXII) W. Bonrath, et al.,.Angew. Chem.

Int. Ed. Engl., vol. 29, p. 298-300 (1990).

(XXXXIV) H. tom Dieck, et al., Z, Natruforsch., vol. 366, p. 823-832 (1981); and M.

Svoboda, et al., J. Organometal. Chem., vol. 191, p.

321-328 (1980).

(XXXXV) G. van Koten, et al., Adv.

Organometal. Chem., vol. 21, p. 151-239 (1982).

In polymerizations using (XIV), the same preferred monomers and groups (such as R, R 3

R

4

R

5 and X) as are preferred for the polymerization using (II) are used and preferred. Likewise, the conditions used and preferred for polymerizations with (XIV) are similar to those used and preferred for except that higher olefin pressures (when the olefin is a gas) are preferred. Preferred pressures are about 2.0 to about MPa. (XIV) may be prepared by the reaction of one mole of [Pd(RI 3

CN)

4

]X

2 with one mole of (VIII) in acetonitrile or nitromethane.

.Novel compound (XIV) is used as an olefin polymerization catalyst. In preferred forms of (XIV), the preferred groups R 2

R

3

R

5 and X are the same as are preferred for compound (II).

Another type of compound which is an olefin polymerization catalyst are n-allyl and n-benzyl compounds of the formula

R

N

A

R'

X

R

5

XXXVII

wherein M is Ni.(II) or Pd(II); R 2 and R 5 are hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen 5 0J o 06/03.sw133 lispa, 4 atom has at least two,carbon atoms bound to it; R' ana

R

4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R' taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; X is a weakly coordinating anion; and A is a nallyl or n-benzyl group. By a n-allyl group is meant a monoanionic with 3 adjacent sp carbon atoms bound to a metal center in an T3 fashion. The three sp 2 carbon atoms may be substituted with other hydrocarbyl groups or functional groups. Typical n-allyl groups include

CO'R

COR

SCI

wherein R is hydrocarbyl. By a n-benzyl group is meant n-allyl ligand in which two of the sp 2 carbon atoms are part of an aromatic ring. Typical n-benzyl groups include T-Benzyl compounds usually initiate polymerization of the olefins fairly readily even at room temperature, but i-allyl compounds may not necessarily do so.

46 006/03.swI33 Ipa,46 Initiation of 7-allyl compounds can be improved by using one or more of the following methods: Using a higher temperature such as about 800C.

Decreasing the bulk of the a-diimine ligand, such as R 2 and R 5 being 2,6-dimethylphenyl instead of 2,6-diisopropylphenyl.

Making the n-allyl ligand more bulky, such as using rather than the simple n-allyl group itself.

Having a Lewis acid present while using a functional 7-ailyl or r-benzyl group. Relatively weak Lewis acids such a triphenylborane, tris(pentafluorophenyl)borane, and trifluoromethylphenyl)borane, are preferred. Suitable functional groups include chloro and ester. "Solid" acids such as montmorillonite may also be used.

When using (XXXVII) as a polymerization catalyst, it is preferred that ethylene and/or a linear a-olefin Sis the monomer, or cyclopentene, more preferred if the monomer is ethylene and/or propylene, and ethylene is especially preferred. A preferred temperature for the polymerization process using (XXXVII), is about +20 0 C to about 100 0 C. It is also preferred that the partial pressure due to ethylene or propylene monomer is at least about 600 kPa.It is also noted that (XXXVII) is a novel compound, and preferred items for (XXXVII) for the polymerization process are also preferred for the compound itself.

Another catalyst for the polymerization of olefins is a compound of the formula 47 02AW6/03,sw1331 lspa 4 7 RSs

RS

N Z X' R I

(XXXVIII)

and one or more monomers selected from the.group consisting of ethylene, an olefin of the formula

R

17 CH=CH or RiCH=CHRl, cyclobutene, cyclopentene, substituted norbornene, and norbornene, wherein: R and R 4 are each independentlv hydrogen, hydrocarbyl, substituted hydrocarbyl or R' and R' taken together are hydrocarbylene or substizuted hydrocarbylene to form a ring; R 54 is hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; each R 55 is independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or a functional group; W is alkylene or substituted alkylene containing 2 or more carbon atoms; Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur, or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound (measured in water) is less than aboit 6, cr an olefin of the formula R"'CH=CHR 7 each R" is independently alkyl cr substituted alkyl; and X is a weakly coordinating anion. It is preferred that in compound (XXXV:III' that: R s4 is phenyl or substituted phenyl, and preferred substituents are.alkyl groups; each R S5 is independently hydrogen or alkyl containing 1 to carbon atoms; W contains 2 carbon atoms between the phenyl ring and metal atom it is bonded to or w is a divalent polymeric group derived from the polymerization of R CH=CHR 7 and it is especially preferred that it is -CH(CH 3

)CH

2 or -C(CH3) 2

CH

2 and Z is a dialkyl ether or an olefin of the formula -4 02/06/03.sw3311 spa47 R=CH=CHR"; and combinations thereof. W is an alkylene group in which each of the two free valencies are to different carbon atoms of the alkylene group.

When W is a divalent group formed by the polymerization of R"CH=CHR" 7 and Z is R"CH=CHR', the compound (XXXVIII) is believed to be a living ended polymer. That end of W bound to the phenyl ring actually is the original fragment from R 56 from which the "bridge" W originally formed, and the remaining part of W is formed from the olefin(s) R'CH=CHR". In a sense this compound is similar in function to compound (VI).

By substituted phenyl in (XXXVIII) and (XXXIX) is meant the phenyl ring can be substituted with any grouping which does not interfere with the compound's stability or any of the reactions the compound undergoes. Preferred substituents in substituted phenyl are alkyl groups, preferably containing 1 to carbon atoms.

Preferred monomers for this polymerization are ethylene and linear a-olefins, or cyclopentene, particularly propylene, and ethylene and propylene or both are more preferred, and ethylene is especially preferred.

It is noted that (XXXVII:) is a novel compound, and preferred compounds and groupings'are the same as in the polymerization process.

Compound (XXXVIII) can be made by heating compound

(XXXIX),

RSS

I

NI X' R4

(XXXIX)

49 0206/3.,sw3311spa,49 wherein: R and R' are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R' and R' taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; R is hydrocarbyl or Ssubstituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; each Rss is independentlyhydrogen, hydrocarbyl, substituted hydrocarbyl, or a functional group; R 56 is alkyl containing 2 to carbon atoms; T is alkyl; Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur, or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound (measured in water) is less than about 6; and X is a weakly coordinating anion. Preferred groups are the same as those in (XXXVIII). In addition it is preferred that T S contain 1 to 10 carbon atoms, and more preferred that it is methyl. A preferred temperature for the conversion of (XXXIX) to (XXXVIII) is about -30 0 C to about 50 0 C. Typically the reaction takes about 10 min. to about 5 days, the higher the temperature, the faster the reaction. Another factor which affects the reaction rate is the nature of Z.

The weaker the Lewis basicity of Z, the faster the desired reaction will be.

When (III), VII), (VIII) or a combination of compounds that will generate similar compounds, (subject to the conditions described above) is used in the polymerization of olefins, cyclolefins, and optionally olefinic esters or carboxylic acids, polymer having what is believed to be similar to a "living end" is formed. This molecule is that from which the polymer grows to its eventual molecular weight. This compound may have the structure -02/0603,sw331

(VI)

wherein: M is Ni(II) or Pd(II); R 2 and R' are hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and

R

4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R' taken together are hydrocarbylene or substituted hydrocarbylene to fcrm a ring; each R: is independently hydrogen, alkyl or

-(CH

2 )mCO 2 R; T i is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, R5 R or

-CH

2

CHCH

2

CO

2 Re; R" is hydrocarbyl not containing olefinic or acetylenic unsaturation; P is a divalent group containing one or more repeat units derived from the polymerization of one or more of ethylene, an -olefin of the formula R"~CH=CH 2 or R"CH=CHR', cyclobutene, cyclopentene, substituted ncrbornene, or norbornene and, when M is Pd(II), optionally one or more compounds of the formula R' is hydrocarbyl; each R 17 is independently hydrocarbyl or substituted hydrocarbyl provided that any olefinic bond in said olefin is separated from any other olefinic bond or aromatic ring by a quaternary carbon atom or at least two saturated carbon atoms; m is 0 or an integer from 1 to 16; R 1 is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to 10 carbon atoms; and X is a weakly coordinating anion; and that when M is Ni(II), R" is not -CO 2

R

e and when M is Pd a diene is not present. By an "olefinic ester or carboxylic acid" is meant a compound of the formula St £'-Oii3 5w:? spIsFja

CH

2

=CH(CH),),CO

2 R, wherein m and R 1 are as definec immediately above.

This molecule will react with additional monomer (olefin, cyclic olefin, olefinic ester or olefinic carboxylic acid) to cause further polymerization. In other words, the additional monomer will be added to P, extending the length of the polymer chain. Thus P may be of any size, from one "repeat unit" to many repeat units, and when the polymerization is over and P is removed from M, as by hydrolysis, P is essentially the polymer product of the polymerization. Polymerizations with that is contact of additional monomer with this molecule takes place under the same conditions as described above for Ehe polymerization process using (III), (VII) or (VIII), or combinations of compounds that will generate similar molecules, and where appropriate preferred conditions and structures are the same.

The group T 3 in (VI) was originally the group T 1 in (II) or (III), or the group which included Rs in It in essence will normally be one of the end groups of the eventual polymer product. The olefinic group which is coordinated to M, R:CH=CHR1 is normally one of the monomers, olefin, cyclic olefin, or, if Pd(III is M, an olefinic ester or carboxylic acid. If more than one of these monomers is present in the reacticn, it may be.any one of them. It is preferred that T" is alkyl and especially preferred that it is methyl, and it is also preferred that R n is hydrogen or n-alkyl. It is-also preferred that M is Pd(II).

Another "form" for the living end is (XVI).

R

2 R N H r -R' R N 1 NTR1 (XVI) (X)a 52 02/06/03sw133 spa52 This type of compound is sometimes referred to as a compound in the "agostic state". In fact both (VI) and (XVI) may coexist together in the same polymerization, both types of compound representing living ends. It is believed that (XVI)-type compounds are particularly favored when the end of the growing polymer chain bound to the transition metal is derived from a cyclic olefin such as cyclopentene. Expressed in terms of the structure of (XVI) this is when both of R 11 are hydrocarbylene to form a carbocyclic ring, and it is preferred that this be a five-membered carbocyclic ring.

For both.t-he polymerization process -using (XVI) and the structure of (XVI) itself, the same conditions and groups as are used and preferred for (VI) are also used and preferred for (XVI), with the exception that for R" it is preferred in (XVI) that both of R"1 are hydrocarbylene to form a carbocyclic ring.

This invention also concerns a compound of the formula R2 R3

I

rN r M

CHR

14 R4 R14HC X- Rs

(IX)

wherein: M is Ni(II-) or Pd(II); R and R 5 are hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; R' and R' are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R' taken together are hydrocarbylene or substituted hydrocarbylene to form a 153 02/06/03,sw1331 spa.53 ring; each R 14 is independently hydrogen, alkyi or [when M is Pd(II) (CH 2

),CO

2 R R is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to carbon atoms; T 4 is alkyl, -R60C(O) OR, R or R is hydrocarbyl not containing olefinic or acetylenic bonds; R60 is alkylene not containing olefinic or acetylenic bonds; Re is hydrocarbyl; and X is a weakly coordinating anion.

(IX) may also be used to polymerize olefins, cyclic olefins, and optionally olefinic esters and carboxylic acids. The same conditions (except as noted below) apply to the polymerizations using (IX) as they do for It is preferred that M is Pd(II) and T" is methyl.

A compound of formula may also be used as a catalyst for the polymerization of olefins, cyclic olefins, and optionally olefinic esters and/or carboxylic acids. In this process is contacted with one or more of the essential monomers. Optionally a source of a relatively weakly coordinating anion may also be present. Such a source could be an alkali metal salt of BAF or AgX (wherein X is the anion), etc.

Preferably about 1 mole of the source of X, such as AgX, will be added per mole of This will usually be done in the liquid phase, preferably in which (V) and the source of the anion are at least partially soluble. The conditions of this polymerization are otherwise the same as described above for (III), (IV) and (VII), including the preferred conditions and ingredients.

In polymerizations using (XX) as the catalyst, a first compound which is a source of a relatively noncoordinating monoanion is present. Such a source can be an alkali metal or silver salt of the monoanion.

-54- 0206/03.sw13311spa54 R3 ~N T'

P

R4

N

(XX)

It is preferred that the alkali metal cation is sodium or potassium. It is preferred that the monoanion is SbF 6 BAF, PF 6 or BF4-, and more preferred that it is BAF. It is preferred that "T is methyl and/or S is chlorine. All other preferred groups and conditions for these polymerizations are the same as for polymerizations with (II).

In all of the above polymerizations, and the catalysts for making them it is preferred that R 2 and

R

5 if present, are 2,6-diisopropylphenyl and R 3 and R' are hydrogen or methyl. When cyclopentene is polymerized, is preferred that R 2 and R 5 (if present) are 2,6-dimethylphenyl or 2,4,6-trimethylphenyl and that R 3 and R 4 taken together are An. R 2 R' and R and other groups herein may also be substituted hydrocarbyl. As previously defined, the substituent groups in substituted hydrocarbyl groups (there may be one or more substituent groups) should not substantially interfere with the polymerization or other reactions that the compound is undergoing.

Whether a particular group will interfere can first be judged from the artisans general knowledge and the particular polymerization or other reaction that is involved. For instance, in polymerizations where an alkyl aluminum compound is used may not be compatible with the presence of groups containing an active (relatively acidic) hydrogen atom, such as hydroxyl or carboxyl because of the known reaction of alkyl aluminum compounds with such active hydrogen containing groups (but such polymerizations may be possible if 55 02/06/03,sw 3311 enough "extra" alkyl aluminum compound is added to react with these groups). However, in very similar polymerizations where alkyi aluminum compounds are not present, these groups containing active hydrogen may be present. Indeed many of the polymerization processes described herein are remarkably tolerant to the presence of various functional groups. Probably the most important considerations as to the operability of compounds containing any particular functional group are the effect of the group on the coordination of the metal atom (if present), and side reaction of the group with other process ingredients (such as noted above).

Therefore of course, the further away from the metal atom the functional group is, the less likely it is to influence, say, a polymerization. If there is doubt as to whether a particular functional group, in a particular position, will affect a reaction, simple minimal experimentation will provide the requisite answer. Functional groups which may be present in R', R and other similar radicals herein include hydroxy, halo (fluoro, chloro, bromo and iodo), ether, ester, dialkylamino, carboxy, oxo (keto and aldehyo), nitre, amide, thioether, and imino. Preferred functional groups are hydroxy, halo, ether and dialkylamino.

Also in all of the polymerizations, the (cyclo)olefin may be substituted hydrocarbyl. Suitable substituents include ether, keto, aldehyde, ester, carboxylic acid.

In all of the above polymerizations, with the exceptions noted below, the following monomer(s), to produce the corresponding homo- or copolymers, are preferred to be used: ethylene; propylene; ethylene and propylene; ethylene and an a-olefin; an a-olefin; ethylene and an alkyl acrylate, especially methyl acrylate; ethylene and acrylic acid; ethylene and carbon monoxide; ethylene, and carbon monoxide and an acrylate ester or acrylic acid, especially methyl -56- 02106/03,swl331 spa,56 acrylate; propylene and alkyl acrylate, especially methyl acrylate; cyclopentene; cyclopentene and ethylene; cyclopentene and propylene. Monomers which contain a carbonyl group, including esters, carboxylic acids, carbon monoxide, vinyl ketones, etc., can be polymerized with Pd(II) containing catalysts herein, with the exception of those that require the presence of a neutral or cationic Lewis acid or cationic Bronsted acid, which is usually called the "first compound" in claims describing such polymerization processes.

Another useful "monomer" for these polymerization processes is a C 4 refinery catalytic cracker stream, which will often contain a mixture of n-butane, isobutane, isobutene, l-butene, 2-butenes and small amounts of butadiene. This type of stream is referred to herein as a "crude butenes stream". This stream may act as both the monomer source and "solvent" for the polymerization. It is preferred that the concentration of 1- and 2-butenes in the stream be as high as possible, since these are the preferred compounds to be polymerized. The butadiene content should be minimized because it may be a polymerization catalyst poison. The isobutene may have been oreviously removed for other uses. After being used in the polymerization (during which much or most of the ibutene would have been polymerized), the butenes stream can be returned to the refinery for further processing.

In many of the these polymerizations certain general trends may be noted, although for all of these trends there are exceptions. These trends (and exceptions) can be gleaned from the Examples.

Pressure of the monomers (especially gaseous monomers such as ethylene) has an effect on the polymerizations in many instances. Higher pressure often affects the polymer microstructure by reducing branching, especially in ethylene containing polymers.

This effect is more pronounced for Ni catalysts than Pd -57- 02/06/03,sw13311 spa,7 catalysts. Under certain conditions higher pressures also seem to give higher productivities and higher molecular weight. When an acrylate is present and a Pd catalyst is used, increasing pressure seems to decrease the acrylate content in the resulting copolymer.

Temperature also affects these polymerizations.

Higher temperature usually increases branching with Ni catalysts, but often has little such effect using Pd catalysts. With Ni catalysts, higher temperatures appear to often decrease molecular weight. With Pd catalysts, when acrylates are present, increasing temperature usually increases the acrylate content of the polymer, but also often decreases the productivity and molecular weight of the polymer.

Anions surprisingly also often affect molecular weight of the polymer formed. More highly coordinating anions often give lower molecular weight polymers.

Although all of the anions useful herein are relatively weakly coordinating, some are more strongly coordinating than others. The coordinating ability of such anions is known and has been discussed in the literature, see for instance W. Beck., et al., Chem.

Rev., vol. 88 p. 1405-1421 (1988), and S. H. Strauss, Chem. Rev., vol. 93, p. 927-942''(1993), both of which are hereby included by reference. The results found herein in which the molecular weight of the polymer produced is related to the coordinating ability of the anion used, is in line.with the coordinating abilities of these anions as described in Beck 1411) and Strauss 932, Table II).

In addition to the "traditional" weakly coordinating anions cited in the paragraph immediately above, heterogeneous anions may also be employed. In these cases, the true nature of the counterion is poorly defined or unknown. Included in this group are MAO, MMAO and related aluminoxanes which do not form true solutions. The resulting counterions are thought to bear anionic aluminate moieties related to those -58- 02/06/3,sw1331 IspM58 cited in the paragraph immediately above. Polymeric anionic materials such as Nafion" polyfluorosulfonic acid can function as non-coordinating counterions. In addition, a wide variety of heterogeneous inorganic materials can be made to function as non-coordinating counterions. Examples would include aluminas, silicas, silica/aluminas, cordierites, clays, MgC12, and many others utilized as traditional supports for Ziegler- Natta olefin polymerization catalysts. These are generally materials which have Lewis or Bronsted acidity. High surface area is usually desired and often these materials will have been activated through some heating process. Heating may remove excess surface water and change the surface acidity from Bronsted to Lewis type. Materials which are not active in the role may often be made active by surface treatment. For instance, a surface-hydrated silica, zinc oxide or carbon can be treated with an organoaluminum compound to provide the required functionality.

The catalysts described herein can be heterogenized through a variety of means. The heterogeneous anions in the paragraph immediately above will all serve to heterogenize the catalysts.

Catalysts can also be heterogenized by exposing them to small quantities of a monomer to encapsulate them in a polymeric material through which additional monomers will diffuse. Another method is to spray-dry the catalyst with its suitable non-coordinating counterion onto a polymeric support. Heterogeneous versions of the catalyst are particularly useful for running gasphase polymerizations. The catalyst is suitably diluted and dispersed on the surface of the catalyst support to control the heat of polymerization. When applied to fluidized-bed polymerizations, the heterogeneous supports provide a convenient means of catalyst introduction.

-59- 02/06/03,sw 13311spa,59 Another item may effect the incorporation of polar monomers such as acrylic esters in olefin copolymers.

It has been found that catalysts containing less bulky a-diimines incorporate more of the polar monomer into the polymer (one obtains a polymer with a higher percentage of polar monomer) than a catalyst containing a more bulky a-diimine, particularly when ethylene is the olefin comonomer. For instance, in an a-diimine of formula (VIII), if R 2 and R 5 are 2,6-dimethylphenyl instead of 2,6-diisopropylphenyl, more acrylic monomer will be incorporated into the polymer. However, another common effect of using a less bulky catalyst is to produce a polymer with lower molecular weight.

Therefore one may have to make a compromise between polar monomer content in the polymer and polymer molecular weight..

When an olefinic carboxylic acid is polymerized into the polymer, the polymer will of course contain carboxyl groups. Similarly in an ester containing polymer, some or all of the ester groups may be hydrolyzed to carboxyl groups (and vice versa). The carboxyl groups may be partially or completely converted into salts such as metallic salts. Such polymeric salts are termed ionomers. Ionomers are useful in adhesives, as ionomeric elastomers, and as molding resins. Salts may be made with ions of metals such as Na, K, Zn, Mg, Al, etc. The polymeric salts may be made by methods known to the artisan, for instance reaction of the carboxylic acid containing polymers with various compounds of the metals such as bases (hydroxides, carbonates, etc.) or other 60- 02/06/03.sw13311 spa.6 0 compounds, such as acetylacetonates. Novel polymers that contain carboxylic acid groups herein, also form novel ionomers when the carboxylic acid. groups are partially or fully converted to carboxylate salts.

When copolymers of an olefinic carboxylic acid or olefinic ester and selected olefins are made, they may be crosslinked by various methods known in the art, depending on the specific monomers used to make the polymer. For instance, carboxyl or ester containing polymers may be crosslinked by reaction with diamines to form bisamides. 'Certain functional groups which may be present on the polymer may be induced to react to crosslink the polymer. For instance epoxy groups (which may be present as glycidyl esters) may be crosslinked by reaction of the epoxy groups, see for instance Example 135.

It has also been found that certain fluorinated olefins, some of them containing other functional groups may be polymerized by nickel and palladium catalysts. Note that these fluorinated olefins are included within the definition of H 2

C=CHR

17 wherein R' 1 can be considered to be substituted hydrocarbyl, the substitution being fluorine and possibly other substituents. Olefins which may be polymerized include HC=CH(CH2)aRfR 42 wherein a is an integer of 2 to 20, R.

is perfluoroalkylene optionally containing one or more ether.groups, and R 42 is fluorine or a functional group. Suitable functional groups include hydrogen, chlorine, bromine or iodine, ester, sulfonic acid

SO

3 and sulfonyl halide. Preferred groups for R 42 include fluorine, ester, sulfonic acid, and sulfonyl fluoride. A sulfonic acid group containing monomer does not have to be polymerized directly. It is preferably made by hydrolysis of a sulfonyl halide group already present in an already made polymer. It is preferred that the perfluoroalkylene group contain 2 to 20 carbon atoms and preferred perfluoroalkylene groups are -(CF 2 wherein b is 2 to 20, and 61 0 06/D3,sw1331 spa,61 (CF,)dOCF 2

CF

2 wherein d is 2 to 20. A preferrea olefinic comonomer is ethylene or a linear a-olefin, and ethylene is especially preferred.. Polymerizations may be carried out with many of the catalysts described herein, see Examples 284 to 293.

As described herein, the resulting fluorinated polymers often don't contain the expected amount of branching, and/or the lengths of the branches present are not those expected for a simple vinyl polymerization.

The resulting polymers may be useful for compatibilizing fluorinated and nonfluorinated polymers, for changing the surface characteristics of fluorinated or nonfluorinated polymers (by being mixed with them), as molding resins, etc. Those polymers containing functional groups may be useful where those functional groups may react or be catalysts. For instance, if a polymer is made with a sulfonyl fluoride group (R 42 is sulfonyl fluoride) that group may be hydrolyzed to a sulfonic acid, which being highly fluorinated is well known to be a very strong acid.

Thus the polymer may be used as an acid catalyst, for example for the polymerization of cyclic ethers such as tetrahydrofuran.

In this use it has been found that this polymer is more effective than a completely fluorinated sulfonic acid containing polymer. For such uses the sulfonic acid content need not be high, say only 1 to 20 mole percent, preferably about 2 to 10 mole percent of the repeat units in the' polymer having sulfonic acid groups. The polymer may be crosslinked, in which case it may be soluble in the medium (for instance tetrahydrofuran), or it may be crosslinked so it swollen but not dissolved by the medium, Or it may be coated onto a substrate and optionally chemically attached and/or crosslinked, so it may easily be separated from the other process ingredients.

62 02/06/03,swl3311spa.62 One of the monomers that may be polymerizea by the above catalysts is ethylene either by itself to form a homopolymer, or with a-olefins and/or olefinic esters or carboxylic acids. The structure of the polymer may be unique in terms of several measurable properties.

These polymers, and others herein, can have unique structures in terms of the branching in the polymer..

Branching may be determined by NMR spectroscopy (see the Examples for details), and this analysis can determine the total number of branches, and to some extent the length of the branches. Herein the amount of branching is expressed as the number of branches per 1000 of the total methylene groups in the polymer, with one exception. Methylene groups that are in an ester grouping, i.e. -CO 2 R, are not counted as part of the 1000 methylenes. These methylene groups include those in the main chain and in the branches.

These polymers, which are E homopolymers, have a branch content of about 80 to about 150 branches per 1000 methylene groups, preferably about 100 to about 130 branches per 1000 methylene groups. These branches do not include polymer end groups. In addition the distribution of the sizes (lengths) of the branches is unique. Of the above total branches, for every 100 that are methyl, about 30 to about 90 are ethyl, about 4 to about 20 are propyl, about 15 to about SO butyl, about 3 to about 15 are amyl, and about 30 to about 140 are hexyl or longer, and it is preferred that for every 100 that are methyl, about 50 to about 75 are ethyl, about 5 to about 15 are propyl, about 24 to about are butyl, about.5 to 10 are amyl, and about 65 to about 120 are hexyl or larger. These E homopolymers are often amorphous, although in some there may be a small amount of crystallinity.

Another polyolefin, which is an E homopolymer that can be made by these catalysts has about 20 to about 150 branches per 1000 methylene groups, and, per 100 -63- 02t/06/3,sw 1331 spa,61 methyl groups, about 4 to about 20 ethyl grours, about 1 to about 12 propyl groups, about 1 to about 12 butyl group, about 1 to about 10 amyl groups, and C to about hexyl or larger groups. Preferably this polymer has about 40 to about 100 methyl groups per 1000 methylene groups, and per 100 methyl groups, about 6 tc about ethyl groups, about 2 to about 10 propyl groups, about 2 to about 10 butyl groups, about 2 to about S amyl groups, and about 2 to about 15 hexyl or larger groups.

Many of the polyolefins herein, including homopolyethylenes, may be crosslinked by various methods known in the art, for instance by the use of peroxide or other radical generating species which can crosslink these polymers. Such crosslinked polymers are novel when the uncrosslinked polymers from which they are derived are novel, because for the most part the structural feature(s) of the uncrosslinked polymers which make them novel will be carried over into the crosslinked forms.

In addition, some of the E homopolymers have an exceptionally low density, less than about 0.86 g/mL, preferably about 0.85 g/mL or less, measured at 25 0

C.

This density is based on solid polymer.

Homopolymers of polypropylene can also. have unusual structures. Similar effects have been observed with other a-olefins 1-hexene). A "normal" P homopolymer will have one methyl group for.each methylene group (or 1000 methyl groups per 1000 methylene groups), since the normal repeat unit is CH(CH3)CH 2 However, using a catalyst of formula (I) in which M is Ni(II) in combination with an alkyl aluminum compound it is possible to produce a P homopolymer with about 400 to about 600 methyl groups per 1000 methylene groups, preferably about 450 to about 550 methyl groups per 1000 methylene groups.

Similar effects have been observed with other a-oiefins 1-hexene).

64 0206/03 ,sw 13311 p64 In the polymerization processes described herein olefinic esters and/or carboxylic acids may also be present, and of course become part of the copolymer formed. These esters may be copolymerized with one or more of E and one or more a-olefins. When copolymerized with E alone polymers with unique structures may be formed.

In many such E/olefinic ester and/or carboxylic acid copolymers the overall branching level and the distribution of branches of various sizes are unusual.

In addition, where and how the esters or carboxylic acids occur in the polymer is also unusual. A relatively high proportion of the repeat units derived from the olefinic esters are at the ends of branches.

In such copolymers, it is preferred that the repeat units derived from the olefinic esters and carboxylic acids are about 0.1 to 40 mole percent of the total repeat units, more preferably about 1 to about 20 mole percent. In a preferred ester, m is 0 and R 1 is hydrocarbyl or substituted hydrocarbyl. It is preferred that R 1 is alkyl containing 1 to 20 carbon atoms, more preferred that it contains 1 to 4 carbon atoms, and especially preferred that R 1 is methyl.

One such preferred dipolymer has about 60 to 100 methyl groups (excluding methyl groups which are esters) per 1000 methylene groups in the polymer, and contains, per 100 methyl branches, about 45-to about ethyl branches, about 1 to about 3 propyl branches, about 3 to about 10 butyl branches, about 1 to about 3 amyl branches, and about 15 to about 25 hexyl or longer branches. In addition, the ester and carboxylic acid containing repeat units are often distributed mostly at the ends of the branches as follows. If the branches, and the carbon atom to which they are attached to the main chain, are of the formula -CH(CH 2

),CO

2

R

1 wherein the CH is part of the main chain, then in some of these polymers about 40 to about 50 mole percent of ester groups are found in branches where n is 5 or more, 076/03.w 1331 about 10 to about 20 mole percent when n is 4, about to 30 mole percent when n is 1, 2 and 3 and about 5 to about 15 mole percent when n is 0. When n is 0, an acrylate ester has polymerized "normally" as part of the main chain, with the repeat unit -CH 2

-CHCO

2

R-.

These branched polymers which contain olefin and olefinic ester monomer units, particularly copolymers of ethylene and methyl acrylate and/or other acrylic esters are particularly useful as viscosity modifiers for lubricating oils, particularly automotive lubricating oils.

Under certain polymerization conditions, some of the polymerization catalysts described herein produce polymers whose structure is unusual, especially considering from what compounds (monomers) the polymers were made, and the fact that polymerization catalysts used herein are so-called transition metal coordination catalysts (more than one compound may be involved in the catalyst system, one of which must include a transition metal). Some of these polymers were described in a somewhat different way above, and they may be described as "polyolefins" even though they may contain other monomer units which are not olefins olefinic esters). In the polymerization of an 2$ unsaturated compound of the formula H 2

C=CH(CH

2 )eG, wherein e is 0 or an integer of 1 or more, and G is hydrogen or -CO 2

R

1 the usual ("normal") polymeric repeat unit obtained would be -CH 2 -CHI(CH2)eG] wherein the branch has the formula -(CH 2 )eG. However, with somne of the ins.-ant catalysts a polymeric unit may be -CH 2

CH[(CH

2 wherein f e, and f is 0 or an integer of 1 or more. If f<e, the "extra" methylene groups may be part of the main polymer chain. If f>e (parts of) additional monomer molecules may be incorporated into that branch. Ip other words, the structure of any polymeric unit may be irregular and different for monomer molecules incorporated into the polymer, and the structure of such a polymeric unit obtained could 66- 02/06/O3,sw13l Ispa,66 be rationalized as the result of "migration c: the active polymerizing site" up and down the polymer chain, although this may not be the actual mechanism.

This is highly unusual, particularly for polymerizations employing transition metal coordination catalysts.

For "normal" polymerizations, wherein the polymeric unit -CH 2

-CH[(CH

2 is obtained, the theoretical amount of branching, as measured by the number of branches per 1000 methylene groups can be calculated as follows which defines terms "theoretical branches" or "theoretical branching" herein: Theoretical branches I000Total mole rarrion of o-olef'ns {[S(2*mole fraction e-0 (mole fraction u-olefinee j In this equation, an a-olefin is any olefinic compound

HC=CH(CH

2 )eG wherein e*0. Ethylene or an acrylic compound are the cases wherein e=0. Thus to calculate the number of theoretical branches in a polymer made from 50 mole percent ethylene 30 mole percent propylene and 20 mole percent methyl would be as follows: Tneoretical crancnes oo 238 (branches;ic0 mechyienes [12*0.5)J) (030 11.!O.20O44IJ The "1000 methylenes" include all of the methylene groups in the polymer, including methylene groups in the branches.

For some of the polymerizations described herein, the actual amount of branching present in the polymer is considerably greater than or less than the above theoretical branching calculations would indicate. For instance, when an ethylene homopolymer is made, there should be no branches, yet there are often many such branches. When an a-olefin is polymerized, the -67- 02/06/03,sw 133 I spa.67 branching level may be much lower or higher than the theoretical branching level. It is preferred that the actual branching level is at 90% or less of the theoretical branching level, more preferably about or less of the theoretical branching level, or 110% or more cf the theoretical branching level, more preferably about 120% or more of the theoretical branching level. The polymer should also have at least about 50 branches per 1000 methylene units, preferably about 75 branches per 1000 methylene units, and more preferably about 100 branches per 1000 methylene units.

In cases where there are branches theoretically present, as in ethylene homopolymers or copolymers with acrylics, excess branches as a percentage cannot be calculated. In that instance if the polymer has 50 or more, preferably 75 or more branches per 1000 methylene groups, it has excess branches in branches in which f>0).

These polymers also have "at least two branches of different lengths containing less than 6 carbon atoms each." By this is meant that branches of at least two different lengths number of carbon atoms), and containing less than 6 carbon atoms, are present in the polymer. For instance the polymer may contain ethyl and butyl branches, or methyl and amyl branches.

As will be understood from the above discussion, the lengths of the branches do not necessarily correspond to the original sizes of the monomers used Indeed branch lengths are often present which do net correspond to the sizes of any of the monomers used and/or a branch length may be present "in excess".

By "in excess" is meant there are more branches of a particular length present than there were monomers which corresponded to that branch length in the polymer. For instance, in the copolymerization of mole percent ethylene and 25 mole percent 1-butene it would be expected that there would be 125 ethyl branches per 1000 methylene carbon atoms. If there -68- 02/06/03sw 13311 I spa,68 were more ethyl branches than that, theykAoiuld be i:: excess compared to the theoretical branching. There may also be a deficit of specific length branches. If there were less than 125 ethyl branches per 1000 methylene groups in this polymer there would be a deficit. Preferred polymers have 90% or less or 110% or more of the theoretical amount of any branch length present in the polymer, and it is especially preferred if these branches are about 80% or less or about 120% or more of the theoretical amount of any branch length.

In the case of the 75 mole percent ethylene/25 mole percent 1-butene polymer, the 90% would be about 113 ethyl branches or less, while the 110% would be about 138 ethyl branches or more. 'Such polymers may also or exclusively contain at least 50 branches per 1000 methylene atoms with lengths which should not theoretically (as described above) be present at all.

These polymers also have "at least two branches of different lengths containing less than 6 carbon atoms each." By this is meant that branches of at least two different lengths number of carbon atoms), and containing less than 6 carbon atoms, are present in the polymer. For instance the polymer may contain ethyl and butyl branches, or methyl and amyl branches.

Some of the polymers produced herein are novel because cf unusual structural features- Normally, in polymers of alpha-olefins of the formula CH 2

=CH(CH

2 )aH wherein a is an integer of 2 or more made by coordination polymerization, the most abundant, and often the only, branches present in such polymers have the structure -(CH2)aH. Some of the polymers produced herein are novel because methyl branches comprise about to about 75% of the total branches in the polymer.

Such polymers are described in Examples 139, 162, 173 and 243-245. Some of the polymers produced herein are novel because in addition to having a high percentage (25-75%) of methyl branches (of the total branches present), they also contain linear branches of the -69- D2/06/03,sw1331 lspa, 69 structure -(CH 2 )nH wherein n is an integer cf six or greater. Such polymers are described in Examples 139, 173 and 243-245. Some of the polymers produced herein are novel because in addition to having a high Spercentage (25-75%) of methyl branches (of the total branches present), they also contain the structure (XXVI), preferably in amounts greater than can be accounted for by end groups, and more preferably greater than 0.5 (XXVI) groups per thousand methyl groups in the polymer greater than can be accounted for by end groups.

CH

3

-CH;

2 -CH-(CH2)aH (XXVI) Normally, homo- and copolymers of one or more alpha-olefins of the formula CH 2

=CH(CH

2 )aH wherein a is an integer of 2 or more contain as part of the polymer backbone the structure (XXV) R36 I I

-CH-CH

2 -CH-

(XXV)

wherein R 3 5 and R 3 6 are alkyl groups. In most such polymers of alpha-olefins of this formula (especially those produced by coordination-type polymerizations), both of R 35 and R 36 are -(CH2)aH. However, in certain of these polymers described herein, about 2 mole percent or more, preferably about 5 mole percent or more and more preferably about 50 mole percent or more of the total amount of (XXV) in said polymer consists of the structure where one of R 35 and R 36 is a methyl group and the other is an alkyl group containing two or more carbon atoms. Furthermore, in certain of these polymers described herein, structure (XXV) may occur in side chains as well as in the polymer backbone.

Structure (XXV) can be detected by 13 C NMR. The signal 02/06/03,swl331 1sp,70 -fr the carbon atom of the methylene group between the zwo methine carbons in (XXV) usually occurs in the 13

C

NMR at 41.9 to 44.0 ppm when one of R 35 and R 3 6 is a methyl group and the other is an alkyl group containing two or more carbon atoms, while when both R 35 and R 3 6 contain 2 or more carbon atoms, the signal for the methylene carbon atom occurs at 39.5 to 41.9 ppm.

Integration provides the relative amounts of these structures present in the polymer. If there are interfering signals from other carbon atoms in these regions, they must be subtracted from the total integrals to give correct values for structure (XXV).

Normally, homo- and copolymers of one or more alpha-olefins of the formula CH 2 =CH(CH2)aH wherein a is an integer of 2 or more (especially those made by coordination polymerization) contain as part of the polymer backbone structure (XXIV) wherein n is 0, 1, or 2. When n is 0, this structure is termed "head to head" polymerization. When n is 1, this structure is termed "head to tail" polymerization. When n is 2, this structure is termed "tail to tail" polymerization.

In most such polymers of alpha-olefins of this formula *especially those produced by coordination-type polymerizations), both of R 37 and R 38 are -(CH2)aH.

Ecwever some of the polymers of alpha-olefins of this formula described herein are novel in that they also contain structure (XXIV) wherein n a, R 37 is a methyl group, and R 38 is an alkyl group with 2 or more carbon atoms.

R37 R38 -CH- (C H)n-CH-

(XXIV)

Normally polyethylene made by coordination pcivmerization has a linear backbone with either no -71 02/06/03,swl331 lspa71 branching, or small amounts of linear branches. Some of the polyethylenes described herein are unusual in that they contain structure (XXVII) which has a methine carbon that is not part of the main polymer backbone.

CH

3

I

-CH

2

-CH-CH

2

CH

3

(XXVII)

Normally, polypropylene made by coordination polymerization has methyl branches and few if any branches of other sizes. Some of the polypropylenes described herein are unusual in that they contain one or both of the structures (XXVIII) and (XXIX).

CH

3

CH

3 1 -CH2CH 2

-CH-CH

3

(XXIX)

As the artisan understands, in coordination polymerization alpha-olefins of the formula

CH

2

=CH(CH

2 )aH may insert into the growing polymer chain in a 1,2 or 2,1 manner. Normally these insertion steps lead to 1,2- enchainment or 2,1-enchainment of the monomer. Both of these fundamental steps form a

(CH

2 )aH branch. However, with some catalysts herein, some of the initial product of 1,2 insertion can rearrange by migration of the coordinated metal atom to the end of the last inserted monomer before insertion of additional monomer occurs. This results in omega,2enchainment and the formation of a methyl branch.

-72- 0206/03,swl3 I spa,72 1.2 insertion polymer-M CH2=CH(CH 2

),H

CH, CH, p CH_ rearrangement polymerCH, (CH. polymer (CH2).H polymer (CH2),M 1.2-enchainment c.2-enchainment

-(CH

2 branch -CH, branch It is also known that with certain other catalysts, some of the initial product of 2,1 insertion can rearrange in a similar manner by migration of the coordinated metal atom to the end of the last inserted monomer. This results in omega,1-enchainmenz and no branch is formed.

2.1 insertion polymer-M CH,=CH(CH 2

M

polymers. ,CH rearranement o er H CH; (CH 2 )aH CH 2

(CH

2

),M

2.1-enchainment 1-enchanment

-(CH

2 branch no branch Of the four types of alpha-olefin enchainment, omega,1-enchainment is unique in that it does not generate a branch. In a polymer made from an alphaolefin of the formula CH2=CH(CH 2 )aH, the total number of branches per 1000 methylene groups can be expressed as: B (1000) X ,1i(a 2)] where X,,I is the fraction of omega,1-enchainment Solving this expression for X,,i gives: Xw, I (1000 aB)/(1000 2B) This equation provides a means of calculating the fraction of omega,l-enchainment in a polymer of a linear alpha-olefin from the total branching B. Total branching can be measured by 1 H NMR or 13C NMR.

Similar equations can be written for branched alpha- -73 02/06/03,swl3311 ip.73 olefins. For example, the equaticn for 4-methyl-1pentene is: Xw,1 (2000 2B)/(1000 2B) Most polymers of alpha-olefins made by other Scoordination polymerization methods have less than omega,1-enchainment. Some of the alpha-olefin polymers described herein have unusually large amounts (say of omega,i-enchainment. In essence this is similar to stating that a polymer made from an a-olefin has much less than the "expected" amount of branching. Although many of the polymerizations described herein give substantial amounts of c,l- and other unusual forms of enchainment of olefinic monomers, it has surprisingly been found that "unsymmetrical" a-diimine ligands of formula (VIII) give especially high amounts of- ,lenchainment. In particular when R 2 and R s are phenyl, and one or both of these is substituted in such a way as different sized groups are present in the 2 and 6 position of the phenyl ring(s), w,1-enchainment is enhanced. For instance, if one or both of R 2 and R are 2-t-butylphenyl, this enchainment is enhanced. In this context when R 2 and/or R 5 are "substituted" phenyl the substitution may be not only in the 2 and/or 6 positions, but on any other position in the phenyl ring. For instance, 2,5-di-t-butylphenyl, and 2-tbutyl-4,6-dichlorophenyl would be included in substituted phenyl.

The steric effect of various groupings has been quantified by a parameter called Es, see R. W. Taft, Jr., J. Am. Chem. Soc., vol. 74, p. 3120-3128, and M.S.

Newman, Steric Effects in Organic Chemistry, John Wiley Sons, New York, 1956, p. 598-603. For the purposes herein, the Es values are those for o-substituted benzoates described in these publications. If the value fcr E, for any particular group is not known, it can be determined by methods described in these publicaricns. For the purposes herein, the value of hydrogen is defined to be the same as for methyl. It -74 0206/03,swl3311spa,74 is preferred that difference in Es, when R" :ana preferably also R 5 is phenyl, between the. groups substituted in the 2 and 6 positions of the phenyl ring is at least 0.15, more preferably at least about 0.20, and especially preferably about 0.6 or more. These phenyl groups may be unsubstituted or substituted in any other manner in the 3, 4 or 5 positions.

These differences in E, are preferred in a diimine such as (VIII), and in any of the polymerization processes herein wherein a metal complex containing an a-diimine ligand is used or formed. The synthesis and use of such a-diimines is illustrated in Examples 454- 463.

Because of the relatively large amounts of w,1enchainment that may be obtained using some ct the polymerization catalysts reported herein novel polymers can be made. Among these homopolypropylene In some of the PP's made herein the structure CaHCH 2

CH

2 CdH 2 (CbH2)nCdH 2

CH

2 CH2Ca H--

(XXXX)

may be found. In this structure each C4 is a methine carbon atom that is a branch point, while each C b is a methylene group that is more than 3 carbon atoms removed from any branch point Herein methylene groups of the type -CbH2- are termed 5+ (or delta+) methylene groups. Methylene groups of the type -CtH-, which are exactly the third carbon atom from a branch point, are termed y (gamma) methylene groups. The NMR signal for the 6+ methylene groups occurs at about 29.75 ppm, while the NMR signal for the y methylene groups appears at about 30.15 ppm. Ratios of these types of methylene groups to each other and the total number of methylene groups in the PP is done by the usual NMR integration techniques.

026/03w 13311 It is preferred that PP's made herein have about to about 300 6+ methylene groups per 1000 methylene groups (total) in the PP.

It is also preferred that the ratio of methylene groups in the PP be 0.7 to about The above ratios involving 6+ and y methylene groups in PP are of course due to the fact that high relatively high w,1 enchainment can be obtained. It is preferred that about 30 to 60 mole percent of the monomer units in PP be enchained in an co,l fashion.

Using the above equation, the percent w,I enchainment for polypropylene can be calculated as: u,i (100) (1000-B)/(1000+2B) wherein B is the total branching (number of methyl groups) per 1000 methylene groups in the polymer.

Homo- or copolymers of one or more linear Qolefins containing 3 to 8 carbon atoms may also have 6+ carbon atoms in them, preferably at least about 1 or more 6+ carbon atoms per 1000 methylene groups.

The above polymerization processes can of course be used to make relatively random copolymers (except for certain CO copolymers) of various possible monomers. However, some of them can also be used to make block polymers. A block polymer is conventionally defined as a polymer comprising molecules in which there is a linear arrangement of blocks, a block being a portion of a polymer molecule which the monomeric units have at least one constitutional or configurational feature absent from adjacent portions (definition from H. Mark, et al., Ed., Encyclopedia of Polymer Science and Engineering, Vol. 2, John Wiley Sons, New York, 1985, p. 324). Herein in a block copolymer, the constitutional difference is a difference in monomer units used to make that block, while in a block homopolymer the same monomer(s) are used but the repeat units making up different blocks are different structure and/or ratios of types of structures.

02/06/03,sw 133 11s 76 Since it is believed that many of the polymerization processes herein have characteristics that often resemble those of living polymerizations, making block polymers may be relatively easy. One method is to simply allow monomer(s) that are being polymerized to be depleted to'a low level, and then adding different monomer(s) or the same combination of monomers in different ratios. This process may be repeated to obtain polymers with many blocks.

Lower temperatures, say about less than CCC, preferably about -10° to about tends to enhance the livingness of the polymerizations. Under these conditions narrow molecular weight distribution polymers may be obtained (see Examples 367-369 and 371), and block copolymers may also be made iExample 370).

As pointed out above, certain polymerization conditions, such as pressure, affect the microstructure of many polymers. The microstructure in turn affects many polymer properties, such as crystallization.

Thus, by changing polymerization conditions, such as the pressure, one can change the microstructure of the part of the polymer made under those conditions. This of course leads to a block polymer, a polymer have defined portions having structures different from other defined portions. This may be done with more than one monomer to obtain a block copolymer, or may be.done with a single monomer or single mixture of monomers to obtain a block homopolymer. For instance, in the polymerization of ethylene, high pressure sometimes leads to crystalline polymers, while lower pressures give amorphous polymers. Changing the pressure repeatedly could lead to an ethylene homopolymer containing blocks of amorphous polyethylene and blocks of crystalline polyethylene. If the blocks were of the correct size, and there were enough of them, a thermoplastic elastomeric homopolyethylene could be -77- 02106103,sw 1331 Ispa,77 produced. Similar polymers could possibly be made trom other monomer(s), such as propylene.

Homopolymers of a-olefins such as propylene, that is polymers which were made from a monomer that j consisted essentially of a single monomer such as propylene, which are made herein, sometimes exhibit unusual properties compared to their "normal" homopolymers. For instance, such a homopolypropylene usually would have about 1000 methyl groups per 1000 methylene groups. Polypropylenes made herein typically have about half that many methyl groups, and in addition have some longer chain branches. Other aolefins often give polymers whose microstructure is analogous to these polypropylenes when the above catalyscs are used for the polymerization.

These polypropylenes often exhibit exceptionally low glass transition temperatures "Normal" polypropylene has a Tg of about -170C, but the polypropylenes herein have a Tg of -30°C or less, preferably about -35 0 C or less, and more preferably about -40 0 C or less. These Tg's are measured by Differential Scanning Calorimetry at a heating rate of C/min, and the Tg is taken as the midpoint of the transition. These polypropylenes preferably have at least 50 branches (methyl groups) per 1000 carbon atoms, more preferably at least about 100 branches per 1000 methylene groups.

Previously, when cyclopentene was coordination polymerized to higher molecular weights, the resulting polymer was essentially intractable because of its very high melting point, greatly above 300 0 C. Using the catalysts here to homopolymerize cyclopentene results in a polymer that is tractable, may be reformed, as by melt forming. Such polymers have an end of melting point of about 320 0 C or less, preferably about 300CC or less, or a melting point of about 275 C or less, preferably about 250 0 C or less. The melting point is determined by Differential Scanning -78- 0206/03,sw13311 spa, 7 8 Calorimetry at a heating rate of 15C/min, and taking the maximum of the melting endotherm as the melting point. However these polymers tend to .have relatively diffuse melting points, so it is preferred to measure the "melting point" by the end of melting point. The method is the same, except the end of melting is taken as the end (high temperature end) of the melting endotherm which is taken as the point at which the DSC signal returns to the original (extrapolated) baseline.

Such polymers have an average degree of polymerization (average number of cyclopentene repeat units per polymer chain) of about 10 or more, preferably about 3C or more, and more preferably about 50 or more.

In these polymers, enchainment of the cyclopentene repeat units is usually as cis-1,3-pentylene units, in contrast to many prior art cyclopentenes which were enchained as 1,2-cyclopentylene units. It is preferred that about 90 mole percent or more, more preferably about 95 mole percent or more of the enchained cyclopentene units be enchained as 1,3-cyclopentylene units, which are preferably cis-1,3-cyclopentylene units.

The X-ray powder diffraction pattern of the instant poly(cyclopentenes) is also unique. To produce cyclopentene polymer samples of uniform thickness for X-ray measurements, powder samples were compressed into disks approximately 1 mm thick and 32 mm in diameter.

X-ray powder diffraction patterns of the samples were collected over the range 10-500 28. The diffraction data were collected using an automated Philips diffractometer (Philips X'pert System) operating in the symmetrical transmission mode (Ni-filtered CuKa radiation, equipped with a diffracted beam collimator (Philips Thin Film Collimator system), Xe filled proportional detector, fixed step mode (0.05 0 /step) 12.5 sec./step, 1/40 divergence slit). Reflection positions were identified using the peak finding routine in the APD suite of programs provided with the 02/06/03,sw331 Ispa,79 X'pert System. The X-ray powder diffraction pattern had reflections at approximately 17.3°, 19.30, 24.20, and 40.70 20, which correspond to d-spacings of approximately 0.512, 0.460, 0.368 and 0.222 nm, Srespectively. These polymers have a monoclinic unit cell of the approximate dimensions: a=0.561 nm; b=0.607 nm; c=7.37 nm; and g=123.2.

Copolymers of cyclopentene and various other olefins may also be made. For instance a copolymer of ethylene and cyclopentene may also be made. In such a copolymer it is preferred that at least 50 mole percent, more preferably at least about 70 mole percent, of the repeat units are derived from cyclopentene. As also noted above, many of the polymerization systems described herein produce polyethylenes that have considerable branching in them.

Likewise the ethylene units which are copolymerized with the cyclopentene herein may also be branched, so it is preferred that there be at least 20 branches per 1000 methylene carbon atoms in such copolymers. In this instance, the "methylene carbon atoms" referred to in the previous sentence do not include methylene groups in the cyclopentene rings. Rather it includes methylene groups only derived from ethylene or other olefin, but not cyclopentene.

Another copolymer that may be prepared is one from cyclopentene and an a-olefin, more preferably a linear a-olefin. It is preferred in such copolymers that repeat units derived from cyclopentene are 50 mole percent or more of-the repeat units. As mentioned above, a-olefins may be enchained in a l,c fashion, and it is preferred that at least 10 mole percent of the repeat units derived from the a-olefin be enchained in such a fashion. Ethylene may also be copolymerized with the cyclopentene and a-olefin.

Poly(cyclopentene) and copolymers of cyclopentene, especially those that are (semi)crystalline, may be used as molding and extrusion resins. They may contain 02/06/03,sw 1331 various materials normally found in resins, such as fillers, reinforcing agents, antioxidants, antiozonants, pigments, tougheners, compatibilizers, dyes, flame retardant, and the like. These polymers may also be drawn or melt spun into fibers. Suitable tougheners and compatibilizers include polycyclopentene resin which has been grafted with maleic anhydride, an grafted EPDM rubber, a grafted EP rubber, a functionalized styrene/butadiene rubber, or other rubber which has- been modified to selectively bond to components of the two phases.

In all of the above homo- and copolymers of cyclopentene, where appropriate, any of the preferred state may be combined any other preferred state(s).

The homo- and copolymers of cyclopentene described above may used or made into certain forms as described below: 1. The cyclopentene polymers described above may be part of a polymer blend. That is they may be mixed in any proportion with one or more other polymers which may be thermoplastics and/or elastomers.

Suitable polymers for blends are listed below in the listing for blends of other polymers described herein.

One preferred type of polymer which may be blended is a toughening agent or compatibilizer, which is often elastomeric and/or contains functional groups which may help compatibilize the mixture, such as epoxy or carboxyl.

2. The polycyclopentenes described herein are useful in a nonwoven fabric comprising fibrillated three-dimensional network fibers prepared by using of a polycyclopentene resin as the principal component. It can be made by flash-spinning a homogeneous solution containing a polycyclopentehe. The resultant nonwoven fabric is excellent in heat resistance, dimensional stability and solvent resistance.

3. A shaped part of any of the cyclopentene containing resins. This part may be formed by -81 0206/03.sw133 11 sp,81 injection molding, extrusion, and thermoformong.

Exemplary uses include molded part for automotive use, medical treatment container, microwave-range container, food package container such as hot packing ccntainer, oven container, retort container, etc., and heatresisting transparent container such as heat-resisting bottle.

4. A sheet or film of any of the cyclopentene containing resins. This sheet or film may be clear and may be used for optical purposes breakage resistant glazing). The sheet or film may be oriented or unoriented. Orientation may be carried out by any of the known methods such a uniaxial or biaxial drawing. The sheet or film-may be stampable or thermoformable.

The polycyclopentene resins are useful in nonwoven fabrics or microfibers which are produced by melt-blowing a material containing as a main component a polycyclopentene. A melt-blowing process for producing a fabric or fiber comprises supplying a polycyclopentene in a molten form from at least one orifice of a nozzle into a gas stream which attenuates the molten polymer into microfibers. The nonwoven fabrics are excellent in heat-resistant and chemical resistant characteristics, and are suitable for use as medical fabrics, industrial filters, battery separators and so.forth. The microfibers are particularly useful in the field of high temperature filtration, coalescing and insulation.

6. A laminate in which one or more of the layers comprises a cyclopentene resin. The laminate may also contain adhesives, and other polymers in some or all of the layers, or other materials such as paper, metal foil, etc. Some or all of the layers, may be oriented in the same or different directions. The laminate as a whole may also be oriented. Such materials are useful for containers, or other uses where barrier properties are required.

-82- 02/06/03,sw13311spa, 8 2 7. A fiber of a cyclopentene poiymer. .This fiber may be undrawn or drawn to further orient it. It is useful for apparel and in industrial application where heat resistance and/or chemical resistance are important.

8. A foam or foamed object of a cyclopentene polymer. The foam may be formed in any conventional manner such as by using blowing agents.

9. The cyclopentene resins may be .microporous membranes. They may be used in process wherein semipermeable membranes are normally used.

In addition, the cyclopentene resins may be treated or mixed with other materials to improve certain properties, as follows: 1; i. They may further be irradiated with electron rays. This often improves heat resistance and/or chemical resistance, and is relatively inexpensive.

Thus the molding is useful as a material required to have high heat resistance, such as a structural material, a food container material, a food wrapping material or an electric or electronic part material, particularly as an electric or electronic part material, because it is excellent in soldering resistance.

2. Parts with a crystallinity of at least may be obtained by subjecting cyclopentene polymers having an end of melting point between 240 and 300 0 C to heat treatment (annealing) at a temperature of 120 0 C to just below the melting point of the polymer. Preferred conditions are a temperature of 150 to 280 0 C. for a period of time of 20 seconds to 90 minutes, preferably to give a cyclopentene polymer which has a heat deformation temperature of from 200 to 260°C. These parts have good physical properties such as heat resistance and chemical resistance, and thus are useful for, for example, general construction materials, electric or electronic devices, and car parts.

-83 02/06/03,swl3311 spa,83 3. Cyclopentene resins may be nucleated to promote crystallization during processing. An example would be a polycyclopentene resin composition containing as main components 100 parts by weight of a poiycyclopentene and 0.01 to 25 parts by weight cf one or more nucleating agents selected from the group consisting of metal salts of organic acids, inorganic compounds, organophosphorus compounds, and/or metal salts of ionic hydrocarbon copolymer. Suitable nucleating agents may be sodium methylenebis(2,4-di-tertbutylphenyl) acid phosphate, sodium bis(4-tert-butylphenyl) phosphate, aluminum p- (tert-butyl) benzoate, talc, mica, or related species.

These could be used in a process for producing polycyclopentene resin moldings by molding the above polycyclopentene resin composition at a temperature above their melting point.

4. Flame retardants and flame retardant combinations may be added to a cyclopentene polymer.

Suitable flame retardants include a halogen-based or phosphorus-based flame retardant, antimony trioxide, antimony pentoxide, sodium antimonate, metallic antimony, antimony trichloride, antimony pentachloride, antimony trisulfide, antimony pentasulfide, zinc borate, barium metaborate or zirconium oxide. They may be used in conventional amounts.

Antioxidants may be used in conventional amounts to improve the stability of the cyclopentene polymers. For instance 0.005 to 30 parts by weight, per 100 parts by weight of the cyclopentene polym'er, of an antioxidant selected from the group consisting of a phosphorous containing antioxidant, a phenolic antioxidant or a combination thereof. The phosphorous containing antioxidant may be a monophosphite or diphosphite or mixture thereof and the phenolic antioxidant may be a dialkyl phenol, trialkyl phenci, diphenylmonoalkoxylphenol, a tetraalkyl phenol, or a mixture thereof. A sulfur-containing antioxidant may -84- 02o/0i/3,sw1331 spaS4 also be used alone or in combination with o-rte antioxidants.

6. Various fillers or reinforcers, such as particulate or fibrous materials, may be added to improve various physical properties.

7. "Special" physical properties can be obtained by the use of specific types of materials.

Electrically conductive materials such as fine metallic wires or graphite may be used to render the polymer electrically conductive. The temperature coefficient of expansion may be regulated by the use of appropriate fillers, and it may be possible to even obtain materials with positive coefficients of expansion.

Such materials are particularly useful in electrical and electronic parts.

8. The polymer may be crosslinked by irradiation or chemically as by using peroxides, optionally in the presence of suitable coagents.

Suitable peroxides include benzoyl peroxide, lauroyl peroxide, dicumyl peroxide, tert-butyl peroxide, tertbutylperoxybenzoate, tert-butylcumyl peroxide, tertbutylhydroperoxide, 2,5-dimethyl-2,5-di(tertbutylperoxy)hexane, 2,5-dimethyl-2,5-di(tertbutylperoxy)hexyne-3,1,1-bis(tertbutylperoxyisopropyl)benzene, 1,1-bis(tertbutylperoxy)-3,3,5- trimethylcyclohexane, n-butyl-4,4bis(tert-butylperoxy)valerate, 2,2-bis(tertbutylperoxy)butane and tert-butylperoxybenzene.

When polymerizing cyclopentene, it has been found that some of the impurities that may be found in cyclopentene poison or otherwise interfere with the polymerizations described herein. Compounds such as 1,3-pentadiene (which can be removed by passage through molecular sieves), cyclopentadiene (which can be removed by distillation from Na), and methylenecyclobutane (which can be removed by distillation from polyphosphoric acid), may interfere 006/03.swi33 s I with the polymerization, and their level should be kept as low as practically possible.

The above polymers (in general) are useful in many applications. Crystalline high molecular weight polymers are useful as molding resins, and for films for use in packaging. Amorphous resins are useful as elastomers, and may be crosslinked by known methods, such as by using free radicals. When such amorphous resins contain repeat units derived from polar monomers they are oil resistant. Lower molecular weight polymers are useful as oils, such as in polymer processing aids. When they contain polar groups, particularly carboxyl groups, they are useful in adhesives.

In many of the above polymerizations, the transition metal compounds employed as (part of the) catalysts contain(s) metal atom(s) in a positive oxidation state. In addition, these complexes may have a square planar configuration about the metal, and the metal, particularly nickel or palladium, may have a d s electronic configuration. Thus some of these catalysts may be said to have a metal atom which is cationic and has a ds-square planar configuration.

In addition these catalysts may have a bidentate ligand wherein coordination to the transition metal is through two different nitrogen atoms or through a nitrogen atom and a phosphorus atom, these nitrogen and phosphorus atoms being part of the bidentate ligand.

It is believed that some of these compounds herein are effective polymerization catalysts at least partly because the bidentate ligands have sufficient steric bulk on both sides of the coordination plane (of the square planar complex). Some of the Examples herein with the various catalysts of this type illustrate the degree of steric bulk which may be needed for such catalysts. If such a complex contains a bidentate ligand which has the appropriate steric bulk, it is -86- 02/06-03,swl33 I spa,86 believed that it produces polyethylene with a degree cf polymerization of at least about 10 or more.

It is also believed that the polymerization catalysts herein are effective because unpolymerized S lefinic monomer can only slowly displace from the complex a coordinated olefin which may be formed by fhydride elimination from the growing polymer chain which is attached to the transition metal. The displacement can occur by associative exchange.

Increasing the steric bulk of the ligand slows the rate of associative exchange and allows polymer chain growth. A quantitative measure of the steric bulk of the bidentate ligand can be obtained by measuring at 0 C the rate of exchange of free ethylene with complexed ethylene in a complex of formula (XI) as shown in equation 1 using standard 1H NMR techniques, which is called herein the Ethylene Exchange Rate *EER). The neutral bidentate ligand is represented by YN where Y is either N or P. The EER is measured in this system. In this measurement system the metal is always Pd, the results being applicable to other metals as noted below. Herein it is preferred for catalysts to contain bidentate ligands for which the second order rate constant for Ethylene Exchange Rate is about 20,000 L-mol-Is- 1 or less when the metal used in the polymerization catalyst is palladium, more preferably about 10,000 L-mcl-s- 1 or less, and more preferably about 5,000 L-mols or less. When the metal in the polymerization catalyst is nickel, the second order rate constant (for-the ligand in EER measurement) is about 50,000 L-mol's' 1 more preferably about 25,000 Lmol's' or less, and especially preferably about 10,000 l-mol ss' or less. Herein the EER is measured using the compound (XI) in a procedure including temperature: described in Examples 21-23.

-87- 02106/03,sw 133t spa87 X CH 3 k X ,CH3 Pd- Pd (1) N' II N II (XI) X=Nor P In these polymerizations it is preferred if the bidentate ligand is an a-diimine. It is also preferred.

if the olefin has the formula R 1 CH=CH, wherein R 17 is hydrogen or n-alkyl.

In general for the polymers described herein, blends may be prepared with other polymers, and such other polymers may be elastomers, thermoplastics or thermosets. By elastomers are generally meant polymers whose Tg (glass transition temperature) and Tm (melting point}, if present, are below ambient temperature, usually considered to be about 20 0 C. Thermoplastics are those polymers whose Tg and/or Tm are at or above ambient temperature. Blends can be made by any of the common techniques known to the artisan, such as solution blending, or melt blending in a suitable apparatus such as a single or twin-screw extruder.

Specific uses for the polymers of this application in the blends or as blends are listed below.

Blends may be made with almost any kind of elastomer, such as EP, EPDM, SBR, natural rubber, polyisoprene, polybutadiene, neoprene, butyl rubber, styrene-butadiene block copolymers, segmented polyester-polyether copolymers, elastomeric polyurethanes, chlorinated or chlorosulfonated polyethylene, (per)fluorinated elastomers such as copolymers of vinylidene fluoride, hexafluoropropylene and optionally tetrafluoroethylene, copolymers of tetrafluoroethylene and perfluoro(methyl vinyl ether), and copolymers of tetrafluoroethylene and propylene.

Suitable thermoplastics which are useful for blending with the polymers described herein include: polyesters such as poly(ethylene terephthalate), poly(butylene terephthalate), and poly(ethylene 88 020603.swl3311spS.B adipate); polyamides such as nylon-6, nylon-,o, nyion- 12, nylon-12,12, nylon-11, and a copolymer of hexamethylene diamine, adipic acid and terephthalic acid; fluorinated polymers such as copolymers of ethylene and vinylidene fluoride, copolymers of tetrafluoroethylene and hexafluoropropylene, copolymers of tetrafluoroethylene and a perfluoro(alkyl vinyl ether) such as perfluoro(propyl vinyl ether), and poly(vinyl fluoride); other halogenated polymers such a poly(vinyl chloride) and poly(vinylidene chloride) and its copolymers; polyolefins such as polyethylene, polypropylene and polystyrene, and copolymers thereof; (meth)acrylic polymers such a poly(methyl methacrylate) and copolymers thereof; copolymers of olefins such as ethylene with various (meth) acrylic monomers such as alkyl acrylates, (meth)acrylic acid and ionomers thereof, and glycidyl (meth)acrylate); aromatic polyesters such as the copolymer of Bisphenol A and terephthalic and/or isophthalic acid; and liquid crystalline polymers such as aromatic polyesters or aromatic poly(ester-amides).

Suitable thermosets for blending with the polymers described herein include epoxy resins, phenolformaldehyde resins, melamine resins, and unsaturated polyester resins (sometimes called thermoset polyesters). Blending with thermoset polymers will often be done before the thermoset is crosslinked, using standard techniques.

The polymers described herein may also be blended with uncrosslinked polymers which are not usually considered thermoplastics for various reasons, for instance their viscosity is too high and/or their melting point is so high the polymer decomposes below the melting temperature. Such polymers include poly(tetrafluoroethylene), aramids such as poly(pphenylene terephthalate) and poly(m-phenylene isophthalate), liquid crystalline polymer such as -89- 026/03,sw 1331] spa89 poly(benzoxazoles), and non-melt processinie polyimiaes which are often aromatic polyimides.

All of the polymers disclosed herein may be mixed with various additives normally added to elastomers and thermoplastics Isee EPSE (below), vol. 14, p. 327-410].

For instance reinforcing, non-reinforcing and conductive fillers, such as carbon black, glass fiber, minerals such as clay, mica and talc, glass spheres, barium sulfate, zinc oxide, carbon fiber, and aramid fiber or fibrids, may be used. Antioxidants, antiozonants, pigments, dyes, delusterants, compounds to promote crosslinking may be added. Plasticizers such as various hydrocarbon oils may also be used.

The following listing is of some uses for polyolefins, which are made from linear olefins and do not include polar monomers such as acrylates, which are disclosed herein. In some cases a reference is given which discusses such uses for polymers in general. All of these references are hereby included by reference.

For the references, refers to w. Gerhartz, et ai., Ed., Ullmann's Encyclopedia of Industrial Chemistry, Ed. VCH Verlagsgesellschaft mBH, Weinheim, for which the volume and page number are given, "ECT3" refers to the H. F. Mark, et al., Ed., Kirk-Othmer Encyclopedia of Chemical Technology, 4th Ed., John Wiley Sons, New York, "ECT4" refers to the J. I Kroschwizz, et al., Ed., Kirk-Othmer Encyclopedia of Chemical Technology, 4th Ed., John Wiley Sons, New York, for which the volume and page number are given, "EPST" refers to H. F. Mark, et al., Ed., Encyclopedia of Polymer Science and Technology, 1st Ed., John Wiley Sons, New York, for which the volume and page number are given, "EPSE" refers to H. F. Mark, et al., Ed., Encyclopedia of Polymer Science and Engineering, 2nd Ed., John Wiley Sons, New York, for which volume and page numbers are given, and "PM" refers to J. A.

Brydscn, ed., Plastics Materials, 5 Ed., Butterworth- Heinemann, Oxford, UK, 1989, and the page is given. In 02106/0s3sw133 these uses, a polyethylene, polypropylene and a copolymer of ethylene and propylene are preferred.

1. Tackifiers for low strength adhesives (U, vol. Al, p. 235-236) are a use for these polymers.

Elastomeric and/or relatively low molecular weight polymers are preferred.

2. An oil additive for smoke suppression in single-stroke gasoline engines is another use.

Elastomeric polymers are preferred.

3. The polymers are useful as base resins for hot melt adhesives vol. Al, p. 233-234), pressure sensitive adhesives vol. Al, p. 235-236) or solvent applied adhesives. Thermoplastics are preferred for hot melt adhesives. The polymers may also be used in a carpet installation adhesive.

4. Lubricating oil additives as Viscosity Index Improvers for multigrade engine oil (ECT3, Vol 14, p.

495-496) are another use. Branched polymers are preferred. Ethylene copolymer with acrylates or other polar monomers will also function as Viscosity Index Improvers for multigrade engine oil with the additional advantage of providing some dispersancy.5. Polymer for coatings and/or penetrants for the protection of various porous items such as lumber and masonry, particularly out-of-doors. The polymer may be in a suspension or emulsion, or may be dissolved in a solvent.

6. Base polymer for caulking of various kinds is another use. An elastomer is preferred. Lower molecular weight polymers are often used.

7. The polymers may be grafted with various compounds particularly those that result in functional groups such as epoxy, carboxylic anhydride (for instance as with a free radically polymerized reaction with maleic anhydride) or carboxylic acid (EPSE, vol.

12, p. 445). Such functionalized polymers are particularly useful as tougheners for various thermoplastics and thermosets when blended. When the -91 02/06/03,sw 1331 1spi,9l polymers are elastomers, the functional groups whicn are grafted onto them may be used as curesites to crosslink the polymers. Maleic anhydride-grafted randomly-branched polyolefins are useful as tougheners for a wide range of materials (nylon, PPO, PPO/styrene alloys, PET, PBT, POM, etc.); as tie layers in multilayer constructs such as packaging barrier films; as hot melt, moisture-curable, and coextrudable adhesives; or as polymeric plasticizers. The maleic andhydride-grafted materials may be post reacted with, for example; amines, to form other functional materials. Reaction with aminopropyl trimethoxysilane would allow for moisture-curable materials. Reactions with di- and tri-amines would allow for viscosity modifications.

8. The polymers, particularly elastomers, may be used for modifying asphalt, to improve the physical properties of the asphalt and/or extend the life of asphalt paving.

9. The polymers may be used as base resins for chlorination or chlorosulfonation for making the corresponding chlorinated or chlorosulfonated elastomers. The unchlorinated polymers need not be elastomers themselves.

10. Wire insulation and jacketing may be made from any of the polyolefins (see EPSE, vol. 17, p. 828- 842). In the case of elastomers it may be preferable to crosslink the polymer after the insulation or jacketing is formed, for example by free radicals.

11. The polymers, particularly the elastomers, may be used as tougheners for other polyolefins such as polypropylene and polyethylene.

12. The base for synthetic lubricants (motor oils) may be the highly branched polyolefins described herein (ECT3, vol. 14, p. 496-501).

13. The branched polyolefins herein can be used as drip suppressants when added to other polymers.

-92- 02/06/03.sw1331 IspA,92 14. The branched poilyolefins herein are especially useful in blown film applications because of their particular rheologicai properties (EPSE, vol. 7, p. 88-106). It is preferred that these polymers have some crystallinity.

The polymer described herein can be used to blend with wax for candles, where they would provide smoke suppression and/or drip control.

16. The polymers, especially the branched polymers, are useful as base resins for carpet backing, especially for automobile carpeting.

17. The polymers, especially those which are relatively flexible, are useful as capliner resins for carbonated and noncarbonated beverages.

18. The polymers, especially those having a relatively low melting point, are useful as thermal transfer imaging resins (for instance for imaging teeshirts or signs).

19. The polymers may be used for extrusion or coextrusion coatings onto plastics, metals, textiles or paper webs.

The polymers may be used as a laminating adhesive for glass.

21. The polymers are useful as for blown or cast films or as sheet (see EPSE, vol. 7 p. 88-106; ECT4, vol. 11, p. 843-856; PM, p. 252 and p. 432ff) The films may be single layer or multilayer, the multilayer films may include other polymers, adhesives, etc. For packaging the films may be stretch-wrap, shrink-wrap or cling wrap. The films are useful form many applications such as packaging foods, geomembranes and pond liners. It is preferred that these polymers have some crystallinity.

22. The polymers may be used to form flexible or rigid foamed objects, such as cores for various sports items such as surf boards and liners for protective headgear. Structural foams may also be made. It is preferred that the polymers have some -93- 0/06/03.swl 331 ]spa.93 crystallinity. The polymer of the foams may be crosslinked.

23. In powdered form the polymers may be used to coat objects by using plasma, flame spray or fluidized bed technicues.

24. Extruded films may be formed from these polymers, and these films may be treated, for example drawn. Such extruded films are useful for packaging of various sorts.

25. The polymers, especially those that are elastomeric, may be used in various types of hoses, such as automotive heater hose.

26. The polymers, especially those that are branched, are useful as pour point depressants for fuels and oils.

27. These polymers may be flash spun to nonwoven fabrics, particularly if they are crystalline (see EPSE vol. 10, p. 202-253) They may also be used to form spunbonded polyolefins (EPSE, vol. 6, p. 756- 760). These fabrics are suitable as house wrap and geotextiles.

28. The highly branched, low viscosity polyolefins would be good as base resins for masterbatching of pigments, fillers, flame-retardants, and related additives for polyolefins. 29. The polymers may be grafted with a compound containing ethylenic unsaturation and a functional group such as a carboxyl group or a derivative of a carboxyl group, such as ester, carboxylic anhydride of carboxylate salt. A minimum grafting level of about 0.01 weight percent of grafting agent based on the weight of the grafted polymer is preferred. The grafted polymers are useful as compatibilizers and/or tougheners. Suitable grafting agents include maleic, acrylic, methacrylic, itaconic, crotonic, alpha-methyl crotonic and cinnamic acids, anhydrides, esters and their metal salts and fumaric acid and their esters, anhydrides (when appropriate) and metal salts.

94 0 2 0 6 /03,sw1331 spa,94 Copolymers of linear olefins with 4vinylcyclohexene and other dienes may generally be used for all of the applications for which the linear olefins polymers(listed above) may be used. In they may be sulfur cured, so they generally can be used for any use for which EPDM polymers are used, assuming the olefin/4-vinylcyclohexene polymer is elastomeric.

Also described herein are novel copolymers of linear olefins with various polar monomers such as acrylic acid and acrylic esters. Uses for these polymers are given below. Abbreviations for references describing these uses in general with polymers are the same as listed above for polymers made from linear olefins.

1. Tackifiers for low strength adhesives (U, vol. Al, p. 235-236) are a use for these polymers.

Elastomeric and/or relatively low molecular weight polymers are preferred.

2. The polymers are useful as base resins for hot melt adhesives vol. Al, p. 233-234), pressure sensitive adhesives vol. Al, p. 235-236) or solven: applied adhesives. Thermoplastics are preferred for hot melt adhesives. The polymers may also be used in a carpet installation adhesive.

3. Base polymer for caulking of various kinds is another use. An elastomer is preferred. Lower molecular weight polymers are often used.

4. The polymers, particularly elastomers, may be used for modifying asphalt, to improve the physical properties of the asphalt and/or extend the life of asphalt paving, see U.S. patent 3,980,598.

Wire insulation and jacketing may be made from any of the polymers (see EPSE, vol. 17, p. 828- 342). In the case of elastomers it may be preferable to crosslink the polymer after the insulation or jacketing is formed, for example by free radicals.

02/06/03,sw1331 6. The polymers, especially the branched polymers, are useful as base resins for carpet backing, especially for automobile carpeting.

7. The polymers may be used for extrusion or coextrusion coatings onto plastics, metals, textiles or paper webs.

8. The polymers may be used as a laminating adhesive for glass.

9. The polymers are useful as for blown or cast films or as sheet (see EPSE, vol. 7 p. 88-106; ECT4, vol. I1, p. 843-856; PM, p. 252 and p. 432ff). The films may be single layer or multilayer, the multilayer films may include other polymers, adhesives, etc. For packaging the films may be stretch-wrap, shrink-wrap or cling wrap. The films are useful form many applications such as packaging foods, geomembranes and pond liners. It is preferred that these polymers have some crystallinity.

The polymers may be used to form flexible or rigid foamed objects, such as cores for various sports items such as surf boards and liners for protective headgear. Structural foams may also be made. It is preferred that the polymers have some crystallinity. The polymer of the foams may be crosslinked.

11. In powdered form the polymers may be used to coat objects by using plasma, flame spray or flu:dized bed techniques.

12. Extruded films may be formed from these polymers, and these films may be treated, for example drawn. Such extruded films are useful for packaging of various sorts.

13. The polymers, especially those that are elastomeric, may be used in various types of hoses, such as automotive heater hose.

14. The polymers may be used as reactive diluents in automotive finishes, and for this purpose -96- 02/06/03,swl331 I spa.96 it is preferred that they have a relatively low molecular weight and/or have some crystallinity.

The polymers can be converted to ionomers, which when the possess crystallinity can be used as resins. Exemplary uses for these ionomeric molding resins are golf ball covers, perfume caps, sporting goods, film packaging applications, as tougheners in other polymers, and usually extruded) detonator cords.

16. The functional groups on the polymers can be used to initiate the polymerization of other types of monomers or to copolymerize with other types of monomers. If the polymers are elastomeric, they can act as toughening agents.

17. The polymers can act as compatibilizing agents between various other polymers.

18. The polymers can act as tougheners for various other polymers, such as thermoplastics and thermosets, particularly if the olefin/polar monomer polymers are elastomeric.

19. The polymers may act as internal plasticizers for other polymers in blends. A polymer which may be plasticized is poly(vinyl chloride).

The polymers can serve as adhesives between other polymers.

21. With the appropriate functional groups, the polymers may serve as curing agents for other polymers with complimentary functional groups the functional groups of the two polymers react with each other).

22. The polymers, especially those that are branched, are useful as pour point depressants for fuels and oils.

23. Lubricating oil additives as Viscosity Index Improvers for multigrade engine oil (ECT3, Vol 14, p. 495-496) are another use. Branched polymers are preferred. Ethylene copolymer with acrylates or other polar monomers will also function as Viscosity Index 97 02/6/03,sw 3311spa,97 Improvers for multigrade engine oil with the additicnal advantage of providing some dispersancy.

24. The polymers may be used for roofing membranes.

The polymers may be used as additives to various molding resins such as the so-called thermoplastic olefins to improve paint adhesion, as in automotive uses.

Polymers with or without polar monomers present are useful in the following uses. Preferred polymers with or without polar monomers are-those listed above in the uses for each "type".

1. A flexible pouch made from a single layer or multilayer film (as described above) which may be used for packaging various liquid products such as milk, or powder such as hot chocolate mix. The pouch may be heat sealed. It may also have a barrier layer, such as a metal foil layer.

2. A wrap packaging film having differential cling is provided by a film laminate, comprising at least two layers; an outer reverse which is a polymer (or a blend thereof) described herein, which contains a tackifier in sufficent amount to impart cling properties; and an outer obverse which has a density of at least about 0.916 g/mL which has little or no cling, provided that a density of the outer reverse layer is at least 0.008 g/mL less than that of the density of the outer obverse layer. It is preferred that the outer obverse layer is linear low density polyethylene, and the polymer of the outer obverse layer have a density of less than 0.90 g/mL. All densities are measured at 25 0

C.

3. Fine denier fibers and/or multifilaments.

These may be melt spun. They may be in the form of a filament bundle, a non-woven web, a woven fabric, a knitted fabric or staple fiber.

98 0206/03,sw 13311sp,.98 4. A composition comprising a mixture of the polymers herein and an antifogging agent. This composition is especially useful in film or sheet form because of its antifogging properties.

5. Elastic, randomly-branched olefin polymers are disclosed which have very good processability, including processing indices (PI's) less than or equal to 70 percent of those of a comparative linear olefin polymer and a critical shear rate at onset of surface melt fracture of at least 50 percent greater than the critical shear rate at the onset of surface melt fracture of a traditional linear olefin polymer at about the same 12 and Mw/Mn. The novel polymers may have higher low/zero shear viscosity and lower high I shear viscosity than comparative linear olefin polymers made by other means. These polymers may be characterized as having: a) a melt flow ratio, 110/12, 5.63, b) a molecular weight distribution, Mw/Mn, defined by the equation: Mw/Mn (110/12)-4.63, and c) a critical shear rate at onset of surface melt fracture of at least 50 percent greater than the critical shear rate at the onset of surface melt fracture of a linear olefin polymer having about the same 12 and Mw/Mn.

Some blends of these polymer are characterized as havins: a) a melt flow ratio, 110/12, 5.63, b) a molecular weight distribution, Mw/Mn, defined by the equation: Mw/Mn (110/12)-4.63, and c) a critical shear rate at onset of surface melt fracture of at least 50 percent greater than the critical shear rate at the onset of surface melt fracture of a linear olefin polymer having about the same 12 and Mw/Mn and at least one other natural or synthetic polymer chosen from the polymer of claims 1, 3, 4, 6, 332, or 343, a conventional high density polyethylene, low density polyethylene or linear low density polyethylene polymer. The polymers may be further characterized as having a melt flow ratio, 110/12, 5.63, a molecular weight distribution, Mw/Mn, defined by the equation: -99- 02/06/03.sw 133 I Ispa,99 Mw/Mn S (110/I2)-4.63, and a critical shear stress at onset of gross melt fracture of greater than about 400 kPa (4x106 dyne/cm 2 and their method of manufacture are disclosed. The randomly-branched olefin polymers preferably have a molecular weight distribution from about 1.5 to about 2.5. The polymers described herein often have improved processability over conventional olefin polymers.and are useful in producing fabricated articles such as fibers, films, and molded parts. For this paragraph, the value 12 is measured in accordance with ASTM D-1238-190/2.16 and 110 is measured in -accordance with ASTM D-1238-190/10; critical shear rate at onset of surface melt fracture and processing index (PI) are defined in U.S. Patent 5,278,272, which is hereby included by reference.

In another process described herein, the product of the process described herein is an a-olefin. It is preferred that in the process a linear a-olefin is produced. It is also preferred that the a-olefin contain 4 to 32, preferably 8 to 20, carbon atoms.

R2 R3 Q

S

(XXXI)

When (XXXI) is used as a catalyst, a neutral Lewis acid or a cationic Lewis or Bronsted acid whose counterion is a weakly coordinating anion is also present as part of the catalyst system (sometimes called a "first compound" in the claims).. By a "neutral Lewis acid" is meant a compound which is a Lewis acid capable for abstracting X' from to form a weakly coordinating anion. The neutral Lewis acid is originally uncharged not ionic). Suitable neutral Lewis acids include SbFs, Ar 3 B (wherein Ar is 100- 0 26/03,w3sw3311 spa.o aryl), and BF. By a cationic Lewis acid is meant a cation with a positive charge such as Ag*, and Na'.

A preferred neutral Lewis acid is an alkyl aluminum compound, such as R 3A1, R 2AlC1, R'AlCl1, and "R'A10" (alkylaluminoxane), wherein R 9 is alkyl containing 1 to 25 carbon atoms, preferably 1 to 4 carbon atoms. Suitable alkyl aluminum ccmpounds include methylaluminoxane,

(C

2

H

5 2 ACl, CH.AlCln, and

[(CH

3 2 CHCH) 3A Relatively noncoordinating anions are known in the art, and the coordinating ability of such anions is known and has been discussed in the literature, see for instance W. Beck., et al., Chem. Rev., vol. 88 p. 1405- 1421 (1988), and S. H. Strauss, Chem. Rev., vol. 93, p..

927-942 (1993), both of which are hereby included by reference. Among such anions are those formed from the aluminum compounds in the immediately preceding paragraph and including R5,A1X R' 2 AlClX, R'AICI 2

X,

and "R 9 AlOX'". Other useful noncoordinating anions include BAF" (BAF bis(trifluoromethyl)phenyl]borate), SbF6", PF/, and BF4 trifluoromethanesulfonate, p-toluenesulfonate, (RfSO, 2 2 N, and (C 6 Fs) 4

B'.

The temperature at which the process is carried out is about -100°C to about +200 0 C, preferably about 0 0 C to about 150C, more preferably about 25'C to about 100°C. It is believed that at higher temperatures, lower molecular weight a-olefins are produced, all other factors being equal. The pressure at which th? polymerization is carried out is not critical, atmospheric pressure to about 275 MPa being a suitable range. It is also believed that increasing the pressure increases the relative amount of a-olefin (as opposed to internal olefin) produced.

The process to make a-olefins may be run in a solvent (liquid), and that is preferred. The solvent may in fact be the a-olefin produced. Such a process may be started by using a deliberately added solvent 101 0206/03,sw1331 Ispa, 101 which is gradually displaced as the reaction proceeas.

By solvent it is not necessarily meant that any or all of the starting materials and/or products are soluble in the (liquid) solvent.

In it is preferred that R 3 and R 4 are both hydrogen or methyl or R' and R 4 taken together are (An) It is also preferred that each of Q and S is independently chlorine or bromine, and it is more preferred that both of Q and S in (XXXI) are chlorine or bromine.

In (XXXI) R' and R 5 are hydrocarbyl or substituted hydrocarbyl. What these groups are greatly determines whether the a-olefins of this process are made, or whether higher polymeric materials, materials containing over 25 ethylene units, are coproduced or produced almost exclusively. If R 2 and R 5 are highly sterically hindered about the nickel atom, the tendency is to produce higher polymeric material. For instance, when R' and R 5 are both 2,6-diisopropylphenyl mostly higher polymeric material is produced. However, when R' and R 5 are both phenyl, mostly the a-olefins of this process are produced. Of course this will also be influenced by other reaction conditions such as temperature and pressure, as noted above. Useful groups for R' and R 5 are phenyl, and p-methylphenyl.

As is understood by the artisan, in cligomerization reactions of ethylene to produce aolefins, usually a mixture-of such a-olefins is obtained containing a series of such a-olefins differing from one another by two carbon atoms (an ethylene unit). The process for preparing a-olefins described herein produces products with a high 102 0 2 /06103.sw13311spa,o02 percentage of terminal olefinic groups (as opposed to internal olefinic groups). The product mixture also contains a relatively high percentage of molecules which are linear. Finally relatively high catalyst efficiencies can be obtained.

The a-olefins described as being made herein may also be made by contacting ethylene with one of the compounds R2 R3 T R4 Z x-

(III)

or N U r x

(XXXIV)

wherein R 2

R

3

R

4 and R 5 are as defined (and creferred) as described above (for the preparation of a -olefins), and T' is hydrogen or n-alkyl containing up to 38 carbon atoms, Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur, or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound (measured in water) is less than about 6, U is n-alkyl containing up to 38 carbon atoms, and X is a noncoordinating anion isee above). The process conditions for making aolefins using (III) or (XXXIV) are the same as for using (XXXI) to make these compounds except a Lewis or Bronsted acid need not be present. Note that the double line in (XXXIV) represents a coordinated 103 02/0603.sw13311p II.103 ethylene molecule. (XXXIV) may be made-rm (II) by reaction of (III) with ethylene. In other words, (XXXIV) may be considered an active intermediate in the formation of a-olefin from (III). Suitable groups for Z include dialkyl ethers such as diethyl ether, and alkyl nitriles such as acetonitrile.

In general, a-olefins can be made by this process using as a catalyst a Ni[II] complex of an a-diimine of formula (VIII), wherein the Ni[II] complex is-made by any of the methods which are described above, using Ni[0], Ni[I) or Ni[II] precursors. All of the process conditions, and preferred groups on (VIII), are the same as described above in the process for making aolefins.

EXAMPLES

In the Examples, the following convention is used for naming a-diimine complexes of metals, and the adiimine itself. The a-diimine is indicated by the letters "DAB". To the left of the "DAB" are the two groups attached to the nitrogen atoms, herein usually called R 2 and R s To the right of the "DAB" are the groups on the two carbon atoms of the a-diimine group, herein usually termed R 3 and R4 To the right of all this appears the metal, ligands attached to the metal (such as Q, S and and finally any anions which when "free" anions are designated by a superscript minus sign Of course if there is a "free" anion present, the metal containing moiety is cationic.

Abbreviations for these groups are as described in the Specification in the Note after Table 1. Analogous abbreviations are used for a-diimines, etc.

In the Examples, the following abbreviations are used: AHf heat of fusion acac acetylacetonate Bu butyl t-BuA t-butyl acrylate 104 0206/03,sw 13311 spa. l04 DMA Dynamic Mechanical Analysis DME 1,2-dimethoxyethane DSC Differential Scanning Calorimetry E ethylene EOC end of chain Et ethyl perfluoro(n-butyltetrahydrofuran) FOA fluorinated octyl acrylate GPC gel permeation chromatography MA methyl acrylate MAO methylaluminoxane Me methyl MeOH methanol MMAO a modified methylaluminoxane in which about 25 mole percent of the methyl groups have been replaced by isobutyl groups M-MAO see MMAO MMAO-3A see MMAO Mn number average molecular weight MVK methyl vinyl ketone Mw- weight average molecular weight Mz viscosity average molecular weight PD or P/D polydispersity, Mw/Mn Ph phenyl PMAO see MAO PMMA poly(methyl methacrylate) Pr propyl PTFE polytetrafluoroethylene RI refractive index RT (or rt) room temperature TCE 1,1,2,2-tetrachloroethane Tc temperature of crystallization Td temperature of decomposition Tg glass transition temperature TGA Thermogravimetric Analysis THF tetrahydrofuran Tm melting temperature 105 02/06/03.sw133 I Ispa 105 TO turnovers, the number of moles of monomer polymerized per g-atom of metal in the catalyst used UV ultraviolet Unless otherwise noted, all pressures are gauge Spressures.

In the Examples, the following procedure was used to quantitatively determine branching, and the distribution of branch sizes in the polymers (but not necessarily the simple number of branches as measured by total number Of methyl groups per 1000 methylene groups). 100 MHz 13 C NMR spectra were obtained on a Varian Unity 400 MHz spectrometer using a 10 mm probe on typically 15-20 wt% solutions of the polymers and 0.05 M Cr(acetylacetonate)3 in 1,2,4-trichlorobenzene (TCB) unlocked at 120-140 0 C using a 90 degree pulse of 12.5 to 18.5 psec, a spectral width of 26 to 35 kHz, a relaxation delay of 5-9 s, an acquisition time of 0.64 sec and gated decoupling. Samples were preheated for at least 15 min before acquiring data. Data acquisition time was typically 12 hr. per sample. The

T

i values of the carbons were measured under these conditions to be all less than 0.9 s. The longest T 1 measured was for the Bu, end of chain resonance at 14 ppm, which was 0.84 s. Occasionally about 16 vol. benzene-dr was added to the TCB and the sample was run locked. Some samples were run in chloroform-dl, CDCl 3 dl, (locked) at 30 0 C under similar acquisition parameters. T 1 's were also measured in CDC13 at ambient temperature on a typical sample with 0.05 M Cr(aceylacetonate) 3 to be all less than 0.68 s. In rare cases when Cr(acetylacetonate) 3 was not used, a 30-40 s recycle delay was used to insure quantitation.

The glycidyl acrylate copolymer was run at 100 0 C with Cr(acetylacetonate) 3 Spectra are referenced to the solvent either the TCB highfield resonance at 127.8 ppm or the chloroform-dl triplet at 77 ppm. A DEPT 135 spectrum was done on most samples to distinguish methyls and methines from methylenes. Methyls were 106 02/06/03,swl3311spa,106 .istinguished from methines by chemical shift. EOC is end-of-chain. Assignments reference to following naming scheme: 1. xBy: By is a branch of length y carbons; x is carbon being discussed, the methyl at the end of the branch is numbered 1. Thus the second carbon from the end of a butyl branch is 2B4. Branches of length y or greater are designated as y'.

2. xEBy: EB is an ester ended branch containing y methylenes. x is the carbon being discussed, the first methylene adjacent to the ester carbonyl is labeled 1.

Thus the second methylene from the end of a 5 methylene ester terminated branch would be 2EB5. 13 C NMR of model compounds for EBy type branches for y=0 and y=5 confirm the peak positions-and assignments of these branches. In addition, a model compound for an EB1 branch is consistent with 2 dimensional NMR data using the well know 2D NMR techniques of hsqc, hmbc, and hsqc-tocsy; the 2D data confirms the presence of the EB5, EBO, EB1 and other intermediate length EB branches 3. The methylenes in the backbone are denoted with Greek letters which determine how far from a branch point methine each methylene is. Thus pp (beta beta) B denotes the central methylene in the following

PCHRCH

2

CH

2

CH

2 CHRP. Methylenes that are three or more carbons from a branch point are designated as y' (gamma+).

4. When x in xBy or xEBy is replaced by a M, the methine carbon of that branch is denoted.

Integrals of unique carbons in each branch were measured and were reported as number of branches per 1000 methylenes (including methylenes in the backbone and branches). These integrals are accurate to relative for abundant branches and 10 or relative for branches present at less than 10 per 1000 methylenes.

107- 02106/03.w 13311 spa, 107 Such types of analyses are generally~ irnon, see for instance "A Quantitative Analysis of Low Density (Branched) Polyethylenes by Carbon-12 Fourier Transform Nuclear Magnetic Resonance at 67.9 MHz", D. E. Axelson, et al., Macromolecules 12 (1979) pp. 41-52; "Fine Branching Structure in High-Pressure, Low Density Polyethylenes by 50.10-MHz 13C NMR Analysis", T. Usayri et al., Macromolecules 17 (1984) pp. 1757-1761; and "Quantification of Branching in Polyethylene by 13C NMR Using Paramagnetic Relaxation Agents", J. V. Prasad, et al., Eur. Polym. J. 27 (1991) pp. 251-254 (Note that this latter paper is believed to have some significant.

typographical errors in it).

it is believed that in many of the polymers described herein which have unusual branching, i.e., they have more or fewer branches than would be expected for "normal" coordination polymerizations, or the distribution of sizes of the branches is different from that expected, that "branches on branches" are also present. By this is meant that a branch from the main chain on the polymer may itself contain one or more branches. It is also noted that the concept of a "main chain" may be a somewhat semantic argument if there are sufficient branches on branches in any particular polymer.

By a polymer hydrocarbyl branch is meant a methyl group to a methine or quaternary carbon atom or a group of consecutive methylenes terminated at one end by a methyl group and connected at the other end to a methine or quaternary carbon atom. The length of the branch is defined as the number of carbons from and including the methyl group to the nearest methine or quaternary carbon atom, but not including the methine or quaternary carbon atom. if the number of consecutive methylene groups is then the branch contains (or the branch length is) n+1. Thus the structure (which represents part of a polymer) W8 lo 2O61O3.swI1331 I spa, 108

H

2 CCCHH [CH,CH 2 CHCHCCH,CHH) CCH3 CH 2 CHCHCH:- contains 2 branches, a methyl and an ethyl branch.

For ester ended branches a similar definition is used. An ester branch refers to a group of consecutive methylene groups terminated at one end by an ester COOR group, and connected at the other end to a methine or quaternary carbon atom. The length of the branch is defined as the number of consecutive methylene groups from the ester group to the nearest methine or quaternary carbon atom, but not including the methine or quaternary carbon atom. If the number of methylene 1 groups is then the length of the branch is n.

Thus -CHCH,CH [CH 2

CH

2 CCH2CH (CH 3

CH

2 COOR] CHCH-CHCH 2 contains 2 branches, a methyl and an n=l ester branch.

The 3 C NMR peaks for.copolymers of cyciopentene and ethylene are described based on the labeling scheme and assignments of A. Jerschow et al, Macromolecules 1995, 28, 7095-7099. The triads and pentads are described as 1-cme, 1,3-ccmcc, 1,3-cmc, 2-cme, 2-cmc, 1,3-eme,3-cme, and 4,5-cmc, where e ethylene, c cyclopentene, and m meta cyclopentene 1,3 enchainment). The same labeling is used for cyclopentene/l-pentene copolymer substituting p pentene for e. The synthesis of diimines is reported in the literature (Tom Dieck, Svoboda, Grieser, T. Z. Naturforsch 1981, 36b, 823-832. Kliegman, J. M.; Barnes, R. K. J. Org. Chem. 1970, 35, 3140-3143.) Example 1 [(2,6-i-PrPh) 2DABMe 2 PdMeCl Et 2 0 (75 mL) was added to a Schlenk flask containing CODPdMeCl (COD 1,5-cyclooctadiene) (3.53 g, 13.3 mmol) and a slight excess of (2,6-i- PrPh) 2 DABMe- (5.43 g, 13.4 mmol, 1.01 equiv). An orange precipitate began to form immediately upon mixing. The reaction mixture was stirred overnight and the Et 2 0 and free COD were then removed via filtration.

The product was washed with an additional 25 mL of and then dried overnight in vacuo. A pale orange -109- 0206/03.swl33 11spa.109 .,owder (7.18 g, 95.8%) was isolated: 'H NMR (CD 2 C12, 400 MHz) 6 7.4 7.2 6, Haryi), 3.06 (septet, 2, J 6.81, CHMe 2 3.01 (septet, 2, J 6.89, C'HMe 2 2.04 and 2.03 1.40 6, J 6.79, C'HMeMe'), 1.36 6, J 6.76, CHMeMe'), 1.19 6, J 6.83, CHMeMe'), 1.18 6, J 6.87, C'HMeMe'), 0.36 3, PdMe); 1 3 C NMR (CD 2 C1 2 400 MHz) 6 175.0 and 170.3 142.3 and 142.1 (Ar, Ar': Cipso), 138.9 and 138.4 (Ar, Ar': Co), 128.0 and 127.1 (Ar, Ar': Cp), 124.3 and 123.5 (Ar, Ar': Cm), 29.3 (CHMe 2 28.8 (C'HMe 2 23.9, 23.8, 23.5 and 23.3 (CHMeMe', C'HMeMe'), 21.5 and 20.1 5.0 (JcH 135.0, PdMe).

110- 02/06/03,swl331 spa, Examnle 2 [(2,6-i-PrPh) 2 DAnH 2 ]PdMecl Following the procedure of Example 1, an orange powder was isolated in 97.1% yield: 1H NMR (CD 2 Cl 2 400 MHz) 6 8.31 and 8,.15 I each, 7.3 7.1 6, Haryl), 3.22 (septet, 2, J 6.80, CHlMe 2 3.21 (septet, 2, J 6.86, C'HMe 2 1.362, 1.356, 1.183 and 1.178 6 each, J 7.75 6.90; CHMeMe', C'HMeMe'), 0.67 3, PdMe); PC NMR

(CD

2

C

2 100 MHz) 6 164.5 (JCH 179.0, 160.6 (JC 178.0, 144.8 and 143.8 (Ar, Ar': Cips o 140.0 and 139.2 (Ar, Ar': CO), 128.6 and 127.7 (Ar, Ar': Cp), 124.0 and 123.4 (Ar, Ar': Cm), 29.1 (CMe2), 28.6 (C'HMe 2 24.7, 24.1, 23.1 and 22.7 (CHMeMe', C'HMeMe'), 3.0 (JCH 134.0, PdMe). Anal.

Calcd for (C 2 7

H

39 C1N 2 Pd): C, 60.79; H, 7.37; N, 5.25.

Found: C, 60.63; H, 7.24; N, 5.25.

Example 3 6 -MePh), 2 DABMe2J PdMeCl Following the procedure of Example 1, a yellow 'powder was isolated in 90.6% yield: 1H NMR (CD 2 C1 2 400 MHz) 6 7.3 6.9 6, Ha-,ryl), 2.22 6, Ar, Ar' Me), 2.00 and 1.97 0.25 3, PdMe).

Example 4 [(2,6-MePh) 2 DABMe 2 PdMeC1 Following the procedure of Example 1,.an orange powder was isolated in 99.0% yield: 1 H NMR (CD 2 Cl 2 400 MHz, 41 OC) 8 8.29 and 8.14 7.2 7.1 6, Haryl), 2.33 and 2.30 6 each, Ar, Ar': Me), 0.61 3, PdMe); 1 3 C NMR (CD 2 Cl 2 100 MHz, 41 OC) 6 165.1 (JCH 179.2, 161.0 (JCH 177.8 147.3 and 146.6 (Ar, Ar': Cipso), 129.5 and 128.8 (Ar, Ar': Co), 128.8 and 128.5 (Ar, Ar': Cm), 127.9 and 127.3 (Ar, Ar': Cp), 18.7 and 18.2 (Ar, Ar': Me), 2.07 (JCH 136.4, PdMe).

11 0206/03sw13311 Ispal I Example 5 -3 [4 -MePh) 2 DABMe,] PdMeCl Following the procedure of Example 1, a yellow powder was isolated in 92.1% yield: 1 H NMR (CD 2 C12, 400 MHz) 6 7.29 2, J 8.55, Ar:'Hm), 7.26 2, J 7.83, Ar': Hm), 6.90 2, J 8.24, Ho), 6.83 2, J 8.34, Ar: Ho), 2.39 6, Ar, Ar': Me), 2.15 and 2.05 3 each, 0.44 (s, 3, PdMe);' 13 C NMR (CD 2 C1 2 100 MHz) 6 176.0 and 169.9 144.9 and 143.7 (Ar, Ar': Cipso), 137.0 and 136.9 (Ar, Ar': Cp), 130.0 and 129.3 (Ar, Ar': Cm), 122.0 and 121.5 (Ar, Ar': Co), 21.2 20.1 (Ar, Ar': Me), 19.8 2.21 (JCH 135.3, PdMe). Anal. Calcd for (Ci9H 23 C1N 2 Pd): C, 54.17; H, 5.50; N, 6.65. Found: C, 54.41; H, 5.37; N, 6.69.

Example 6 [(4-MePh) 2

DABH

2 PdMeC1 Following the procedure of Example 1, a burnt orange powder was isolated in 90.5% yield: Anal. Calcd for (C 17

H

9 C1N 2 Pd): C, 51.93; H, 4.87; N, 7.12. Found: C, 51.36; H, 4.80; N, 6.82.

Example 7 [(2,6-i-PrPh) 2DABMe 2 ]PdMe 2 (-Cl))BAF- (25 mL) was added to a mixture of PrPh),DABMe,]PdMeCl (0.81 g, 1.45 mmol) and 0.5 equiv of NaBAF (0.64 g, 0.73 mmol) at room temperature. A golden yellow solution and NaC1 precipitate formed immediately upon mixing. The reaction mixture was stirred overnight and then filtered. After the EtO2 was removed in vacuo, the product was washed with 25 mL of hexane. The yellow powder was then dissolved in mL of CH 2 C1 2 and the resulting solution was filtered in order to removed traces of unreacted NaBAF. Removal of

CH

2 C1 2 in vacuo yielded a golden yellow powder (1.25 g, 1H NMR (CD 2 C1 2 400 MHz) 8 7.73 8, BAF: Ho), 7.57 4; BAF: Hp), 7.33 2, J 7.57, Ar: Hp), 7.27 4, J 7.69, Ar: Ho), 7.18 2, J 7.64, Ar: Hp), 7.10 4, J 7.44, Ar': Ho), 2.88 112- 02/0603,sw13311spa, 112 ts. -tet, 4, J 6.80, CHMe 2 2.75 (septet, 4, J 6 82, C'HMe 2 2.05 and 2.00 6 each, N=C(Me)- 1.22, 1.13, 1.08 and 1.01 12 each, J 6.61-6.99, CHMeMe', C'HMeMe'), 0.41 6, PdMe); 13

C

NMR (CD 2 C1 2 100 MHz) 6 177.1 and 171.2 162.2 JBC 49.8, BAF: Cipso), 141.4 and 141.0 (Ar, Ar': Cipso) 138.8 and 138.1 (Ar, Ar': Co), 135.2 (BAF: Cp), 129.3 JCF 31.6, BAF: Cm), 128.6 and 127.8 (Ar, Ar': Cp), 125.0 JCF 272.5, BAF: CF 3 124.5 and 123.8 (Ar, Ar': Cm), 117.9 (BAF: Cp), 29.3 (CHMe 2 29.0 (C'HMe 2 23.8, 23.7, 23.6 and 23.0 (CHMeMe', C'HMeMe'), 21.5 and 20.0 9.8 (JCH 136.0, PdMe). Anal. Calcd for '(C 90

H

98 BC1F 24

N

4 Pd 2

C,

55.41; H, 5.06; N, 2.87. Found: C, 55.83; H, 5.09; N, 2.63.

Example 8 [(2,6-i-PrPh) 2

DABH

2 PdMe) 2 (p-Cl))BAF- The procedure of Example 7 was followed with one exception, the removal of CH 2 C1 2 in vacuo yielded a product that was partially an oil. Dissolving the compound in EtO2 and then removing the EtO2 in vacuo yielded a microcrystalline red solid 1 H NMR

(CD

2 Cl 2 400 MHz) 6 8.20 and 8.09 2 each, N=C(H)- C' 7.73 8, BAF: Ho), 7.57 4, BAF: Hp), 7.37 2, J 7.73, Ar: Hp), 7.28 4, J 7.44, Ar: Ha), 7.24 2, Ar': Hp), 7.16 4, J 7.19, Ar': Hm), 3.04 (septet, 4, J 6.80, CHMe 2 2.93 (septet, 4, J 6.80, C'HMe 2 1.26 12, J 6.79, CHMeMe'), 1.14 .12, J 6.83, CHMeMe'), 1.11 12, J 6.80, C'HMeMe'), 1.06 12, J 6.79, C'HMeMe'), 0.74 6, PdMe); 13C NMR (CD 2 C1 2 100 MHz) 6 166.0 (JCH 180.4, 161.9 JBC 49.6, BAF: Cipso), 160.8 (JCH 179.9, 143.5 and 143.0 (Ar, Ar': Cipso), 139.8 and 138.9 (Ar, Ar': Co), 135.2 (BAF: Co), 129.3 JCF 31.4, BAF: Cm), 129.3 and 128.5 (Ar, Ar': Cp), 125.0 JCF 272.4, BAF: CF 3 124.3 and 123.7 (Ar, Ar': Cm), 117.9 (BAF: Cp), 29.2 and 28.9 (CHMe2, C'HMe 2 24.5, 24.1, 23.0, and 22.5 113- 02/0603.swl3311 sp, 113 (CHMeMe', C'HMeMe'), 10.3 (PdMe) Anal. C.-cd for (C8gH9oBC1F 2 4

N

4 Pd 2 C, 54.52; H, 4.97; N, 2.96.

Found: C, 54.97; H, 4.72; N, 2.71.

Example 9 Alternatively, the products of-Examples 7 and 8 have been synthesized by stirring a 1:1 mixture of the appropriate PdMeCl compound and NaBAF in Et2O for -1 h.

Removal of solvent yields the dimer 0.5 equiv of Na+(OEt 2 2 BAF Washing the product mixture with hexane yields ether-free NaBAF, which is insoluble in

CH

2 C1 2 Addition of CH 2 C12 to the product mixture and filtration of the solution yields salt-free dimer: 1H NMR spectral data are identical with that reported above.

For a synthesis of CODPdMe 2 see: Rudler- Chauvin, and Rudler, H. J. Organomet. Chem. 1977, 134, 115-119.

Example [(2,6-i-PrPh) 2 DABMe 2 PdMe 2 A Schlenk flask containing a mixture of PrPh) 2 DABMe 2 PdMeCl (2.00 g, 3.57 mmol) and 0.5 equiv of Me 2 Mg (97.2 mg, 1.79 mmol) was cooled to -78 OC, and the reaction mixture was then suspended in 165 mL of Et 2 O. The reaction mixture was allowed to warm to room temperature and then stirred for 2 h, and the resulting brown solution was then filtered twice. Cooling the solution to -30 oC yielded brown single crystals (474.9 mg, 24.6%, 2 crops): 1 H NMR (C 6

D

6 400 MHz) 6 7.2-7.1 6, Haryl), 3.17 (septet, 4, J 6.92, CHMe 2 1.39 12, J 6.74, CHMeMe'), 1.20 1.03 12, J 6.89, CHMeMe'), 0.51 6, PdMe); 3

C

NMR (C 6

D

6 100 MHz) 6 168.4 143.4 (Ar: Cipso) 138.0 (Ar: Co), 126.5 (Ar: Cp), 123.6 (Ar: Cm), 28.8 (CHMe 2 23.6 and 23.5 (CHMeMe'), 19.5 (N=C(Me)- -4.9 (JCH 127.9, PdMe). Anal. Calcd for

(C

3 oH 4 6

N

2 Pd): C, 66.59; H, 8.57; N, 5.18. Found: C, 66.77; H, 8.62; N, 4.91.

114 02 0 6 03 ,sw, 33 1 I sp.l 4 Example 11 [(2,6-i-PrPh) 2

DABH

2 )PdMe 2 The synthesis of this compound in a manner analogous to Example 10, using 3.77 mmol of ArN=C(H)- C(H)=NAr and 1.93 mmol of Me 2 Mg yielded 722.2 mg of a deep brown microcrystalline powder upon recrystallization of the product from a hexane/toluene solvent mixture.

This compound was also synthesized by the following method: A mixture of Pd(acac) 2 (2.66 g, 8.72 mmol) and corresponding diimine (3.35 g, 8.90 mmol) was suspended in'100 mL of Et20, stirred for 0.5 h at room temperature, and then cooled to -78°C. A solution of Me 2 Mg (0.499 g, 9.18 mmol) in 50 mL of EtO2 was then added via cannula to the cold reaction mixture. After stirring for 10 min at -780C, the yellow suspension was allowed to warm to room temperature and stirred for an additional hour. A second equivalent of the diimine was then added to the reaction mixture and stirring was continued for -4 days. The brown Et20 solution was then filtered and the solvent was removed in vacuo to yield a yellow-brown foam. The product was then .extracted with 75 mL of hexane, and the resulting solution was filtered twice, concentrated, and cooled to -30C overnight to yield 1.43 g of brown powder: -H NMR (C 6

D

6 400 MHz) 6 7.40 2, N=C(H)- 7.12 6, Haryl), 3.39 (septet, 4, J 6.86, CHMe 2 1.30 12, J 6.81, CHMeMe'), 1.07 12, J 6.91, CHMeMe'), 0.77 6, PdMe); 13 C NMR (C6D 6 100 MHz) 6 159.9 (JCH 174.5, 145.7 (Ar: Cipso) 138.9 (Ar: Co), 127.2 (Ar: Cp) 123.4 (Ar: Cm), 28.5 (CHMe 2 24.4 and 22.8 (CHMeMe'), -5.1 (JcH 128.3, PdMe). Anal. Calcd for (C 2 sH 4 2

N

2 Pd) C, 65.55, H, 8.25; N, 5.46. Found: C, 65.14; H, 8.12; N, 5.14.

115- 02A)6/03.sw13311 Ispl 11 [(2,6-MePh)2DABH 2 PdMe 2 This compound was synthesized in a manner similar to the second procedure of Example 11 (stirred for 5 h at rt) using 5.13 mmol of the corresponding diimine and 2.57 mmol of Me 2 Mg. After the reaction mixture was filtered, removal of Et 2 0 in vacuo yielded 1.29 g of a deep brown microcrystalline solid: 1H NMR

(C

6

D

6 100 MHz, 120C) 6 6.98 2, 6.95 6, Haryl), 2.13 12, Ar: Me), 0.77 6, PdMe); 13C NMR (C 6 Ds, 400 MHz, 120C) 6 160.8 (JCH 174.6, 147.8 (Ar: Cipso), 128.2 (Ar: Cm), 128.15 (Ar: Co), 126.3 (Ar: Cp), 18.2 (Ar: Me), (JCH 127.6, Pd-Me).

Example 13 (2,6-i-PrPh) 2 DABH2]NiMe 2 The synthesis of this compound has been reported (Svoboda, tom Dieck, H. J. Organomet. Chem. 1980, 191, 321-328) and was modified as follows: A mixture of Ni(acac) 2 (1.89 g, 7.35 mmol) and the corresponding diimine (2.83 g, 7.51 mmol) was suspended in 75 mL of Et 2 O and the suspension was stirred for 1 h at room temperature. After cooling the reaction mixture to 78C, a solution of Me 2 Mg (401 mg, 7.37 mmol) in 25 mL of Et20 was added via cannula. The reaction mixture was stirred for 1 h at -780C and then for 2 h at 0°C to give a blue-green solution. After the solution was filtered, the Et20 was removed in vacuo to give a bluegreen brittle foam. The product was then dissolved in hexane and the resulting solution was filtered twice, concentrated, and then cooled to -300C to give 1.23 g (35.9% one crop) of small turquoise crystals.

Example 14 [(2,6-i-PrPh) 2 DABMe 2 ]NiMe 2 The synthesis of this compound has been reported (Svoboda, tom Dieck, H. J. Organomet. Chem. 1980, 191, 321-328) and was synthesized according to the above modified procedure (Example 13) using Ni(acac)2 116- OM2o 0 3,sw 1331 sp 116 ;3.02 g, 11.75 mmoi), the corresponding diamine ;4.80 g, 11.85 mmol) and Me 2 Mg (640 mg, 11.77 mmol). A turquoise powder was isolated (620 mg, 10.7%).

Example (2,6-MePh) DABMe2 PdMe (MeCN) }BAF' To a mixture of [(2,6-MePh) 2 DABMe 2 ]PdMeCl (109.5 mg, 0.244 mmol) and NaBAF (216.0 mg, 0.244 mmol) were added 20 mL each of Et2O and CH 2 C1 2 and 1 mL of CH3CN.

The reaction mixture was then stirred for 1.5 h and then the NaC1 was removed via filtration. Removal of the solvent in vacuo yielded a yellow powder, which was washed with 50 mL of hexane. The product (269.6 mg, 83.8%) was then dried in vacuo: 1 H NMR (CD 2 C1 2 400 MHz) 5 7.73 8, BAF: Ho), 7.57 4, BAF: Hp), 7.22-7.16 6, Haryl), 2..23 6, Ar: Me), 2.17 (s, 6, Ar': Me), 2.16, 2.14, and 1.79 3 each, N=C(Me)- NCMe), 0.38 3, PdMe); 1 3 C NMR (CD 2 Ci 2 100 MHz) 6 180.1 and 172.2 162.1 JBC 49.9, BAF: Cipso), 142.9 (Ar, Ar': Co), 135.2 (BAF: Co), 129.3 (Ar: Cm), 129.2 JCF 30.6, BAF: Cm), 129.0 Cm), 128.4 (Ar: Cp), 128.2 (Ar: Co), 127.7 (Ar': Cp), 127.4 Co), 125.0 JCF 272.4, BAF: CF 3 121.8 (NCMe), 117.9 (BAF: Cp), 20.2 and 19.2 (N=C(Me)- 18.0 (Ar: Me),17.9 Me), 5.1 and 2.3 (NCMe, PdMe). Anal. Calcd for (CssH 4 2

BF

2 4

N

3 Pd) C, 50.12; H, 3.21; N, 3.19. Found: C, 50.13; H, 3.13, N, 2.99.

Example 16 (4 -MePh) 2 DABMe 2 PdMe (MeCN) }BAF' Following the procedure of Example 15, a yellow powder was isolated in 85% yield: IH NMR (CD 2 C1 2 400 MHz) 5 7.81 8, BAF: Ho), 7.73 4, BAF: Hp), 7.30 4, J 8.41, Ar, Ar': Hm), 6.89 2, J 8.26, Ar: Ho), 6.77 2, J 8.19, Ar': Ho), 2.39 6, Ar, Ar': Me), 2.24, 2.17 and 1.93 3 each, N=C(Me)- C' NCMe)Pd-Me; 1 3 C NMR (CD 2 C1 2 100 MHz) 6 180.7 and 171.6 162.1 JBC 49.8, BAF: Cipso), 143.4 and 142.9 (Ar, Ar': Cipso), 138.6 and 138.5 (Ar, -117 02/063,sw133JIspa 117 Cp), 135.2 (BAF: 130.6 and 130.4 (Ar, Ar': Cm), 129.3 JCF 31.6, BAF: Cm), 125.0 JCF 272.5, BAF: CF 3 122.1 (NCMe), 121.0 and 120.9 (Ar, Ar': CO), 117.9 (BAF: Cp), 21.5 (ArN=C(Me)), 21.1 (Ar, Ar': Me), 19.7 6.2 and 3.0 (NCMe, PdMe).

Anal. Calcd for (CS 3

H

3 8BF 24

N

3 Pd): C, 49.34; H, 2.97: N, 3.26. Found: C, 49.55; H, 2.93; N, 3.10.

Example 17 6-MePh) 2 DABMe 2 PdMe (Et, 2

BAF

A Schlenk flask containing a mixture of PrPh),DABMe 2 JPdMe 2 (501 mg, 0.926 mmol) and H'(OEt 2 2 BAF- (938 mg, 0.926 mmol) was cooled to -78 0

C.

Following the addition of 50 mL of Et20, the solution was allowed to warm and stirred briefly (-15 min) at room temperature. The solution was then filtered and the solvent was removed in vacuo to give a pale orange powder (1.28 g, which was stored at -30 0 C under an inert atmosphere: 11 NMR (CD 2 C1 2 400 MHz, -60 0

C)

6 7.71 8, BAF: H o 7.58 4, BAF: Hp), 7.4 6, Haryl), 3.18 4, J 7.10, O(CH 2

CH

3 2 2.86 (septet, 2, J 6.65, CHMe 2 2.80 (septet, 2, J 6.55, CIHMe 2 2.18 and 2.15 1.34, 1.29, 1.14 and 1.13 6 each, J 6.4-6.7, CHMeMe', C'HMeMe'), 1.06 J 6.9, O(CH 2

CH

3 2 0.33 3, PdMe); 1 3 C NMR (CD 2 Cl 2 100 MHz, -60 0 C) 5 179.0 and 172.1 161.4 JBC 49.7, BAF: Cipso), 140.21 and 140.15 (Ar, Ar': Cipso), 137.7 and 137.4 (Ar, Ar': Co), 134.4 (BAF: Cp), 128.3 JcF 31.3, BAF: Cm), 128.5 and 128.2 (Ar, Ar': Cp), 124.2

JCF

272.4, BAF: CF 3 117.3 (BAF: Cp), 71.5 (O(CH2CH3), 28.7 (CHMe 2 28.4 (C'HMe 2 23.7, 23.6, 23.1 and 22.6 (CHMeMe', C'HMeMe'), 21.5 and 20.7 14.2 (O(CH 2

CH

3 2 2 8.6 (PdMe). Anal. Calod for (CsH6 5

BF

24

N

2 OPd) C, 53.35; H, 4.48; N, 1.91. Found: C, 53.01; H, 4.35; N, 1.68.

118 O2/0603,sw 3311spl I1s Example 19 [(2,6-MePh) 2 DABH,] PdMe (Et 2 O) BAF Following the procedure of Example 17, an orange powder was synthesized in 94.3% yield and stored at 300C: 'H NMR (CD 2 Cl 2 400 MHz, -60 0 C) 6 8.23 and 8.20 1 each, 7.72 8, BAF: Ho), 7.54 4, BAF: Hp), 7.40 7.27 6, Haryi), 3.32 4, J 6.90, O(CH 2

CH

3 2 3.04 and 3.01 (septets, 2 each, J 6.9 7.1, CHMe 2 and C'HMe 2 1.32, 1.318, 1.14 and 1.10 6 each, J 6.5 6.8, CHMeMe' and C'HMeMe'), 1.21 6, J 6.93, O(CH 2

CH

3 2 0.70 3, PdMe); 1 3 C NMR (CD 2 C1 2 100 MHz, -600C) 5 166.9 (JCH 182.6, 161.5 (JBC 49.7, BAF: Cipso). 161.3 (JCH 181.6, N=C' 143.0 and 141.8 (Ar, Ar': Cipso), 138.7 and 137.8 (Ar, Ar': Co), 134.4 (BAF: Co), 129.1 and 128.8 (Ar, Ar': Cp), 128.3 (JCF 31.3, BAF: Cm), 124.0 and 123.9 (Ar, Ar': Cm), 117.3 (BAF: Cp), 72.0

(O(CH

2

CH

3 2 28.5 and 28.4 (CHMe 2 CHMe 2 25.2, 24.1, 21.9 and 21.7 (CHMeMe', C'HMeMe'), 15.2 (O(CH 2

CH

3 2 11.4 (JH 137.8, PdMe). Anal. Calcd for (Cs 63

H

1

BF

24

N

2 OPd): C, 52.72; H, 4.28; N, 1.95. Found: C, 52.72; H, 4.26; N, 1.86.

Example 9 [(2,6-MePh) ,DABMe,]NiMe(Et 2

O)BAF

Following the procedure of Example 17, a magenta powder was isolated and stored at -30 0 C: 1 H NMR

(CD

2 Cl2, 400 MHz, -60 0 C; A H 2 0 adduct and free were observed.) 5 7.73 8, BAF: Ho), 7.55 4, BAF: Hp), 7.4 7.2 6, Hayl), 3.42 2, OH 2 3.22 4, O(CH 2

CH

3 2 3.14 and 3.11 (septets, 2 each, J 7.1, CHMe 2 C'HMe 2 1.95 and 1.78 3 each, 1.42, 1.39, 1.18 and 1.11 (d, 6 each, 3 6.6 6.9, CHMeMe' and C'HMeMe'), 0.93 (t, J 7.5, C(CH 2 CH3) 2 -0.26 (s NiMe); 13C NMR

(CD

2 C1 2 100 MHz, -58oC) 6 175.2 and 170.7 161.6 JBC 49.7, BAF: Cipso), 141.2 (Ar: Cipso), 139-.16 and 138.68 (Ar, Ar': Co), 136.8 Cipso) 134.5 (BAF: Co), 129.1 and 128.4 (Ar, Ar': Cp), 128.5 119- 02MOW03.sw1331 Isr, 19 JCF 32.4, BAF: C) 125.0 and 124.2 (Ar, Ar': Cm), 124.3 JCF 272.5, BAF: CF3), 117.4 (BAF: Cp), 66.0 (0(CH 2

CH

3 2 29.1 (CHMe 2 28.9 (C'HMe 2 23.51, 23.45, 23.03, and 22.95 (CHMeMe', C'HMeMe'), 21.0 and 19.2 14.2 (OCH 2

CH

3 2 -0.86 (JCH 131.8, NiMe). Anal. Calcd for (C 65

H

65

BF

24

N

2 NiO) C, 55.15; H, 4.63; N, 1.98. Found: C, 54.74; H, 4.53; N, 2.05.

Example (-(2,6-MePh) 2DABH 2 NiMe (Et,0) BAF Following the procedure of Example 17, a purple powder was obtained and stored at -30 0 C: 1 H NMR

(CD

2 C1 2 400 MHz, -80 0 C; H20 and Et20 adducts were observed in an 80:20 ratio, respectively.) 6 8.31 and 8.13 0.8 each, H20 Adduct), 8.18 and 8.00 0.2 each, Et20 Adduct), 7.71 8 BAF: Co), 7.53 4, BAF: Cp), 7.5 6, Haryl), 4.21 1.6, OH 2 3.5 3.1 8,

O(CH

2

CH

3 2 CHMe 2 C'HMe 2 1.38, 1.37, 1.16 and 1.08 4.8 each, CHMeMe', C'HMeMe'; H20 Adduct; These peaks overlap with and obscure the CHMe 2 doublets of the Et 2 0 adduct.), 0.27 2.4, PdMe; H20 Adduct), 0.12 0.6, PdMe: Et20 Adduct).

Examples 21-23 The rate of exchange of free and bound ethylene was determined by IH NMR line broadening experiments at 0 C for complex see the Table below. The NMR instrument was a 400 MHz Varian® NMR spectrometer.

Samples were prepared according to the following procedure: The palladium ether adducts PrPh) 2 DABMe 2 PdMe(OEt 2 }BAF, PrPh) 2 An]PdMe(OEt 2 }BAF, and PrPh)2DABH 2 ]PdMe(OEt 2 )}BAF were used as precursors to and were weighed (-15 mg) in a tared 5 mm dia.

NMR tube in a nitrogen-filled drybox. The tube was then capped with a septum and Parafilm® and cooled to -800C. Dry, degassed CD 2 C1 2 (700 pL) was then added to the palladium complex via gastight syringe, and the 120 0 2 06 /03,sw 3 tspa,12 0 cube was shaken and warmed briefly to give a homogeneous solution. After acquiring a -850C NMR spectrum, ethylene was added to the solution via gastight syringe and a second NMR spectrum was acquired at -85 0 C. The molarity of the BAF counterion was calculated according to the moles of the ether adduct placed in the NMR tube. The molarity of (XI) and free ethylene were calculated using the BAF peaks as an internal standard. Line-widths were measured at half-height in units of Hz for the complexed ethylene signal (usually at 5 to 4 ppm) and were corrected for line widths (Wo) in the absence of exchange.

For (XI) the exchange rate was determined from the standard eauation for the slow exchange approximation: k (W where is the molar concentration of ethylene.

These experiments were repeated twice and an average value is reported below.

Rate Constants for Ethylene Exchange a k Ex. (XI) (L-M s-1 21 [(2,6-i-PrPh) 2 DABMe 2 PdMe() }BAF 22 [(2,6-i-PrPh) 2 An]PdMe(=))BAF 520 23 ({(2,6-i-PrPh) 2 DABH2]PdMe(=))BAF 8100 aThe Ti of free ethylene is 15 sec. A pulse delay of 60 sec and a 300 pulse width were used.

Example 24 Anhydrous FeC 2 1 (228 mg, 1.8 mmol) and (2,6-i- PrPh) 2 DABAn (1.0 g, 2.0 mmol) were combined as solids and dissolved in 40 ml of CH 2 C1 2 The mixture was stirred at 25CC for 4 hr. The resulting green soluzion was removed from the unreacted FeC1 2 via filter cannula. The solvent was removed under reduced 121 02/06/03.sw13 3 11 spa121 aressure resulting in a green solid (0.95 g, 84% yield).

A portion of the green solid (40 mg) was immediately transferred to another Schlenk flask and dissolved in 50 ml of toluene under 1 atm of ethylene.

The solution was cooled to 0°C, and 6 ml of a 10% MAO solution in toluene was added. The resulting purple solution was warmed to 25 0 C and stirred for 11 hr. The polymerization was quenched and the polymer precipitated by acetone. The resulting polymer was washed with 6M HC1, water and acetone. Subsequent drying of the polymer resulted in 60 mg of white polyethylene. H NMR (CDC1 3 200 MHz) 61.25 (CH, CH) 6 0.85 CH,).

Example (2-t-BuPh)2DABMe 2 A Schlenk tube was charged with 2-t-butylaniline (5.00 mL, 32.1 mmol) and 2,3-butanedione (1.35 mL, 15.4 mmol). Methanol (10 mL) and formic acid (1 mL) were added and a yellow precipitate began to form almost immediately upon stirring. The reaction mixture was allowed to stir overnight. The resulting yellow solid was collected via filtration and dried under vacuum.

The solid was dissolved in ether and dried over Na2S04 for 2-3 h. The ether solution was filtered, condensed and placed into the freezer (-300C). Yellow crystals were isolated via filtration and dried under vacuum overnight (4.60 g, 1 H NMR (CDC13, 250 MHz) 6 7.41(dd, 2H, J 7.7, 1.5 Hz, Hm), 7.19 (td, 2H, J= 1.5 Hz, Hm or Hp), .7.07 (td, 2H, J 7.6, 1 6 Hz, Hm or Hp), 6.50 (dd, 2H, J 7.7, 1.8 Hz, Ho), 2.19 6H, N=C(Me)-C(Me)=N) 1.34 18H, C(CH3)3) Examples 26 and 27 General Polymerization Procedure for Examples 26 and 27: In the drybox, a glass insert was loaded with [(13-C 3

H

5 )Pd(p-Cl)] 2 (11 mg, 0.03 mmol), NaBAF (53 mg, 0.06 mmol), and an a-diimine ligand (0.06 mmol). The insert was cooled to -350C in the drybox freezer, 5 mL 122- 02/0603,sw133 I sp,12 2 jf C 6 D6 was added to the cold insert, and the insert was then capped and sealed. Outside of the drybox, the cold tube was placed under 6.9 MPa of ethylene and allowed to warm to RT as it was shaken mechanically for 18 h. An aliquot of the solution was used to acquire a 1H NMR spectrum. The remaining portion was added to mL of MeOH in order to precipitate the polymer.

The polyethylene was isolated and dried under vacuum Example 26 a-Diimine was (2,6-i-PrPh) 2 DABMe 2 Polyethylene mg) was isolated as a solid. 1 H NMR spectrum

(C

6

D

6 is consistent with the production of 1- and 2butenes and branched polyethylene.

Example 27 a-Diimine was (2,6-i-PrPh) 2 DABAn. Polyethylene (17 mg) was isolated as a solid. 1 H NMR spectrum

(C

6

D

6 is consistent with the production of branched polyethylene.

Example 28 [(2,6-i-PrPh) 2

DABH

2 ]NiBr 2 The corresponding diimine (980 mg, 2.61 mmol) was dissolved in 10 mL of CH 2 C1l in a Schlenk tube under a

N

2 atmosphere. This solution was added via cannula to a suspension of (DME)NiBr 2 (DME 1,2-dimethoxyethane) (787 mg, 2.55 mmol) in CH 2 Cl 2 (20 mL). The resulting red/brown mixture was stirred for 20 hours. The solvent was evaporated under reduced pressure resulting in a red/brown solid. The product was washed with 3 x mL of hexane and dried in vacuo. The product was isolated as a red/brown powder (1.25 g, 82% yield).

Example 29 6-i-PrPh) DABMe 2 ]NiBr 2 Using a procedure similar to that of Example 28, 500 mg (1.62 mmol) (DME)NiBr 2 and 687 mg (1.70 mmol) of the corresponding diimine were combined. The product was isolated as an orange/brown powder (670 mg, 67% yield).

123- OQ2 03,sw13 3 1 I sp.12 3 Example 6-MePh) 2

DABH

2 ]NiBr, Using a procedure similar to that of Example 28, 500 mg (1.62 mmol) (DME)NiBr 2 and 448 mg (1.70 mmol) of the corresponding diimine were combined. The product was isolated as a brown powder (622 mg, 80% yield).

Example 31 [(2,6-i-PrPh) 2 DABAn]NiBr 2 Using a procedure similar to that of Example 28, 500 mg (1.62 mmol) (DME)NiBr 2 and 850 mg (1.70 mmol) of the corresponding diimine were combined. The product was isolated as a red powder (998 mg, 86% yield).

Anal. Calcd. for C36H 40

N

2 Br 2 Ni: C, 60.12; H, 5.61; N, 3.89. Found C, 59.88; H, 5.20; N, 3.52.

Example 32 [(2,6-MePh) 2 DABAn)NiBr 2 The corresponding diimine (1.92 g, 4.95 mmol) and (DME)NiBr 2 (1.5 g, 4.86 mmol) were combined as solids in a flame dried Schlenk under an argon atmosphere. To this mixture 30 mL of CH 2 C1 2 was added giving an orange solution. The mixture was stirred for 18 hours resulting in a red/brown suspension. The CHC1 2 was removed via filter cannula leaving a red/brown solid.

The product was washed with 2 x 10 mL of CHC1 2 and dried under vacuum. The product was obtained as a red/brown powder (2.5 g, 83% yield).

Example 33 [(2,6-MePh)2DABMe2]NiBr 2 Using a procedure similar to that of Example 32, the title compound was made from 1.5 g (4.86 mmol) (DME)NiBr 2 and 1.45 g (4.95 mmol) of the corresponding diimine. The product was obtained as a brown powder (2.05 g, 81% yield).

Example 34 [(2,6-i-PrPh) 2DABMe 2 PdMeCl (COD)PdMeCl (9.04 g, 34.1 mmol) was dissolved in 200 ml of methylene chloride. To this solution was added the corresponding diimine (13.79 g, 34.1 mmol) -7 124 02/06/03,sw 3311sp. 124 .he resulting solution rapidly changed color from yellow to orange-red. After stirring at room temperature for several hours it was concentrated to form a saturated solution of the desired product, and Scooled to -40°C overnight. An orange solid crystallized from the solution, and was isolated by filtration, washed with petroleum ether, and dried to afford 12.54 g of the title compound as an orange powder. Second and third crops of crystals obtained from the mother liquor afforded an additional 3.22 g of product. Total yield 87%.

Examples 35-39 The following compounds were made by a method similar to that used in Example 34.

Example Compound [(2,6-i-PrPh) 2 DABH PdMeC1 36 (2,6-i-PrPh) 2 DABAn] PdMeC1 37 2 DABMe] PdMeCl 38 [(2,6-EtPh) 2 DABMe] PdMeCl 39 6-MePh) 2 DABMe,] PdMeCl Note: The diethyl ether complexes described in Examples 41-46 are unstable in'non-coordinating solvents such as methylene chloride and chloroform.

They are characterized by 1H NMR spectra recorded in

CD

3 CN; under these conditions the acetonitrile adduct of the Pd methyl cation is formed. Typically, less than a whole equivalent of free diethylether is observed by IH NMR when 2 DAB(R')2]PdMe (OEt 2 )X is dissolved in CD 3 CN. Therefore, it is believed the complexes designated as "{[(R)2DAB(R')2]PdMe(OEt 2

)X"

below are likely mixtures of 2

DAB(R')

2 ]PdMe(OEt 2 and (R) 2

DAB(R')

2 ]PdMeX, and in the latter complexes the X ligand (SbF 6

BF

4 or

PF

6 is weakly coordinated to palladium. A formula of the type [(R)2DAB(R')2]PdMe(OEt) is a "formal" way of conveying the approximate overall composition of 125 02/06/03,sw3311 spa,125 this compound, but may not accurately depict the exact coordination to the metal atom.

Listed below are the 13 C NMR data for Example 36.

13C NMR data £req-ppm 46.5568 44.9321 40.8118 40.3658 39.5693 38.7782 38.6295 38.2844 38.1198 37.8384 37.5198 37.2384 37.1163 36.7446 36.0012 35.7198 34.2278 32.9216 32.619 32.4172 32.1995 31.9765 31.8809 30.4686 30.3199 30.0225 29.7411 29.311 28.7111 28.2597 27.1659 27.0067 26.1146 24.5642 22.6368 20.1413 19.7271 17.5236 14.2528 13.8812

TCB,

intensity 24.6005 3.42517 55.4341 145.916 18.458 4.16118 5.84037 8.43098 8.29802 3.83966 13.4977 23.,4819 16.8339 114.983 6.19217 5.17495 4.83958 20.2781 3.6086 2.98497 10.637 42.2547 143.871 27.9974 47.1951 36.1409 102.51 4.83244 117.354 9.05515 22.5725 5.81855 13.5772 2.59695 12.726 3.7815 20.0959 7.01554 3.03535 12.3635 120C, 0.05M CrAcAc 1 cmp and/or 1,3 ccmcc 1,3 cmc 2 pmp 1,3 pmp methylenes from- 2 cmp and/or 2 cmc 3B6+, 3EOC

POB

2B 5 2EOC 2B 3

IB

1 end group 1B 3

IB

4 1EOC ExampleAa C (4-Me 2 NPh) 2 DABMe 2 PdMe (MeCN) }SbF 6 -MeCN 126 0 2 /6/0 3 ,swl33tIspa,126 A procedure analogous to that used in Example 54, using (4-Me 2 NPh) 2 DABMe 2 in place of (2-C6H 4 -tBu) 2 DABMe 2 afforded {[(4-NMe 2 Ph) 2 DABMe 2 ]PdMe(MeCN) JSbF 6 .MeCN as a purple solid (product was not recrystallized in this instance). 1 H NMR (CD 2 Cl 2 5 6.96 2H, Haryl), 6.75 (mult, 6H, Haryl), 3.01 6H, NMe 2 2.98 6H, NMe' 2 2.30, 2.18, 2.03, 1.96 3H each, N=CMe, N=CMe', and free and coordinated NMCMe), 0.49 3H, Pd-Me).

Example 41 [(2,6-i-PrPh) 2 DABMe] PdMe (Et 2 0),JSbF 6 [(2,6-i-PrPh) 2 DABMe 2 ]PdMeCI (0.84 g, 1.49 mmol) was suspended in 50 mL of diethylether and the mixture cooled to -40 0 C. To this was added AgSbF 6 (0.52 g, 1.50 mmoli. The reaction mixture was allowed to warm to room temperature, and stirred at room temperature for 90 min. The reaction mixture was then filtered, giving a pale yellow filtrate and a bright yellow precipitate. The yellow precipitate was extracted with 4 x 20 mL 50/50 methylene chloride/diethyl ether. The filtrate and extracts were then combined with an additional 30 mL diethyl ether. The resulting solution was then concentrated to half its original volume and 100 mL of petroleum ether added. The resulting precipitate was filtered off and dried, affording 1.04 g of the title compound as a yellow-orange powder (83% yield). IH NMR (CD 3 CN) 6 7.30 (mult, 6H, Haryl), 3.37 free O(CH 2

CH

3 2 3.05-2.90 (overlapping sept's, 4H, CHMe:), 2.20 3H, N=CMe), 2.19 3H, N=CMe'), 1.35-1.14 (overlapping d's, 24H, CHMe 2 1.08 free

O(CH

2

CH

3 2 0.28 3H, Pd-Me). This material contained 0.4 equiv of Et20 per Pd, as determined by 1H NMR integration.

Example 42 6-i-PrPh) 2 DABMe 2 )PdMe(Et 2 BF4 A,procedure analogous to that used in Example 41, using AgBF 4 in place of AgSbF 6 afforded the title compound as a mustard yellow powder in 61% yield. This 127- 02/06/03.swl331 Ispa,127 material contained 0.3 equiv of Et20 per Pd, as determined by 1- NMR integration. 1H NMR in CD 3 CN was otherwise identical to that of the compound made in Example 41.

Example 43 S[(2,6-i-PrPh) 2 DABMe 2 PdMe (Et 2 0),)PF, A procedure analogous to that used in Example 41, using AgPF 6 in place of AgSbF 6 afforded the title compound as a yellow-orange powder in 72% yield. This material contained 0.4 equiv of Et20 per Pd, as determined by 1H NMR integration. 1H NMR in CD 3 CN was identical to that of the compound of Example 41.

Example 44 [(2,6-i-PrPh) DABH) PdMe (Et 2 0)n}SbF6 A procedure analogous to that used in Example 41, using [(2,6-i-PrPh) 2 DABH2] PdMeCl in place of PrPh) 2 DABMe 2 ]PdMeCl, afforded the title compound in 71% yield. 1H NMR (CD 3 CN) 8 8.30 2H, N=CH and N=CH'), 7.30 6H, Haryl), 3.37 free O(CH 2

CH

3 2 1, 3.15 (br, 4H, CRMe 2 1.40-1.10 (br, 24H, CHMe 2 1.08 (t, free O(CH 2

CH

3 2 0.55 3H, Pd-Me). This material contained 0.5 equiv of EtO2 per Pd, as determined by 1H NMR integration.

Example [(2,4,6-MePh) 2DABMe2 PdMe (Et 2 O)n}SbF6 1(2,4,6-MePh) 2 DABMe 2 ]PdMeCl (0.50 g, 1.05 mmol) was partially dissolved in 40 mL 50/50 methylene chloride/diethylether. To this mixture at room temperature was added AgSbF 6 (0.36 g, 1.05 mmol). The resulting reaction mixture was stirred at room temperature for 45 min. It was then filtered, and the filtrate concentrated in vacuo to afford an oily solid.

The latter was washed with diethyl ether and dried to afford the title compound as a beige powder. H NMR

(CD

3 CN) 8 6.99 4H, Haryl), 3.38 free

O(CH

2

CH

3 2 2.30-2.00 (overlapping s's, 24H, N=CMe, N=CMe' and aryl Me's), 1.08 free O(CH 2

CH

3 2 0.15 128- 020603sw1331spa,128 .4H, CHMe 2 2.29 3H, N=CMe), 2.28 TH, N=CMe'), 1.81 3H, N-CMe), 1.37-1.19 (overlapping d's, 24H, CHMe's), 0.40 3H, Pd-Me). This compound can also be prepared by addition of acetonitrile to PrPh) 2 DABMe 2 PdMe (EtO) )SbF6 Example 49 DABMe 2 PdMe (MeCN) }SbFr A procedure analogous to that used in Example 48, using [(Ph) 2 DABMe 2 ]PdMecl in place of PrPh) 2 DABMe 2 ]PdMeCl, afforded the title compound as a yellow microcrystalline solid upon recrystallization from methylene chloride petroleum ether. This complex crystallizes as the acetonitrile solvate from acetonitrile solution at -40 0 C. 1H NMR of material recrystallized from methylene chloride/petroleum ether: (CDC13) 6 7.46 (mult, 4H, Haryl), 7.30 2H, Haryl), 7.12 2H, Haryl), 7.00 2H, Haryl), 2.31 3H, N=CMe), 2.25 3H, N=CMe'), 1.93 3H, N=CMe), 0.43 3H, Pd-Me).

Example S[(2,6-EtPh) 2 DABMe2J PdMe (MeCN) }BAF' [(2,6-EtPh) 2 DABMe 2 ]PdMeCl (0.200 g, 0.396 mmol) was dissolved in 10 mL of acetonitrile to give an orange solution.. To this was added NaBAF (0.350 g, 0.396 mmol). The reaction mixture turned bright yellow and NaC1 precipitated. The reaction mixture was stirred at room temperature for 30 min and then filtered through a Celite® pad. The Celite® pad was extracted with 5 mL of acetonitrile. The combined filtrate and extract was concentrated in vacuo to afford an orange solid, recrystallization of which from methylene chloride petroleum ether at -40 0 C afforded 0.403 g of the title compound as orange crystals (Yield 1H NMR (CDC1 3 5 7.68 8H, Hortho of anion), 7.51 4H, Hpara of anion), 7.33-7.19 (mult, 6H, Haryl of cation), 2.56-2.33 (mult, 8H, CH 2 CH3), 2.11 3H, N=CMe), 2.09 3H, N=CMe'), 1.71 3H, NsCMe), 1.27-1.22 (mult, 12H, CH 2

CH

3 0.41 3H, Pd-Me).

129- 02/06/03,sw1331 Isp, 12 9 3H, Pd-Me). This material contained-'.7 equiv of per Pd, as determined by 1 H MR integration.

Example 46 [(2,6-i-PrPh) DABAn] PdMe (Et 2 0)nSbF 6 A procedure analogous to that used in Example 41, using [(2,6-i-PrPh) 2 DABAn]PdMeC1 in place of PrPh) 2 DABMe 2 ]PdMeCl, afforded the title compound in 92% yield. 1 H NMR (CD 3 CN) 6 8.22 (br t, 2H, Haryl), 7.60- 7.42 (br mult, 8H, Haryl), 6.93 (br d, 1H, Haryl), 6.53 (br d, 1H, Haryl), 3.38 free O(CH 2

CH

3 2 3.30 (br mult, 4H, CHMe 2 1.36 (br d, 6H, CHMe 2 1.32 (br d, 6H, CHMe 2 1.08 free O(CH 2

CH

3 2 1.02 (br d, 6H, CHMe 2 0.92 (br d, 6H, CHMe 2 0.68 3H, Pd-Me).

The amount of ether contained in the product could not be determined precisely by-1H NMR integration, due to overlapping resonances.

Example 47 i PrPh) 2 DABMe 2 PdMe (OSOzCF 3 A procedure analogous to that used in Example 41, using AgOSO 2

CF

3 in place of AgSbF 6 afforded the title compound as a yellow-orange powder. 1H NMR in CD 3

CN

was identical to that of the title compound of Example 41, but without free ether resonances.

Example 48 [(2,6-i-PrPh) 2 DABMe2]PdMe(MeCN) }SbF 6 [(2,6-i-PrPh) 2 DABMe 2 ]PdMeCl (0.40 g, 0.71 mmoil was dissolved in 15 mL acetonitrile to give-an orange solution. To this was added AgSbF 6 (0.25 g, 0.71 mmol) at room temperature. AgC1 immediately precipitated from the resulting bright yellow reaction mixture. The mixture was stirred at room temperature for 3 h. It was then filtered and the AgC1 precipitate extracted with 5 mL of acetonitrile. The combined filtrate and extract were concentrated to dryness affording a yellow solid. This was recrystallized from methylene chloride/petroleum ether affording 0.43 g of the title compound as a bright yellow powder (Yield 1H NMR (CDC13) 5 7.35-7.24 (mult, 6H, Haryl), 2.91 (mult, 130- 0210603.sw1331 I sl. 1 3 0 Example 51 {[(2,6-EtPh) 2 DABMe2]PdMe(MeCN) }SbF( A procedure analogous to that used in Example using AgSbF 6 in place of NaBAF, afforded the title compound as yellow crystals in 99% yield after recrystallization from methylene chloride/petroleum ether at Example 52 [(COD)PdMe(NCMe)]SbF 6 To (COD)PdMeCl (1.25 g, 4.70 mmol) was added a solution of acetonitrile (1.93 g, 47.0 mmol) in 20 mL methylene chloride. To this clear solution was added AgSbF 6 (1.62 g, 4.70 mmol). A white solid immediately precipitated. The reaction mixture was stirred at room temperature for 45 min, and then filtered. The yellow filtrate was concentrated to dryness, affording a yellow solid. This was washed with ether and dried, affording 2.27 g of [(COD)PdMe(NCMe)]SbF 6 as a light yellow powder (yield 1 H NMR (CD 2 C1 2 6 5.84 (mult, 2H, CH=CH), 5.42 (mult, 2H, 2.65 (mult, 4H, CHH'), 2.51 (mult, 4H, CHH'), 2.37 3H, NCMe), 1.18 3H, Pd-Me).

Example 53 [(COD)PdMe(NCMe) BAF A procedure analogous to that used in Example 52, using NaBAF in place of AgSbF 6 afforded the title compound as a light beige powder in 96% yield.

131 02/06O3,swI 31 Ispa.1 3 1 Example 54 [(2-t-BuPh)DABMe2 PdMe (MeCN) }SbF, To a suspension of (2-t-BuPh) 2 DABMe 2 (0.138 g, 0.395 mmol) in 10 mL of acetonitrile was added [(COD)PdMe(NCMe)]SbF 6 (0.200 g, 0.395 mmol). The resulting yellow solution was stirred at room temperature for 5 min. It was then extracted with 3 x mL of petroleum ether. The yellow acetonitrile phase was concentrated to dryness, affording a bright yellow powder. Recrystallization from methylene chloride/petroleum ether at -40 °C afforded 180 mg of the title product as a bright yellow powder (yield 1H NMR (CD 2 C1 2 6 7.57 (dd, 2H, Haryl) 7.32 (mult, 4H, Haryl), 6.88 (dd, 2H, Haryl), 6.78 (dd, 2H, Haryl), 2.28 3H, N=CMe)-, 2.22 3H, N=CMe'), 1.78 3H, NsCMe), 1.48 18H, tBu), 0.52 3H, Pd- Me).

Example [(Np) 2 DABMe 2 PdMe (MeCN) }SbF 6 A procedure analogous to that used in Example 54, using (Np) 2 DABMe 2 in place of (2-t-BuPh) 2 DABMe 2 afforded the title compound as an orange powder in 52% yield after two recrystallizations from methylene chloride/petroleum ether. 1H NMR (CD 2 Cl 2 6 8.20-7.19 (mult, 14 H, Haromatic), 2.36 J 4.3 Hz, 3H, N=CMe), 2.22 J 1.4 Hz, 3H, N=CMe'), 1.32 3H, NCMe), 0.22 3H, Pd-Me).

Example 56 [(Ph 2 CH) DABH 2 PdMe (MeCN) }SbF 6 A proced-re analogous to that used in Example 54, using (PhCH) 2

DABH

2 in place of (2-t-BuPh) 2 DABMe 2 afforded the title compound as a yellow microcrystalline solid. -H NMR (CDC1 3 6 7.69 1H, N=CH), 7.65 1H, 7.44-7.08 (mult, Haryl), 6.35 2H, CHPh 2 1.89 3H, NCMe), 0.78 3H, Pd-Me).

132 02/06/03,swl33lspa,132 Example 57 S[(2-PhPh),DABMe 2 ]PdMe(MeCN) }SbF 6 A procedure analogous to that used in Example 54, using (2-PhPh) 2 DABMe 2 in place of (2-t-BuPh) 2 DABMe 2 afforded the title compound as a yellow-orange powder in 90% yield. Two isomers, due to cis or trans orientations of the two ortho phenyl groups on either side of the square plane, were observed by 1I NMR. 1

H

NMR (CD 2 C!2) 5 7.80-6.82 (mult, 18H, Haryl), 1.98, 1.96, 1.90, 1.83, 1.77, 1.73 (singlets, 9H, N=CMe, N=CMe', NCMe for cis and trans isomers), 0.63, 0.61 (singlets, 3H, Pd-Me for cis and trans isomers).

Example 58 [(Ph)2DAB (cyclo-CMe2CH 2 CMe,-) PdMe(MeCN) }BAF To a solution of [(COD)PdMe(NCMe)]BAF- (0.305 g, 0.269 mmol) dissolved in 15 mL of acetonitrile was added N,N'-diphenyl-2,2',4,4'-tetramethylcyclopentyldiazine (0.082 g, 0.269 mmol). A gold colored solution formed rapidly and was stirred at room temperature for 20 min. The solution was then extracted with 4 x 5 mL petroleum ether, and the acetonitrile phase concentrated to dryness to afford a yellow powder. This was recrystallized from methylene chloride/petroleum ether at -40 0 C to afford 0.323 g of the title compound as a yellow-orange, crystalline solid. 1H NMR (CDC1 3 5 7.71 8H, Hortho of anion), 7.54 4H, Hpara of anion), 7.45-6.95 (mult, 10H, Haryl of cation), 1.99 2H, CH2), 1.73 3H, NCMe), 1.15 6H, Me 2 1.09 6H, Me' 2 0.48 3H, Pd-Me).

Example 59 ([(2,6-i-PrPh) 2 DABMe 2 ]Pd(CH 2

CH

2 CH2CO2Me) }SbF6 Under a nitrogen atmosphere PrPh) 2 DABMe2]PdMe(EtO0)}SbF 6 (3.60 g, 4.30 mmol) was weighed into a round bottom flask containing a magnetic stirbar. To this was added a -40°C solution of methyl acrylate (1.85 g, 21.5 mmol) dissolved in 100 ml of methylene chloride. The resulting orange solution was 133- 0206/03,sw 1311 spa 133 itirred for 10 min, while being allowed to warm to room temperature. The reaction mixture was then concentrated to dryness, affording a yellow-brown solid. The crude product was extracted with methylene chloride, and the- orange-red extract concentrated, layered with an equal volume of petroleum ether, and cooled to -400C. This afforded 1.92 g of the title compound as yellow-orange crystals. An additional 1.39 g was obtained as a second crop from the mother liquor; total yield 91%. IH NMR (CD 2 Cl 2 6 7.39-7.27 (mult, 6H, Haryl), 3.02 3H, OMe), 2.97 (sept, 4H, CHMe 2 2.40 (mult, 2H, CH 2 2.24 3H, N=CMe), 2.22 3H, N=CMe'), 1.40-1.20 (mult, 26H, CHMe 2 and CH2'), 0.64 (mult, 2H, CH 2 Example [(2,6-i-PrPh)2DABH2]Pd(CH2CH2CH2CO2Me) }SbF, AgSbF6 (0.168 g, 0.489 mmol) was added to a -400C solution of {[(2,6-i-PrPh)2DABH2]PdMeCl (0.260 g, 0.487 mmol) and methyl acrylate (0.210 g, 2.44 mmol) in 10 mL methylene chloride. The reaction mixture was stirred for 1 h while warming to room temperature, and then filtered. The filtrate was concentrated in vacuo to give a saturated solution of the title compound, which was then layered with an equal volume of petroleum ether and cooled to -40 0 C. Red-orange crystals precipitated from the solution. These were separated by filtration and dried, affording 0.271 g of the title compound (68% yield). 1H NMR (CD 2 C1 2 6 8.38 1H, N=CH), 8.31 1H, 7.41-7.24 (mult, 6H, Haryl), 3.16 (mult, 7H, OMe and CHMe 2 2.48 (mult, 2H,

CH

2 1.65 2H, CH 2 1.40-1.20 (mult, 24H, CHMe 2 0.72 (mult, 2H, CH2' Example 61 PrPh) 2 DABMe 2 Pd (CH2CH2CH2CO2Me) [B(C 6

F

5 3 Cl) [(2,6-i-PrPh)2DABMe 2 ]PdMeCl (0.038 g, 0.067 mmol) and methyl acrylate (0.028 g, 0.33 mmol) were dissolved in CD 2 C1 2 To this solution was added B(C6F 5 3 (0.036 134 02/0603.sw13311spa,134 0.070 mmol) 1 H NMR of the resulting reaction mixture showed formation of the title compound.

ExampD1e 62 A 100 mL autoclave was charged with chloroform mL), {[(2-t-BuPh) 2 DABMe 2 )PdMe(NCMe)}SbFe- (0.090 g, 0.12 mmol), and ethylene (2.1 MPa). The reaction mixture was stirred at 25 0 C and 2.1 MPa ethylene for 3 h. The ethylene pressure was then vented and volatiles removed from the reaction mixture in vacuo to afford 2.695 g of branched polyethylene. The number average molecular weight calculated by 1 H NMR integration of aliphatic vs. olefinic resonances, was 1600. -The degree of polymerization, DP, was calculated on the basis of the 1H NMR spectrum to be 59; for a linear polymer this would result .in 18 methyl-ended branches per 1000 methylenes. However, based on the iH NMR spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 154. Therefore, it may be concluded that this material was branched polyethylene. 1H NMR (CDC1 3 6 5.38 (mult, vinyl H's), 1.95 (mult, allylic methylenes), 1.62 (mult, allylic methyls),- 1.24 (mult, non-allylic methylenes and methines), 0.85 (mult, non-allylic methyls).

Example 63 A suspension of BuPh) 2 DABMe 2 ]PdMe(NCMe)}SbF 6 (0.015 g, 0.02 mmol) in mL FC-75 was agitated under 2.8 MPa of ethylene for min. The pressure was then increased to 4.1 MPa and maintained at this pressure for 3 h. During this time the reaction temperature varied between 25 and 40 0 C. A viscous oil was isolated from the reaction mixture by decanting off the FC-75 and dried in vacuo. The number average molecular weight calculated by 1H NMR integration of aliphatic vs. olefinic resonances, was 2600. DP for this material was calculated on the basis of the 1 H NMR spectrum to be 95; for a linear polymer this would result in 11 methyl-ended branches per 1000 methylenes. However, based on the 1 H NMR 135 02/06/03,sw13311 spl 135 spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 177.

Example 64 A 100 mL autoclave was charged with chloroform mL), [(2-hPPh) 2 DABMe 2 )PdMe(NCMe)}SbF6" (0.094 g, 0.12 mmol), and ethylene (2.1 MPa). The reaction mixture was stirred at 25 0 C and 2.1 MPa ethylene for 3 h. The ethylene pressure was then vented and volatiles removed from the reaction mixture in vacuo to afford 2.27 g of a pale yellow oil. Mn was calculated on the basis of 1 H NMR integration of aliphatic vs. olefinic resonances to be 200. The degree of polymerization, DP, was calculated on the basis of the 1H NMR spectrum to be 7.2; for a linear polymer this would result in 200 methyl-ended branches per -1000 methylenes. However, based on the 1 H NMR spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 283.

Example A suspension of [(2-PhPh) 2 DABMe 2 ]PdMe(NCMe) )SbF 6 (0.016 g, 0.02 mmol) in 5 mL FC-75 was agitated under 1.4 MPa of ethylene for 3 h 40 min. During this time the reaction temperature varied between 23 and 410C. A viscous oil (329 mg) was isolated from the reaction mixture by decanting off the FC-75 and dried in vacuo.

Mn was calculated on the basis of 1 H NMR integration of aliphatic vs. olefinic resonances to be 700. The degree of polymerization, DP, was calculated on -the basis of the 1 H NMR spectrum to be 24.1; for a linear polymer this would result in 45 methyl-ended branches per 1000 methylenes. However, based on the IH NMR spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 173.

Example 66 A 100 mL autoclave was charged with FC-75 (50 mL), (Ph 2 DABMe 2 )PdMe(NCMe)}SbF 6 (0.076 g, 0.12 mmol) and ethylene (2.1 MPa). The reaction mixture was stirred at 24 0 C for 1.5 h. The ethylene pressure was then vented, and the FC-75 mixture removed from the reactor.

136 02/06/03.sw13311spI36 Ssmall amount of insoluble oil was isolated from the mixture by decanting off the FC-75. The reactor was washed out with 2 x 50 mL CHC1 3 and the washings added to the oil. Volatiles removed from the resulting solution in vacuo to afford 144 mg of an oily solid.

Mn was calculated on the basis of 1H NMR integration of aliphatic vs. olefinic resonances to be 400. The degree of polymerization, DP, was calculated on the basis of the 1H NMR spectrum to be 13.8; for a linear polymer this would result in 83 methyl-ended branches per 1000 methylenes. However, based on the 1H NMR spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 288.

Example 67 A 100 mL autoclave was charged with chloroform mL), {[(2,6-EtPh) 2 DABMe2]PdMe(NCMe)}BAF" (0.165 a, 0.12 mmol), and ethylene (2.1 MPa). The reaction mixture was stirred under 2.1 MPa of ethylene for 60 min; during this time the temperature inside the reactor increased from 22 to 480C. The ethylene pressure was then vented and volatiles removed from the reaction mixture in vacuo to afford 15.95 g of a viscous oil.

IH NMR of this material showed it to be branched polyethylene with 135 methyl-ended branches per 1000 methylenes. GPC analysis in trichlorobenzene (vs. a linear polyethylene standard) gave Mn 10,400, Mw 22,100.

Example 68 This was run identically to Example 67, but with [(2,6-EtPh) 2 DABMe 2 ]PdMe(NCMe)}SbF 6 (0.090 g, 0.12 mmol) in place of the corresponding BAF salt. The temperature of the reaction increased from 23 to 30 0

C

during the course of the reaction. 5.25 g of a viscous oil was isolated, 1H NMR of which showed it to be branched polyethylene with 119 methyl-ended branches per 1000 methylenes.

137- 0/06/03.sw1331 spa 137 Example 69 A suspension of 2 DABMe 2 PdMe(NCMe)}SbF- (0.027 g, 0.02 mmol) in 5 mL FC-75 was agitated under 1.4 MPa of ethylene for 3 h; during this time the temperature inside the reactor varied between 25 and Two FC-75 insoluble fractions were isolated from the reaction mixture. One fraction, a non-viscous oil floating on top of the FC-75, was removed by pipette and shown by IH NMR to be branched ethylene oligomers for which Mn 150 and with 504 methyl-ended branches per 1000 methylenes. The other fraction was a viscous oil isolated by removing FC-75 by pipette; it was shown by IH NMR to be polyethylene for which Mn 650 and with 240 methyl-ended branches per 1000 methylenes.

Example A suspension of {[(Ph 2 CH) 2

DABH

2 PdMe (NCMe) }SbF- (0.016 g, 0.02 mmol) in 5 mL FC-75 was agitated under 1.4 MPa of ethylene for 3 h 40 min. During this time the reaction temperature varied between 23 and 41 0 C. A viscous oil (43 mg) was isolated from the reaction mixture by decanting off the FC-75 and dried in vacuo.

Mn was calculated on the basis of IH NMR integration of aliphatic vs. olefinic resonances to be approximately 2000. The degree of polymerization, DP, was calculated on the basis of the IH NMR spectrum to be 73; for a linear polymer this would result in 14 methyl-ended branches per 1000 methylenes. However, based on the IH NMR spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 377.

Example 71 A 100 mL autoclave was charged with FC-75 (50 mL), ({Ph 2 DAB(cyclo -CMe 2

CH

2 CMe 2 }PdMe(MeCN))BAF (0.160 g, 0.12 mmol) and ethylene (2.1 MPa). The reaction mixture was stirred at 24-25 0 C for 3.5 h. The ethylene pressure was then vented, and the cloudy FC-75 mixture removed from the reactor. The FC-75 mixture was extracted with chloroform, and the chloroform extract concentrated to dryness affording 0.98 g of an oil. Mn 138- 0206/03.sw1331 spa. 138 gas calculated on the basis of IH NMR integration of aliphatic vs. olefinic resonances to be 500. The degree of polymerization, DP, was calculated on the basis of the 1 H NMR spectrum to be 19.5; for a linear polymer this would result in 57 methyl-ended branches per 1000 methylenes. However, based on the 1 H NMR spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 452.

Example 72 A 100 mL autoclave was charged with FC-75 (50 mL), {[(4-NMePh)2DABMe 2 ]PdMe(MeCN) }SbF" (MeCN) (0.091 g, 0.12 mmol) and ethylene (2.1 MPa). The reaction mixture was stirred at 24 0 C for 1.5 h. The ethylene pressure was then vented, and the cloudy FC-75 mixture removed from the reactor. -The FC-75 was extracted with 3 x 25 mL of chloroform. The reactor was washed out with 3 x 40 mL CHCI 3 and the washings added to the extracts. Volatiles removed from the resulting solution in vacuo to afford 556 mg of an oil. Mn was calculated on the basis of 1H NMR integration of aliphatic vs. olefinic resonances to be 200. The degree of polymerization, DP, was calculated on the basis of the IH NMR spectrum to be 8.4; for a linear polymer this would result in 154 methyl-ended branches per 1000 methylenes. However, based on the 18 NMR spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 261.

Example 73 Under nitrogen, a 250 mL Schlenk flask was charged with 10.0 g of the monomer CH 2

=CHCO

2

CH

2

CH

2

(CF

2 )nCF3 (avg n 40 mL of methylene chloride, and a magnetic stirbar. To the rapidly stirred solution was added [(2,6-i-PrPh)2DABMe2]PdMe(OEt2)}SbF (0.075 g, 0.089 mmol) in small portions. The resulting yellow-orange solution was stirred under 1 atm of ethylene for 18 h.

The reaction mixture was then concentrated, and the viscous product extracted with 300 mL of petroleum ether. The yellow filtrate was concentrated to 139- 02V0603.sw33 I spa, 139 3ryness, and extracted a second time with 150 mL petroleum ether. 500 mL of methanol was added to the filtrate; the copolymer precipitated as an oil which adhered to the sides of the flask, and was isolated by decanting off the petroleum ether/ methanol mixture.

The copolymer was dried, affording 1.33 g of a slightly viscous oil. Upon standing for several hours, an additional 0.70 g of copolymer precipitated from the petroleum ether/ methanol mixture. By 1H NMR integration, it was determined that the acrylate content of this material was 4.2 mole%, and that it contained 26 ester and 87 methyl-ended branches .per 1000 methylenes. GPC analysis in tetrahydrofuran (vs.

a PMMA standard) gave Mn 30,400, Mw 40,200. 1H NMR.

(CDC1 3 6 4.36 CH2CH2CO2CH 2

CH

2 Rf), 2.45 (mult,

CH

2

CH

2 CO2CH 2

CH

2 Rf), 2.31 CH2CH2C2CH 2

CH

2 Rf) 1.62 (mult, CH2CH 2 CO2CH 2

CH

2 Rf), 1.23 (mult, other methylenes and methines), 0.85 (mult, methyls). 13C NMR gave branching per 1000 CH 2 Total methyls Methyl Ethyl(20), Propyl Butyl Amyl >Hex and end of chains GPC analysis in THF gave Mn 30,400, Mw 40,200 vs. PMMA.

Example 74 A 100 mL autoclave was charged with ~Pd(CH 3

CH

2

CN)

4 (BF4)2 (0.058 g, 0.12 mmol) and chloroform (40 mL). To this was added a solution of ;2,6-i-PrPh) 2 DABMe 2 (0.070 g, 0.17 mmol) dissolved in mL of chloroform under ethylene pressure (2.1 MPa).

The pressure was maintained at 2.1 MPa for.1.5 h, during which time the temperature inside the reactor increased from 22 to 35 C. The ethylene pressure was then vented and the reaction mixture removed from the reactor. The reactor was washed with 3 x 50 mL of chloroform, the washings added to the reaction mixture, and volatiles removed from the resulting solution in vacuo to afford 9.77 g of a viscous oil. IH NMR of this material showed it to be branched polyethylene with 96 methyl-ended branches per 1000 methylenes.

140- 02/06/03,sw1331 sp, 14 0 Example A 100 mL autoclave was charged with [Pd(CH 3

CN)

4 J (BF 4 2 (0.053 g, 0.12 mmol) and chloroform mL). To this was added a solution of (2,6-i- PrPh) 2 DABMe 2 (0.070 g, 0.17 mmol) dissolved in 10 mL of chloroform under ethylene pressure (2.1 MPa). The pressure was maintained at 2.1 MPa for 3.0 h, during which time the temperature inside the reactor increased from 23 to 52 0 C. The ethylene pressure was then vented and the reaction mixture removed from the reactor. The reactor was washed with 3 x 50 mL of chloroform, the washings added to the reaction mixture, and volatiles removed from the resulting solution in vacuo to afford 25.98 g of a viscous oil. 1 H NMR of this material showed it to be branched polyethylene with 103 methylended branches per 1000 methylenes. GPC analysis in trichlorobenzene gave Mn 10,800, Mw 21,200 vs.

linear polyethylene.

Example 76 A mixture of 20 mg (0.034 mmol) of PrPh)DABH,]NiBr 2 and 60 mL dry, deaerated toluene was magnetically-stirred under nitrogen in a 200-mL threenecked flask with a gas inlet tube, a thermometer, and a gas exit tube which vented through a mineral oil bubbler. To this mixture, 0.75 mL (65 eq) of 3M poly(methylalumoxane) (PMAO) in toluene was.added via syringe. The resulting deep blue-black catalyst solution was stirred as ethylene was bubbled through at about 5 ml and 1 atm for 2 hr. The temperature of the mixture rose to 60°C in the first 15 min and then dropped to room temperature over the course of the reaction.

The product solution was worked up by blending with methanol; the resulting white polymer was washed with 2N HC1, water, and methanol to yield after drying purge) 5.69g (6000 catalyst turnovers) of polyethylene which was easily-soluble in hot chlorobenzene. Differential scanning calorimetry 141 02/0O.sw1331 Ispa, 141 exhibited a broad melting point at 107 0 C (67 Gel permeation chromatography (trichlorobenzene, 1350C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=22,300; Mw=102,000; Mw/Mn=4.56. 13C NMR analysis: branching per 1000 CH 2 total Methyls Methyl Ethyl Propyl Butyl Amyl _Hexyl and end of chain chemical shifts were referenced to the solvent: the high field carbon of 1,2,4-trichlorobenzene (127.8 ppm). A film of polymer (pressed at 2000C) was strong and could be stretched and drawn without elastic recovery.

Example 77 In a Parr 600-mL stirred autoclave under nitrogen was combined 23 mg (0.039 mmol) of PrPh)DABH 2 ]NiBr 2 60 mL of dry toluene, and 0.75 mL of poly(methylalumoxane) at 280C. The mixture was stirred, flushed with ethylene, and pressurized to 414 kPa with ethylene. The reaction was stirred at 414 kPa for 1 hr; the internal temperature rose to 310C over this time. After 1 hr, the ethylene was vented and 200 mL of methanol was added with stirring to the autoclave. The resulting polymer slurry was filtered; the polymer adhering to the autoclave walls and impeller was scraped off and added to the filtered polymer. The product was washed with methanol and acetone and dried (800C/vacuum/nitrogen purge) to yield 5.10g (4700 catalyst turnovers) of polyethylene.

Differential scanning calorimetry exhibited a melting point at 1270C (170 Gel permeation chromatography (trichlorobenzene, 1350C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=49,300; Mw=123,000; Mw/Mn=2.51. Intrinsic viscosity (trichlorobenzene, 1350C): 1.925 dL/g. Absolute molecular weight averages corrected for branching: Mn=47,400; Mw=134,000; Mw/Mn=2.83. 13C NMR analysis; branching per 1000 CH 2 total Methyls Methyl Ethyl Propyl -142- 0206103,swl3311spat142 Butyl 2Butyi and end of chain chemical shifts were referenced to the solvent: the high field carbon of 1,2,4-trichlorobenzene (127.8 ppm) A film of polymer (pressed at 2000C) was strong and stiff and could be stretched and drawn without elastic recovery.

This polyethylene is much more crystalline and linear than the polymer of Example 76. This example shows that only a modest pressure increase from 1 atm to 414 kPa allows propagation to successfully compete with rearrangement and isomerization of the polymer chain by this catalyst, thus giving a less-branched, morecrystalline polyethylene.

Example 78 A mixture of 12 mg (0.020 mmol) of PrPh)DABHJNiBr 2 and 40 mL.dry, deaerated toluene was magnetically-stirred under nitrogen at 15 0 C in a 100-mL three-necked flask with an addition funnel, a thermometer, and a nitrogen inlet tube which vented through a mineral oil bubbler. To this mixture, 0.5 mL of poly(methylalumoxane) in toluene was added via syringe; the resulting burgundy catalyst solution was stirred for 5 min and allowed to warm to room temperature. Into the addition funnel was condensed (via a Dry Ice condenser on the top of the funnel) mL (about 10g) of cis-2-butene. The catalyst solution was szirred as the cis-2-butene was'added as a liquid all at once, and the mixture was stirred for 16 hr.

The product solution was treated with 1 mL of methanol and was filtered through diatomaceous earth; rotary evaporation yielded 0.35g (300 catalyst turnovers) of a light yellow grease, poly-2-butene. 13 C NMR analysis; branching per 1000 CH 2 total Methyls (365), Methyl (285), Ethyl Butyl and end of chain chemical shifts were referenced to the solvent chloroform-d i (77 ppm).

Listed below are the 1 C NMR data upon which the above analysis is based.

143- 02/06103,sw1331 sp, 143 Freq ppm 41.6071 41.1471 38.6816 37.1805 36.8657 36.7366 36.6196 36.2645 35.9094 35.8004 35.5785 34.7351 34.4325 34.3114 34.1177 33.9886 33.8837 33.5326 33.004 32.7377 32.657 32.3705 31.5876 31.3818 31.0066 30.0946 29.9736 29.7072 29.3602 29.2512 29.114 28.9769 27.9358 27.7501 27.0682 26.7333 26.3257 26.015 25.3008 25.0627 22,.4801 22.3308 19.6192 19.4618 19.3085 18.9937 18.8525 13.7721 11.0484 10.4552 10.1283 9.99921 13C NNR Data CDC1 3 RT, 0.05M CnAcAc Intensity 11.2954 13.7193 3.55568 7.07882 33.8859 35.1101 33.8905 12.1006 13.3271 11.8845 4.20104 24.9682 39.3436 59.2878 125,698 121.887 120.233 49.8058 132.842 51.2221 55.6128 18.1589 9.27643 16.409 15.1861 41.098 42.8009 106.314 60.0884 35.0694 26.6437 29.1226 3.57351 3.56527 14.6121 81.0769 14.4591 11.8399 8.17451 5.98833 3.60955 2B4 10.4951 2B5+, EOC 90.3272 151 154.354 IB1 102.085

IB.

34.7667 IB1 38.7651

IB

1 11.2148 1B4+, EOC, IB 3 54.8771 IB2 10.8437 IB2 11.0735 IB2 9.36226 IB2 144- 0 2 0 6 3.sw 1331 tspa. 144 Example 79 A mixture of 10 mg (0.017 mmol) of PrPh)DABH2]NiBr2 and 40 mL dry, deaerated toluene was magnetically-stirred under nitrogen at 5°C in a 100-mL three-necked flask with an addition funnel, a thermometer, and a nitrogen inlet tube which vented through a mineral oil bubbler. To this mixture, 0.5 mL of 3M poly(methylalumoxane) in toluene was added via syringe; the resulting burgundy catalyst solution was stirred at 50C for 40 min. Into the addition funnel was condensed (via a Dry Ice condenser on the top of the funnel) 20 mL (about 15 g) of 1-butene. The catalyst solution was stirred as the 1-butene was added as a liquid all at once. The reaction temperature rose to 50 0 C over 30 min and then dropped to room temperature as the mixture was stirred for 4 hr. The product solution was treated with 1 mL of methanol and was filtered through diatomaceous earth; rotary evaporation yielded 6.17 g (1640 catalyst turnovers) of clear, tacky poly-l-butene rubber. Gel permeation chromatography (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=64,700; Mw=115,000; Mw/Mn=1.77. 13 C NMR analysis; branching per 1000 CH2: total Methyls (399), Methyl Ethyl (272), !Butyl and end of chain chemical shifts were referenced to the solvent chloroform-di (77 ppm). This example demonstrates the polymerization of an alpha-olefin and shows the differences in branching between a polymer derived from a 1-olefin (this example) and a polymer derived from a 2-olefin (Example 78). This difference shows that the internal olefin of Example 78 is not first isomerized to an alpha-olefin before polymerizing; thus this catalyst is truly able to polymerize internal olefins.

Listed below are the 13 C NMR data upon which the above analysis is based.

145- 02/6/03,sw133 I sp, 145 Freq ppm 43.8708 41.5304 41.0825 38.7623 38.1247 37.3338 36.8173 35.756 35.0337 34.1419 33.8514 33.4116 33.0645 32.7094 32.431 30.946 30.1551 29.7516 29.4248 27.6008 27.2417 27.1207 26.7777 26.0755 25.6599 24.3807 23.4809 22.8393 22.1372 19.4981 19.3609 15.132 13.8448 12.2509 12.037 11.0766 10.2938 10.1364 13C NMR Data CDC1 3 RT, 0.0SM CrAcAc Intensity 6.42901 11.1597 16.1036 103.647 50.3288 24.6017 30.0925 55.378 22.3563 64.8431 55.3508 90.2438 154.939 51.3245 23.0013 12.8866 3B 6 26.1216 54.6262 40.7879 8.64277 20.1564 21.9735 45.0824 66.0697 77.1097 8.9175 32.0249 2B 4 2B5+, 2EOC 8.06774 16.4732 57.7003 IB1 70.588 IB1 17.2402 1B4+ 7.9343 1B4+ 27.8653 27.0118 6.61931 IB2 98.0101 IB2 104.811 IB2 Example A 22-mg (0.037-mmol) sample of PrPh)DABH 2 ]NiBr, was introduced into a 600-mL stirred Parr® autoclave under nitrogen. The autoclave was sealed and 75 mL of dry, deaerated toluene was introduced into the autoclave via gas tight syringe through a port on the autoclave head. Then 0.6 mL of 3M poly(methylalumoxane) was added via syringe and stirring was begun. The autoclave was pressurized with 146- 02/06/03.swl3311 Ispa,146 ropylene to 414 kPa and stirred with continuous propylene feed. There was no external cooling. The internal temperature quickly rose to 33°C upon initial propylene addition but gradually dropped back to 24°C over the course of the polymerization. After about 7 min, the propylene feed was shut off and stirring was continued; over a total polymerization time of 1.1 hr, the pressure dropped from 448 kPa to 358 kPa. The propylene was vented and the product, a thin, honeycolored solution, was rotary evaporated to yield 1.65g of a very thick, brown semi-solid. This was dissolved in chloroform and filtered through diatomaceous earth; concentration yielded 1.3 g (835 catalyst turnovers) of tacky, yellow polypropylene rubber. Gel permeation chromatography (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polypropylene using universal calibration theory): Mn=7, 940; Mw=93,500; Mw/Mn=ll.78.

Example 81 A mixture of 34 mg (0.057 mmol) of PrPh)DABH]NiBr 2 and 20 mL dry, deaerated toluene was magnetically-stirred under nitrogen at 5°C in a 100-mL three-necked flask with a thermometer and a nitrogen inlet tube which vented through a mineral oil bubbler.

To this mixture, 0.7 mL of 3M poly(methylalumoxane) in toluene was added via syringe and the resulting deep blue-black solution was stirred for 30 min at 5°C. To this catalyst solution was added 35 mL of dry, deaerated cyclopentene, and the mixture was stirred and allowed to warm to room temperature over 23 hr. The blue-black mixture was filtered through alumina to remove dark blue-green solids (oxidized aluminum compounds from PMAO); the filtrate was rotary evaporated to yield 1.2 g (310 catalyst turnovers) of clear liquid cyclopentene oligomers.

FExamplg 82 A 20-mg (0.032 mmol) sample of PrPh)DABMe2]NiBr 2 was placed in Parr® 600-mL stirred 147- 02/06/03.sw|331 Isps, 147 autoclave under nitrogen. The autoclave was sealed and 100 mL of dry, deaerated toluene and 0.6 mL of 3M poly(methylalumoxane) were injected into the autoclave through the head port, and mixture was stirred under nitrogen at 20 0 C for 50 min. The autoclave body was immersed in a flowing water bath and the autoclave was then pressurized with ethylene to 2.8 MPa with stirrihg as the internal temperature rose to 53 0 C. The autoclave was stirred at 2.8 MPa (continuous ethylene feed) for 10 min as the temperature dropped to 29 0

C,

and the ethylene was then vented. The mixture stood at 1 atm for 10 min; vacuum was applied to the autoclave for a few minutes and then the autoclave was opened.

The product was a stiff, swollen polymer mass which was scraped out, cut up, and fed in portions to 500 mL methanol in a blender. The polymer was then boiled with a mixture of methanol (200 mL) and trifluoroacetic acid (10 mL), and finally dried under high vacuum overnight to yield 16.8g (18,700 catalyst turnovers) of polyethylene. The polymer was somewhat heterogeneous with respect to crystallinity, as can be seen from the differential scanning calorimetry data below; amorphous and crystalline pieces of polymer could be picked out of the product. Crystalline polyethylene was found in the interior of the polymer mass; amorphous polyethylene was on the outside. The crystalline polyethylene was formed initially when the ethylene had good access to the catalyst; as the polymer formed limited mass transfer, the catalyst became ethylene-starved and began to make amorphous polymer. Differential scanning calorimetry: (crystalline piece of polymer): mp: 130 0 C (150J/g); (amorphous piece of polymer): -48oC mp: 42 0

C

960C (11J/g). Gel-permeation chromatography (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=163,000; Mw=534,000; Mw/Mn=3.27. This example demonstrates the effect of -148- 02/&3.,s13311sp,148 ethylene mass transfer on the polymerization and-shows that the same catalyst can make both amorphous and crystalline polyethylene. The bulk of the polymer was crystalline: a film pressed at 200 0 C was tough and stiff.

Example 83 A 29-mg (0.047 mmol) sample of PrPh)DABMe 2 ]NiBr 2 was placed in Parr@ 600-mL stirred autoclave under nitrogen. The autoclave was sealed and 100 mL of dry, deaerated toluene and 0.85 mL of 3M poly(methylalumoxane) .were injected into the autoclave through the head port. The mixture was stirred under nitrogen at 23 0 C for 30 min. The autoclave body was immersed in a flowing water bath and the autoclave was pressurized with ethylene -to 620 kPa with stirring.

The internal temperature peaked at 38 0 C within 2 min.

The autoclave was stirred at 620 kPa (continuous ethylene feed) for 5 min as the temperature dropped to 32 0 C. The ethylene was then vented, the regulator was readjusted, and the autoclave was pressurized to 34.5 kPa (gauge) and stirred for 20 min (continuous ethylene feed) as the internal temperature dropped to 22 0 C. In the middle of this 20 min period, the ethylene feed was temporarily shut off for 1 min, during which time the autoclave pressure dropped from 34.5 kPa (gauge) to 13.8 kPa; the pressure was then restored to 34.5 kPa.

After stirring 20 min at 34.5 kPa, the autoclave was once again pressurized to 620 kPa for 5 min; the internal temperature rose from 22 0 C to 34°C. The ethylene feed was shut off for about 30 sec before venting; the autoclave pressure dropped to about 586 kPa.

The ethylene was vented; the product was a dark, thick liquid. Methanol (200 mL) was added to the autoclave and the mixture was stirred for 2 hr. The polymer, swollen with toluene, had balled up on the stirrer, and the walls and bottom of the autoclave were coated with white, fibrous rubbery polymer. The 149- 02106/03,sw133 I spa. 149 .polymer was scraped out, cut up, and blended with methanol in a blender and then stirred with fresh boiling methanol for 1 hr. The white rubber was dried under high vacuum for 3 days to yield 9.6 g (7270 catalyst turnovers) of rubbery polyethylene. 1H NMR analysis (CDC1 3 95 methyl carbons per 1000 methylene carbons.

Differential scanning calorimetry: -51 0 C mp: 39.5°C mp: 76.40C Gel permeation chromatography (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=223,000; Mw=487,000; M,/Mn=2.19.

The polyethylene of Example 83 could be cast from hot chlorobenzene or pressed at 2000C to give a strong, stretchy, hazy, transparent film with good recovery.

It was not easily chloroform-soluble. This example demonstrates the use of the catalyst's ability (see Example 82) to make both amorphous and crystalline polymer, and.to make both types of polymer within the same polymer chain due to the catalyst's low propensity to chain transfer. With crystalline blocks (due to higher ethylene pressure) on both ends and an amorphous region (due to lower- pressure, mass transf e r-limited polymerization) in the center of each chain, this polymer is a thermoplastic elastombr.

Example 84 A Schlenk flask containing 147 mg (0.100 mmol) of S[(2,6-i-PrPh)DABMe2]PdMe(OEt) }BAF was cooled to 78 0 C, evacuated, and placed under an ethylene atmosphere. Methylene chloride (100 ml) was added to the flask and the solution was then allowed to warm to room temperature and stirred. The reaction vessel was warm during the first several hours of mixing and the solution became viscous. After being stirred for 17.4 h, the reaction mixture was added to -600 mL of MeOH in order to precipitate the polymer. Next, the MeOH was decanted off of the sticky polymer, which was then 150 0 2/oW03.sw133 I sp.,150 dissolved in -600 mL of petroleum etner. After being filtered through plugs of neutral alumina and silica gel, the solution appeared clear and almost colorless.

The solvent was then removed and the viscous oil (45.31 g) was dried in vacuo for several days: 'H NMR (CDC1 3 400 MHz) 6 1.24 (CH 2 CH), 0.82 CH3); Branching: -128 CH 3 per 1000 CH2; DSC: Tg -67.70C. GPC: Mn 29,000; Mw 112,000.

Example Following the procedure of Example 84 PrPh)DABMe 2 ]PdMe(OEt 2 )}BAF (164 mg, 0.112 mmol) catalyzed the polymerization of ethylene for 24 h in mL of CH 2 C12 to give 30.16 g of polymer as a viscous oil. 1H NMR (C 6

D

6 6 1.41 (CH 2 CH), 0.94 (CH 3 Branching: -115 CH 3 per 1000 CH2; GPC Analysis (THF, PMMA standards, RI Detector): Mw 262,000; Mn 121,000; PDI 2.2; DSC: Tg -66.8oC.

Example 86 The procedure of Example 84 was followed using 144 mg (0.100 mmol) of {[(2,6-i-PrPh)DABH2]PdMe(OEt 2

)}BAF-

in 50 mL of CH 2 C1 2 and a 24 h reaction time. Polymer (9.68 a) was obtained as a free-flowing oil. 1 H NMR (CDC1 3 400-MHz) 6 5.36 RHC=CHR'), 5.08 (br s, RR'C=CHR''), 4.67 (br s, H 2 C=CRR'), 1.98 allylic 1.26 (CH2, CH), 0.83 CH 3 Branching: -149 CH3 per 1000 CH2; DSC: T 9 -84.6 0

C.

Example 87 A 30-mg (0.042-mmol) sample of PrPh)DABAn]NiBr 2 was placed in Parr® 600-mL stirred autoclave under nitrogen. The autoclave was sealed and 150 mL of dry toluene and 0.6 mL of 3M polymethylalumoxane were injected into the autoclave through the head port. The autoclave body was immersed in a flowing water bath and the mixture was stirred under nitrogen at 20 0 C for 1 hr. The autoclave was then pressurized with ethylene to 1.31 MPa with stirring for 5 min as the internal temperature peaked at 30 0 C. The ethylene was then vented to 41.4 kPa 151 02/06/03,swl331 1spa 151 .gauge) and the mixture was stirred and fed ethylene at 41.4 kPa for 1.5 hr as the internal temperature dropped to 19 0 C. At the end of this time, the autoclave was again pressurized to 1.34 MPa and stirred for 7 min as the internal temperature rose to 350C.

The ethylene was vented and the autoclave was briefly evacuated; the product was a stiff, solventswollen gel. The polymer was cut up, blended with 500 mL methanol in a blender, and then stirred overnight with 500 mL methanol containing 10 mL of 6N HC1. The stirred suspension in methanol/HCl was then boiled for 4 hr, filtered, and dried under high vacuum overnight to yield 26.1 g (22,300 catalyst turnovers) of polyethylene. Differential scanning calorimetry: -490C (Tg) mp: 116 0 C (42J/g). The melting transition was very broad and appeared to begin around room temperature. Although the melting point temperature is higher in this Example than in Example 76, the area under the melting endotherm is less in this example, implying that the polymer of this Example is less crystalline overall, but the crystallites that do exist are more ordered. This indicates that the desired block structure was obtained. Gel permeation chromatography (trichlorobenzene, 1350C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=123,000; Mw=601,000; Mw/Mn=4.87. The polyethylene of this example could be pressed at 200 0 C to give a strong, tough, stretchy, hazy film with partial elastic recovery. When the stretched film was plunged into boiling water, it completely relaxed to its original dimensions.

Example 88 A 6.7-mg (0.011-mmol) sample of PrPh)DABMe,]NiBr 2 was magnetically-stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of dry, deaerated toluene as 0.3 mL of 3M poly(methylalumoxane) was injected via syringe. The mixture was stirred at 23 0 C for 40 min to give a deep blue-green solution of -152- 02/06/03,sw 1331 lsp. 152 atalyst. Dry, deaerated cyclopentene (10 mL was injected and the mixture was stirred for 5 min. The flask was then pressurized with ethylene at 20.7 MPa and stirred for 22 hr. The resulting viscous solution was poured into a stirred mixture of 200 mL methanol and 10 mL 6N HC1. The methanol was decanted off and replaced with fresh methanol, and the polymer was stirred in boiling methanol for 3 hr. The tough, stretchy rubber was pressed between paper -towels and dried under vacuum to yield 1.0g of poly[ethylene/cyclopentene]. By 1H NMR analysis(CDCl3): 100 methyl carbons per 1000 methylene carbons. Comparison of the peaks attributable to cyclopentene (0.65 ppm and 1.75 ppm) with the standard polyethylene peaks (0.9 ppm and 1.3 ppm) indicates about a 10 mol% cyclopentene incorporation. This polymer yield and composition represent about 2900 catalyst turnovers. Differential scanning calorimetry: -44 0 C Gel permeation chromatography (trichlorobenzene, 135 0 polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=122,000; Mw=241,000; Mw/Mn=1.97.

Listed below are the 13 C NMR data upon which the above analysis is based.

13 C NMR data TCB, 120C, 0.05M CrAcAc Freq ppm Intensity 50.9168 5.96663 46.3865 3.27366 1 cme and/or 1,3 ccmcc 40.7527 40.5963 2 eme 40.567 41.9953 1,3 eme 40.3336 45.8477 1,3 eme 37.1985 60.1003 36.6998 41.2041 36.0579 11.2879 35.607 25.169 34.4771 19.0834 34.0845 22.8886 33.1243 20.1138 32.8962 27.6778 31.8406 75.2391 30.0263 76.2755 153- 02/06103.sw1331 Ispa, 1 5 3 29.6921 170.41 28.9494 18.8754 28.647 25.8032 27.4588 22.2397 27.1086 48,0806 24.3236 3.31441 22.5783 4.64411 2B 5 2 EOC 19.6712 43.1867 1BI 17.5546 1.41279 end group 14.3399 1.74854 IB3 13.8518 5.88699 1B4+, 1EOC 10.9182 2.17785 2B 1 Example ;9 A 7.5-mg (0.013-mmol) sample of BuPh)DABMe 2 ]NiBr 2 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 40 mL of dry, deaerated toluene as 0.5 mL of 3M poly(methylalumoxane).

was injected via syringe.. The mixture was stirred at 23 0 C for 1 hr to give a deep blue-green solution of catalyst. The flask was pressurized with ethylene at 20.7 kPa (gauge) and stirred for 20 hr. The solution, which had become a reddish-brown suspension, was poured into a stirred mixture of 200 mL methanol and 10 mL 6N HC1 and was stirred at reflux for 1 hr. The methanol was decanted off and replaced with fresh methanol, and the white polymer was stirred in boiling methanol for 1 hr. The stiff, stretchy rubber was pressed between paper towels and then dried under vacuum to yield 1.25 g (3380 catalyst turnovers) of polyethylene. IH-i NMR analysis (CGD6): 63 methyl carbons per 1000 methylene carbons. Differential scanning calorimetry: -34°C mp: 44 0 C (31J/g); mp: 101°C (23J/g).

Example A 5.5 mg (0.0066 mmol) sample of PrPh) 2 DABMe 2 PdMe(Et20)}SbF

G

was allowed to stand at room temperature in air for 24 hr. A 100-mL three-neck flask with a magnetic stirrer and a gas inlet dip tube was charged with 40 mL of reagent methylene chloride and ethylene gas was bubbled through with stirring to saturate the solvent with ethylene. The sample of [(2,6-i-PrPh),DABMe 2 )PdMe(Et2O) }SbF6" was then rinsed 154- 02/06/03,sw331 I spa, 154 .nto the flask with 5 mL of methylene chloride ana ethylene was bubbled through with stirring for 5 hr.

The clear yellow solution was rotary evaporated to yield 0.20 g (1080 catalyst turnovers) of a thick yellow liquid polyethylene.

Example 21 A 600-mL stirred Parr® autoclave was sealed and flushed with nitrogen, and 100 mL of dry, deaerated toluene was introduced into the autoclave via gas tight syringe through a port on the autoclave head. The autoclave was purged with propylene gas to saturate the solvent with propylene. Then 45 mg (0.054 mmol) of (2,6-i-PrPh) 2 DABMe 2 ]PdMe(Et 2 O) SbF 6 was introduced into the autoclave in the following manner: a gas tight syringe with a syringe valve was loaded with mg of{[(2,6-i-PrPh) 2 DABMe 2 ]PdMe (Et20)}SbF 6 under nitrogen in a glove box; then 1-2 mL of dry, deaerated methylene chloride was drawn up into the syringe and the contents were quickly injected into the autoclave through a head port. This method avoids having the catalyst in solution with no stabilizing ligands.

The autoclave was pressurized with propylene to 414 MPa and stirred for 2.5 hr, starting with continuous propylene feed. The autoclave was cooled in a running tap water bath at 220C. The internal temperature quickly rose to 30 0 C updn initial propylene addition but soon dropped back to 22 0 C. After 0.5 hr, the propylene feed was shut off and stirring was continued. Over 2 hr, the pressure dropped from 41.4 MPa to 38.6 MPa. The propylene was then vented. The product was a thin, honey-colored solution. Rotary evaporation yielded 2.3 g (1010 catalyst turnovers) of very thick, dark-brown liquid polypropylene which was almost elastomeric when cool. Gel permeation chromatography (trichlorobenzene, 135°C, polystyrene reference, results calculated as polypropylene using universal calibration theory): Mn8, 3 0 0 Mw=15,300; Mw/Mn=1.84. 13 C NMR analysis; branching per 1000 CH2: 155- 02/06/W3.sw 1 3311 spa 155 cotal Methyls (545), Propyl >Buryi and end cf chain chemical shifts. The polymer exhibited a glass transition temperature of -44 0 C by differential scanning calorimetry.

Listed below are the C NMR data upon which the above analysis is based.

13 C NMR data Freq ppm CDcl1 3

RT,

Intensity 46.4978 45.8683 45.3639 45.1783 44.5568 44.4398 44.3026 44.1372 43.5036 42.4262 41.6918 39.1537 38.7179 37.8664 37.6727 37.0755 36.781 36.559 34.5495 34.3195 33.5488 33.351 32.7982 32.4108 31.8701 31.5957 29.8364 29.7072 29.3925 29.0293 27.6089 27.4193 27.0763 26.9552 26.7615 26.3661 24-.8529 23.1217 22.6779 22.5245 13.2699 11.9947 10.959 11.3339 8.41708 7.69019 6.29108 6.73541 5.49837 5.03113 3.72552 4.23147 25.2596 10.0979 14.3755 17.623 42.0719 10.0773 5.34388 7.48969 12.6148 20.5271 4.10612 22.781 5.90488 10.6988 44.4935 103.844 152.645 6.71341 38.7993 10.3543 66.8261 92.859 55.7233 20.1674 16.9056 12.5439 13.0147 9.16236 0.05M CrAcAc Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes .Methylenes Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines Methines anc and and and and and and and and and and and and and and and and and and and and and and and and SMethylenes Methylenes I Methylenes I Methylenes Metbylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methylenes Methyleres Methylenes Methylenes Methylenes Methylenes Methine Carbon of XXVIII Methine carbons of XXVIII and XXIX, 2B4+, EOC Methine carbons of XXVIII and XXIX, 2B4+, EOC Methine carbons of XXVIII and XXIX, 2B4+, EOC -156- 02oV06/03.sw13311 sp.15 6 WO 96/23010 22.3389 77.3342 Methine carbons of XXVII: and XXIX, 254+, EOC 21.9757 9.85242 Methine carbons of XXVIII and XXIX, 2B4+, EOC 21.1405 10.0445 Methylb 20.4182 8.49663 Methyls 19.9743 25.8085 Methyls 19.825 31.4787 Methyls 19.3811 44.9986 Methyls 19.1995 31.3058 Methyls 13.8569 6.37761 Methyls 13.8004 7.67242 Methyls 137.452 22.0529 Methyls 128.675 44.6993 Methyls 127.88 43.8939 Methyls 124.959 22.4025 Methyls 122.989 3.3312 Methyls Example 92 A 600-mL stirred Parr® autoclave was sealed, flushed with nitrogen, and heated to 60 0 C in a water bath. Fifty mL (48 g; 0.56 mol) of dry, deaerated methyl acrylate was introduced into the autoclave via gas tight syringe through a port on the autoclave head and ethylene gas was passed through the autoclave at a low rate to saturate the solvent with ethylene before catalyst addition. Then 60 mg (0.07 mmol) of PrPh) 2 DABMe2]PdMe(Et 2 0)}SbF6 was introduced into the autoclave in the following manner: a 2.5-mL gas tight syringe with a syringe valve was loaded with 60 mg of {[(2,6-i-PrPh) 2 DABMe2)PdMe(Et 2 0))SbF 6 under nitrogen in a glove box; then 1 mL of dry, deaerated methylene chloride was drawn up into the syringe and the contents were quickly injected into the autoclave through a head port. This method avoids having the catalyst in solution with no stabilizing ligands.

The autoclave'was pressurized with ethylene to 689 kPa and continuously fed ethylene with stirring for hr; the internal temperature was very steady at 60 0

C.

The ethylene was vented and the product, a clear yellow solution, was rinsed out of the autoclave with chloroform, rotary evaporated, and held under high vacuum overnight to yield 1.56 g of thin light-brown liquid ethylene/methyl acrylate copolymer. The 157 02/ 0 6 0 3.swI3311pa. 157 infrared spectrum of the product exhibited a strona ester carbonyl stretch at 1740 cm- 1 1 H-I NMR analysis (CDC13): 61 methyl carbons per 1000 methylene carbons.

Comparison of the integrals of the ester methoxy (3.67ppm) and ester methylene (CH2COOMe; 2 .30ppm) peaks with the integrals of the carbon chain methyls (0.8- 0.9ppm) and methylenes (1.2-1.3ppm) indicated a methyl acrylate content of 16.6 mol% (37.9 This product yield and composition represent 480 ethylene turnovers and 96 methyl acrylate turnovers. 13 C NMR analysis; branching per 1000 CH 2 total methyls Methyl Ethyl Propyl Butyl Amyl and End of Chain methyl acrylate esterbearing -CH(CH 2 )nCO 2 CH, branches as a of total ester: n 5 n=4 n=1,2,3 n=0 (20.3); chemical shifts were referenced to the solvent: the high field carbon of 1, 2 ,4-trichlorobenzene (127.8 ppm). Gel permeation chromatography (tetrahydrofuran, 0 C, polymethylmethacrylate reference, results calculated as polymethylmethacrylate using universal calibration theory): Mn=3,370; Mw=5,450; Mw/Mn=1.62.

Listed below are the "C NMR data upon which the above analysis is based.

-158 o0206/03,sw 31Ispa.58 13 C NMR data TCB 120C, 0.05M CrAcAc Freq ppm Intensity 53.7443 2.19635 CH 2 C1 2 solvent impurity 50.9115 8.84408 50.641 132.93 45.5165 7.55996 MEB 0 43.8 ppm:2 adjacent MEB 0 39.6917 2.71676 39.2886 7.91933 38.1639 13.843 37.7926 26.6353 37.1666 20.6759 36.6733 8.65855 34.6256 17.6899 34.4612 16.7388 34.1429 85.624 33.9095 124.997 1EB 4 33.676 40.0271 Contributions from EB 33.2888 11.4719 Contributions from EB 32.8644 14.4963 Contributions from EB 32.3498 17.58863 Contributions from EB 32.0475 9.83096 Contributions from EB 31.8459 30.9676 Contributions from EB 31.7079 12.7737 Contributions from EB 31.5912 13.8792 Contributions from EB 31.0873 19.6266 Contributions from EB 30.6258 10.5512 30.1324 58.6101 29.6497 169.398 29.4322 48.5318 29.1934 95.4948 27.8619 8.70181 27.4269 32.9529 26.9283 78.0563 26.5145 27.0608 26.3554 14.0683 25.4588 21.9081 2EB 4 (tent) 25.33:5 9.04646 2EB 4 (tent) 24.9761 64.2333 2EB 5 24.2069 10.771 BBB (beta-beta-B) 23.0451 9.50073 2B4 22.9337 6.90528 2B4 22.5518 30.0427 2B5+, EOC 19.9842 1.87415 2B3 19.6288 17.125 IBI 19.1673 6.0427 1B1 16.7695 2.23642 14.3 1B3 13.7882 34.0749 1B4+, EOC 11.0774 4.50599 IB2 10.8705 10.8817 IB2 189.989 1.04646 EB 0 Carbonyl 175.687 3.33867 EB 0 Carbonyl 175.406 14.4124 EB 0 Carbonyl 175.22 5.43832 EBO Carbonyl 175.061 3.53125 EBo Carbonyl -159- 02/06/03,sw1331 Ispa,159 172.859 11.2356

EB

2 Carbonyl 172.605 102.342 EBI+ Carbonyl 172.09 7.83303 EBI+ Carbonyl 170.944 3.294 EBI Carbonyl Examp-le 9-3 A 45-mg (0.048-mmol) sample of PrPh) 2 DABAn]JPdMe(Et20) }SbF 6 -was placed in a 600-mL Parr stirred autoclave under nitrogen. To this was added mL of dry, deaerated methylene chloride, and the autoclave was pressurized to 414 kPa with ethylene.

Ethylene was continuously fed at 414 kPa with stirring at 23-25 0 c for 3 hr; then the feed was shut off and the reaction was stirred for 12 hr more. At the end of this time, the autoclave was under 89.6 kPa (absolute), The autoclave was repressurized to 345 kPa with ethylene and stirred for 2 hr more as the pressure dropped to 255 kPa, showing that the catalyst was still active; the ethylene was then vented. The brown solution in the autoclave was rotary evaporated, taken up in chloroform, filtered through alumina to remove catalyst, and rotary evaporated and then held under high vacuum to yield 7.35 g of thick, yellow liquid polyethylene. IH NMR analysis (CDC13): 131 methyl carbons per 1000 methylene carbons. Gel permeation chromatography (trichlorobenzene, 135°C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=10,300; Mw=l8,100; Mw/Mn=1.76.

Examp]2 94 A 79-mg (0.085-mmol) sample of PrPh) 2 DABAn]PdMe(Et 2 o0) }sbF6 was placed in a 600-mL Parr stirred autoclave under nitrogen. To this was added 50 mL of dry, deaerated methyl acrylate, and the autoclave was pressurized to 689 kPa with ethylene.

The autoclave was warmed to 50°C and the reaction was stirred at 689 kPa for 70 hr; the ethylene was then vented. The clear yellow solution in the autoclave was filtered through alumina to remove catalyst, rotary 160 02/06/03.sw133 I sptMO160 evaporated, and held under high vacuum to yield C.27 g of liquid ethylene/methyl acrylate copolymer. The infrared spectrum of the product exhibited a strong ester carbonyl stretch at 1740cm 1 1 H NMR analysis (CDC13): 70 methyl carbons per 1000 methylene carbons; 13.5 mol% (32 wt%) methyl acrylate. This yield and composition represent 12 methyl acrylate turnovers and ethylene turnovers.

Example A 67-mg (0.089-mmol) of MePh) 2 DABMe2]PdMe(Et 2 O) SbF 6 was placed in a 200-mL glass centrifuge bottle with a magnetic stir bar under nitrogen. To this was added 40 mL of dry, deaerated methylene chloride. The bottle was immediately pressurized to 207 kPa with ethylene. Ethylene was continuously fed at 207 kPa with stirring at 23-250C for 4 hr. After 4 hr, the ethylene feed was shut off and the reaction was stirred for 12 hr more. At the end of this time, the bottle was under zero pressure (gauge). The brown'solution was rotary evaporated and held under high vacuum to yield 5.15 g of thick, brown liquid polyethylene. 1H NMR analysis (CDC13): 127 methyl carbons per 1000 methylene carbons. Gel permeation chromatography (trichlorobenzene, 135 0

C,

polystyrene reference, results calculated as polyethylene using universal calibration theory): 200 Mw=32,1 00 Mw/Mn=1.5 9 Example 96 A 56-mg (0.066-mmol) sample of PrPh) 2 DABMe 2 )PdCHzCH 2 C(0)CH 3 )}SbFs was placed in a 600mL Parr® stirred autoclave under nitrogen. To this was added 30 mL of dry, deaerated perfluoro(propyltetrahydrofuran). The autoclave was stirred and pressurized to 5.9 MPa with ethylene. The internal temperature peaked at 29 0 C; a cool water bath was placed around the autoclave body. The reaction was stirred for 16 hr at 230C and 5.9 MPa and the ethylene was then vented. The autoclave contained a light 161- 02/06/03,swl3311spa. 161 yellow granular rubber; this was scraped out cf the autoclave and held under high vacuum to yield 29.0 g (15,700 catalyst turnovers) of spongy, non-tacky, rubbery polyethylene which had good elastic recovery and was very strong; it was soluble in chloroform or chlorobenzene.

The polyethylene was amorphous at room temperature: it exhibited a glass transition temperature of -57 0 C and a melting endotherm of -16 0

C

(35J/g) by differential scanning calorimetry. On cooling, there was a crystallization exotherm with a maximum at 1°C (35J/g). Upon remelting and recooling the melting endotherm and crystallization exotherm persisted, as did the glass transition. Dynamic mechanical analysis at 1Hz. showed a tan 6 peak at -51lC and a peak in the loss modulus E" at -65OC; dielectric analysis at 1000 Hz showed a tan d peak at -35 0 C. 1

H

NMR analysis (CDC1 3 86 methyl carbons per 1000 methylene carbons. 13 C NMR analysis: branching per 1000 CH2: total Methyls Methyl Ethyl Propyl Butyl >Am and End Of Chain chemical shifts were referenced to the solvent: the high field carbon of 1,2,4-trichlorobenzene (127.8 ppm). Gel permeation chromatography (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=137,000; Mw=289,000; Mw/Mn=2.10. Intrinsic viscosity (trichlorobenzene, 135 0 2.565 dL/g.

Absolute molecular weight averages corrected for branching: Mn=196,000; Mw=425,000; Mw/Mn=2.17. Density (determined at room temperature with a helium gas displacement pycnometer): 0.8546 0.0007 g/cc.

Example 97 A 49-mg (0.058 mmol) Sample of PrPh) 2 DABMe:]PdCHCH 2 C(0)CH3)SbF6 was placed in a 600-mL Parr® stirred autoclave under nitrogen. To this was added 30 mL of dry, deaerated hexane. The autoclave was stirred and pressurized to 5.9 MPa with ethylene.

162- 02/06/03,sw133 I Ispa 162 The internal temperature peaked briefly at 34°C; a cool water bath was placed around the autoclave body. The reaction was stirred for 16 hr at 23°C. At 14 hr, the ethylene feed was shut off; the autoclave pressure dropped to 5.8 MPa over 2 hr; the ethylene was then vented. The autoclave contained a light yellow, gooey rubber swollen with hexane, which was scraped out of the autoclave and held under high vacuum to yield 28.2 g (17,200 catalyst turnovers) of spongy, non-tacky, rubbery polyethylene which had good elastic recovery and which was very strong.

The polyethylene was amorphous at room temperature: it exhibited a glass transition temperature of -610C and a melting endotherm of -12°C (27J/g) by differential scanning calorimetry. Dynamic mechanical analysis at 1Hz showed a tan d peak at -52 0

C

and a peak in the loss modulus E" at -70 0 C; dielectric analysis at 1000 Hz showed a tan d peak at -37 0 C. 1

H

NMR analysis (CDC13): 93 methyl carbons per 1000 methylene carbons. 13 C NMR analysis: branching per 1000 CH2: total Methyls Methyl Ethyl Propyl Butyl Amyl >Hex and End Of Chain chemical shifts were referenced to the solvent: the high field carbon of 1,2,4-trichlorobenzene (127.8 ppm). Gel permeation chromatography (trichlorobenzene, 135C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=149,000; Mw=3 47 ,000; Mw/Mn=2.

33 Density (determined at room temperature with a helium gas displacement pycnometer): 0.8544 0.0007 g/cc.

Example 98 Approximately 10-mesh silica granules were dried at 200 0 C and were impregnated with a methylene chloride solution of {[(2,6-i-PrPh)2DABMez]PdCH2

CH

2 C(O)CH})SbFe6 to give a 10 wt% loading of the catalyst on silica.

A 0.53-g (0.063 mmol) sample of silica gel containing 10 wt% 163 02/0603,sw 13311 spa163 rPh)2DABMeJPdCH 2 CHC(0)CH,}SbF- was placed in a 600 -mL Parr® stirred autoclave under nitrogen. To this was added 40 mL of dry, deaerated hexane. The autoclave was stirred and pressurized to 5.5 MPa with ethylene; the ethylene feed was then turned off. The internal temperature peaked briefly at 31 0 C. The reaction was stirred for 14 hr at 23°C as the pressure dropped to 5.3 MPa; the ethylene was then vented. The autoclave contained a clear, yellow, gooey rubber swollen with hexane. The product was dissolved in 200 mL chloroform, filtered through glass wool, rotary evaporated, and held under high vacuum to yield 7.95 g.

(4500 catalyst turnovers) of gummy, rubbery polyethylene. 1H NMR analysis (CDC1 3 96 methyl carbons per 1000 methylene carbons. Gel permeation chromatography (trichlorobenzene, 1350C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=6,900; Mw=118,000; Mw/Mn=17.08.

ExampIp 99 A 108-mg (0.073 mmol) sample of PrPh) 2 DABMe 2 ]PdCHCHC(O)CH3)BAF- was placed in a 600-mL Parr® stirred autoclave under nitrogen. To this was added via syringe 75 mL of deaerated reagent grade methyl acrylate containing 100 ppm hydroquinone monomethyl ether and 100 ppm of phenothiazine. The autoclave was pressurized to 5.5 MPa with-ethylene and was stirred at 35 0 C as ethylene was continuously fed for 90 hr; the ethylene was then vented. The product consisted of a swollen clear foam wrapped around the impeller; 40 mL of unreacted methyl acrylate was poured off the polymer. The polymer was stripped off the impeller and was held under high vacuum to yield 38.2 g of clear, grayish, somewhat-tacky rubber. 1H NMR analysis (CDCI 3 99 methyl carbons per 1000 methylene carbons. Comparison of the integrals of the ester methoxy (3.67ppm) and ester methylene (CH2COOMe; 2.30ppm) peaks with the integrals of the carbon chain 164 o0mW3,sw133 I sp,6 4 nLethyls (0.8-0.9ppm) and methylenes (1.2-1.3ppm) indicated a methyl acrylate content of 0.9 mol% (2.6 This product yield and composition represent 18,400 ethylene turnovers and 158 methyl acrylate turnovers. 13 C NMR analysis: branching per 1000 CH 2 total Methyls (105.7), Methyl Ethyl (22), Propyl Butyl Amyl ;Hex and End Of Chain methyl acrylate ester-bearing -CH(CH2)nCO2CH3 branches as a of total ester: n n=1,2,3 n=0 chemical shifts were referenced to the solvent: the high field carbon of 1,2,4-trichlorobenzene (127.8 ppm). Gel permeation chromatography (tetrahydrofuran, 30 0

C,

polymethylmethacrylate reference, results calculated as polymethylmethacrylate using universal calibration theory): Mn=151,000; Mw=2 72 ,000; Mw/Mn=l.

8 1.

Example 100 A 62-mg (0.074-mmol) sample of [(2,6-i-PrPh) 2 DABMe2]PdMe(Et20) )SbF 6 was placed in a 600-mL Parr® stirred autoclave under nitrogen with 200 mL of deaerated aqueous 10% n-butanol. The autoclave was pressurized to 2.8 MPa with ethylene and was stirred for 16 hr. The ethylene was vented and the polymer suspension was filtered. The product consisted of a fine gray powdery polymer along with some larger particles of sticky black polymer; the polymer was washed with acetone and dried to yield 0.60 g (290 catalyst turnovers) of polyethylene. The gray polyethylene powder was insoluble in chloroform at RT; it was soluble in hot tetrachloroethane, but formed a gel on cooling to RT. 1 H NMR analysis (tetrachloroethane-d2; 100oC): 43 methyl carbons per 1000 methylene carbons. Differential scanning calorimetry exhibited a melting point at 89 0 C (78J/g) with a shoulder at 70 0 C; there was no apparent glass transition.

Example 101 165- 02/O613.sw13311 sp,165 A 78-mg (0.053-mmol) sample of PrPh) 2 DABMe2]PdCH2CH 2 C(0)CH3BAF- was placed in a 600-mL Parr® stirred autoclave under nitrogen. To this was added 40 mL of dry, deaerated t-butyl acrylate containing 100 ppm hydroquinone monomethyl ether. The autoclave was pressurized with ethylene to 2.8 MPa and was stirred and heated at 35 0 C as ethylene was continuously fed at 2.8 MPa for 24 hr; the ethylene was then vented. The product consisted of a yellow, gooey polymer which was dried under high vacuum to yield 6.1 g of clear, yellow, rubbery ethylene/t-butyl acrylate copolymer which was quite tacky. 1 H NMR analysis (CDC13): 102 methyl carbons per 1000 methylene carbons.

Comparison of the integral of the ester t-butoxy (1.44 ppm) peak with the integrals of the carbon chain methyls (0.

8 -0.9ppm) and methylenes (1.

2 -1.3ppm) indicated a t-butyl acrylate content of 0.7 mol% (3.3 This yield and composition represent 3960 ethylene turnovers and 30 t-butyl acrylate turnovers.

Gel permeation chromatography (tetrahydrofuran, 30 0

C,

polymethylmethacrylate reference, results calculated as polyrmethylmethacrylate using universal calibration theory): Mn=112,000; Mw=179,000; Mw/Mn=1.60.

Example 102 A 19-mg (0.022-mmol) sample of {[(2,6-i-PrPh) 2 DABMe 2 PdCH 2

CH

2

C(O)CH

3 }SbF~ was placed in a 600-mL Parr® stirred autoclave under nitrogen. The autoclave was pressurized to 5.2 MPa with ethylene and was stirred for 2 hr; the ethylene feed was then shut off. The autoclave was stirred for 16 hr more as the ethylene pressure dropped to 5.0 MPa; the ethylene was then vented. The autoclave contained a light yellow, granular sponge rubber growing all over the walls and head of the autoclave; this was scraped out to yield 13.4 g (21,800 catalyst turnovers) of spongy, nontacky, rubbery polyethylene which was very strong and elastic. 1 H NMR analysis (CDC 3 90 methyl carbons per 1000 methylene carbons.

166- 02/06/03.sw331 spa. 166 Differential scanning calorimetry exhibitea a glass transition at -50 0 C. Gel permeation chromatography (trichlorobenzene, 1350C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=175,000; Mw=476,000; Mw/Mn=2.72.

Example 103 A 70-mg (0..047-mmol) sample of PrPh) 2 DABMe] PdCH 2

CH

2

C(O)CH

3 }BAF- was placed in a 600-mL Parr® stirred autoclave under nitrogen. To this was added 70 mL of deaerated reagent grade methyl acrylate containing 100 ppm each hydroquinone monomethyl ether and phenothiazine and 0.7 mL (1 wt%; 4.7 mol%) deaerated, deionized water. The autoclave was stirred at 35 0 C as ethylene was continuously fed at 4.8 MPa for 16 hr; the ethylene was then vented. The product consisted of a clear solution. Rotary evaporation yielded 1.46 g of ethylene/methyl acrylate copolymer as a clear oil. The infrared spectrum of the product exhibited a strong ester carbonyl stretch at 1740cm- 1 1H NMR analysis (CDC1 3 118 methyl carbons per 1000 methylene carbons. Comparison of the integrals of the ester methoxy (3.67ppm) and ester methylene (CH2COOMe; 2.30ppm) peaks with the integrals of the carbon chain methyls (0.8-0.9ppm) and methylenes (1.2-1.3ppm) indicated a methyl acrylate content of 0.7 mol% (2.2 This product yield and composition represent 1090 ethylene turnovers and 8 methyl acrylate turnovers. Gel permeation chromatography (trichlorobenzene, 135°C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=362; Mw=908; Mw/Mn=2.51.

Example 104 A 53-mg (0.036-mmol) sample of PrPh) 2 DABMe 2 ]PdCHCH2C(O)CH 3 }BAF' was placed in a 600-mL Parr® stirred autoclave under nitrogen. To this was added 100 mL of dry, deaerated methylene chloride. The autoclave was immersed in a cool water bath and stirred 167- 02/06/03,sw1331 ]sps,167 as it was pressurized to 4.8 MPa with ethylene.

Ethylene was continuously fed with stirring at 4.8 MPa and 23 0 C for 23 hr; the ethylene then was vented. The product consisted of a clear rubber, slightly swollen with methylene chloride. The polymer wastdried under high vacuum at room temperature to yield 34.5 g (34,100 catalyst turnovers) of clear rubbery polyethylene. 1H NMR analysis (CDC13): 110 methyl carbons per 1000 methylene carbons. Gel permeation chromatography (trichlorobenzene, 135C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=243,000; Mw=676,000; Mw/Mn=2.78.

Example 104A A 83-mg (0.056-mmol) sample of PrPh) 2 DABMe 2 ]PdCH 2

CH

2 C (O)CH 3 }BAF was placed in a 600-mL Parr® stirred autoclave under nitrogen. To this was added 70 mL of dry, deaerated, ethanol-free chloroform.

The autoclave was immersed in a cool water bath and stirred as it was pressurized to 4.7 MPa with ethylene.

Ethylene was continuously fed with stirring at 4.7 MPa and 23 0 C for 21 hr; the ethylene then was vented. The product consisted of a pink, rubbery, foamed polyethylene, slightly swollen with chloroform. The polymer was dried under vacuum at 40 0 C to yield 70.2 g (44,400 catalyst turnovers) of pink, rubbery polyethylene which was slightly tacky. 1 H NMR analysis (CDC13): 111 methyl carbons per 1000 methylene carbons.

Gel permeation chromatography (trichlorobenzene, 135 0

C,

polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=213,000; Mw=728,000; Mw/Mn=3.41.

Example 105 A 44-mg (0.052-mmol) sample of PrPh) zDABMez]PdCH 2

CH

2 C(0)CH3}SbF 6 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with mL of dry, deaerated methylene chloride. To this was added 5 mL (5.25 g; 73 mmol) of freshly distilled 168- 02/06/03,swl331 Ispa. 168 acrylic acid (contains a few ppm of phenothiazine as a radical polymerization inhibitor) via syringe and the mixture was immediately pressurized with ethylene at 5.52 kPa and stirred for 40 hr. The dark yellow solution was rotary evaporated and the residue was stirred with 50 mL water for 15 min to extract any acrylic acid homopolymer. The water was drawn off with a pipette and rotary evaporated to yield 50 mg of dark residue. The polymer which had been water-extracted was heated under high vacuum to yield 1.30 g of ethylene/acrylic acid copolymer as a dark brown oil.

The infrared spectrum showed strong COOH absorbances at 3400-2500 and at 1705cm 1 as well as strong methylene absorbances at 3000-2900 and 1470cm 1 A 0.2-g sample of the ethylene/acrylic acid copolymer was treated with diazomethane in ether to esterify the COOH groups and produce an ethylene/methyl acrylate copolymer. The infrared spectrum of the esterified copolymer showed a strong ester carbonyl absorbance at 1750cm-l;.the COOH absorbances were gone.

1 H NMR analysis (CDC1 3 87 methyl carbons per 1000 methylene carbons. Comparison of the integrals of the ester methoxy (3.67ppm) and ester methylene (CH2COOMe; 2.30ppm) peaks with the integrals of the carbon chain methyls (0.8-0.9ppm) and methylenes (1.2-1.3ppm) indicated a methyl acrylate content'of 5.3 mol% (14.7 wt% methyl acrylate 12.3 wt% acrylic acid in the original copolymer). This product yield and composition represent 780 ethylene turnovers and 43 acrylic acid turnovers. Gel permeation chromatography (tetrahydrofuran, 30 0 C, polymethylmethacrylate reference, results calculated as polymethylmethacrylate using universal calibration-theory): Mn=25,000; Mw=42,800; Mw/Mn=1.71.

Listed below are the 13 C NMR data upon which the above analysis is based.

13C NMR Data CDC1 3 0.05M CrAcAc, Freq ppm Intensity 169- 02/06/03,sw331 I spa,169 51.0145 45.434 38.8925 38.5156 37.3899 37.0713 36.7634 36.4182 36.2961 34.459 34.0289 33.7369 33.3705 32.8926 32.3935 32.0271 31.5705 31.1723 29.813 29.3511 29.1387 28.9953 28.613 27.2007 26.744 26.3777 26.006 25.5547 25.0609 24.9175 24.6042 23.7547 23.3777 22.7936 22.6768 22.3211 19.3477 18.8645 14.1814 13.7407 11.0274 10.5124 176.567 174.05 173.779 24.9141 1.11477 2.29147 6.51271 10.7484 17.3903 17.6341 3.57537 6.0822 2.158 9.49713 34.4456 49.2646 18.2918 10.5014 3.5697 30.6837 1.54526 46.4503 117.987 21.034 30.603 7.18386 8.02265 23.8731 46.8498 5.42389 8.13592 5.46013 2.30355 15.7434 2.78914 5.63727 8.07071 3.78032 33.1603 15.4369 5.97477 1.99297 38.5361 6.19758 10.4707 9.61122 9.03673 85.021

MEBO

3B 3BG+, 3EOC 2 EB 4 (tentative) 2 EB4(tentative) 2 EBs+ 2B4 2B4 2B5+, 2EOC 1B1 IB1 1B3 1B4+, 1EOC 182 1B2 EBg carbonyl EBI+ carbonyl EB1+ carbonyl Example 106 A 25-mg (0.029-mmol) sample of PrPh) DABMe2]PdCH 2 CH2C(O)CH3)SbFj was magnetically stirred under 55.2 kPa of ethylene in a 50-mL Schlenk flask with 20 mL of dry methylene chloride and 5 mL g; 39 mmol) of methyl 4-pentenoate for 40 hr at room temperature. The yellow solution was rotary -170- 02106R 3,swl31 evaporated to yield 3.41 g of ethylene/methyl 4pentenoate copolymer as a yellow oil. The infrared spectrum of the copolymer showed a strong ester carbonyl absorbance at 1750cm 1 IH NMR analysis (CDC13): 84 methyl carbons per 1000 methylene carbons.

Comparison of the integrals of the ester methoxy (3.67ppm) and ester methylene (CH2COOMe; 2.30ppm) peaks with the integrals of the carbon chain methyls (0.8- 0.9ppm) and methylenes (1.2-1.3ppm) indicated a methyl 4-pentenoate content of 6 mol% (20 This yield and composition represent about 3400 ethylene turnovers and 200 methyl 4-pentenoate turnovers. 13 C NMR quantitative analysis: branching per 1000 CH 2 total Methyls Methyl Ethyl(18.7), Propyl Butyl Am and end of chains Bu and end of chains ester-bearing branches -CH(CH)nCO 2

CH

3 as a of total ester: n25 n=4 n=1,2,3 n=0 chemical shifts were referenced to the solvent: chloroform-dl (77 ppm). Gel permeation chromatography (tetrahydrofuran, 30 0

C,

polymethylmethacrylate reference, results calculated as polymethylmethacrylate using universal calibration theory): Mn=32,400; Mw=52,500; Mw/Mn=1.

62 Example 107 A 21-mg (0.025-mmol) sample of PrPh) 2 DABMe 2 ]PdCHCH 2 C(0)CH3}SbF6 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with mL of dry methylene chloride and 5 mL (4.5 g; 39 mmol) of methyl 4-pentenoate for 74 hr. The yellow solution was rotary evaporated to yield 0.09 g of a yellow oil, poly[methyl 4-pentenoate].. The infrared spectrum showed a strong ester carbonyl absorbance at 1750cm 1 The 1H NMR (CDC13) spectrum showed olefinic protons at 5.4-5.5ppm; comparing the olefin integral with the integral of the ester methoxy at 3.67ppm indicates an average degree of polymerization of 4 to 5. This example demonstrates the ability of this catalyst to 171 02/06/03,sw13311spa,171 .omopolymerize alpha olefins bearing polar functional groups not conjugated to the carbon-carbon double bond.

Example A 53-mg (0.063-mmol) sample of PrPh) 2 DABMe)PdCHCH 2 C(0)CH3}SbF6 was placed in a 600-mL Parr® stirred autoclave under nitrogen. To this was added 25 mL of dry, deaerated toluene and 25 mL (26 g; 0.36 mol) of freshly distilled acrylic acid containing about 100 ppm phenothiazine. The autoclave was pressurized to 2.1 MPa with ethylene and was stirred for 68 hr at 230C; the ethylene was then vented. The autoclave contained a colorless, hazy solution. The solution was rotary evaporated and the concentrate was taken up in 50 mL of chloroform, filtered through diatomaceous earth, rotary.evaporated, and then held under high vacuum to yield 2.23 g of light brown, very viscous liquid ethylene/acrylic acid copolymer. The infrared spectrum showed strong COOH absorbances at 3400-2500 and at 1705cm-1, as well as strong methylene absorbances at 3000-2900 and 1470cm- 1 A 0.3-g sample of the ethylene/acrylic acid copolymer was treated with diazomethane in ether to esterify the COOH groups and produce an ethylene/methyl acrylate copolymer. The infrared spectrum showed a strong ester carbonyl absorbance at 1750cm-1; the COOH absorbances were gone. 1 H NMR analysis (CDC13): 96 methyl carbons per 1000 methylene carbons. Comparison of the integrals of the ester methoxy (3.67ppm) and ester methylene (CH2COOMe; 2.30ppm) peaks with the integrals of the carbon chain methyls (0.8-0.9ppm) and methylenes. (1.2-1.3ppm) indicated a methyl acrylate content of 1.8 mol% (5.4 wt% methyl acrylate 4.5 wt% acrylic acid in the original copolymer). This product yield and composition represent 1200 ethylene turnovers and 22 acrylic acid turnovers. Gel permeation chromatography (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polyethylene using -172- 0216/03.swI33lspa, 172 aniversal calibration theory): Mn=5,3 3 0; Iw=1.,000; Mw/Mn= 2 82 Example 109 A 600-mL stirred Parr® autoclave was sealed and flushed with nitrogen. Fifty mL (48 g; 0.56 mcl) of dry, deaerated methyl acrylate was introduced into the autoclave via gas tight syringe through a port on the autoclave head. Then 60 mg (0.07 mmol) of PrPh) 2 DABMe 2 ]PdMe(Et2O)}BAF" was introduced into the autoclave in the following manner: a 2.5-mL gas tight syringe with a syringe valve was loaded with 60 mg of {[(2,6-i-PrPh) 2 DABMe 2 PdMe(Et 2 O) }BAF" under nitrogen in a glove box; then 1 mL of dry, deaerated methylene chloride was drawn up into the syringe and the contents were quickly injected into. the autoclave through a head port. This method avoids having the catalyst in solution with no stabilizing ligands.

The autoclave body was immersed in a running tap water bath; the internal temperature was very steady at 22 0 C. The autoclave was pressurized with ethylene to 2.8 MPa and continuously fed ethylene with stirring for hr. The ethylene was then vented and the product, a mixture of methyl acrylate and yellow gooey polymer, was rinsed out of the autoclave with chloroform, rotary evaporated, and held under high vacuum overnight to yield 4.2 g of thick, light-brown liquid ethylene/methyl acrylate copolymer. The infrared spectrum of the product exhibited a strong ester carbonyl stretch at 1740cm- 1 1H NMR analysis (CDC13): 82 methyl carbons per 1000 methylene carbons.

Comparison of the integrals of the ester methoxy (3.67ppm) and ester methylene (CH2COOMe; 2.30ppm) peaks with the integrals of the carbon chain methyls (0.8- 0.9ppm) and methylenes (1.2-1.3ppm) indicated a methyl acrylate content of 1.5 molk (4.4 This product yield and composition represent 2000 ethylene turnovers and 31 methyl acrylate turnovers. 13 C NMR analysis: branching per 1000 CH2: total Methyls Methyl 173- 02/6/03,sw 1331 spa.173 Ethyl Propyl Butyl Ener and End Of Chain methyl acrylate Esterbearing -CH(CH2)nCO2CH3 branches as a of total ester: n 5 n=4 n=1,2,3 n=0 Mole%: Sethylene methyl acrylate chemical shifts were referenced to the solvent: the high field carbon of 1, 2 ,4-trichlorobenzene (127.8 ppm). Gel permeation chromatography (tetrahydrofuran, 30 0

C,

polymethylmethacrylate reference, results.calculated as polymethylmethacrylate using universal calibration theory): Mn=22,000; Mw=45,500; Mw/Mn=2.07.

A mixture of 1.45 g of this ethylene/methyl acrylate copolymer, 20 mL dioxane, 2 mL water, and 1 mL of 50% aqueous NaOH was magnetically stirred at reflux under nitrogen for 4.5 hr. The liquid was then decanted away from the swollen polymer and the polymer was stirred several hours with three changes of boiling water. The polymer was filtered, washed with water and methanol, and dried under vacuum (80oC/nitrogen purge) to yield 1.2 g soft of ionomer rubber, insoluble in hot chloroform. The FTIR-ATR spectrum of a pressed film (pressed at 125°C/6.9 MPa) showed a strong ionomer peak at 1570cm- 1 and virtually no ester carbonyl at 1750cm- 1 The pressed film was a soft, slightly tacky rubber with about a 50% elongation to break. This example demonstrates the preparation of an-ionomer from this ethylene/methyl acrylate polymer.

Example 110 The complex [(2,6-i-PrPh)2DABMe2]PdMeCl (0.020 g, 0.036 mmol) was weighed into a vial and dissolved in 6 ml CH 2 C1 2 NaBAF (0.032g, 0.036 mmol) was rinsed into the stirring mixture with 4 ml of CH2C1 2 There was an immediate color change from orange to yellow. The solution was stirred under 6.2 MPa ethylene in a Fisher Porter tube with temperature control at 19 0 C. The internal temperature rose to 22 0 C during the first minutes. The temperature controller was raised to 0 C. After 35 minutes, the reaction was consuming 174- 021/03.sw 1331 spa, 174 :thylene slowly. After a total reaction'tihe or anout h, there was no longer detectable ethylene consumption, but the liquid level in the tube was noticeably higher. Workup by addition to excess MeOH gave a viscous liquid precipitate. The precipitate was redissolved in CH2C12, filtered through a 0.5 micron PTFE filter and reprecipitated by addition to excess MeOH to give 7.208 g dark brown viscous oil (7180 equivalents of ethylene per Pd). 1H NMR (CDC13) 0.8- 1.0 CH3); 1.0-1.5 CH and CH2). Integration allows calculation of branching: 118 methyl carbons per 1000 methylene carbons. GPC in THF vs. PMMA standard: Mn=12, 7 00 Mw= 28 ,800, Mw/Mn= 2 26 Example 111 The solid complex PrPh) 2 DABMe 2 ]PdMe(Et 2 0) SbF 6 (0.080 g, 0.096 mmol) was placed in a Schlenk flask which was evacuated and refilled with ethylene twice. Under one atm of ethylene, black spots formed in the center of the solid complex and grew outward as ethylene was polymerized in the solid state and the resulting exotherm destroyed the complex. Solid continued to form on the solid catalyst that had not been destroyed by the exotherm, and the next day the flask contained considerable solid and the reaction was still slowly consuming ethylene.

The ethylene was disconnected and 1.'808 g of light gray elastic solid was removed from the flask (644 equivalents ethylene per Pd). The 1H NMR in CDC13 was similar to example 110 with 101 methyl carbons per 1000 methylene carbons. Differential Scanning Calorimetry (DSC): first heat 25 to 1500C, 150C/min, no events; second heat -150 to 150°C, Tg -530C with an endothermic peak centered at -200C; third heat -150 to 2750C, Tg -51°C with an endothermic peak centered at -200C. GPC (trichlorobenzene, 135°C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=1 3 ,000 Mw= 3 1 3 ,000 Mw/Mn= 24 175- 0206103.s1331Ispa. 175 Example 1j The complex [(2,6-i-PrPh) 2 DABMe,)PdMe(Et,0)}sbF,- (0.084 g, 0.100 mmol) was loaded into a Schlenk flask in the drybox followed by 40 ml of dry dioxane. The septum-capped flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene. The light orange mixture was stirred under an ethylene atmosphere at slightly above 1 atm by using a mercury bubbler. There was rapid uptake of ethylene.

A room temperature water bath was used to control the temperature of the reaction. After 20 h, the reaction was worked up by removing the solvent in vacuo to give 10.9 g of a highly viscous fluid (3870 equivalents of ethylene per Pd). Dioxane is a solvent for the Pd complex and a non-solvent .for the polymer product. 1H NMR (CDC1 3 0.8-1.0 CH3); 1.0-1.5 CH and CH 2 Integration allows calculation of branching: 100 methyl carbons per 1000 methylene carbons. GPC (trichlorobenzene, 1350C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Partially resolved trimodal distribution with Mn=16300, Mw=151000 Mw/Mn=9.25. DSC (second heat,-150OC to 150°C, Tg=-63*C, endothermic peak centered at 30°00C.

Example 113 Polymerization of ethylene was carried out according to example 112, using pentane as solvent.

Pentane is a non-solvent for the Pd complex and a solvent for the polymer product. The reaction gave 7.47 g of dark highly viscous fluid (2664 equivalents of ethylene per Pd). 1H NMR analysis (CDCI 3 126 methyl carbons per 1000 methylene carbons. 13C NMR analysis, branching per 1000 CH2: Total methyls (128.8), Methyl Ethyl Propyl Butyl Amyl ZHexyl and end of chain average number of carbon atoms for Hexyl branches 16.6 (calculated from intrinsic viscosity -176- 02/06/03,sw1331 Ispa,176 and GPC molecular weight data). Quantitation of the

CH

2 CH(CH3)CH 2

CH

3 structure per 1000 CH2's: 8.3. These side chains are counted as a Methyl branch and an Ethyl branch in the quantitative branching analysis. GPC (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=9,800, Mw=16,100, Mw/Mn=1.6 4 Intrinsic viscosity (trichlorobenzene, 135 0 C) 0.125 g/dL. Absolute molecular weights calculated by GPC (trichlorobenzene, 135 0 C, polystyrene reference, corrected for branching using measured intrinsic viscosity): Mn=34,900, Mw=58,800, Mw/Mn=1.68.

DSC (second heat, -150°C to 150 0 C, 15 0 C/min)

T

g 71 0 C, endothermic peak centered at -43 °C.

Example 114 Polymerization of ethylene was carried out according to example 112, using distilled degassed water as the medium. Water is a non-solvent for both the Pd complex and the polymer product. The mixture was worked up by decanting the water from the product which was then dried in vacuo to give 0.427 g of dark sticky solid (152 equivalents of ethylene per Pd). 1H NMR analysis (CDCl3): 97 methyl carbons per 1000 methylene carbons. GPC (trichlorobenzene, 135 0

C,

polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=25,100, Mw=208,000, Mw/Mn=8.31.

Example 115 Polymerization of ethylene was carried out according to example 112, using 2-ethylhexanol as the solvent. The Pd complex is sparingly soluble in this solvent and the polymer product is insoluble. The polymer product formed small dark particles of high viscosity liquid suspended in the 2-ethylhexanol. The solvent was decanted and the polymer was dissolved in CHC13 and reprecipitated by addition of excess MeOH.

The solvent was decanted, and the reprecipitated polymer was dried in vacuo to give 1.66 g of a dark 177- 026/03,swI33 I spa, 177 .ighly viscous fluid (591 equivalents of ethylene per Pd). IH NMR analysis (CDC1 3 122 methyl carbons per 1000 methylene carbons. GPC (trichlorobenzene, 1350C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=7,890, Mw=21,600, Mw/Mn=2.74.

Examnle 116 The solid complex PrPh) 2 DABMe 2 ]PdMe(Et 2 0)}SbFe- (0.084 g, 0.100 mmol) was loaded into a Schlenk flask in the drybox. The flask was connected to a Schlenk line under I atm of ethylene, and cooled to -78°C. Solvent,(CH 2 C12, 40 ml) was added by syringe and after equilibrating at -780C under ethylene, the mixture was warmed to room temperature under ethylene. The mixture was stirred under an ethylene atmosphere at slightly above 1 atm by using a mercury bubbler. There was rapid uptake of ethylene. A room temperature water bath was used to control the temperature of the reaction. After 24 h, the reaction was worked up by removing the solvent in vacuo to give 24.5 g of a highly viscous fluid (8730 equivalents of ethylene per Pd). CH2Cl2 is a good solvent for both the Pd complex and the polymer product. The polymer was dissolved in CH2C12, and reprecipitated by addition to excess MeOH in a tared flask. The solvent was decanted, and the reprecipitated polymer was dried in vacuo to give 21.3 g of a dark highly viscous fluid. 1H NMR analysis (CDC13): 105 methyl carbons per 1000 methylene carbons.

C-13 NMR analysis, branching per 1000 CH2: Total methyls (118.6), Methyl Ethyl Propyl Butyl Amyl Hexyl and end of chains average number of carbon atoms for 2 Hexyl branches 22.5 (calculated from intrinsic viscosity and GPC molecular weight data). Quantitation of the -CH 2

CH(CH

3 )CH2CH 3 structure per 1000 CH 2 8.1.

These side chains also counted as a Methyl branch and an Ethyl branch in the quantitative branching analysis.

178- 02/06/03,sw 13311 spa, 178 3PC (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=25,800, Mw=45,900, Mw/Mn=1.78. Intrinsic viscosity (trichlorobenzene, 1350C) 0.24 g/dL. Absolute molecular weights calculated by GPC (trichlorobenzene, 135°C, polystyrene reference, corrected for branching using measured intrinsic viscosity): Mn=104,000, Mw=188,000, Mw/Mn=1.81.

Listed below are the 13 C NMR data upon which the above analysis is based.

179- 02906/03.sw 33 I spa,1 7 9 13C NMR Data TCB, 120C, 0.06M CrAcAc req ppml intensity 39.7233 39.318 38.2022 37.8369 37.2469 36.8335 36.7452 34.9592 34.6702 34.5257 34.2006 33.723 33.3136 32.9323 32.4266 31.9409 31.359 31.0981 30.6606 30.2271 30.1188 29.7455 29.5809 29.3361 29.2157 27.6424 27.526 27.3534 27.1607 27.0042 26.5908 26.3941 25.9446 24.4034 24.2428 23.1391 23.0227 22.6494 20.0526 19.7355 19.2017 14.4175 13.9118 11.1986 10.9617 5.12305 17.6892 17.9361 32.3419 43.1136 10.1653 14.674 10.3554 24.015 39.9342 109.158 36.1658 12.0398 20.7242 6.47794 96.9874 15.2429 19.2981 15.8689 96.7986 54.949 307.576 36.2391 79.3542 23.0783 24.2024 29.8995 23.1626 70.8066 109.892 7.13232 23.945 4.45077 9.52585 11.1161 21.2608 11.2909 103.069 5.13224 37.8832 14.8043 4.50604 116.163 18.5867 32.3855

MB

2

MB

3

MB

3 cB 1 3B3

QB

1 3B3 aB 1 3B 3 ay+B, (4B4, 525, etc.) ay7+, (4B 4 5B5, etc.) ay+B, (4B 4 5B5, etc.) ay+B, (4B4, 5B5, etc.) ay+B, (4B 4

SB

5 etc.)

MB

1

MB

1 3B 3B6+, 3EOC 7+Y+B, 3B4 y+y+B, 354 Y+Y+B, 3B 4 y+y+B, 3B 4 y-y+B, 3B4 T+Y+B, 3B4 747+B, 324 3B4 y+y+B, 3B2, (4 Py+B, 2B 2 (4B5, etc.) Dy+B, 2B2, (4B5, etc.) PY+B, 2B 2 (4B5, etc.) 2B2, (4B 5 etc.) 2B2, (485, etc.) PY+B, 2B2, (4B5, etc.) Py+B, 2B2, etc.) PY+B, 2B2 (4B5, etc.)

DOB

PPB

284 2B4 2B5+, 2EOC 283 18 1 181, Structure XXVII 183 184+, IEOC 182, Structure XXVII 18 2 180- 02A6103,sw133 I spa. 180 Example 117 Polymerization of ethylene was carried out according to example 116, at a reaction temperature of 0 C and reaction time of several hours. The polymer product formed a separate fluid phase on the top of the mixture. The reaction was quenched by adding 2 ml acrylonitrile. The product was moderately viscous fluid, 4.5 g (1600 equivalents of ethylene per Pd). 1 NMR analysis (CDC13): 108 methyl carbons.per 1000 methylene carbons. 13C NMR analysis, branching per 1000 CH2: Total methyls (115.7), Methyl Ethyl Propyl Butyl Amyl >Hexyl and end of chain Quantitation of the

CH

2 CH(CH3)CH 2

CH

3 structure per 1000 CH 2 7.C. These side chains are counted as a Methyl branch and an Ethyl branch in the quantitative branching analysis. GPC (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory: Mn=15, 200 Mw=23, 7 00 Mw/Mn=1.5 6 Example 118 The Pd complex PrPh) 2 DABMe2]PdCH2CH2

CH

2

C(O)OCH

3 )SbF 6 (0.084 g, 0.100 mmol) was loaded into a Schlenk flask in the drybox, and 40 ml of FC-75 was added. The septum-capped flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. The mixture was stirred under an ethylene atmosphere at slightly above 1 atm by using a mercury bubbler. Both the Pd initiator and the polymer are insoluble in FC-75. After 15 days, the reaction flask contained a large amount of gray elastic solid.

The FC-75 was decanted, and the solid polymer was then dissolved in CHC13 and precipitated by addition of the solution to excess MeOH. The polymer was dried in vacuo, and then dissolved in o-dichlorobenzene at 100 0 C. The hot solution was filtered through a 10 pm PTFE filter. The filtered polymer solution was shaken 181 02/06/3,sw13311Ispa. 181 .n a separatory funnel with concentrated sulfuric acid, followed by distilled water, followed by 5% NaHCO 3 solution, followed by two water washes. The polymer appeared to be a milky suspension in the organic layer during this treatment. After washing, the polymer was precipitated by addition to excess MeOH in a blender and dried at room temperature in vacuo to give 19.6 g light gray elastic polymer fluff (6980 equivalents of ethylene per Pd). 1H NMR analysis (CDC13): 112 methyl carbons per 1000 methylene carbons. 13 C NMR analysis, branching per 1000 CH2: Total methyls (114.2), Methyl Ethyl Propyl Butyl Amyl >Hexyl and end of chain average number of carbon atoms for Hexyl branches 14.4 (calculated from intrinsic viscosity and GPC molecular weight data). GPC (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory: Mn=110,000, Mw=265,000, Mw/Mn=2.40. Intrinsic viscosity (trichlorobenzene, 135 0 C) 1.75 g/dL. Absolute molecular weights calculated by GPC (trichlorobenzene, 135 0 C, polystyrene reference, corrected for branching using measured intrinsic viscosity): Mn=214,000, Mw=535,000, Mw/Mn=2.51.

Example 119 Polymerization of ethylene was carried out according to example 112, using the complex PrPh)2DABMe 2 ]PdCH 2

CH

2

CHC(O)OCH

3 }SbF6 (0.084 g, 0.100 mmol) as the initiator and CHC13 as the solvent. The reaction gave 28.4 g of dark viscous fluid (10,140 equivalents of ethylene per Pd). 1 H NMR analysis (CDC1 3 108 methyl carbons per 1000 methylene carbons.

13 C NMR analysis, branching per 1000 CH2: Total methyls (119.5), Methyl Ethyl Propyl Butyl Amyl Hexyl and end of chain GPC (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as linear polyethylene 182- 02/06/3.sw13311 sp,182 .equivalents of ethylene per Pd). Mn estimated by integration of olefin end groups is 300.

Examplp 122 The complex [(2,6-i-PrPh),DABMe 2 )PdMeCl (0.056 g, 0.10 mmol) was loaded into a Schlenk flask in the drybox followed by 40 ml of dry toluene. A solution of ethyl aluminum dichloride (1.37 ml of 0.08 M solution in o-dichlorobenzene) was added while stirring.

Polymerization of ethylene was carried out using this solution according to example 112. The reaction gave 0.255 g of low viscosity fluid, after correcting for the catalyst residue this is 0.200 g (71 equivalents of ethylene per Pd). Mn estimated by integration of olefin end groups is 1300.

1 3 1 Example 124 Methyl acrylate was sparged with argon, dried over activated 4A sieves, passed through activity 1 alumina B in the drybox, and inhibited by addition of 20 ppm phenothiazine. The solid complex PrPh) 2 DABMe2]PdMe(Et 2 0)}SbF,- (0.084 g, 0.100 mmol) was loaded into a Schlenk flask in the drybox. The flask was connected to a Schlenk line under 1 atm of ethylene, and cooled to -78 0 C. Forty ml of CH2C1 2 was added by syringe and after equilibrating at -78 0 C under ethylene, 5 ml of methyl acrylate was added by syringe and the mixture was warmed to room"temperature under ethylene. After 40 h, the reaction was worked up by removing the solvent in vacuo to give 3.90 g of moderately viscous fluid. Integration of the 1H NMR spectrum showed that this copolymer contained 6.9 mole methyl acrylate. No poly(methyl acrylate) homopolymer could be detected in this sample by 1H NMR.

1H NMR shows that a significant fraction of the ester groups are located at the ends of hydrocarbon branches: 3.65(s, -C0 2

CH

3 area=4.5), 2.3(t, -CH2CO2CH3, ester ended branches, area=3), 1.6(m, -CH2CH2CO 2

CH

3 ester ended branches, area=3), 0.95-1.55(m, CH and other CH2, area=73), 0.8-0.95(m, CH3, ends of branches or ends of 184 02/06/o03swl33I Isp..1S4 .sing universal calibration theory): Mn=10,800, Mw=26,800, Mw/Mn=2.47.

Example 120 Polymerization of ethylene was carried out according to example 112, using the complex PrPh) 2 DABMe 2 ]PdMe(OS0 2

CF

3 (0.068g, 0.10 mmol) as the initiator and CHC1 3 as the solvent. The reaction gave 5.98 g of low viscosity fluid (2130 equivalents of ethylene per Pd). 1 H NMR (CDC1 3 0.8-1.0 CH3); 1.0-1.5 CH and CH2); 1.5-1.7 CE3CH=CH- 1.9- 2.1 (broad, -CH2CH=CHCH2- 5.3-5.5 -CH=CH- Integration of the olefin end groups assuming one olefin per chain gives.Mn 630 (DP 24). A linear polymer with this molecular weight and methyl groups at both ends should have 46 methyl carbons per 1000 methylene carbons. The value measured by integration is 161, thus this polymer is highly branched.

Example 121 Polymerization of ethylene was carried out according to example 112, using the complex PrPh) 2

DABH

2 ]PdCH 2

CH

2

CH

2 C(0)OCH 3 }SbF6 (0.082 g, 0.10 mmol) as the initiator and CHC1 3 as the solvent. The reaction gave 4.47 g of low viscosity fluid (1600 equivalents of ethylene per Pd). 1 H NMR (CDC13) is similar to example 120. Integration of the olefin end groups assuming one olefin per chain gives Mn 880 (DP 31). A linear polymer with this molecular weight and methyl groups at both ends should have 34 methyl carbons per 1000 methylene carbons. The value measured by integration is 156, thus this polymer is highly branched.

Example 122 Polymerization of ethylene was carried out according to example 112, using the complex PrPh) 2 DABMel2PdCH 2

CH

2

CH

2 C(O)OCH3.}BC1(C 6

F

s 3 (0.116 g, 0.10 mmol) as the initiator and CHC13 as the solvent.

The reaction gave 0.278 g of low viscosity fluid, after correcting for the catalyst residue this is 0.160 g (57 183 02/06/03,swl331 Ispa. 183 .chains, area=9.5) This is confirmed by the 3 C NMR quantitative analysis: Molet: ethylene methyl acrylate Branching per 1000 CH 2 Total methyls Methyl Ethyl Propyl Butyl Amyl >_Hexyl and end of chain methyl acrylate Ester branches

CH(CH

2 )nCO 2

CH

3 as a of total ester: n25 n=4 n=1,2,3 n=0 GPC of this sample was done in THF vs. PMMA standards using a dual UV/RI detector. The outputs of the two detectors were very similar. Since the UV detector is only sensitive to the ester functionality, and the RI detector is a relatively nonselective mass detector, the matching of the two detector outputs shows that the ester functionality of the methyl acrylate is distributed throughout the entire molecular weight range of the polymer, consistent with a true copolymer of methyl acrylate and ethylene.

A 0.503 g sample of the copolymer was fractionated by dissolving in benzene and precipitating partially by slow addition of MeOH. This type of fractionation experiment is a particularly sensitive method for detecting a low molecular weight methyl acrylate rich component since it should be the most soluble material under the precipitation conditions.

The precipitate 0.349 g, contained 6.9 mole methyl acrylate by 1 H NMR integration, GPC (THF, PMMA standard, RI detector): Mn=19,600, Mw=29,500, Mw/Mn=1.51. The soluble fraction 0.180g (36%) contained 8.3 mole methyl acrylate by 1 H NMR integration, GPC (THF, PMMA standard, RI detector): Mn=11l,700, Mw=19,800, Mw/Mn=1.70. The characterization of the two fractions shows that the acrylate content is only slightly higher at lower molecular weights. These results are also consistent with a true copolymer of the methyl acrylate with ethylene.

185- 02/0603,sw1331 Ispa,185 Example 125 Methyl acrylate was sparged with argon, dried over activated 4A sieves, passed through activity 1 alumina B in the drybox, and inhibited by addition of 20 ppm phenothiazine. The complex PrPh) 2 DABMe 2 ]PdMe(OSO 2

CF

3 (0.068 g, 0.10 mmol) was loaded into a Schlenk flask in the drybox, and 40 ml of CHC13 was added followed by 5 ml of methyl acrylate.

The septum capped flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. The light orange mixture was stirred under an ethylene atmosphere at slightly above 1 atm by using a mercury bubbler. After h, the reaction was worked up by removing the solvent and unreacted methyl acrylate .in vacuo to give 1.75 g of a low viscosity copolymer.

13 C NMR quantitative analysis: Mole%: ethylene methyl acrylate Branching per 1000 CH2: Total methyls (100.9), Methyl Ethyl (19.8), Propyl Butyl Amyl >Hexyl and end of chains methyl acrylate This sample is low molecular weight total methyls does not Sinclude end of chain methyls. Ester branches CH(CH2)nCO2CH 3 as a of total ester: nS5 n=4 n=1,2,3 n=0 6.3).

Example 126 Ethylene and methyl acrylate were copolymerized according to example 125 with catalyst PrPh) 2 DABMe]PdCH 2

CH

2

CH

2

C(O)OCH

3 }BAF- (0.136 g, 0.10 mmol) in CH 2

CI

2 solvent with a reaction time of 72 hours to give 4.93 g of copolymer.

Example 127 Ethylene and methyl acrylate were copolymerized according to example 125 with catalyst PrPh) 2 DABMe2)PdCH 2

CH

2

CH

2 C(0)OCH 3 )SbFj" (0.084 g, 0.10 mmol) with a reaction time of 72 hours to give 8.19 g of copolymer.

-186- 02/O O3.swi331I pa.,l Example 128 Ethylene and methyl acrylate were copolymerized according to example 125 with catalyst PrPh) 2 DABH,]PdCH 2

CH

2

CH

2

C(O)OCH

3 }SbF(" (0.082 g, 0.10 mmol) to give 1.97 g of copolymer.

Example 129 Ethylene and methyl acrylate were copolymerized according to example 125 with catalyst PrPh),DABMe 2 }PdMe(CH 3 CN)}SbF 6 e (0.080 g, 0.10 mmol) to give 3.42 g of copolymer. The 1H NMR shows primarily copolymer, but there is also a small amount of poly(methyl acrylate) homopolymer.

Example 130 Ethylene and methyl acrylate (20 ml) were copolymerized in 20 ml of -CHC1 3 according to example 125 using catalyst PrPh) 2 DABMe2]PdCH2CH2CHCC(O)OCH3}SbF" (0.339 g, 0.40 mmol) to give 2.17 g of copolymer after a reaction time of 72 hours. 13 C NMR quantitative analysis: Mole%: ethylene methyl acrylate Branching per 1000 CH2: Total methyls Methyl Ethyl Propyl Butyl Amyl and end of chains methyl acrylate (138.1). Ester branches CH(CH2)nCO2CH3 as a of total ester: n>5 n=4 n=1,2,3 n=0 (25.4).

Example 131 Ethylene and methyl acrylate (20 ml) were copolymerized in 20 ml of CHC13 at 50°C for 20 hours according to example 125 using catalyst PrPh) 2 DABMe2]PdCH2CH 2

CH

2 C(O)OCH3}SbFs (0.339 g, 0.40 mmol) to give 0.795 g of copolymer. DSC (two heats, 150 to +150 0 C, 15°C/min) shows Tg= -480C.

Example 132 A solution of the ligand (2,6-i-PrPh)2DAB(Me2) (0.045 g, 0.11 mmol) dissolved in 2 ml of CHC13 was added to a solution of the complex [PdMe(CH 3 cyclooctadiene)H+SbF6 (0.051 g, 0.10 mmol) in 2 ml of CHC1 3 This mixture was combined with 35 ml of 187- 0206/03,swl3311 spa,187 additional CHC13 and 5 ml of methyl acrylate in a Schlenk flask in a drybox, and then a copolymerization with ethylene was carried out according to example 125 to give 1.94 g of copolymer.

Example 133 Methyl acrylate (5 ml) was added to the solid catalyst 6-i-PrPh) 2 DABMe 2 PdMe (Et20) )BF, (0 069g, 0.10 mmol) followed by 40 ml of CHCl 3 The addition of methyl acrylate before the CHC13 is often.important to avoid deactivation of the catalyst. A copolymerization with ethylene was carried out according to example 125 to give 2.87 g of copolymer.

Characrerization of polv(ethvlene-co-methvl ac-rIm-ae b~y -IH NMR NMR spectra in CDC1 3 were integrated polymer compositions and branching ratios calculated. See example 124 for chemical assignments.

and the were shifts and Example Yield(g) methyl acrylate CH 3 per C0 2

CH

3 per S _(mole 1000 CH 2 1000 CH2 124 3.9 6.9 80 42 125 1.75 7.1 104 126 4.93 5.6 87 34 127 8.19 6.1 87 37 128 1.97 7.3 159 129 3.42 9.5 86 59 130 2.17 22.8 29 137 131 0.795 41 14 262 132 1.94 6.1 80 36 133 2.87 8.2 70 49 Molecular Weight Characterization GPC was done in THF using PMMA standards and an RI detector except for example 133 which was done in trichlorobenzene at 135°C vs. polystyrene reference 188- o 0 206/03.swI33 sp., with results calculated as linear polyethylene using universal calibration theory. When polymer end groups could be detected by 1H NMR (5.4 ppm, multiplet, CH=CH-, internal double bond), Mn was calculated Sassuming two olefinic protons per chain.

Example M n

M

w Mw/Mn Mn 1 H NMR) 124 15,500 26,400 1.70 125 1,540 2,190 1.42 850 126 32,500 49,900 1.54 127 12,300 22,500 1.83 128 555 595 1.07 360 129 16.100 24,900 1.55 130 800 3,180 3.98 1.800 131 1,100 132 15,200 26,000 1.71 133 5,010 8,740 1.75 Example 134 Ethylene and t-butyl acrylate (20 ml) were copolymerized according to example 130 to give 2.039 g of viscous fluid. 1H NMR of the crude product showed the desired copolymer along with residual unreacted tbutyl acrylate. The weight of polymer corrected for monomer was 1.84 g. The sample was reprecipitated to remove residual monomer.by slow addition of excess MeOH to a CHC13 solution. The reprecipitated polymer was dried in vacuo. 1H NMR (CDC13): 2.2(t, -CH 2 CO2C(CH3)3, ester ended branches), 1.6(m, -CH 2

CH

2 CO2C(CH3)3, ester ended branches), 1.45(s, -C(CH3)3), 0.95-1.45(m, CH and other CH2), 0.75-0.95(m, CH3, ends of hydrocarbon branches or ends of chains). This spectrum shows that the esters are primarily located at the ends of hydrocarbon branches; integration gave 6.7 mole tbutyl acrylate. 13 C NMR quantitative analysis, branching per 1000 CH 2 Total methyls Methyl Ethyl Propyl Butyl ?Amyl 189- 0206/03,swl331 Ispa, 18 9 :nd end of chains -C02C(CH 3 3 ester (43.2).

Ester branches -CH(CH2)nC02C(CH 3 3 as a of total ester: n 5 n=1,2,3,4 n=0

GPC

(THF, PMMA standard): Mn=6000 Mw=83i0 Mw/Mn 1.39.

Example 135 Glycidyl acrylate was vacuum distilled and inhibited with 50 ppm phenothiazine. Ethylene and glycidyl acrylate (5 ml) were copolymerized according to Example 125 using catalyst PrPh) 2 DABMe 2 )PdCHCHCH 2 C(O)OCH3)SbF' (0.084 g, 0.10 mmol). The reaction mixture was filtered through a fritted glass filter to remove chloroform insolubles, and the chloroform was removed in vacuo to give 14.1 g viscous yellow oil which still contained residual unreacted glycidyl acrylate. The sample was reprecipitated to remove residual monomer by slow addition of excess acetone to a CHC13 solution. The reprecipitated polymer was dried in vacuo to give 9.92 g of copolymer containing 1.8 mole glycidyl acrylate.

1 H NMR (CDC1 3 4.4, 3.9, 3.2, 2.85, 2.65 (multiplets, 1H each -CH 2

CHCH

2 0 2.35 (t,

S

-CH2CO 2

CH

2

CHCH

2 0, ester ended branches), 1.65(m1 L i -CH2CH2CO 2

CH

2

CHCH

2 0, ester ended branches), 0.95-1.5(m.C H and other CH2), 0.

7 5-0.95(m, CH 3 ends of hydrocarbon branches or ends of chains). This spectrum shows that the epoxide ring is intact, and that the glycidyl ester groups are primarily located at the ends of hydrocarbon branches. GPC (THF, PMMA standard): Mn=63,100 Mw=179,000 Mw/Mn 2.85.

1 3 C NMR quantitative analysis, branching per 1000

CH

2 Total methyls (101.7), Methyl Ethyl Propyl Butyl Amyl Hexyl and end of chains Ester branches -CH(CH 2 )nCO 2

R

as a of total ester: n5 n=4 (small amount), n=1,2,3 n=0 190- 02J06/03,sw133 I spa. A 3.24-g sample of the copolymer was dissolved in mL of refluxing methylene chloride. A solution of 0.18 g oxalic acid dihydrate in 5 mL of 1:1 chloroformacetone was added to the solution of copolymer and the solvent was evaporated off on a hot plate. The thick liquid was allowed to stand in an aluminum pan at room temperature overnight; the pan was then placed in an oven at 70 0 C for 1.5 hr followed by 110°C/vacuum for hr. The cured polymer was a dark, non-tacky soft rubber which tore easily (it had a very short elongation to break despite its rubberiness).

Example 136 1-Pentene (20 ml) and methyl acrylate (5 ml) were copolymerized in 20 ml chloroform for 96 hours using catalyst [(2,6-i-PrPh) 2 DABMe 2 ]PdCH 2 CH2CH 2 C(O)OCH}SbF.

(0.084 g, 0.10 mmol). The solvent and unreacted monomers were removed in vacuo to give 0.303 g copolymer (0.219 g after correcting for catalyst residue). The 1 H NMR spectrum was similar to the ethylene/methyl acrylate copolymer of example 124 suggesting that many of the ester groups are located at the ends of hydrocarbon branches. Integration shows that the product contains 21 mole methyl acrylate.

There are 65 acrylates and 96 methyls per 1000 methylene carbons. GPC (THF, PMMA standard): Mn=6 400 Mw=11 200 Mw/Mn 1.76.

Example 137 Benzyl acrylate was passed through activity 1 alumina B, inhibited with 50 ppm phenothiazine, and stored over activated 4A molecular sieves. Ethylene and benzyl acrylate (5 ml) were copolymerized according to example 135 to give 11.32 g of viscous fluid. 1

H

NMR of the crude product showed a mixture of copolymer and unreacted benzyl acrylate (35 wt The residual benzyl acrylate was removed by two reprecitations, the first by addition of excess MeOH to a chloroform solution, and the second by addition of excess acetone to a chloroform solution. 1H NMR (CDCl 3 7.35 (broad 191 02/06/03,swt331 I spa. 191 -CH2C6H5), 5.1(s, -CH2C6H5), 2.35(t, -CH2CO2CH 2 C6H 5 ester ended branches), 1.6(m, -CH2CH 2

CO

2

CH

2 C6H5, ester ended branches), 0.95-1.5(m, CH and other CH2), 0.75- 0.95(m, CH3, ends of hydrocarbon branches or ends of chains). Integration shows that the product contains 3.7 mole benzyl acrylate. There are 21 acrylates and 93 methyls per 1000 methylene carbons. GPC (THF, PMMA standard): Mn=46,200 Mw=73,600 Mw/Mn 1.59.

13C NMR quantitative analysis, Branching per 1000

CH

2 Total methyls Methyl Ethyl (20.3), Propyl Butyl Amyl Hexyl and end of chains benzyl acrylate Ester branches -CH(CH 2 )nCO 2 R as a of total ester: n n=4 n=1,2,3 n=0 (6) Example 138 l-Pentene (10 ml) and ethylene (1 atm) were copolymerized in 30 ml chloroform according to example 125 using catalyst PrPh) 2 DABMe,]PdCH2CH 2 CH2

C

(0)OCH})SbF, (0.084 g, 0.10 mmol) to give 9.11 g highly viscous yellow oil The 1I NMR spectrum was similar to the poly(ethylene) of example 110 with 113 methyl carbons per 1000 methylene carbons. 13 C NMR quantitative analysis, branching per 1000 CH2: Total methyls (119.5), Methyl Ethyl Propyl Butyl Amyl Hexyl and end of chains GPC (trichlorobenzene, 135°C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=25,000, Mw=44,900, Mw/Mn=1.79.

Listed below are the 1C NMR data upon which the above analysis is based.

13 C NMR Data TCB, 120C, 0.05M CrAcAc Freq ppm Intensity 39.6012 5.53532 39.4313 6.33425

MB

2 38.3004 8.71403 MB3+ 37.9446 17.7325 MB3+ 37.2809 36.416 OB1, 3B3 36.7659 5.10586 aB 1 3B 3 192- 021A03.sw1331 sp. 192 34.3181 56.1758 ay+B 33.8243 15.6271 ay+B 33.3942 8.09189 MB1 32.9854 20.3523 MB 1 32.6721 4.35239 MB 1 32.327 4.06305 3B 31.9394 27.137 3B6+, 3 EOC 31.4031 9.62823 y+y+E. 3B 4 30.235 52.8404 Y+Y+B, 3B 4 29.7518 162.791 y+y+B, 3B 4 29.3164 26.506 y+y+B. 3B 4 27.5695 15.4471 By+B, 2B 2 27.1341 59.1216 By+B, 2B 2 26.4811 8.58222 By+B, 2B 2 24.4475 5.93996 PPB 23.12 5.05181 2B 4 22.6369 29.7047 2B5+, 2 EOC 20.1626 6.29481 2B3 19.7378 31.9342 1B 1 19.2068 3.93019 IB 1 14.2582 5.59441 IB 3 13.8706 36.3938 1B4+, 1 EOC 10.9768 9.89028 IB 2 Example 139 1-Pentene (20 ml) was polymerized in 20 ml chloroform according to example 138 to give 2.59 g of viscous fluid (369 equivalents 1-pentene per Pd).

Integration of the 1H NMR spectrum showed 118 methyl carbons per 1000 methylene carbons. DSC (two heats, 150 to +150°C, 15°C/min) shows Tg= -58 0 C and a low temperature melting endotherm from -50°C to 30 0 C (32 J/g).

13C NMR quantitative analysis, branching per 1000 CH2: Total methyls (118), Methyl Ethyl (none detected), Propyl Butyl (non detected), .Amyl and end of chains GPC (trichlorobenzene, 135cC, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn= 22 ,500, Mw= 43 ,800, Mw/Mn,1.94.

Listed below are the 3C NMR data upon which the above analysis is based.

193- 02/06 3,sw1331 spa,193 13C NMR data TCB, 120C, 0.05M CrAcAc Frea ppm Intensity 42.6277 4.69744 aa for Me Et+ 39.5428 9.5323 3 rd carbon of a 6+ carbon side chain that has a methyl branch at the 4 position 38.1357 3.59535 37.8384 13.9563 MB3 37.5888 28.4579 37.2224 54.6811 aB 1 ,3B 3 35.5287 6.51708 35.2419 3.55603 34.6366 7.35366 34.2437 22.3787 32.911 45.2064

MB

1 32.5977 10.5375 32.38 4.02878 31.8809 14.1607 3B 6 3EOC 30.6916 8.44427 y+Y+B 30.0703 63.1613 y+y+B 29.6987 248 yy+B 29.2633 17.9013 y+y+B 28.8916 3.60422 27.1182 66.2971 Py+B, (4B 5 etc.) 24.5324 16.8854 22.5784 16.0395 2B5+, 2EOC 20.1041 13.2742 19.6952 54.3903 IB1, 2B3 14.2104 12.2831 13.8281 16.8199 1B 4 +,EOC,1B 3 Integration of the CH2 peaks due to the structure -CH(R)CH2CH(R')- where R is an alkyl group, and R' is an alkyl group with two or more carbons showed that in 69% of these structures, R Me. The region integrated for the structure where both R and R' are 2Ethyl was 39.7 ppm to 41.9 ppm to avoid including an interference from another type of methylene carbon on a side chain.

Example 140 [(2,6-i-PrPh) DABMe,]PdMeCl (0.020 g, 0.036 mmol) was dissolved in 4 ml CH 2 C1 2 and methyl acrylate (0.162 g, 0.38 mmol, inhibited with 50 ppm phenothiazine) was added while stirring. This solution was added to a stirred suspension of NaBAF (0.033 g, 0.038 mmol) in 4 ml of CH2C12. After stirring for 1 194- 0 2/06/03.swl331 Ispa, 194 our, the mixture was filtered through a 0.5 pm PTFE membrane filter to remove a flocculant gray precipitate. The solvent was removed from the filtrate in vacuo to give a solid which was recrystallized from a CH2Cl2/pentane mixture at -40 0 C to give 0.39 g yield) of orange crystalline PrPh) 2 DABMe 2 PdCH 2 CH2CH 2 C (O)OCH 3 BAF'. 18 NMR (CDC1 3 0.65(m, CH2, 2H); 1.15-1.45(four sets of doublets for -CH(CH3)2 and multiplet at 1.4 for a CH2, .total area 26H); 2.19,2.21 CH 3 of ligand backbone, 6H); 2.40(m, CH2, 2H); 2.90 -CH(CH3)2, 4H) 3.05(s, CO2CH3, 3H); 7.25-7.75(m, aromatic H of ligand and counterion, 19H).

All GPC data reported for examples 141-170, 177, and 204-212 were run in trichlorobenzene vs.

polyethylene standards unless otherwise indicated. All DSC data reported for examples 141-170, 177, and 204- 212 (second heat, -150 0 C to 1500, 10 or 15 0 C/min) Example 141 A Schlenk flask containing PrPh) 2

DABH

2 ]NiMe(Et 2 O) }BAF' (1.3 mg, 8.3 x 10- 7 mol) under an argon atmosphere was cooled to -78 0 C. Upon cooling, the argon was evacuated and the flask backfilled with ethylene (1 atm). Toluene (75 mL) was added via syringe. The polymerization mixture was then warmed to 0 C. The solution was stirred for 30 minutes Polymer began to precipitate from the solution within minutes. After 30 minutes, the polymerization was terminated upon exposing the catalyst to air. The polymer was precipitated from acetone, collected by filtration and washed with 6 M HCI, water, and acetone.

The polymer was dried in vacuo. The polymerization yielded 1.53 g of polyethylene (1.3 x 105 TO). Mn 91,900; Mw 279,000; Mw/Mn 3.03; Tm 129 0 C. 1H NMR

(C

6

D

5 C1, 142 0 C) 0.6 methyls per 100 carbons.

Example 142 The reaction was done in the same way as in Example 141 using 1.3 mg of 195- 02/0.6/.10sw33 I spa. 195 rPh)2DABMe] NiMe (Et20) }BAF (8.3 x 10- 7 mol). The polymer was isolated as a white solid (0.1 g).

Examples 143-148 General procedure for the polymerization of 3 ethylene by the methylaluminoxane (MAO) activation of nickel complexes containing bidentate diimine ligands: Polymerization at 0 C: The bisimine nickel dihalide complex (1.7 x 10 5 mol) was combined with toluene (100 mL) in a flame dried Schlenk flask under 1 atmosphere ethylene pressure. The polymerization was cooled to 0 C in an ice-water bath. The mixture was stirred at 0°C for 15 minutes prior to activation with MAO.

S Subsequently, 1.5 mL of a 10% MAO (100 eq) solution in toluene was added onto the nickel dihalide suspension.

The solution was stirred at 0°C for 10, 30, or minutes. Within minutes increased viscosity and/or precipitation of polyethylene was observed. The polymerization was quenched and the polymer precipitated from acetone. The polymer was collected by suction filtration and dried under vacuum for 24 hours. See Table I for a detailed description of molecular weight and catalyst activity data.

Example No. Catalyst 143 [(2,6-i-PrPh) 2 DABH2] NiBr 2 144 [(2,6-i-PrPh) 2 DABMe 2 NiBr 2 145 (2,6-MePh) 2

DABH

2 NiBr 2 146 (2,6 -i-PrPh) 2 DABAn]NiBr 2 147 [(2,6-MePh) DABAn] NiBr 2 148 [(2,6-MePh) 2 DABMe 2 NiBr, Exam, Condi- Yield TO/ M n Mw M,/Mn Thermal tionsl hr-mol Analysis catalyst

(CC)

143 0C. 30 m 5.3 22,700 80,900 231.000 2.85 119 (TmJ 144= 0C. 30 m 3.8 16,300 403,000 795,000 1.97 115 (T m 145- 0C. 30 m 3.4 14,300 42,900 107,000 2.49 131 (Tm) 146, 0-C.30m 7.0 29,900 168,000 389,000 2.31 107 (Tm, 147 0'C.0Om 3.7 47,500 125,000 362,000 2.89 122 (Tm) 148 O'C. 10m 5.1 65,400 171,000 440,000 2.58 115 (Tm) 196- 07 2 06/03.swl33 I sp, 196 1 Polymerization reactions run at 1 atmosphere ethylene pressure.

2 Branching Analysis by 13CNMR per 1000 CH 2 Ex. 144: Total methyls Methyl (43.4), Ethyl Propyl Butyl >Butyl and end of chains Ex. 146: Total methyls Methyl (65.3), Ethyl Propyl Butyl Amyl 2 Hexyl and end of chains (10.2).

3 Ex. 145: 'H NMR (C 6 DsCl), 1420C) 0.1 methyl per 100 carbon atoms.

Examples 149-154 Polymerization at Ambient Temperature The general procedure described for the MAO activation of the diimine-nickel dihalides was followed in the polymerizations detailed below, except all polymerizations were run between 25-300C.

Example No. Catalyst 149 [(.2,6-i-PrPh) 2 DABH2]NiBr 2 150 [(2,6-i-PrPh) 2 DABMe 2 NiBr 2 151 (2,6-MePh) 2

DABH

2 NiBr 2 152 [(2,6-i-PrPh) 2 DABAn]NiBr 2 153 -MePh) 2 DABAn] NiBr 2 154 [(2,6-MePh),DABMe2] NiBr Exam. Condi- Yield TO/ Mn w MwM n Thermal tions hr-mol Analysis catalyst

C

149 30°C.30 2.5 12,200 .15500 34,900 2.25 m 150' 25 C,30 3.4 14,500 173,000 248,000 1.44 -51 (Tg) m 151 25C.30 7.2 30,800 13,900 39,900 2.88 90,112 m (Tm) 152' 25OC.30 4.2 18,000 82;300 175,000 2.80 39 (Tm) m 153 25C .10 4.9 62,900 14,000 25,800 1.85 m 154 25 0 C.10 3.7 47,500 20,000 36,000 1.83 m 197- 02/06/03,sw13311 spa.197 1 Polymerization reactions run at 1 atmosphere ethylene pressure.

2 Branching Analysis by "C NMR per 1000 CH 2 Ex. 150: Total methyls (116.3), Methyl (93.5), Ethyl Propyl Butyl Am -Hex and end of chains (11.2).

Ex. 152: Total methyls (141.9), Methyl (98.1), Ethyl Propyl Butyl Amyl Hex and end of chains Quantitation of the

CH

2

CH(CH

3

)CH

2

CH

3 structure per 1000 CH 2 8.

3 Ex. 151: IH NMR (C 6

D

s Cl), 142°C) 3 methyl per 100 carbon atoms.

Example 155 A standard solution of [(2,6-i-PrPh) 2 DABAn]NiBr, was prepared as follows: 1,2-difluorobenzene (10 mL) was added to 6.0 mg of [(2,6-i-PrPh) 2 DABAn]NiBr 2 (8.4 x 6 mol) in a 10 mL volumetric flask. The standard solution was transferred to a Kontes flask and stored under an argon atmosphere.

The standard catalyst solution (1.0 mL, 8.4 x 7 mol catalyst) was added to a Schlenk flask which contained 100 mL toluene, and was under 1 atmosphere ethylene pressure. The solution was cooled to 0 0 C, and mL of a 10% solution of MAO (21000 eq) was added.

The solution was stirred for 30 minutes. Polymer began to precipitate within minutes. The polymerization was quenched and the polymer precipitated from acetone.

The resulting polymer was dried in vacuo (2.15 g, 1.84 x 10 S TO). Mn 489,000; Mw 1,200,000; Mw/Mn 2.47 Example 1 IS The polymerization of ethylene at 250C was accomplished in an identical manner to that described in Example 155. The polymerization yielded 1.8 g of polyethylene (1.53 x 105 TO). Mn 190,000; Mw 410,000; Mw/Mn 2.16; 1H NMR (C 6 DsCI, 142 0 C) 7 methyls per 100 carbons.

Example 157 198 0 2 0 603swl331hsp, 98 A standard solution of [(2,6-MePh) 2 DABAnJNiBr 2 was prepared in the same way as described for the complex in Example 155 using 5.0 mg of [(2,6-MePh)2DABAn]NiBr 2 (8.4 x 10- 6 mol).

Toluene (100 mL) and 1.0 mL of the standard solution of complex 5 (8.3 x 10- 7 mol catalyst) were combined in a Schlenk flask under 1 atmosphere ethylene pressure. The solution was cooled to 0°C, and 1.5 mL of a 10% solution of MAO(Z1000 eq) was added. The polymerization mixture was stirred for 30 minutes. The polymerization was terminated and the polymer precipitated from acetone. The reaction yielded 1.60 g of polyethylene (1.4 x 10 s TO). Mn 590,000; Mw 1,350,000; Mw/Mn 2.29.

Example Toluene (200 mL) and 1.0 mL of a standard solution of [(2,6-i-PrPh) 2 DABAn]NiBr 2 (8.3 x 10- mol catalyst) were combined in a Fisher-Porter pressure vessel. The resulting solution was cooled to 0°C, and 1.0 mL of a 10% MAO 1000 eq) solution in toluene was added to activate the polymerization. Subsequent to the MAO addition, the reactor was rapidly pressurized to 276 kPa. The solution was stirred for 30 minutes at 0°C.

After 30 minutes, the reaction was quenched and polymer precipitated from acetone. The resulting polymer was dried under reduced pressure. The polymerization yielded 2.13 g of white polyethylene (1.82.x 105 TO).

Mn 611,000; Mw 1,400,000; Mw/Mn 2.29; Tm 123°C; IH NMR (C6DsCI, 142 0 C) 0.5 methyls per 100 carbons.

Examples 159-160 Polymerization of Propylene The diimine nickel dihalide complex (1.7x10- 5 mol) was combined with toluene (100 mL) in a Schlenk flask under i atmosphere propylene pressure. The polymerization was cooled to 0 C, and 1.5 mL of a MAO (100 eq) solution in toluene was added. The solution was stirred for 2 hours. The polymerization -199- 02/06/03,sw1331 Ispa,199 'as quenched and the polymer precipitated from acetone.

The polymer was dried under vacuum.

Example No. Catalyst 159 (2,6-i-PrPh) 2 DABH2] NiBr 2 160 [(2,6-i-PrPh)iDABAn NiBr 2 Exam. Condi- Yield TO/ M n Mw M,/M n Thermal tionsI hr.mol Analysis catalyst_ (Oc) 159 0°C. 2 h 1.3 900 131.000 226,000 1.72 -20 (T a 160 00C.2h 4.3 2,900 147,000 235,000 1.60 -78, (To) Ex. 159: carbon atoms.

Ex. 160: carbon atoms.

per 1000 CH2: aGPC (toluene, polystyrene standard) H NMR (C 6

D

s C1), 142 0 C) 30 methyls per 100 H NMR (C 6

D

s Cl), 142 0 C) 29 methyls per 100 Quantitative 13 C NMR analysis, branching Total methyls (699). Based on the total methyls, the fraction of 1,3-enchainment is 13%.

Analysis of backbone carbons (per 1000 CH 2 8+ (53), 5+/y (0.98).

Listed below above analysis is are the 'C NMR data upon which the based.

13 C NMR Data TCB, 140C, 0.05M CrAcAc Intensity Freq ppm 47.3161 46.9816 46.4188 45.84 38.4702 38.0985 37.472 37.2915 35.3747 34.5623 33.3145 32.996 30.9464 30.6703 30.081 53.1767 89.3849 82.4488 23.1"84 12.8395 29.2643 18.6544 24.8559 15.6971 14.6353 14.2876 12.2454 24.2132 57.4826 30.122 y to single branch -200- 026/03,swl33 1 tspa,200 29.6987 29.2186 6* to branch 28.3659 298.691 27.4792 33.2539 27.1235 29.7384 24.5324 9.45408 21.1554 20.0541 20.6244 110.077 19.9926 135.356 16.9342 8.67216 16.4829 8.81404 14.9962 8.38097 Example 161 [(2,6-i-PrPh) 2 DABH2]NiBr2 (10 mg, 1.7 x 10- 5 mol) was combined with toluene (40 mL) under a N 2 atmosphere. A 10% solution of MAO (1.5 mL, 100 eq) was added to the solution. After 30 minutes, the Schlenk flask was backfilled with propylene. The reaction was stirred at room temperature for 5.5 hours. The polymerization was quenched, and the resulting polymer dried under vacuum (670 mg, 213 Mn 176,000; Mw 299,000; Mw/Mn 1.70. Quantitative 13C NMR analysis, branching per 1000 CH2: Total methyls (626), Methyl (501), Ethyl >Butyl and end of chain Based on the total methyls, the fraction of 1,3enchainment is 22%. Analysis of backbone carbons (per 1000 CH2) 6 (0.76).

Examples 162-165 The diimine nickel dihalide catalyst precursor (1.7xIO' 5 mol) was combined with toluene (40 mL) and 1hexene (10 mL) under a N 2 atmosphere. Polymerization reactions of 1-hexene were run at both 0 C and room temperature. A 10% solution of MAO (1.5 mL, 100 eq) in toluene was added. Typically the polymerization reactions were stirred for 1-2 hours. The polymer was precipitated from acetone and collected by suction filtration. The resulting polymer was dried under vacuum.

-201- 02/06/03.sw 1331 IspB.201 Ex. No.

162 163 164 165 Catalyst [(2,6-i-PrPh),DABH NiBr, [(2,6-i-PrPh) 2 DABAn]NiBr S(2, 6-i-PrPh) 2

DABH

2 ]NiBr, [(2,6-i-PrPh) 2 DABAn NiBr, Exam. Condi- Yield TO/ Mna Mw M/M n Thermal tions 1 hr-mol Analysis catalyst

(C)

I, 162 25C. I h 2100 173,000 318,000 -4g (7 1.84 163 250C, Ih 1.2 860 314,000 642,000 2.05 -54 (Tg) -19 (Tm) 164 0 0 C. 2h 3.0 1100 70,800 128,000 1.80 -45 165 0*C. 2h 1.5 540 91,700 142,000 1.55 -49 aGPC (toluene, polystyrene standards).

Branching Analysis Ex. 162: by 13 C NMR per 1000

CH

2 Total methyls (157.2), Methyl Ethyl Propyl Butyl (101.7), Am and end of chain -202o02O0603,sw 1331 I spa.202 13C NM data (Example 162) Frea nm 42.8364 41.3129 40.5759 37.8831 37.2984 36.6684 35.5773 34.655 34.3091 33.8356 33.428 32.9957 31.9169 31.5546 31.1552 30.5993 30.274 30.1258 29.747 29.1047 28.8823 28.1289 27.5648 27.1777 27.0213 26.9142 26.4572 23.2085 22.6074 20.0669 19.6963 15.9494 14.3477 13.8742 TCB, 120C, 0.05M CrAcAc Intensity 7.99519 Me 27.5914 a 19.6201 aa 14.7864 Me 93.6984 Me 6.99225 Me 36.067 Me 55.825 Me 63.3862 Me 24.1992 Me 53.7439 Me 51.1648 Me 17.4373 Mel 14.008 Mel 10.6667 Mel 34.6931 Mel 56.8489 Mel 42.1332 Mel 97.9715 Mel 47.1924 Mel 64.5807 Mel 13.6645 Mel 61.3977 Mel 50.9087 Mel 31.6159 Mel 31.9306 Mel 4.715666 Mel 154.844 2B 12.0719 2B, 8.41495 1B 57.6935 18 17.7108 8.98123 248 IB, thine to two Eth' branches to two Eth* branches thines and Methylenes thines and Methylenes thines and Methylenes' thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes.

thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes thines and Methylenes 4

;+,EOC

1 1 4+,EOC Example 166 (2,6-i-PrPh)2DABMe2]NiBr 2 (10.4 mg, 1.7 x 10mol) was combined with toluene (15 mL) and 1-hexene mL) under 1 atmosphere ethylene pressure. The solution was cooled to 0°C, and 1.5 mL of a 10% MAO (100 eq) solution in toluene was added. The reaction was stirred at 0°C for 2.5 hours. The polymerization was quenched and the polymer precipitated from acetone.

The resulting polymer was dried under reduced pressure Mn 299,000; Mw 632,000; Mw/Mn 2.12.

-203 02/06/03,swl331 I spa,203 Branching Analysis by 13 C NMR per 1000 CH 2 Total methyls (101.3), Methyl Ethyl Propyl Butyl Amyl and end of chains (11.5).

Example 167 [(2,6-i-PrPh) 2

DABH

2 )NiBr 2 (10 mg, 1.7 x 10- 5 mol) was added to a solution which contained toluene (30 mL) and 1-octene (20 mL) under 1 atm ethylene. A solution of MAO (1.5 mL, 100 eq) in toluene was added.

The resulting purple solution was allowed to stir for 4 hours at room temperature. Solution viscosity increased over the duration of the polymerization. The polymer was precipitated from acetone and dried under vacuum resulting in 5.3 g of copolymer. Mn 15,200, Mw 29,100, Mn/Mw 1.92.

Example 1fi [(2,6-i-PrPh),DABAn]NiBr 2 (12 mg, 1.7x10- 5 mol) was combined with toluene (75 mL) in a Schlenk flask under 1 atmosphere ethylene pressure. The mixture was cooled to 0°C, and 0.09 mL of a 1.8 M solution in toluene of Et 2 AlC1 (10 eq) was added. The resulting purple solution was stirred for 30 minutes at 0 0 C. The polymerization was quenched and the polymer precipitated from acetone. The resulting polymer was dried under reduced pressure (6.6 g, 2.8 x 104 TO). Mn 105,000; Mw 232,000; Mw/Mn 2.21 Example _19 [(2,6-i-PrPh) 2 DABAn]NiBr 2 (12 mg, 1.7x10- 5 mol) was combined with toluene (75 mL) under 1 atmosphere propylene pressure. The solution was cooled to 0°C and 0.1 mL of Et 2 AlC1 (:10 eq) was added. The reaction was stirred at 0 0 C for 2 hours. The polymerization was quenched and the polymer precipitated from acetone.

The resulting polymer was dried under reduced pressure (3.97 c, 2800 TO).

Example 170 [(2,6-i-PrPh) 2 DABAn]NiBr 2 (12 mg, 1.7x10- 5 mol) was combined with toluene (50 mL) and 1-hexene (25 mL) under a N 2 atmosphere. Et 2 AlCI (0.01 mL, 10 eq) was 204 02 10 6/03,sw1331 Ipa,204 idded to the polymerization mixture. The resulting purple solution was allowed to stir for 4 hours. After 4 hours the polymerization was quenched and the polymer precipitated from acetone. The polymerization yielded 1.95 g poly(l-hexene) (348 TO/h). Mn 373,000; Mw 680,000; Mw/Mn 1.81.

Example 171 1-Tetradecene (20 ml) was polymerized in methylene chloride (10 ml) for 20 hr using catalyst PrPh) 2 DABMez]PdCH 2

CH

2

CH

2 C(O)OCH3)SbF6 (0.04 g, 0.05 mmol). The solvent and reacted monomer were removed in vacuo. The polymer was precipitated to remove unreacted monomer, by the addition of acetone to a chloroform solution. The precipitated polymer was dried in vacuo to give a 10.2 g yield. 3C NMR (trichlorobenzene, 120 0 C) integrated to give the following branching analysis per 1000 methylene carbons: Total methyls methyl ethyl propyl butyl amyl 2Hexyl and end of chain Thermal analysis showed Tg -42.7 0 C, and Tm 33.7 0 C (15.2 J/g).

Listed below are the "C NMR data upon which the above analysis is based.

-205 0216/03.swl331 spa.205 C NMR Data TCB, 120C, 0.05M CrAcAc Freq ppm Intensity 39.3416 7.78511 MB2 38.2329 5.03571

MB

3 37.8616 9.01667 MB3+ 37.5857 3.33517 MB3+ 37.2462 31.8174 aB 1 3B 3 36.6415 2.92585 IaB1, 3B 3 34.668 5.10337 ay+B 34.2384 38.7927 ay+B 33.7397 16.9614 3B 33.3471 3.23743 3B6+, 3EOC 32.9387 16.0951 yy+B, 384 31.9148 27.6457 y+y B, 3B 4 31.1297 6.03301 Y+y B, 3B 4 30.212 59.4286 y+Y+B, 3B 4 29.7398 317.201 +Y+yB, 3B4 29.3101 32.1392 7+y+B, 3B 4 27.1511 46.0554 Py+B, 2B 2 27.0185 53.103 pyB, 282 26.419 9.8189 Py*B, 2B 2 24.244 2.46963

OPB

22.6207 28.924 2B5+, 2EOC 20.0479 3.22712 2B 3 19.7084 18.5679 1B 1 14.3929 3.44368 1B 3 13.8677 30.6056 1B4+, 1EOC 10.9448 9.43801 IB2 Example 172 4-Methyl-1-pentene (20 ml) was polymerized in methylene chloride (10 ml) for 19 hr using catalyst 2 ,6-i-PrPh) DABMe,]PdCHCHCHC(0)OCH 3 }SbFr (0.04 g, 0.05 mmol). The solvent and unreacted monomer were removed in vacuo. The polymer was precipitated to remove residual monomer by addition of excess acetone to a chloroform solution. The precipitated polymer was dried in -racuo to give a 5.7 g yield. 1C NMR (trichlorobenzene, 1200C) integrated to give 518 methyls per 1000 methylene carbon atoms. Thermal analysis showed Tg -30.3 0

C.

Listed below are the 1C NMR data upon which the above analysis is based.

-206- OZ/06/3.sw1331spa,2 13C NMR Data TCB, 120C, 0.05M CrAcAc Freq ppm Intensity 47.8896 13.3323 47.4011 8.54293 45.7127 26.142 45.1392 17.4909 43.9658 13.9892 43.1375 12.7089 42.6171 11.5396 41.8207 9.00437 39.203 64.9357 37.9712 24.4318 37.3075 87.438 35.4862 16.3581 34.9553 24,5286 34.35 31.8827 33.3624 25.7696 33.0226 42.2982 31.4403 25.3221 30.6226 38.7083 28.504 26.8149 27.989 81.8147 27.7341 78.3801 27.5802 94.6195 27.458 75.8356 27.0864 35.5524 25.6103 97.0113 23.4333 59.6829 23.0563 41.5712 22.536 154.144 21.9944 5.33517 20.7307 16.294 20.4971 34.7892 20.2953 29.9359 19.7378 62.0082 Fxample 123 1-Eicosene (19.0 g) was polymerized in methylene chloride (15 ml) for 24 hr using catalyst PrPh) 2 DABMe 2 PdCH 2

CH

2 CH2C OCH 3 )SbF6" (0.047 g, 0.05 mmol). -The solvent and unreacted monomer were removed in vacuo. The polymer was precipitated to remove residual monomer by addition of excess acetone to a chloroform solution of the polymer. The solution was filtered to collect the polymer. The precipitated polymer was dried in vacuo to give a 5.0 g yield. 1 3

C

NMR quantitative analysis, branching per 1000 CH2: Total methyls Methyl Ethyl Propyl -207- 20/OC3/O.sw 13 31 spa.

2 0 7 Butyl Amyl 2Hexyl and end of chains (12.4).

Integration of the CH2 peaks due to the structure

-CH(R)CH

2 where R is an alkyl group, and R' is an alkyl group with two or more carbons showed that in 82% of these structures, R Me.

Listed below are the 1C NMR data upon which the above analysis is based.

13 C NMR data TCB, 120C, 0.05M CrAcAc Frea pnm Intensity 37.7853 13.978 MB2+ 37.1428 52.1332 aB 34.1588 41.067 aB4 32.826 26.6707 MB 1 31.8066 24.9262 3B 6 +,3EOC 30.0703 96.4154 y+yB,3B 4 29.6243 1239.8 yy+yB,3B 4 27.0013 78.7094 By+B, (4B 5 etc.) 22.5041 23.2209 2B5+,2EOC 19.605 30.1221

IB

1 13.759 23.5115 1B 4

+,EOC

Example 174 The complex ((2,6-i-PrPh) 2 DA1BH 2 ]PdMeCl (0.010 g, 0.019 mmol) and norbornene (0.882 g, 9.37 mmol) were weighed into a vial and dissolved in 2 ml CH2C12.

NaBAF (0.032g, 0.036 mmol) was rinsed into the stirring mixture with 2 ml of CH 2 C1 2 After stirring about minutes, there was sudden formation of a solid precipitate. Four ml of o-dichlorobenzene was added and the solution became homogenous and slightly viscous. After stirring for 3 days, the homogeneous orange solution was moderately viscous. The polymer was precipitated by addition of the solution to excess MeOH, isolated by filtration, and dried in vacuo to give 0.285 g (160 equivalents norbornene per Pd) bright orange glassy solid. DSC (two heats, 15°C/min) showed no thermal events from -50 to 300 0 C. This is consistent with addition type poly(norbornene). Ringopening polymerization of norbornene is known to 208- 0 2 0 6 1 03.sw13311 ,roduce an amorphous polymer with a glass transition temperature of about 30-55 0

C.

Example 175 The solid complex PrPh) 2

DABH

2 )]PdMe(Et 2 O) SbF': (0.080 g, 0.10 mmol) was added as a solid to a stirring solution of norbornene (1.865 g) in 20 ml of o-dichlorobenzene in the drybox.

About 30 min after the start of the reaction, there was slight viscosity (foam on shaking) and the homogeneous mixture was dark orange/red. After stirring for 20 h, the solvent and unreacted norbornene were removed in vacuo to give 0.508 g orange-red glassy solid (54 equivalents norbornene/Pd). 1 R NMR (CDC13): broad featureless peaks from 0.8-2.4 ppm, no peaks in the olefinic region.. This spectrum is consistent with addition type poly(norbornene). GPC (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=566 Mw=1640 Mw/Mn=2.90.

Example 176 4-Methyl-l-pentene (10 ml) and ethylene (1 atm) were copolymerized in 30 ml of chloroform according to example 125 using catalyst PrPh) 2 DABMe 2 ]PdCH 2 CH2CH2C(O)OCH 3 }SbF 6 (0.084 g, 0.10 mmol) to give 23.29 g highly viscous yellow oil. The 1H NMR spectrum was similar to the poly(ethylene) of example 110 with 117 methyl carbons per 1000 methylene carbons. 13 C NMR quantitative analysis, branching per 1000 CH 2 Total methyls (117.1), Methyl Ethyl Propyl Butyl Amyl >Hexyl and end of chains 2Amyl and end of chains By 13C NMR this sample contains two identifiable branches at low levels attributable to 4methyl-l-pentene. The Bu and >Amyl peaks contain small contributions from isopropyl ended branch structures.

Example 177 CoC1 2 (500 mg, 3.85 mmol) and (2,6-i-PrPh)2 DABAn g, 4.0 mmol) were combined as solids and dissolved -209- 02/06/03,sw 133 I spa.209 .n 50 mL of THF. The brown solution was stirred for 4 hours at 25 0 C. The solvent was removed under reduced pressure resulting in a brown solid (1.97 g, 82% yield).

A portion of the brown solid (12 mg) was immediately transferred to another Schlenk flask and dissolved in 50 mL of toluene under 1 atmosphere of ethylene. The solution was cooled to 0°C, and 1.5 mL of a 10% MAO solution in toluene was added. The resulting purple solution was warmed to 25 0 C and stirred for 12 hours. The polymerization was quenched and the polymer precipitated from acetone. The white polymer (200 mg) was collected by filtration and dried under reduced pressure. Mn 225,000, Mw 519,000, Mw/Mn 2.31, Tg -420, Tm 52 0 C and 99.7 0

C.

Example 178 Ethyl 10-undecenoate (10 ml) and ethylene (1 atm) were copolymerized in 30 ml of CH 2 C12 according to example 125 using catalyst PrPh)2DABMe2]PdCHZCH 2

CH

2 C(O)OCH3)SbF- (0.084 g, 0.10 mmol) The copolymer was precipitated by removing most of the CH 2 C1 2 in vacuo, followed by addition of excess acetone. The solution was decanted and the copolymer was dried in vacuo to give 1.35 g viscous fluid. 1H NMR (CDC1 3 0.

7 5-0.95(m, CH3); 0.95-1.5(m, C(0)OCH2CH 3 CH2, C) 1.5-1.7(m, -CH2CH2C(O)OCH 2

CH

3 1.9-2.0(m, -CH2CH=CH-); -CH2CH 2

C(O)OCH

2 CH3); 4.15(q, -CH2CH 2 C(O)OCH2CH 3 5.40(m, The olefinic and allylic peaks are due to isomerized ethyl 10-undecenoate which has coprecipitated with the copolymer. Adjusting for this, the actual weight of copolymer in this sample is 1.18 g. The copolymer was reprecipitated by addition of excess acetone to a chloroform solution. 1 H NMR of the reprecipitated polymer is similar except there are no peaks due to isomerized ethyl 10-undecenoate at 1.9-2.0 and 5.40 ppm. Based on integration, the reprecipitated copolymer contains 7.4 mole ethyl 10-undecenoate, and -210- 02 0 6/03,sw 33sp,210 .3 methyl carbons per 1000 methylene carbons. 3 C NMR quantitative analysis, branching per 1000 CH 2 Total methyls Methyl Ethyl( 16.9), Propyl Butyl Amyl MHexyl and end of chains GPC (THF, PMMA standard): Mn=20,300 Mw=26,300 Mw/Mn 1.30. 13 C NMR quantitative analysis, branching per 1000 CH2: ethyl ester (37.8), Ester branches -CH(CH2)nCO2CH2CH3 as a of total ester: n25 n=4 n=1,2,3 n=0 (1.2) Listed below are the "C NMR data upon which the above analysis is based.

-211- 02 6/03.swI331 Ispa.21 I 13C NMR Data Freq ppm Intensity 59.5337 39.7234 39.3145 38.2207 37.8437 37.2225 36.7181 34.6792 34.265 33.7181 33.3093 32.9164 32.356 32.0828 31.9075 31.127 30.6757 30.2084 29.9961 29.72 29.5076 29.2899 28.727 27.5164 26.9908 26.5713 26.3749 25.5519 25.0528 24.2457 23.1094 22.9926 22.6156 20.0245 19.6847 19.1643 17.5183 14.2954 13.8653 13.414 11.1521 10.9237 174.945 172.184 171.695 53.217 2'.57361 7.80953 11.9395 20.3066 29.7808 5.22075 17.6322 107.55 21.9369 8.22574 15.0995 8.52655 5.79098 37.468 13.8003 8.38026 52.5908 27.3761 151.164 39.2815 69.7714 6.50082 20.4174 64.4298 9.18236 11.8136 4.52152 43.7554 7.9589 10.0537 4.71618 37.2966 2.4263 25.9312 5.33693 2.20778 66.1759 43.8215 2.52882 5.9183 14.9294 3.27848 125.486 4.57235 The solid complex PrPh) 2

DABH

2 ]PdMe(Et 2 0) }SbF 6 (0.080 g, 0.10 mmol) was added as a solid to a stirring solution of cyclopentene (1.35 g, 20 mmol) in 20 ml of dichlorobenzene in the -212- 02/06/03,swl 3311 spa,212 drybox. AfL r stirring 20 h, the slightly viscous Polution was worked up by removing the solvent in vacuo to give 1.05 g sticky solid (156 equivalents of cyclopentene per Pd). 1H NMR (CDC13): complex spectrum from 0.6-2.6 ppm with maxima at 0.75', 1.05, 1.20, 1.55, 1.65, 1.85, 2.10, 2.25, and 2.50. There is also a multiplet for internal olefin at 5.25-5.35. This is consistent with a trisubstituted cyclopentenyl end group with a single proton M. Kelly et. al., Macromolecules 1994, 27, 4477-4485.) Integration assuming one olefinic proton per polymer chain gives and Mn=540. IR (Thin film between NaC1 plates, cm- 1 3048 (vw, olefinic end group, CH stretch), 1646(vw, olefinic end group, R 2 C=CHR trisubstituted double bond stretch), 1464(vs), 1447(vs), 1364(m), 1332(m), 1257(w), 1035(w), 946(m), 895(w), 882(w), 803 cyclopentenyl end group, R 2 C=CHR trisubstituted double bond, CH bend), 721(vw, cyclopentenyl end group, RHC=CHR disubstituted double bond, CH bend). GPC (trichlorobenzene, 135CC, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=13 8 Mw= 24 6 Mw/Mn=l.

79 Example 180 The solid complex PrPh) 2DABMe 2 ]PdCH 2

CH

2 CHC(O) OCH3)SbF"- (0.084 g, 0.10 mmol) was added to a stirring solution of 10.0 ml cyclopentene in 10 ml CHC13 in the drybox. After stirring for 20 h, the mixture appeared to be separated into two phases. The solvent and unreacted monomer were removed in vacuo leaving 2.20 g off-white solid (323 equivalents cyclopentene per Pd). DSC (25 to 3000C, 15OC/min, first heat): Tg 107 0 C, Tm (onset) 165 Tm (end) 260 Heat of fusion 29 J/g.

similar results were obtained on the second heat.

GPC (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as linear polyethylene using -213- 02/0O/03,swl331 Ispa.,213 niversal calibration theory): Mn=28,700 Mw=33,300 Mw/Mn=1.16.

Listed below are the "C NMR analysis for this polymer.

13C NMR Data TCB, 120C, 0.05M CrAcAc Freq ppm Intensity 46.4873 142.424 38.339 59.7617 30.5886 137.551 Example 181 The solid complex PrPh)2DABMe 2 ]PdCH 2

CH

2

CH

2 C(O)OCH3}SbF6 (0.084 g, 0.10 mmol) was added to a stirring solution of 10.0 ml cyclopentene in 10 ml CHCl- in a Schlenk flask. The flask was evacuated briefly and refilled with ethylene.

It was maintained under slightly above 1 atm ethylene pressure using a mercury bubbler. After 20 h, the solvent and unreacted monomers were removed in vacuo from the homogeneous solution to give 12.89 g of highly viscous fluid. 1 H- NMR (CDC1 3 cyclopentene peaks: 0.65(m, 1H); 1.15( broad s, 2H); 1.5-2.0(m, ethylene peaks: 0.

7 5-0.95(m, CH3); 0.95-1.5(m, CH and

CH

2 Integration shows 24 mole cyclopentene in this copolymer. Analysis of the polyethylene part of the spectrum (omitting peaks due to cyclopentyl units) shows 75 total methyl carbons per 1000 methylene carbons. Based on quantitative 13C analysis, the distribution of branches per 1000 methylene carbons is Methyl Ethyl Propyl Butyl (20) and 2 Amyl DSC (first heat: 25 to 150 0 C, 10 0 C/min; first cool: 150 to -150 0 C, 10 0 C/min; second heat: -150 to 1500C, 10 0 C/min,; values of second heat reported): Tg -33 0 C, Tm 19 0 C (11 GPC (trichlorobenzene, 135°C, polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=3,960 Mw=10,800 Mw/Mn=2.73.

-214- 02 0603,swl3311spa,2j4 Listed below are the -3C NNR data upon wn&icf thne above analysis is based.

Freq ppm intensit) 48.344 46 .5562 44.9064 42 .0842 40.7845 40.5777 40.3336 39,5591 38.7634 38.4716 38.2488 37.2144 36.721 36.2913 35.8776 35.6176 34.5248 34.1959 33 .0182 31,8671 31.4056 30.8433 4613 30.0104 29.7133 29.2359 28. 9653 28.6577 26.9813 26.3925 25.9363 24.2971 22 .9019 22.6048 19.7349 19.1991 17. 5811 13.8783 12.6264 10.9501 1.25262 22.8938 10.8003 16 .824 117 .364 113.702 136.742 15.0962 18.636 .12.384 7 17.3939 17.5837 111.057 11-0136 22.036 7 90. 3685 15. 734 24.7661 14.0261 238.301 20.6401 11.2412 20. 2901 62.2997 78.3272 31.6111 53. S526 64 .0528 17.6335 4.51208 5.6969 1.70709 9.13305 14.3641 10.124 2.00384 2.28331 26.3448 19.6468 4. 96188 13NMR Data TOE. 120C. 0.OSM CrAcAc 1 cme and/or 1,3 ccmac 1,3 cme 2 eme 1,3 eme 1,3 eme methylene from 2 Cifl or/and 2 one 2B4 2B5+. 2EOC 131 end group 1B4+. 1500 end group 132 21 O2/03,sw13I1 1Ispa2 Example 182 1-Pentene (10 ml) and cyclopentene (10 ml) were copolymerized in 20 ml of o-dichlorobenzene solvent according to example 180. After 72 h, the unreacted monomers and part of the solvent were removed in vacuo to give 3.75 g highly viscous fluid. Analysis by 1

H

NMR showed that this material contained 1.81 g of copolymer; the remainder was o-dichlorobenzene. The 1H NMR spectrum was very similar to poly(ethylene-cocyclopentene) in Example 181. Integration shows mole cyclopentene in this copolymer. Analysis of the poly(l-pentene) part of the spectrum (omitting peaks due to cyclopentyl units) shows 62 methyl carbons per 1000 methylene carbons. The fraction of ,1ienchainment (chain straightening) in this section is 72%. Based on quantitative 13C analysis, the distribution of branches per 1000 methylene carbons is Methyl Propyl and Amyl DSC (first heat: -150 to 150 OC, 15 °C/min; first cool: 150 to 150 OC, 15 °C/min; second heat: -150 to 150 0 C, 15 o C/min,; values of second heat reported): Tg -19 oC, Tm 50 OC (24 GPC (trichlorobenzene, 135 0

C,

polystyrene reference, results calculated as linear polyethylene using universal calibration theory): Mn=14,900 Mw=27,300 Mw/Mn=1.82 Example 183 A 100 mL autoclave was charged with chloroform mL), methyl acrylate (10 mL), EtPh) 2 DABMe 2 ]PdMe(NCMe)}BAF (0.100 g, 0.073 mmol), and ethylene (2.1 MPa). The reaction mixture was stirred under 1.4 MPa of ethylene for 180 min; during this time the temperature inside the reactor remained between and 26 0 C. The ethylene pressure was then vented, and the crude reaction mixture discharged from the reactor.

The reactor was washed with 2 x 50 mL of chloroform.

The washings were added to the crude reaction mixture; 250 mL of methanol was added to the resulting solution.

After standing overnight, the polymer product had -216- 02 /06103.sw331Isp216 -recioitated from solution; it was isolated by decanting off the chloroform/methanol solution, and dried giving 3.91 g of an extremely viscous oil. 1

H

NMR of this material showed it to be ethylene/methyl acrylate copolymer, containing 1.1 mole% methyl acrylate. The polymer contained 128 methyl-ended hydrocarbon branches per 1000 methylenes, and 7 methyl ester ended branches per 1000 methylenes.

Example 184 A solution of 2 DABMe 2 ]PdMe(NCMe) SbFe (0.027 g, 0.02 mmol) in 5 mL CDC1 3 was agitated under 1.4 MPa of ethylene for 3 h; during this time the temperature inside the reactor varied between 25 and 40 0 C. 1 H NMR of the solution indicated the presence of ethylene oligomers. Mn was calculated on the basis of 1H NMR integration of aliphatic vs. olefinic resonances to be 100. The degree of polymerization, DP, was calculated on the basis of the 1 H NMR spectrum to be 3.8; for a linear polymer this would result in 500 methyl-ended branches per 1000 methylenes. However, based on the IH NMR spectrum the number of methyl-ended branches per 1000 methylenes was calculated to be 787.

Example 185 [(2-t-BuPh) 2 DABMe 2 J NiBr 2 A Schlenk tube was charged with 0.288 g (0.826 mmol) of (2-t-BuPh)2DABMe2 which was then dissolved in mL of CH2C12. This solution was cannulated onto a suspension of (DME)NiBr2 (0.251 g, 0.813 mmol) in 15 mL of CH 2 C12. The reaction mixture was allowed to stir overnight, resulting in a deep red solution. The solution was filtered and the solvent evaporated under vacuum. The remaining orange, oily residue was washed with ether (2 x 10 mL) and dried under vacuum to give an orange/rust powder (0.36 g, 78%) xample 186 [(2-t-BuPh) 2 DABAn]NiBr 2 (2-t-BuPh),DABAn (0.202 g, 0.454 mmol) and (DME)NiBr2 (0.135 g, 0.437 mmol) were combined and -217- 02/06/03.sw 1331 spa.217 ,tirred in 25 mL of CH 2 C1 2 as in Example 185. An orange/rust solid was isolated (0.18g, 62%).

Example 187 DABAn]NiBr 2 The corresponding diimine (0.559 g, 1:00 mmol) and (DME)NiBr 2 (0.310 g, 1.00 mmol) were combined and stirred in 35 mL of CH 2 C1 2 as was done in Example 185.

An orange solid was isolated (0.64 g, 83%).

Examples 188-190 Polymerizations were carried out at 0 C and under 1 atmosphere of ethylene pressure. The (diimine)NiBr 2 complex (1.4-1.7 x 10-5 mol) was placed into a flamedried Schlenk flask and dissolved in 100 mL of toluene.

The flask was placed under ethylene and cooled in an ice bath. Polymerization was initiated by addition of 100 equivalents (1.5 mL 10% soln in toluene) of methylaluminoxane (MAO). The reaction mixture was stirred for 30 or 120 minutes at constant temperature followed by quenching with 6M HC1. Polymer was precipitated from the resulting viscous solution with acetone, collected via filtration, and dried under vacuum for 24 h. A summary of results is shown below.

Ex No. Catalyst 188 [(2-t-BuPh) DABMe ]NiBr 2 189 [(2-t-BuPh) 2 DABAn]NiBr 2 190 [(2,5-t-BuPh) 2 DABAn].NiBr 2 Exam. Catalyst Conditions Yield TO/hr-mol 5 mol) catalyst 188 0°C.120m 9.88 10.500 189 Oc. 30 m 8.13 40,500 190 0°C.30m 6.60 31,000 Examples 191-196 General Procedure. The procedure of Example 84 for the homopolymerization of ethylene) was followed with the exception that the acrylate was added to the -218- 0 2 06/03,swI31 Ispa,218 eaction mixture a: -78 0 C immediately following the addition of 50 mL of CH 2 C1 2 Polymerizations are at room temperature (rt) and 1 atm ethylene unless stated otherwise. The copolymers were generally purified by filtering an Et2O or petroleum ether solution of the polymer through Celite and/or neutral alumina. 1H and 13 C NMR spectroscopic data and GPC analysis are consistent with the formation of random copolymers. In addition to the polyethylene resonances, the following resonances diagnostic of acrylate incorporation were observed: Methyl Acrylate: 1H NMR (CDC1 3 400 MHz) 6 3.64 OMe), 2.28 J 7.48, OCH 2 1.58 OCH 2

CH

2 1 3 C NMR (C 6 De, 100 MHz) 8 176 50.9 (C(O)OMe).

Fluorinated Octyl Acrylate (FOA. 3M Co.

Minneapolis. MN): 1H NMR (CDCl 3 400 MHz) 5 4.58 J 13.51, OCH 2

(CF

2 6

CF

3 2.40 J 7.32, C(O)CH 2 1.64 C(O)CH 2

CH

2 13C NMR (CDC1 3 100 MHz) 6 172.1 59.3 JCF 27.0, OCH2(CF 2 )6CF 3 Ex. Catalyst Acrylate, Rxn Yield Acry- CH3/ My M n

PDI

cone. Time late Inc. 1000 cone. (Molar) molt/wt% CH 2 (10-3 Molarl 191 Me, 2.3 0 Me. 6.7 2 4 a =0.5 10.9/ 134 27.3 192 Me, 1.4 o Me. 1.1 48 3.94 2.7/ 114 77000 56400 1.4 7.84 b 193 Me, 2.0 FOA, .74 24 27.5 0.80/ 110 S11.58 194 Me, 2.0 FOA, 1.3 24 20.7 0.80/ 126 11. 58 195 H, 2.0 FOA, .74 24 1.49 0.31/ 144 4.85 196 2.0 c FOA. .74 24 2.00 0.71/ 135 10.73 aFinal 3 h at 50 0

C.

bTHF, PMMA standards.

-219- U2/06/3.sw 133.11 spa.2J

C

Catalyst is PrPh) DABAn) PdCHCH 2

CH

2 C OCH2 (CF 2 6

CF

3

}BAF

Examples 197-203 In Examples 197-203, structures -of the type represented by (VI) and (IX) are described.

Example 197 (l(2.6-i-PrPh)2DABMe2)PdMe(H 2

C=CH

2 )}BAF- and fl(2.6-i--PrPh) 2 DABMe 2 )Pd(P)H 2

C=CH

2

)}BAF"

In a drybox under an argon atmosphere, an NMR tube was charged with -0.01 mmol of PrPh) 2 DABMe PdMe 2 (p-C))BAF/ (Na.(OEt2) 2 BAF or NaBAF] or ([{((2,6-i-PrPh)2DABMe,J PdMe(OEt) }BAF. The tube was then capped with a septum, removed from the drybox, and cooled to -78 0 C. Via gastight syringe, 700 AL of

CD

2 C1 2 was then added to the NMR tube and the septum was wrapped with Parafilm. The tube was shaken very briefly in order to dissolve the palladium complex.

After acquiring a spectrum at -80 0 C, 1 10 equiv of olefin was added to the -78 0 C solution via gastight syringe, ant the olefin was dissolved in the solution by briefly shaking the NMR tube. The tube was then transferred to the cold NMR probe and spectra were acquired. This olefin complex was prepared from both precursors using one equiv of ethylene: 18 NMR

(CD

2 C1 2 400 MHz, -60 0 C) 6 7.72 8, BAF: Co), 7.54 BAF: Cp), 7.4 7.0 6, Hiryl), 4.40 4,

H

2

C=CH

2 3.38 (br m, 4, O(CH 2

CH

3 2 2.69 (septet, 2, J 6.73, CRMe 2 2.63 (septet, 2, J 6.80, C'IMe 2 2.34 and 2.23 3 each, 1.33 (d, 6, j 6.80, C'HMeMe'), 1.25 6, J 6.50, CHMeMe'), 1.14 6, J 7.00, CHMeMe'), 1.10 (br m, 6,

O(CH

2

CH

3 1.07 6, J 6.80, C'HMeMe'), 0.18 (PdMe); 1 3 C NMR (CD 2 Cl 2 100 MHz, -60 0 C) 8 180.3 and 174.7 161.5 Jc 49.6, BAF: Cipso, 143.3 and 141.7 (Ar, Ar': Cipso), 134.4 (BAF: Co), 128.6 (Ar: Cp), 128.4 JBC 32.3, BAF: Cm), 127.7 (Ar': Cp), 124.7 and 124.4 (Ar, Ar': Co), 117.3 (BAF: Cp), 91.7 (JCH 160.7, HC=CH 2 65.8 (O(CH 2 CH3) 2 28.9 -220 0 2 /0 6 /03,swl331 Ispa,220 CHMe 2 28.8 (C'HMe 2 24.1, 23.4, 22.9 and 22.7 (CHMeMe', C'HMeMe'), 21.7 and 21.5 15.0 (OCH 2 0CH 3 2 4.3 (PdMe).

In the presence of 5 equiv of ethylene, chain growth was observed at -35 0 C. Spectral data for ([(2,6-i-PrPh) 2 DABMe 2 )Pd(P) (CH 2

=CH

2 )}BAF [wherein P is as defined for intermediates (CD 2 C1 2 400 MHz, 0 C) are reported in the following table: S [(2,6-i-PrPh) DABMe')Pd[(CH2)nCH3](H2C=CH2)}*BAF- HIC=CH2 N=C(Me)-C'(Me)=N Pd(CH2) MAe n mult. 6 mut. mul.t. 6 mult 1 6 0 s 4.42 s 2.35 s 2.24 s 0.22 2 s 4.36 s 2.37 s 2.22 1 7.00 0.39 4 s 4.36 s 2.37 s 2.22 t 7.20 0.62 Addition of 15 more equiv of ethylene and warming to room temperature leads to complete consumption of ethylene and the observance of a single organometallic species: 1 H NMR (CD 2 C1 2 400 MHz, 24.0 0 C) 6 7.74 (s, 8, BAF: Co), 7.19 4, BAF: Hp), 2.85 (br m, 4, CHMe 2 C'HMe 2 2.36 and 2.23 3 each, N=C(Me)- 1.5 1.0 (CHMeMe', C'HMeMe'), 1.29 (Pd(CH 2 )nCH 3 0.89 (Pd(CH 2 )nCH 3 Example 198 (t(2,6-i-PrPh) 2

DABH

2 ]PdMe(H 2

C=CH

2 ))BAF- and ([(2,6-i-PrPh) 2

DABH

2 ]Pd(P)(H 2

C=CH

2

)}BAF-

This olefin complex, PrPh),DABH 2 PdMe(H,C=CH) }BAF was prepared following the procedure of example 197 by both of the analogous synthetic routes used in example 197, using one equiv of ethylene: 1 H NMR (CD 2 C1 2 400 MHz, -60 0 C) 8 8.42 and 8.26 1 each, 7.72 8, BAP: HO), 7.54 4, BAF: Hp), 7.42 7.29 6, Haryl), 4.60

H

2

C=CH

2 3.37 4, J 7.03, (O(CH 2

CH

3 2.89 (septet, 2, J 6.71, CHMe 2 2.76 (septet, 2, J 6.68, C'HMe 2 1.35 6, J 6.72, C'HMeMe'), 1.29 -221- 02/06/03.sw331 Ispa.221 d, 6, J 6.79, CHMeMe'), 1.15 6, J 6.

7 2,CHMeMe'), 1.09 6, J 6.54, C'HMeMe'), 1.15 6, J 7.34,

O(CH

2

CH

3 0.46 3, PdMe); 13

C

NMR (CD 2

C

2 400 MHz, -60 0 C) 6 167.7 *(JE 182, 162.8 (JCH 182, 161.4

J

49.8, BAF: Cipso), 140.2 and 139.8 (Ar, Ar': Cipso), 138.6 and 137.3 (Ar, Ar': 134.4 (BAF: Co), 129.2 and 129.1 (Ar, Ar': Cp), 128.3 JCF 32.2,

BAF:

Cm), 124.3 and 124.0 (Ar, Ar': Cm), 124.2 JCF 272.5; BAF: CF 3 117.3 (BAF: Cp), 92.7 (JcH 162.5,

H

2

C=CH

2 65.8 (O(CH 2

CH

3 2 28.9 and 28.7 (ClMe 2 and C'HMe 2 25.1, 24.0, 22.0 and 21.9 (CIMeMe', C'HMeMe'), 15.12 (Jp 139.2, PdMe), 15.09

(O(CH

2

CH

3 2 In the presence of 10 equiv of ethylene, chain growth was monitored at -35 0 C. Diagnostic 1 H NMR spectral data (CD 2 C1 2 400 MHz, -35C) for the second title compound are reported in the following table: ([(2.6-i-PrPh)2DABII,]Pd(CH 2 )nCH3 ](H2C=CH2)) BAF H2C=CH2 Pd(CH) Me n mult. 6 mult. 5 mult. 8 mut J Oa s 8.42 s 8.27 br s 4.6 s 0.50 2b s 8.41 s 8.24 brs 4.6 t 7.85 0.36 4 s 8.41 s 8.24 br s 4.6 t 7.15 0.62 6 s 8.41 s 8.24 br s 4.6 t 7.25 0.76 >6 s 8.41 s 8.24 br sC 4.6 m 0.85dg 8 For n 0: 6 2.91 and 2.71 (septet, 2 each, ClMe 2 C'RMle 2 1.38, 1.32, 1.18 and 1.12 6 each, CHMeMe', C'HMeMe'). bFor n 0: 8 2.91 and 2.71 (septet, 2 each, ChMe 2 C'HMe 2 1.37, 1.35, 1.16 and 1.11 6 each, CHMeMe', C'HMeMe'). cIn the absence of free ethylene, bound ethylene appears as a sharp singlet at 4.56 ppm. 46 1.27 (Pd(CH 2 )nCH 3 After the ethylene was consumed at -35 0 C, the sample was cooled to -95 0 C. Broad upfield multiplets were observed at -7.2 to -7.5 ppm and 8.0 to ppm. The sample was then warmed to room temperature -222- O/06/03,sw133lt Ispa222 .nd a spectrum was acquired. No olefins were detected, the upfield multiplets were no longer observable, and a single organometallic species was present: 1 H NMR (CD2Cl2, 400 MHz, 19.8 0 C) 6 8.41 and 8228 1 each, 7.72 8, BAF: Ho), 7.56 4, BAF: Hp), 3.09 4, CHMe2, C'HMe2), 1.35, 1.32, 1.26 and 1.22 6 each, J 6.5-6.8, CHMeMe', C'HMeMe'), 1.27 (Pd(CH2)nCH3), 0.88 (Pd(CH2)nCH3).

A second spectrum was acquired 12 minutes later at room temperature. Substantial decomposition of the organometallic species was observed.

Example 199 1[(2,6-i-PrPh) 2 DABH2]PdMe(H 2

C=CH

2

))BAF-

This olefin complex, MePh) 2

DABH

2 PdMe (H,C=CH 2 )BAF was prepared following the procedure in example 197, using MePh),DABH 2 PdMe(OEt2) )BAF and one equiv of ethylene: 1H NMR (CD2C12, 300 MHz, -70 0 C) 6 8.46 and 8.31 1 each, 7.72 8, BAF: Ho), 7.52 (s, 4, BAF: Hp), 7.4 6.4 6, Haryl), 4.56 4,

H

2

C=CH

2 2.19 and 2.16 6 each, Ar, Ar': Me), 0.31 3, PdMe).

In the presence of 10 equiv of ethylene (eq olefin insertion was monitored at -30 0 C and the production of cis- and trans-2-butenes was observed.

Example 200 I[(2,6-i-PrPh) 2 DABMe 2 JdMde(H 2 C=CHMe)IBAF This olefin complex, PrPh), 2 DABMe 2 3 PdMe(H 2 C=CHMe) }BAF, was prepared following the procedure of Example 197, using PrPh),DABMe: PdMe(OEt,) )}BAF- and one equiv of propylene: 1 H NMR (CD2C12, 400 MHz, -61 0 C) 8 7.73 8, BAF: Ho) 7.55 4, BAF: Hp), 7.4 7.0 6, Haryl), 5.00 (m, 1 H2C=CHMe), 4.24 1, J 9.1, HH'C=CHMe), 4.23 (d, 1, J 14.8, HH'C=CHMe), 3.38 (br q, 4, J 6.50, O(CH2CH3)2), 2.84 (septet, 1, J 6.5, Ar: CHMe2), 2.68 3, Ar: C'HMe2; Ar': CHMe2, C'HMe2), 2.32 and 2.22 3 each, 1.63 3, J 6.40, -223- 0 206/03.sw133 I1 spa.223 F-,C=CHMe), 1.35, 1.30, 1.25, 1.1, 1.1, 1.04 3 each, J 6.4 6.7, Ar: C'HMeMe'; Ar': CHMeMe', C'HMeMe'), 1.24 and 1.1 3 each, J 6.4, Ar: CHMeMe'), 1.1 (m, 6, O(CH2CH 3 2 0.28 (PdMe); 13 C NMR iCD2C1 2 100 MHz, -61 0 C) 6 179.9 and 174.7 161.5 JBC 49.7, BAF: Cipso), 138.8, 137.9, 137.8, 137.7, 137.0 and 136.9 (Ar: Cipso, Co, Co'; Ar': Cipso, Co, Co'); 134.4 (BAF: Co), 128.6 and 128.5 (Ar: Cp, 128.4 JCF 31.6, BAF: Cm), 124.8, 124.7, 124.4 and 124.4 (Ar: Cm, Cm'; Ar': Cm, 124.2 JCF 272.5, BAF: CF3), 117.3 (BAF: Cp, 116.1 (JCH 155.8, H2C=CHMe), 85.6 (JCH 161.4, H2C=CHMe), 65.8 (G(CH2C-H 3 2 28.9, 28.7, 28.7, 28.7 (Ar: CHMe 2 C'HMe 2 Ar': C4Me 2 C'HMe2), 24.5, 23.9, 23.5, 23.4, 22.9, 22.9, 22.8, 22.2, 21..71, 21.65, 20.9 (H2C=CHMe; Ar: CHMeMe', C'HMeMe'; Ar': CHMeMe', C'HMeMel, N=C(Me)- 16.9 (JCH 137.5, PdMe), 15.0 (O(CH2CH 3 2 Example 201 1l(2,6-i-PrPh) 2

DABH

2 ]PdMe(H 2 C=CHMe))BAF- and [(2,6-i-PrPh) 2 DABH2]Pd(P)(H 2 C=CHMe) BAF- This olefin complex, PrPh) 2

DABH,

2 PdMe(HC=CHMe)}BAF was prepared following using both of the synthetic routes used in Example 197, using one equiv of propylene: 1H NMR (CD2C12, 400 MHz, -80 0 C) 8 8.40 and 8.24 1 each, 7.72 8, BAF: Ho), 7.53 4, BAF: Hp), 7.40 -7.27 6, Haryl), 5.41 (br m, H2C=CHMe), 4.39 1, J 8.09, H'C=CHMe), 4.14 (br d, 1, J 15.29, HH'C=CHMe), 3.10 (br m, 1, CMe 2 2.87 (overlapping septets, 2, C'BMe2, C'"HRMe2), 2.59 (br septet, 1, C'HRMe2), 1.64 J 6.07, H2C=CHMe), 1.39 and 1.03 3 each, J 6.4, CHMeMe'), 1.27, 1.27, 1.14 and 1.1 3 each, J 5.9 6.7, C'HMeMe', C"'HMeMe'), 1.23 and 1.1 3 each, J 6.8, C" 'HMeMe), 0.47 (PdMe); 13 C NMR

(CD

2 C1 2 100 MHz, -80 0 C) 6 167.1 (JCH 181.6, N=C(Hfl)), 163.0 (JCH 182.1, 161.3 JBC 50.0, BAF: Cipso), 140.5 and 140.0 (Ar, Ar': Cipso), 138.5, 138.3, 137.7 and 137.2 (Ar: Co, CO'; Ar': Co, Co'), -224- 0 2o06/03,sw33r spa,.224 34.2 (BAF: Co), 128.9 and 128.8 (Ar, Ar': Cp), 128.1 JCF 31.1, BAF: Cm), 124.0 JCF 272.5, BAF: CF3), 124.6, 123.8, 123.8 and 123.6 (Ar: Cm, Cm'; Ar': Cm, 117.1 (BAF: Cp), 116.4 (JCH =.160.3,

H

2 C=CHMe), 85.4 (JCH 159.9, H2C-CHMe), 65.7 (O(CH2CH3)2), 29.2, 28.7, 28.5 and 28.0 (Ar: CHMe 2 C'HMe2; Ar': CHMe2, C'HMe2), 26.0, 24.4, 24.03, 23.97, 23.7, 21.9, 21.8, 21.7 and 21.6 (H2C=CHMe; Ar: CEMeMe', C'HMeMe'; Ar': CHMeMe', C'HMeMe'), 16.6 (JCH 142.1, PdMe), 15.0 (O(CH2CH3)2)- In the presence of 10 equiv of propylene, chain growth was monitored at -20 0 C, thus enabling PrPh) 2

DABH

2 Pd (CHMeCH) Me] (H 2 C=CHMe) BAF intermediates to be observed (CD2C12, 400 MHz, -20 0

C):

'[(2.6-i-PrPh)2DABMe 2 ]Pd((CHMeCH)nMe)(H2C=CHMe)

'BAF-

N=CHC'H=N HH'C=CHMe HH'C=CHMe C=CHMe (CHMeCH2)ne n 6 8 mult J 6 mult J S mult i mult 1 6 0 .8.40 8.26 d 14.4 4.25 d 8.6 4.47 m 5.45 s 0.59 1 8.38 8.24 d 14.4 3.98 d 7.4 4.25 m 5.55 t 7.1 0.51 >1 8.39 8.23 d 133.7 4.07 d 8.0 4.41 m 5.42 Example 202 The compound PrPh) 2

DABH

2 PdMe (HC=CHCHMe) }BAF was made using both the synthetic methods described in Example 197, except 1-butene was used. 1 H NMR (CD 2 Cl1 2 400 MHz, -75 0 C) 8 8.44 and 8.28 1 each, 7.74 8, BAF: Co), 7.56 4, BAF: Cp), 7.5 7.2 6, Haryl)t 5.4 1, H 2

C=CHCH

2

CH

3 4.36 1, J 8.2, 1H'C=CHCH 2

CH

3 4.13 (br m, 1, HH'C=CHCH 2

CH

3 3.14, 2.92, 2.92 and 2.62 1 each, Ar, Ar': CHMe 2 C' HMe 2 1.95 and 1.65 1I each, H 2 C=CHCHH'CH3), 1.0 3 each, Ar, Ar': CHMeMe', C'HMeMe'), 0.60 (s, 3, PdMe).

Isomerization to cis- and trans-2-butene began at -780C and was monitored at -15 0 C along with chain -225 0 2/06103.sw1331 Ispa,225 rowth. For Pd[P) species, formation of the l-butene complex occurred selectively in the presence of cisand trans-2-butene. Consumption of all olefins was observed at 20 0

C.

Examples 203 1[(2,6-i-PrPh) 2 DABH2]PdMe(CH 3

CH=CHCH

3

BAF-

Experiments involving the reaction of. the bispalladium(p-Cl) compound/NaBAF (as in Example 197) with trans-2-butene and the bispalladium(p-Cl) compound alone with cis-2-butene led to partial formation of the corresponding olefin complexes. An equilibrium was observed between the ether adduct and the olefin adduct when a compound of the type PrPh),DABHl] PdMe(OEt 2 )}BAF was reacted with one equiv of cis- or trans-2-butene.. Addition of excess 2-butene led to complete formation of the olefin adduct. Chain growth, which was monitored at 0 C to room temperature, led to complete consumption of butenes. Some butene isomerization occurred during the course of the oligomerization and small amounts of P-hydride elimination products (disubstituted internal olefins and trisubstituted olefins) were observed. Oligomer methylene and methyl groups were observed at 1.3 and 0.8 ppm, respectively. Diagnostic 1H NMR spectral data for the butene complexes follows: S[ (2,6 i PrPh) 2

DABH

2 PdMe (trans TCH3CH=CHCH 3 }BAF 1H NMR (CD 2 C12, 400 MHz, -39 0 C) S 8.43 and 8.29 1 each, 5.27 and 4.72 1 each,

CH

3 CH=C'HCH3), 0.73 (PdMe); 13 C NMR (CD 2 C1 2 100 MHz, 95 0 C) S 166.8 (JcH 181.5, 163.2 (JCH 179.8, 161.2 JBC 49.5, BAF: Cipso), 141.3 and 139.9 (Ar, Ar': Cipso), 138.4, 138.2, 138.0 and 137.0 (Ar, Ar': Co, 134.0 (BAF: Co), 128.74 and 128.71 (Ar, Ar': Cp), 128.0 JCF 31.9, BAP: Cm), 125.4 (JcH 150.0, free MeCH=CHMe), 123.8 JCF 272.5, BAF: CF 3 124.8, 123.7, 123.5 and 123.4 (Ar, Ar': Co, 117.0 (BAF: Cp), 107.0 and 106.8 (JcH-152, MeCH=C'HMe), 65.6 (free O(CH2CH 3 2 29.5, 28.3, 27.6, 226 2 /0603.,wl33 Ilspa.226 24.1, 23.6, 23.6, 21.5, 21.3, 21.2, 204, 19.9, 19.6,. 17.9, 17.5 (Ar, Ar': CHMeMe', C'HMeMe'; MeCH=C'HMe), 17.7 (free MeCH=CHMe), 15.0 (PdMe), 14.7

(O(CH

2

CH

3 2 (2,6-i-PrPh) 2

DABH

2 PdMe (cis-CHCH=HCCH 3 )BAF IH NMR (CD 2 C1 2 400 MHz, -75°C) 6 8.37 and 8.25 1 each, 5.18 2, CH3CH=CHCH3), 1.63 6, J 4.9, CH 3 CH=CHCH3), 0.47 (PdMe).

References for the synthesis of bis(oxazoline) ligands and their transition metal complexes: Corey, E. Imai, Zang, H. Y. J. Am. Chem. Soc. 1991, 113, 728-729. Pfaltz, A. Acc. Chem. Res. 1993, 26, 339-345, and references within.

Example 204 2,2-bis{2-[4(S)-methyl-1,3-oxazolinyll propane (500 mg, 2.38 mmol) was dissolved in 10 mL CH 2 C1 2 in a Schlenk tube under a N 2 atmosphere. This solution was added via cannula to a suspension of (1,2dimethoxyethane)NiBr 2 (647 mg, 2.10 mmol) in 30 mL of

CH

2 C1 2 The solution was stirred for 18 hours. The solvent was evaporated under reduced pressure. The product, 2,2-bis{2-[4(S)-methyl-1,3oxazolinyl }propaneNi(Br 2 was washed with 3 x 15 mL of hexane. The product was isolated as a purple powder (0.85 g, 84% yield).

Example 205 The product of Example 204 (14.2 mg, 3.3 x 10 mol) and toluene (75 mL) were combined in a Schlenk flask under 1 atmosphere ethylene pressure. The solution was cooled to 0°C, and 3.0 mL of a 10% MAO (100 eq) solution in toluene was added. The resulting yellow solution was stirred for 40 hours. The oligomerization was quenched by the addition of H 2 0 and a small amount of 6 M HC1. The organic fraction was separated from the aqueous fraction, and the toluene was removed under reduced pressure. A colorless oil resulted (0.95 g of oligomer). This illustrates that polymerization may be effected by such Pd, Ni and/or Co 227 02/0603.swl33I1sp.227 oisoxazoline complexes which are substituted in both 4 positions of the oxazoline ring by hydrocarbyl and substituted hydrocarbyl groups.

Example 206.

[(COD)PdMe(NCMe)

BAF-

To CODPdMeCl (100mg, 0.37 mmol) was added a solution of acetonitrile (0.08 mL, 1.6 mmol) in 25 mL.

CH

2 C1 2 To this colorless solution was added Na BAF- (370 mg, 0.4 mmol). A white solid immediately precipitated. The mixture was stirred at -20 0 C for 2 hours. The solution was concentrated and filtered.

Removal of solvent under reduced pressure resulted in a glassy solid. IH NMR (CD 2 Cl2) 6 5.78 (mult, 2H), 6 5.42 (mult, 2H), 62.65 (mult, 4H), 6 2.51 (9mult, 4H), 6 2.37 3H, NCMe), 6 1.19. 3H, Pd-Me), 8 7.72 (s, 8, BAF-, Ho), 6 7.56 4, BAF-, Hp).

Example 207 [2,6-(i-Pr)2PhDABH 2 ]NiBr 2 (10 mg, 1.7 x 10-5 mol), toluene (13 mL), and 1-hexene (38 mL) were combined in a Schlenk flask under an argon atmosphere. A 10% MAO solution (1.5 mL, 100 eq) in toluene was added to a suspension of the diimine nickel dihalide. The resulting purple solution was stirred at room temperature for 1 hour. The polymerization was quenched and the polymer precipitated from acetone.

The resulting colorless polymer was dried in vacuo GPC (toluene, polystyrene standards) Mn 330,000; Mw 590,000; Mn/Mw 1.8.

Example 2 ,6-i-PrPh),DABH2]NiBr 2 (10 mg, 1.7 x 10- 5 mol) was added to a solution which contained toluene (30 mL) and l-octene (20 mL). A 10% solution of MAO (1.5 mL, 100 eq) in toluene was added. The resulting purple solution was allowed to stir for 4 hours at room temperature. Solution viscosity increased over. the duration of the polymerization. The polymer was precipitated from acetone and dried in vacuo resulting -228- 0 2 06/03.swi33 Ispa,228 n 5.3 g of copolymer. Mn 15,200; Mw 29,100; Mw/Zn 1.92.

Example 209 [(2,6-i-PrPh)2DABMe 2 ]Ni(CH3)2 (20 mg, 4.1 x 10mol) and MAO (35.7 mg, 15eq) were combined as solids in an NMR tube. The solid mixture was cooled to -78°C and dissolved in 700 ±L of CD 2 C12. While cold, 10 gL of ether d 10 was added to stabilize the incipient cation.

1H NMR spectrum were recorded at 253,.273, and 293°K.

It was apparent that the starting nickel dimethyl complex was disappearing and a new nickel complex(es) was being formed. Activation of the dimethyl complex was occurring through methane loss (s,5 0.22). After 2 hours at 293°K all of the starting species had disappeared. To test for ethylene polymerization activity, 5000 iL (0leq) of ethylene was added via gas tight syringe to the solution at -78 0 C. The consumption of ethylene was monitored by 1 H NMR spectroscopy. The onset of ethylene uptake was observed at 223°K and all of the ethylene was consumed upon warming the probe to 293°K. The persistence of the Ni-Me signal during the experiment suggests that under these conditions propagation is faster than initiation. Solid polyethylene was observed upon removing the NMR tube from the probe.

Example 210 [(2,6-i-PrPh) 2 DABAn]NiBr 2 (12 mg, 1.7 x-10 5 mol) was combined with toluene (50 mL) and 1-hexene (25 mL) under a N 2 atmosphere. Et 2 AlCl (0.01 mL, 10 eq) was added to the polymerization mixture. The resulting purple solution was allowed to stir for 4 hours. After 4 hours the polymerization was quenched and the polymer precipitated from acetone. The polymerization yielded 2.05 g poly(l-hexene) (731 TO). (GPC, toluene, polystyrene standards) Mn 305,000; Mw 629,000; Mw/Mn 2.05. Tg -57°C, Tm 52°C. Tm -57°C, Tg 1H NMR (C 6 DsCl, 142°C) 10 methyls per 100 -229- 02/06103,sw133 1 Isp., 2 2 9 arbons. This number is significantly less tnan would be expected for strictly atactic 1-hexene.

Example 211 Concentration dependence on catalyst activity in nickel catalyzed polymerization of a-olefins. A series of homopolymerizations of 1-hexene were run at 20%, 30%, 40%, and 75% 1-hexene by volume. In each of the above cases 10 mg of PrPh) 2

DABH

2 )NiBr 2 was taken up in toluene and 1-hexene (50 mL total volume 1-hexene toluene). All of the polymerizations were run at 25 0 C and activated by the addition of 1.5 mL of a 10% MAO solution in toluene.

The polymerizations were stirred for 1 hour and quenched upon the addition of acetone. The polymer was precipitated from acetone and dried in vacuo. 10% by volume 1-hexene yielded 2.5 g poly(l-hexene), 15% by volume 1-hexene yielded 2.6 g poly(l-hexene), 20% by volume 1-hexene yielded 3.0 g poly(1-hexene), 30% by volume 1-hexene yielded 2.6 g poly(1-hexene), 40% by volume 1-hexene yielded 2.6 g poly(l-hexene), 75% by volume 1-hexene yielded 2.5 g poly(1-hexene).

Example 212 FeC12 (200 mg, 1.6 mmol) and 20 ml of CH 2 C1l were combined in a Schlenk flask under an argon atmosphere.

In a separate flask, 550 mg (2,6-i-PrPh),DABMe 2 and ml CH 2 C, were combined, resulting in a yellow solution. The ligand solution was slowly (2 hr) transferred via cannula into the suspension of FeCl 2 The resulting solution was stirred at 25 0 C. After 4 hr. the solution was separated from the unreacted FeC1d by filter cannula (some purple solid was also left behind). The solvent was removed in vacuo to give a purple solid (0.53 g, 71% yield).A portion of the purple solid was combined with 50 ml of toluene under 1 atm of ethylene. The solution was cooled to 0 C, and 6 ml of a 10% MAO solution in toluene was added. The mixture was warmed to 25 0 C and stirred for 18 hr. The polymer was precipitated by acetone, collected by -230- 02 1 06/03,sw13311 sp.230 suction filtration, and washed with 6M HfL, water ana acetone. The white polymer was dried under reduced pressure. Yield 13 mg.

Example 213 A 58-mg (0.039-mmol) sample of PrPh)2DABMe2]PdCH 2

CH

2

CH

2 C(0)OCH 3 BAF' was placed in a 600-mL stirred autoclave under nitrogen with 150mL of deaerated water. This mixture was pressurized to MPa with ethylene and was stirred at 23CC for 68 hr.

When the ethylene was vented, the autoclave was found to be full of rubbery polymer: on top was a layer of white, fluffy elastomeric polyethylene, while beneath was gray, dense elastomeric polyethylene. The water was poured out of the autoclave; it was a hazy light blue, containing a tiny amount of emulsified polyethylene; evaporation of the whole aqueous sample yielded a few mg of material. The product was dried under high vacuum to yield 85.5g of amorphous elastomeric polyethylene, which exhibited a glass transition temperature of -61 0 C and a melting endotherm of -31 0 C (16J/g) by differential scanning calorimetry.

H-1 NMR analysis (CDC1 3 105 methyl carbons per 1000 'methylene carbons. Gel permeation chromatography (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polyethylene using universal calibration theory): .Mn=42,500; Mw=529,000; Mw/Mn=12.

4 This example demonstrates the use of pure water as a polymerization medium Examle 214 A 73-mg (0.049 mmol) sample of PrPh) 2 DABMe2]PdCH 2

CH

2 CH2C(O)OCH 3 }BAF" was placed in a 600-mL stirred autoclave under nitrogen with 150mL of deaerated water; to this was added 3.1 mL (3.3g) of Triton' X-100 nonionic surfactant. This mixture was pressurized to 5.8 MPa with ethylene and was stirred at 23°C for 17 hr. When the ethylene was vented, most of the emulsion came out the valve due to foaming; it was caught in a flask. There was polymer suspended in the -231 0ZiO/03,-ww133 I Ispa23 I mulsion; this was filtered to give, after MeOH and acetone washing and air-drying, 2.9g of amorphous polyethylene as a fine, gray rubber powder. The filtrate from the suspended polymer was a clear gray solution; this was concentrated on a hot plate to yield recovered Triton- X-100 and palladium black. There was no polymer in the aqueous phase. The elastomeric polyethylene product exhibited a glass transition temperature of -500C and a melting endotherm of 4 8

CC

(5J/g) by differential scanning calorimetry. H-I NMR analysis (CDC1 3 90 methyl carbons per 1000 methylene carbons. Gel permeation chromatography (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=31,000; Mw=311,000; Mw/Mn=O0.0.

This example demonstrates the aqueous emulsion polymerization of ethylene in the presence of a nonionic surfactant.

Example 215 A 93-mg (0.110-mmol) sample of PrPh) 2 DABMe 2 PdCH 2

CH

2

C

2 CC(0) OCHA)}SbFe- was placed in a 600-mL stirred autoclave under nitrogen with 150mL of deaerated water; to this was added 0.75g (1.4 mmol) of anionic fluorosurfactant (potassium perfluorooctansulfonate). This mixture was pressurized to 5.1 MPa with ethylene and was stirred at 23 0 C for hr. The ethylene was vented; the product consisted of polymer suspended in emulsion as well as some polymer granules on the wall of the autoclave; the emulsion was filtered to give, after MeOH and acetone washing and air-drying, 2.4g of amorphous polyethylene as a fine, gray rubber powder. The hazy blue-gray aqueous filtrate was evaporated to yield 0.76g of residue; hot water washing removed the surfactant to leave 0.43g of dark brown sticky polyethylene rubber. H-l NMR (CDC1 3 analysis: 98 CH3's per 1000 CHz.'s. Differentialscanning calorimetry: melting point: 117 0 C (111J/g); glass transition: -310C (second heat; no apparent Tg on -232 02/ 0 6/03.sw133 Ispa,232 -irst heat). This example demonstrates the aqueous emulsion polymerization of ethylene in the presence of a anionic surfactant. This example also demonstrates that a true aqueous emulsion of polyethylene can be obtained by emulsion polymerization of ethylene with these catalysts in the presence of an appropriate surfactant.

Example 216 A 90-mg (0.106-mmol) sample of PrPh) 2 DABMe 2 ]PdCH 2 CH2CH 2 C(0)OCH3)}SbF 6 was placed in a 600-mL stirred autoclave under nitrogen with 150mL of deaerated water; to this was added 0.75g (2.1 mmol) of cetyltrimethylammonium bromide cationic surfactant.

This mixture was pressurized to 5.2 MPa with ethylene and was stirred for 66 hr at 230C. The ethylene was vented; the product consisted of polymer suspended in a dark solution; this was filtered to give, after MeOH and acetone washing and air-drying, 0.13g of amorphous polyethylene as a tacky, gray rubber powder. There was no polymer in the aqueous phase. H-1 NMR (CDC1 3 analysis: 96 CH 3 's per 1000 CH2's. Differential scanning calorimetry: glass transition: -58 0 C; melting endotherms: 400, 860, 120 0 C (total: 20J/g). This example demonstrates the aqueous emulsion polymerization of ethylene in the presence of a cationic surfactant.

Example 217 An 87-mg (0.103-mmol) sample of PrPh) 2 DABMe2]PdCH 2

CH

2

CH

2 C(O)OCHJ3)SbFg- was placed in a 600-mL stirred autoclave under nitrogen. To this was added 100 mL of dry, deaerated methyl acrylate containing 100 ppm of phenothiazine as a free-radical polymerization inhibitor. The autoclave was stirred and pressurized to 300 psig with ethylene over 5 min.

The autoclave was then pressurized to 600 psig with an additional 300 psig of carbon monoxide (300 psig E 300 psig CO 600 psig). The reaction was stirred for hr at 23°C as the autoclave pressure dropped to 270 -233 0206/03,osw 33 I spa.233 .psig. The ethylene was then vented; the autociave contained a yellow solution which was concentrated by rotary evaporation, taken up in methylene chloride, filtered, and again concentrated to yield 0.18g of dark brown viscous oil. The product was washed.with hot acetone to remove the brown catalyst residues and was held under high vacuum to yield 55 mg of a colorless, viscous liquid terpolymer. The infrared spectrum exhibited carbonyl absorbances at 1743 (ester), 1712 (ketone), and 1691 cm- 1 H-1 NMR (CDC1 3 analysis: 76CH 3 's per 1000 CH2; there were peaks at 2.3 (t,

CH

2 COOR), 2.7 CH 2 CO), and 3.66 ppm (COOCH 3 The polymer contained 3.3 mol% MA (9.4 wt% MA). The carbon monoxide content was not quantified, but the absorbance in the infrared spectrum of the polymer due to ketone was about 1/2 to 2/3 the absorbance due to acrylate ester. This example demonstrates the use of carbon monoxide as a monomer.

Example 218 A 20-mg (0.035-mmol) sample of NiBr 2 [2- NpCH=N(CH 2 3 N=CH-2-Np), where Np naphthyl, (see structure below) was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of dry deaerated, toluene. Then 0.6 mL of polymethylalumoxane (3.3M) was injected; the light pink suspension became a dark gray-green solution, eventually with black precipitate. The mixture was immediately pressurized with ethylene to 7 psig and was stirred at 230C for 18 hr, during which time the mixture became a clear yellow solution with black, sticky precipitate. The ethylene was vented; the offgas contained about 3% butenes (90:10 1-butene: trans-2-butene) by gas chromatography Quadrex GSQ® Megabore column; 50-250°C at 0 /min). The toluene solution was stirred with 6N HC1 and methanol and was separated; concentration of the toluene solution followed by acetone rinsing the residue yielded 85 mg of liquid polyethylene. H-i NMR (CDC13) analysis: 209 CH 3 's per 1000 CH 2 This 234 O2/06/03,swl33Ilspas,234 :xample demonstrates the efficacy of a catalyst with a bis-imine ligand in which the imine groups are not alpha to one another.

N N

PMAO

NiBr 2 Example 219 A 17-mg (0.027-mmol) sample of PrPh) 2 DABMe 2 ]ZrC 4 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of dry, deaerated toluene. Then 0.6 mL of polymethylalumoxane (3.3M) was injected; the yellow suspension became an orange-yellow solution. The mixture was pressurized with ethylene to 7 psig and was stirred at 23 0 C for hr, during which time polymer slowly accumulated on the stir bar and eventually rendered the solution unstirrable. The toluene solution was stirred with 6N HC1 and methanol and was filtered to yield (after MeOH and acetone washing and air-drying) 1.01g of white, fluffy polyethylene. Differential scanning calorimetry exhibited a melting point of 131 0 C (124J/g). This example demonstrates the efficacy of a Zr(IV) catalyst bearing a diimine ligand.

Example 220 A 14-mg (0.024-mmol) sample of PrPh) 2 DABMe 2 ]TiCl 4 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of dry, deareated toluene (distilled from Na under N 2 Then 0.6 mL of polymethylalumoxane (3.3M) was injected; the yellow suspension became a dark brown suspension with some precipitate. The mixture was pressurized with ethylene to 7 psig and was stirred at 23 0 C for 3 hr, during which time polymer accumulated and rendered the solution unstirrable. The toluene solution was stirred with 6N HCI and methanol and was filtered to yield, after MeOH and acetone washing and air-drying, 1.09g of 235 02/0603,swl3311 sp.215 .hite, fluffy polyethylene. Differentfal scanning calorimetry exhibited a melting point of 131CC (161J/g). This example demonstrates the efficacy of a Ti(IV) catalyst bearing a diimine ligand.

Example.221 A 28-mg (0.046-mmol) sample of PrPh) 2 DABMe 2 ]CoBr 2 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of dry, deaerated toluene. Then 0.5 mL of polymethylalumoxane ;3.3M) was injected, resulting in a deep purple solution, and the mixture was pressurized immediately with ethylene to 7 psig and stirred at 23 0 C for 17 hr.

The solution remained deep purple but developed some viscosity due to polymer. The ethylene was vented; the cffgas contained 1-butene by gas chromatography (30-m Quadrex GSQ® Megabore column; 50-250 0 C at 10 0 /min). The toluene solution was stirred with 6N HCl/methanol and was separated; concentration of the toluene solution yielded, after drying under high vacuum, 0.18g of elastomeric polyethylene. A film of polymer cast from chlorobenzene was stretchy with good elastic recovery.

Differential scanning calorimetry: glass transition: 41 C; melting endotherm: 43 0 C (15J/g). This example demonstrates the efficacy of a cobalt (II) catalyst bearing a diimine ligand.

Example 222 A 35-mg (0.066-mmol) sample of PrPh)2DABMe 2 ]FeC1 2 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of d:.y, deaerated toluene. Then 0.6 mL of polymethylalumoxane (3.3M) was injected; the deep purple-blue solution became a royal purple solution, which evolved to deep green-black over time. The mixture was immediately pressurized with ethylene to 7 psig and was stirred at 23°C for 70 hr, during which time the mixture became a pale green solution with black, sticky precipitate.

The ethylene was vented; the toluene solution was 236 02/0603.sw1311spa,23 tirred with 6N HCI and methanol and was filtered t: yield 90 mg of polyethylene.

Differential scanning calorimetry: melting endotherm: 128 0 C (84J/g). This example demonstrates the efficacy of a iron (II) catalyst bearing a diimine ligand.

Example 223 A mixture of 3.2g of the polyethylene product of Example 96, 60 mg (1.9 wt%) of dicumyl peroxide, and 50g (1.6 wt%) of triallylisocyanurate (TAIC) was dissolved in 100 mL of THF. The polymer was precipitated by stirring the solution in a blender with water; the peroxide and TAIC are presumed to have stayed in the polymer. The polymer was pressed into a clear, rubbery, stretchy film at 125 0 Strips of this film were subsequently pressed at various temperatures (100'C, 150 0 C, 175°C, 200 0 C) for various times (1 min, min, 10 min) to effect peroxide-induced free-radical crosslinking The cured sheets were all clear and stretchy and shorter-breaking: 100 0 C for 10 min gave no apparent cure, while 150°C/5 min seemed optimal. The cured films came closer to recovering their original dimensions than the uncured films. This example demonstrates peroxide curing of- the amorphous elastomeric polyethylene.

Example 224 A 28-mg (0.050-mmol) sample of TiCl 4 [2- NpCH=N(CH 2 2 N=CH-2-Np], where Np naphthyl, (see structure below) was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of dry, deaerated toluene. Then 0.6 mL of polymethylalumoxane (3.3M) was injected; the orange suspension became reddish-brown. The mixture was immediately pressurized with ethylene to 7 psig and was stirred at 23 0 C for 66 hr. The toluene solution was stirred with 6N HC1 and methanol and was filtered to yield, after methanol washing and air-drying, 1.30g of white, fluffy polyethylene.

237 02/ 0 6/03,swl3,, spa.237 Differential scanning calorimetry: melting endotherm: 135°C (242J/g).

This example demonstrates the efficacy of a catalyst with a bis-imine ligand in Which the imine 3 groups are not alpha to one another.

H H S TiCl 4

PMAO

Example 225 A 33-mg (0.053-mmol) sample of PrPh)2DABMe 2 ]ScC1 3 -THF was -magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of dry, deaerated toluene. Then 0.6 mL of polymethylalumoxane (3.3M) was injected; the pale orange solution became bright yellow. The mixture was immediately pressurized with ethylene to 7 psig and was stirred at 23 0 C for 17 hr, during which time the mixture remained yellow and granular suspended polymer appeared. The ethylene was vented; the toluene solution was stirred with 6N HCI and methanol and was filtered to yield 2.77g of white, granular polyethylene. This example demonstrates the efficacy of a scandium (III) catalyst bearing a diimine ligand.

Example 226 (2-t-BuPh)2DABAN This compound was made by a procedure similar to that of Example 25. Three mL (19.2 mmol) of 2-tbutylaniline and 1.71 g (9.39 mmol) of acenaphthenequinone were partially dissolved in 50 mL of methanol (acenaphthenequinone was not completely soluble). An orange product was crystallized from CH2C12 (3.51 g, 1H NMR (CDC13, 250 MHz)d 7.85 2H, J 8.0 Hz, BIAN: Hp), 7.52 2H, Ar: Hm), 7.35 (dd, 2H, J 8.0, 7.3 Hz, BIAN: Hm), 7.21 4H, 238 02W603swl3311spa,238 tr: Hm and Hp), 6.92 2H, Ar: Ho), 6.81 2H, J 6.9 Hz, BIAN: Ho), 1.38 18H, C(CH3)3).

Example 227 Methyl vinyl ketone was stirred over anhydrous

K

2 C0 3 and vacuum transferred on a high vacuum line to a dry flask containing phenothiazine (50 ppm). Ethylene and methyl vinyl ketone (5 ml) were copolymerized according to Example 16 using catalyst PrPh)2DABMe2] PdCH2CH2CH2C(O)OCH 3 }+SbF6 (0.084 g, 0.10 mmol) to give 0.46 g copolymer (0.38 g after correcting for catalyst residue). 1 H- NMR (CDCl 3 0.

7 5-0.95(m, CH3); 0.95-1.45(m, CH and CH2); 1.55(m, CH2CH2C(O)CH3); 2.15(s, -CH2CH2C(0)CH 3 2.4(t, CH2CH2C(O)CH3). Based on the triplet at 2.15, it appears that much of the ketone functionality is located on the ends of hydrocarbon branches.

Integration shows that the copolymer contains 2.1 mole% methyl vinyl ketone, and 94 methyl carbons (exclusive of methyl ketones) per 1000 methylene carbons. The turnover numbers are 128 equivalents of ethylene and 3 equivalents of methyl vinyl ketone per Pd. GPC (THF, PMMA standard): Mn=5360 Mw=7470 Mw/Mn 1.39.

Example 228 A Schlenk flask containing 122 mg (0.0946 mmol) of {[(4-MePh),DABMe 2 ]PdMe(NCMe) )BAF- was placed under a CO atmosphere. The yellow powder turned orange upon addition of CO, and subsequent addition of 20 mL of

CH

2 C1 2 resulted in the formation of a clear red solution. t-Butylstyrene (10 mL) was added next and the resulting orange solution was stirred for 25.7 h at room temperature. The solution was then added to methanol in order to precipitate the polymer, which was collected by filtration and-dried in a vacuum oven at °C overnight (yield 4.03 GPC Analysis (THF, polystyrene standards): Mw 8,212; Mn 4,603; PDI 1.78. The 1 H NMR spectrum (CDC1 3 400 MHz) of the isolated polymer was consistent with a mixture of copolymer and poly(t-butylstyrene).

239 o 0 2 /063.sw331Isp«.23 Mixtures of alternating copolymer and poly(tbutylstyrene) were obtained from this and the following polymerizations and were separated by extraction of the homopolymer with petroleum ether. When R 2 and R 5 were 4-MePh (this example) atactic alternating copolymer was isolated. When R 2 and R 5 were 2,6-i-PrPh (Example 229) predominantly syndiotactic alternating copolymer was isolated. (Spectroscopic data for atactic, syndiotactic, and isotactic t-butylstyrene/CO alternating copolymers has been reported:

M.

Brookhart, et al., J. Am. Chem. Soc. 1992, 114, 5894- 5895; M. Brookhart, et al., J. Am. Chem. Soc. 1994, 116, 3641-3642.) Petroleum ether (-200 mL) was added to the polymer mixture in order to extract.the homopolymer, and the resulting suspension was stirred vigorously for several h. The suspension was allowed to settle, and the petroleum ether solution was decanted off of the gray powder. The powder was dissolved in CH 2 C12 and the resulting solution was filtered through Celite. The

CH

2 C12 was then removed and the light gray powder (0.61 g) was dried in vacuo. IH and 13C NMR spectroscopic -data are consistent with the isolation of atactic alternating copolymer: IH NMR (CDC1 3 300 MHz) 6 7.6 6.2 (br envelope, 4, Haryi), 4.05 and 3.91 (br, 1, CHAr'), 3.12 and 2.62 (br, 2, CH 2 1.26-1.22 (br envelope, 9, CMe 3 1 3 C NMR (CDC13, 75 MHz) 6 207.5 206.0 (br envelope, 150.0 149.0 (br, Ar': Cp), 135.0 133.8 (br envelope, Ar': Cipso), 127.9 Cm), 126.0 125.0 (br, Ar': Co), 53.0 51.0 (br envelope, CRAr'), 46.0 42.0 (br envelope,

CH

2 34.3 (CMe3), 31.3 (CMe 3 Example 229 The procedure of Example 228 was followed using 134 mg (0.102 mmol) {[(2,6-i-PrPh) 2 DABMe 2 ]PdMe(N= CMe)}+BAF-. A mixture (2.47 g) of copolymer and poly(t-butylstyrene) was isolated. GPC Analysis (THF, polystyrene standards): Mw 10,135; Mn 4 9 2 2 PDI -240- 02/0603,swl3311spa,240 2.06. Following the extraction of the homopolymer with petroleum ether, 0.49 g of off-white powder was isolated. IH and 13 C NMR spectroscopic data are consistent with the isolation of predominantly syndiotactic copolymer, although minor resonances are present: 1H NMR (CDC1 3 300 MHz) 6 7.20 2, J 8.14, Ar': Ho or Hm), 6.87 2, J 7.94, Ar': Ho or Hm), 3.91 (dd, 1, J 9.06, 3.16, CHAr'), 3.15 (dd, 1, J 18.02, 9.96, CRH'), 2.65 (dd, 1, J 17.90, CHH'), 1.25 9, CMe3); 13 C NMR (CDC1 3 75 MHz) 6 207.0 149.8 Cp), 134.5 Cipso) 127.8 (Ar': Cm), 125.6 Co), 51.7 (CHAr'), 45.6 (CH 2 34.3 (CMe3), 31.3 (CMe 3 Example 230 A Schlenk flask containing 74.3 mg (0.0508 mmol) of [(2,6-i-PrPh) 2 DABMe 2 ]PdMe(OEt 2 )BAF- was evacuated, cooled to -78 OC and then placed under an atmosphere of ethylene/CO (1:1 mixture). Following the addition of mL of chlorobenzene, the reaction mixture was allowed to warm to room temperature and stirred. A small amount of white precipitate appeared on the sides of the flask after 0.5 h and more precipitate formed during the next two days. After stirring for 47.2 h, the reaction mixture was added to methanol and the resulting suspension was stirred. The precipitate was then allowed to settle, and the methanol was decanted, leaving behind a cream powder (0.68 which was dried in a vacuum oven at 70 °C for one day. 1 H and 13 C NMR spectroscopic data are consistent with the isolation of an alternating copolymer of ethylene and carbon monoxide: 1 H NMR (CDC13/pentafluorophenol, 400 MHz) 6 2.89 (-C(O)-CH 2 13 C NMR (CDCl 3 /pentafluorophenol, 100 MHz) 6 212.1 35.94 (CH 2 For comparisons of the spectroscopic data of alternating E/CO copolymers herein with literature values, see for example: E. Drent, et al., J.

Organomet. Chem. 1991, 417, 235-251.

241 0 2 /O0603,sw33lsa241 Example 231 A Schlenk flask containing 73.2 mg (0.0500 mmol) of 2 ,6-i-PrPh) 2 DABMeJPdMe(OEt 2 BAF- was evacuated, cooled to -78 oC, and then back-filled with ethylene (1 atm). Chlorobenzene (50 mL) was added via.syringe and the solution was allowed to warm to room temperature.

After 0.5 h, the reaction vessel was very warm and ethylene was being rapidly consumed. The reaction flask was then placed in a room-temperature water bath and stirring was-continued for a total of 3 h. A very viscous solution formed. The atmosphere was then switched to ethylene/carbon monoxide (1:1 mixture, 1 atm) and the reaction mixture was stirred for 47.7 more hours. During this time, the solution became slightly more viscous. The polymer.was then precipitated by adding the chlorobenzene solution to methanol. The methanol was decanted off of the polymer, which was then partially dissolved in a mixture of Et 2 O, CH 2 C12 and THF. The insoluble polymer fraction (2.71 g) was collected on a sintered glass frit, washed with chloroform, and then dried in a vacuum oven at 70 oC for 12 h. The NMR spectroscopic data of the gray rubbery material are consistent with the formation of a diblock of branched polyethylene and linear poly(ethylene-carbon monoxide): 1 H NMR (CDCl3/pentafluorophenol, 400 MHz) 6 2.85 C(0)H2CHC(O)-), 2.77 (-C(O)CH 2 minor), 1.24 (CH2), 0.83 (CH3); Polyethylene Block Branching: -103 CH 3 per 1000 CH2; Relative Block Length[(CH2CH 2 )n- (C(O)CH2CH2)m): n/m 2.0. 1C NMR (CDCl3/pentafluorophenol, 100 MHz; data for ethylene-CO block) 5 211.6 211.5 minor), 35.9

(C(O)-CH

2

CH

2 35.8 (CCO)CH 2 minor).

-242- 02/06/03,swJl33j sp,242 Example 232 A Schlenk flask containing 75.7 mg (0.0527 mmol) of [(2,6-i-PrPh) 2 DABH2]PdMe(OEt 2 BAF- was evacuated, cooled to -78 OC, and then back-filled with ethylene (1 atm). Chlorobenzene (50 mL) was added via syringe, the solution was allowed to warm to room temperature and stirred for 3 h. The solution did not become warm or viscous during this time. The atmosphere was changed to ethylene/carbon monoxide (1:1 mixture, I atm) and the solution was stirred for 47.7 more hours. During this time, the reaction mixture became quite viscous and solvent-swollen polymer precipitated on the sides of the flask. The polymer was precipitated by addition of the reaction mixture to methanol. The methanol was decanted off of the rubbery polymer (4.17 which was then dried in a vacuum oven for one day at 70 oC.

Chloroform was then added.to the polymer and the rubbery insoluble fraction (0.80 g) was collected on a sintered glass frit. A IH NMR spectrum (CDC1 3 400 MHz) of the chloroform-soluble polymer showed no carbon monoxide incorporation; only branched polyethylene was observed. NMR spectroscopic data for the chloroforminsoluble fraction was consistent with the formation of a diblock of branched polyethylene and linear poly(ethylene-carbon monoxide): 1 H NMR (CDCl 3 /pentafluorophenol, 400 MHz) 6S 2.88 (C(0)CH 2

CH

2 1.23 (CH 2 0.83 (CH3); Polyethylene Block Branching: 132 CH 3 per 1000 CH2; Relative Block Length[(CH 2

CH

2 )n-(C(0)CH2CH2)m] n/m 0.30; 1 3 C NMR

(CD

2 Cl 2 /pentafluorophenol, 100 MHz; data for ethylene- CO block) 8 211.3 211.3 minor), 36.5

(-C(O)CH

2

CH

2 36.4 (C(O)CH 2 minor).

Example 233 A 34-mg (0.053-mmol) sample of the crude product of Example 235, was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25 mL of dry, deaerated toluene. Then 0.6 mL of polymethylalumoxane (3.3M) was injected; the purple-pink suspension became a gold- 243 0 2 0 6 /03,swi331,spa.2 4 3 jreen solution with black precipitate. The mixture was pressurized with ethylene to 152 kPa (absolute) and was stirred for 20 hr. Within the first hour, polymer was observed to be accumulating on the stir bar and the walls of the flask. The ethylene was vented and the toluene solution was stirred with 6N HC1 and methanol and was filtered to yield (after MeOH and acetone washing and air-drying) l.37g of white, granular polyethylene. This example demonstrates the efficacy of a catalyst with a 1,3-diimine ligand.

Example 2L4 Synthesis of MeC(=N-2.6-C H.-ipr2jCH=C(NH-2 6 Concentrated HC1 (0.3 ml, 3.6 mmol) was added to a solution of 2,4-pentanedione (1.2 g, 12 mmol) and 2,6diisopropylaniline (5.0 ml, 26.6 mmol) in 15 ml ethanol. The reaction mixture was refluxed for 21 h during which time a white solid precipitated. This was separated by filtration, dried under vacuum and treated with saturated aqueous sodium bicarbonate. The product was extracted with methylene chloride, and the organic layer dried over anhydrous sodium sulfate.

Removal of the solvent afforded 1.43 g of the title compound as a white crystalline product; mp: 140- 142°C; I1 NMR: (CDC1 3 6 12.12 (bs,l H, NH) 7.12 m, 6 H, aromatic), 4.84 1 H, C=CH-C), 3.10 4 H, isopropyl CH, J 7 Hz), 1.72 6 H, CH 3 1.22 (d, 12 H, isopropyl CH3, J 7 Hz), 1.12 12 H, isopropyl CH 3 J 7 Hz). 13C NMR: (CDC1 3 6 161.36 142.63 (aromatic 140.89 (aromatic C-2), 125.27 (aromatic 123.21 (aromatic 93.41 28.43 (isopropyl CH), 24.49 (isopropyl CH 3 23.44 (isopropyl CH 3 21.02 (CH3). MS: m/z 418.333 (calc. 418.335).

-244 02/0 03.swt331n Ispa,244 Example 235 Synthesis of an ethylene polymerization catalyst from Ni(MeOCH 2 CH2OMe)Brj and MeC(=N-2.6-CHjI iPr) CH=C (NH-2. 6-C Hl-iPr IMe Ni(MeOCH2CH20Me)Br2 (0.110 g, 0.356 mmol) and MeC(=N-2,6-C 6 H3-iPr2)CH=C(NH-C6H3-iPr2)Me (0.150 g, 0.359 mmol) were combined in 10 mL of methylene chloride to give a peach-colored suspension. The reaction mixture was stirred at room temperature overnight, during which time a lavender-colored powder precipitated. This was isolated by filtration, washed with petroleum ether and dried affording 0.173 g of material. This compound was used as the catalyst in Example 233.

Example 236 Sf(2,6-i-PrPh) DABMe Pd iMeCN)M l z(Ba [Pd(MeCN) 4 (BF4) 2 (0.423 g, 0.952 mmol) and (2,6i-PrPh)2DABMe2 (0.385 g, 0.951 mmol) were dissolved in mL acetonitrile under nitrogen to give an orange solution. The reaction mixture was stirred at room temperature overnight; it was then concentrated in vacuo to afford a yellow powder. Recrystallization from methylene chloride/petroleum ether at -40 0

C

afforded 0.63 g of the title compound as a yellow crystalline solid. 1H NMR (CD2C12) 6 7.51 2H, Hpara), 7.34 4H, Hmeta), 3.22 (sept,. 4H, CHMe2), 2.52 6H, N=CMe), 1.95 6H, NCEMe), 1.49 12H, CHMe2), 1.31 12H, CHMe2).

Example 237 Ethylene Polymerization Catalyzed by {r 2.6-i- PrPhlDARBMaI Pd ifMeCN)z BFJ2 A 100 mL autoclave was charged with a solution of [2,6-i-PrPh)2DABMe2]Pd(MeCN)2)(BF4)2 (0.043 g, 0.056 mmol) dissolved in 50 mL chloroform and ethylene (2.8 MPa). The reaction mixture was stirred under 2.8 MPa ethylene for 9 h 15 min. During this time, the temperature inside the reactor increased from 23 to 27 0 C. The ethylene pressure was then vented and -245- 0 1331 a,24 02/06/03.swl3311spa,245 'olatiles removed from the reaction mixture to afford 1.65 g of a viscous yellow oil. This was shown by IH NMR to be branched polyethylene containing 94 methylended branches per 1000 methylenes.

Ethylene polymerization by Ni(CODrJ) 2 Example 23o £PEhl2DABIM2*HBAEL2Et 2

QZ

Ni(COD) 2 (0.017 g, 0.06 mmol) and (2,6-i- PrPh)2DABMe 2 HBAF(Et 2 0) 2 (0.085 g, 0.06 mmol) were dissolved in 5 mL of benzene under nitrogen at room temperature. The resulting solution was quickly frozen, and then allowed to thaw under 6.9 MPa of ethylene at 500C. The reaction mixture was agitated under these conditions for 18 h affording a solvent swelled polymer. Drying afforded 5.8 g of a polyethylene as a tough, rubbery material.

Example 239 Ethylene polymerization by Pd(dba I3dba dibenzylideneacetonep)/ (2.6-i--PPh)2DABMea*HBAF iLt Q A sample of (Et 2 O)'HBAF (200 mg, 0.20 mmol) was dissolved in 10 mL of Et 2 0. To this solution was added 1 equivalent of DABMe 2 (or other a-diimine). The solution became red. Removal of the volatiles in vacuo gave a red solid of the acid-a-diimine complex.

Pd2(dba)3 (0.054 g, 0.06 mmol) and (2,6-i- PrPh)2DABMe 2 .HBAF(Et 2 0) 2 (0.076 g, 0.05 mmol) were dissolved in 5 mL of benzene under nitrogen at room temperature. The resulting solution was agitated under 6.9 MPa of ethylene at 50 0 C for 18 h. The product mixture was concentrated to dryness in vacuo, affording an extremely viscous oil. 1 H NMR showed the product to be branched polyethylene containing 105 methyl ended branches per 1000 methylenes.

Example 240 Toluene (30 mL), 4 -vinylcyclohexene (15 mL), and mg of [(2,6-i-PrPh)2DABH2]NiBr 2 (0.03 mmol) were combined in a Schlenk flask under an atmosphere of ethylene. A 10 MAO solution (3 mL) in toluene was -246- 02/ 0 6103,swl331 sp.246 idded. The resulting purple solution was stirred for 16 h. After only a few hours, polymer began to precipitate and adhere to the walls of the flask. The polymerization was quenched and the polymer 3 precipitated from acetone. The polymer was dried in vacuo overnight resulting in 100 mg of a white solid.

Characterization by proton NMR suggests in corporation of 4-vinylcyclohexene as a comonomer. 1 H NMR (CDC1 3 6 5.64 vinyl, cyclohexene), 2.0-0.9 (overlapping m including cyclohexyl methylene, methylene (PE), methine), 0.78 (methyl, PE). There are also some minor signals in the base line that suggests incorporation of the internal olefin (cyclohexene) and free a-olefin (4vinyl).

Example 241 The catalyst PrPh) DABMe 2 ]PdCH 2 CH2CHC(O)OCH3)SbF6, (1.703 g, 2 mmol) was added to a 1 gal Hastalloy@ autoclave. The autoclave was sealed, flushed with nitrogen and then charged with 1500 g of SO,. An over pressure of MPa of ethylene was maintained for 24 hr at 250C. The autoclave was vented to relieve the pressure and the Contents of the autoclave were transferred to a jar.

The polymer was taken up in methylene chloride and purified by precipitation into excess acetone. The precipitated polymer was dried in vacuo to give 2.77 g of polymer. The polymer displayed strong bands attributable to sulfonyl group in the infrared (film on KBr plate) at 1160 and 1330 cm-.

Example 242 Copolymerizaton of Ethylene and Methyl Vinyl Ketone Methyl vinyl ketone (MVK) was stirred over anhydrous K 2

CO

3 and vacuum transferred using a high vacuum line to a dry flask containing phenothiazine ppm). Ethylene and MVK (5 ml) were copolymerized using the procedure of Example 125 using as catalyst i-PrPh) 2 DABMe 2 )PdCH 2

CH

2

CH

2

C(O)OCH

3 )SbF 6 (0.084 g, 0.10 247 06/03.w33 Ip247 .amol) to give 0.46 g of copolymer (0.38 g after correcting for catalyst residue). 1 H NMR (CDC 3 0.75-0.95

CH

3 0.95-1.45 CH and CH 2 1.55 (m,

-CH

2

CH

2

C(O)CH

3 2.15 -CH2CH 2

C(O)CH

3 2.4

CH

2

CH

2 C(0)CH 3 Based on the triplet at 2.15, it appeared that much of the ketone functionality was located on the ends of the hydrocarbon branches.

Integration showed that the copolymer contained 2.1 mole% MVK, and has 94 methyl carbon (exclusive of methyl ketones) per 1000 methyl carbon atoms. The turnover was 128 equivalents of ethylene and 3 equivalents of MVK per Pd. GPC (THF, PMMA standard): Mn=5360, Mw=7470, Mw/Mn=1.39.

Example 243 1-Hexene (20 ml) was polymerized in methylene chloride (10 ml) according to example 173 to give 4.22 g of viscous gel (1002 equivalents 1-hexene per Pd).

Integration of the 1H NMR spectrum showed 95 methyl carbons per 1000 methylene carbons. 13 C NMR quantitative analysis, branching per 1000 CH2: Total methyls (103), Methyl Ethyl(none detected), Propyl (none detected), Butyl Amyl (none detected), Hexyl and end of chains (18.1).

Integration of the CH 2 peaks due to the structure

CH(R)CH

2 where R is an alkyl group, and R' is an alkyl group with two or more carbons showed that in 74% of these structures, R Me.

Listed below are the 13 C NMR data upon which the above analysis is based.

-248- 02/06/03,swl3311spa,.248 Frea nnm 42.6359 37.8987 37.2833 36.8537 35.5381 34.8803 34.5514 34.2755 33.2411 32.9811 31.9467 30.7212 30.2597 30.143 29.7717 29.342 27. 5702 27.1935 27.045 23.0292 22.6526 20.2495 19.7455 13.9049 i3C TCB, 140C, Intensity 4.05957 9.10141 64.4719 8.67514 4.48108 4.30359 5.20522 21.6482 4.13499 32.0944 14.0714 5,48503 28.5961 50.4726 248 17.4732 27.2867 49.5612 23.1776 9.56673 14.1631 5.72164 48.8451 21.5008 NMR data 0.05M CrAcAc aa for Me Et branches MB3 aB 1

MB

1

MB

1 3B6+,3EOC y+y+B, 3B4 y+y+B, 3B4 y+y+B, 3B4 y+y+B, 3B 4 y+y+B,3B4 fy for 2 Me branches Py+B, (4B 5 etc.) 2B4 2B5+, 2EOC 181 IBi 1B4+, 1EOC Example 244 1-Heptene (20 ml) was polymerized in methylene chloride (10 ml) according to example 173 to give 1.29 g of viscous gel (263 equivalents 1-heptene per Pd).

Integration of the 1H NMR spectrum showed 82 methyl carbons per 1000 methylene carbons. 13 C NMR quantitative analysis, branching per 1000 CH2: Total methyls Methyl Ethyl(none detected), Propyl (none detected), Butyl (none detected), Amyl 2Hexyl and end of chains Integration of the CH 2 peaks due to the structure -CH(R)CH 2

CH(R')-

where R is an alkyl group, and R' is an alkyl group with two or more carbons showed that in 71% of these structures, R Me. DSC (two heats, -150-->150 0

C,

shows Tg -42 0 C and a Tm 28 0 C (45 J/g) Listed below are the 13 C NMR data upon which the above analysis is based.

-249- 0 2 /06/03.sw133I spa.249 Frea pnm 42.6041 37.851 37.5963 37.2356 35.4956 34.8219 34.6097 34.2278 33.3418 32.9228 32.2809 31.9148 30.5886 30.4613 30.2173 30.1059 29.7292 29.3049 27.1511 27.0025 26.7267 24.5623 22.6207 20.2176 19.7084 13.8677 13 C NMR data TCB, 120C, 0.05M CrAcAc Intensity 5.16375 aa fo 15.9779 MB3+ 7.67322 99.6734 aB1 7.58713 6.32649 6.37695 37.6181 3.78275

MB

1 60.7999

MB

1 13.6249 21.2367 3B6*,: 13.8482

Y+Y+B,

22.1996 y+y+B, 48.8725 Y+y+B, 80.2189 y+y+B, 496 y+y+B, 26.4277 y+y+B, 114.228 Py+B1 47.5199 20.4817 3.32234 36.4547 2B5* 7.99554 1B 1 70.3654 B11 36.1098 IB4,E r Me Et 3EOC 3B 4 3B4 3B4 3B4 3B4 384 2EOC

DC

Example 245 1-Tetradecene (20 ml) was polymerized in methylene chloride (10 ml) according to ekample 173 to give 6.11 g of sticky solid (622 equivalents 1-tetradecene per Pd). Integration of the 1H NMR spectrum showed 64 methyl carbons per 1000 methylene carbons. 13C NMR quantitative analysis, branching per 1000 CH2: Total methyls Methyl Ethyl(5.6), Propyl Butyl (ncne detected), Amyl 2Hexyl and end of chains Integration of the CH2 peaks due to the structure -CH(R)CH 2

CH(R')-

where R is an alkyl group, and R' is an alkyl group with two or more carbons showed that in 91% of these structures, R Me. The region integrated for the structure where both R and R' are >Ethyl was 40.0 ppm to 41.9 ppm to avoid including a methine carbon interference.

-250 0206/03,sw 3311sp&250 Listed below are the 13 C NMR data upon which the above analysis is based.

Frea pp 39.2826 37.8012 37.2171 34.1694 33.6809 32.9004 31.9022 30.1978 30.0969 29.7252 29.3004 27.1394 26.9748 26.3642 22.6209 19.6952 13.8759 10.929 13 C NMR data TCB, 120C, 0.05M CrAcAc Intensity 6.684

MB

8.13042

MB

24.8352 aB 31.5295 ay 4 13.0926 ay 13.0253

MB]

25.0187 3Be 42.5593 y+y.

34.1982 Y+y.

248 y+y.

26.4627 y+y.

31.8895

PY+

40.5922 Py+] 7.06865 Py+] 25.5043 2B5 15.0868 1B 1 24.9075 1B4 7.63831 1B, 2 3 1, 3B3 B, (4B 4 ,5B 5 etc.) MB 1 B, (4B4,5B5, etc.) MB 1 ;+,3EOC +B,3B4 +B,3B4 +B,3B4 +B,3B4 B,2B2, (4B 5 ,etc.) B,2B2, B,2B2, +,2EOC +,1EOC Examiple 246 This example demonstrates copolymerization of ethylene and 1-octene to give polymer with mostly C6+ branches. Under nitrogen, [(2,6-i-PrPh)2DABH2]NiBr 2 (Q.005 g, 0.0084 mmol) and 9.6 wt. MAO in toluene (0.50 mL) were dissolved in 10 mL of toluene at room temperature. The resulting solution was immediately transferred to a 100 mL autoclave that had previously been flushed with nitrogen and evacuated. 1-Octene mL, 255 mmol) was then added to the reactor, which was subsequently charged with ethylene (320 kPa). The reaction mixture was stirred for 60 min, during which time the temperature inside the reactor varied between 24 and 280C. Ethylene was then vented, and the product polymer was precipitated by addition of the crude reaction mixture to 50 mL of methanol containing 5 mL of concentrated aqueous HC1. The polymer precipitated as a slightly viscous oil; this was removed by pipette and dried affording 3.03 g of amorphous ethylene/loctene copolymer. Branching per 1000 CH2 was -251- 02/ 0 603.swI33 lspa,251 .juantified by 13C NMR (C 6

D

3 C13, 25 0 C) total Methyls Methyl Ethyl(l.6), Propyl Butyl Amyl ;Hex and end of chains Am and end of chains Bu and end of chains (73.7).

GPC (trichlorobenzene vs. linear polyethylene: M 48,200, Mn 17,000. DSC: Tg -63°C.

Example 247 This example demonstrates copolymerization of ethylene and 1-octene to give polymer with mostly methyl and C6+ branches. Under nitrogen, PrPh)2DABH 2 ]NiBr 2 (0.005 g, 0.0084 mmol) and 9.6 wt. MAO in toluene (0.50 mL) were dissolved in 40 mL of toluene at -40°C. The resulting solution was immediately transferred to a 100 mL autoclave that had previously been flushed with nitrogen and evacuated.

1-Octene (10 mL, 64 mmol) was then added to the reactor under 324 kPa of ethylene. The resulting reaction mixture was stirred under 324 kPa of ethylene for 1 h min. During this time the temperature inside the reactor varied between 29 and 40 0 Ethylene was then vented, and the product polymer was precipitated by addition of the crude reaction mixture to methanol.

The polymer was dried affording 6.45 g of ethylene/1octene copolymer. Branching per 1000 CH 2 was quantified by 1 3 C NMR (CsD 3 C1 3 250C) Total methyls Methyl Ethyl(2.4), Propyl Butyl Amyl >Hex and end of chains >Am and end of chains Bu and end of chains GPC (trichlorobenzene vs. linear polyethylene): Mw 116,000, Mn 9,570.

Example 248 Under a nitrogen atmosphere, Ni(COD) 2 (0.017 g, 0.06 mmol) and (2,6-i-PrPh)2DABMe2 (0.024 g, 0.06 mmol) were dissolved in benzene (5.0 mL). To the resulting solution was added HBAF'(Et20) 2 (0.060 g, 0.06 mmol).

The resulting solution was immediately frozen inside a mL shaker tube glass insert. The glass insert was transferred to a shaker tube, and its contents allowed -252- 0 2 /06/03.swl3311 spa,252 o thaw under an ethylene atmosphere. Tfhe reactich mixture was agitated under 6.9 MPa C2H4 for 17.5 h at ambient temperature. The final reaction mixture contained polyethylene, which was washed with methanol and dried; yield of polymer 9.2 g. 1H NMR (CDC12CDC12, 1200C) showed that this sample contained 49 methyl-ended branches per 1000 methylenes. DSC: Tm 118.8 0 C, AHf 87.0 J/g.

Example 249 Under a nitrogen atmosphere, Ni[P(O-2-C6H 4 Me)312(C2H4) (0.047 g, 0.06 mmol) and (2,6-i- PrPh)2DABMe2 (0.024 g, 0.06 mmol) were dissolved in benzene (5.0 mL). To the resulting solution was added HBAF'(Et20)2 (0.060 g, 0.06 mmol). The resulting solution was immediately frozen inside a 40 mL shaker tube glass insert. Theglass insert was transferred to a shaker tube, and its contents allowed to thaw under an ethylene atmosphere. The reaction mixture was agitated under 6.9 MPa C2H4 for 18 h at ambient temperature. The final reaction mixture contained polyethylene, which was washed with methanol and dried; yield of polymer 8.9 g. IH NMR (CDC12CDC12, 120 0

C)

showed that this sample contained 47 methyl-ended branches per 1000 methylenes. DSC: Tm 112.1 0 C, AHf 57.5 J/g.

Example 250 A 100 mL autoclave was charged with a solution of Pd 2 (dba)3 (dba dibenzylideneacetone) (0.054 g, 0.059 mmol) in 40 mL of chloroform. A solution of (2,6-i- PrPh) 2 DABMe2YHBAF'(Et20)2 (0.085 g, 0.059 mmol) (see Example 256) in 10 mL of chloroform was then added under 2.1 MPa of ethylene. The reaction mixture was stirred for 3 h. During this time the temperature inside the reactor varied between 24 and 40 0

C.

Ethylene was then vented, and the product polymer was precipitated by addition of the crude reaction mixture to methanol. The polymer was dried affording 14.7 g of viscous polyethylene. IH NMR (CDC13, 25 0 C) of this 253 0 2 /06/03.swl33 Ispa,253 aterial showed it to be branchea polyethylene with 115 methyl-ended branches per 1000 methylenes. GPC analysis in trichlorobenzene gave Mn 97,300, Mw 225,000 vs. linear polyethylene.

Example 251 A 100 mL autoclave was charged with solid Pd(OAc) 2 (OAc acetate) (0.027 g, 0.12 mmol) and (2,6-i- PrPh) 2 DABMe 2 (0.049 g, 0.12 mmol). The reactor was flushed with nitrogen and evacuated. A solution of 54 wt. HBF4YEt20 (0.098 g, 0.60 mmol) in 10 mL of chloroform was then added under 2.1 MPa of ethylene.

The reaction mixture was stirred for 1.5 h. During this time, the temperature inside the reactor varied between 24 and 37 0 C. Ethylene was then vented, and the product polymer was precipitated by addition of the crude reaction mixture to methanol. The polymer was dried affording 4.00 g of viscous polyethylene. 1H NMR (CDC1 3 25 0 C) of this material showed it to be branched polyethylene with 100 methyl-ended branches per 1000 methylenes. GPC analysis in trichlorobenzene gave Mn 30,500, Mw 43,300 vs. linear polyethylene.

Example 252 (Note: It is believed that in the following experiment, adventitious oxygen was present and acted as a cocatalyst.) Under nitrogen, I(2.6-i-PrPh) 2

DAB

An]Ni(COD) (0.006 g, 0.009 mmol) and 9.6 wt. MAO in toluene (0.54 mL, 1.66 mmol) were dissolved in 50 mL of toluene. This mixture was then transferred to a 100 mL autoclave. The autoclave was then charged with 2.1 MPa 3) of ethylene. The reaction mixture was stirred for 8 min. During this time, the temperature inside the reactor varied between 23 and 51°C. Ethylene pressure was then vented. The product polymer was.washed with methanol and dried, affording 8.44 g of polyethylene.

IH NMR (CDC1 2 120 0 C) showed that this sample contained 77 methyl-ended branches per 1000 methylenes.

Example 253 254- 02/06/03,swl33rspa,254 Under nitrogen, [(2,4,6-MePh)DABAn]NiBr 2 (0.041 g, 0.065 mmol) was suspended in cyclopentene (43.95 g, 645 mmol). To this was added a 1 M solution of EtAlCl 2 in toluene (3.2 mL, 3.2 mmol). The resulting reaction mixture was transferred to an autoclave, and under 700 kPa of nitrogen heated to 60°C. The reaction mixture was stirred at 60°C for 18 h; heating was then discontinued. When the reactor temperature had dropped to -30°C, the reaction was quenched by addition of isopropanol. The resulting mixture was stirred under nitrogen for several minutes. The mixture was then added under air to a 5 aqueous HCI solution (200 mL).

The precipitated product was filtered off, washed with acetone, and dried to afford 6.2 g of polycyclopentene as a white powder. DSC of. this material showed a broad melting transition centered at approximately 190°C and ending at approximately 250°C; AHf 18 J/g. Thermal gravimetric analysis of this sample showed a weight loss starting at 184°C: the sample lost 25% of its weight between 184 and 470°C, and the remaining material decomposed between 470 and 500°C.

Example 24 Under nitrogen, [(2,6-Me-4-BrPh) 2 DABMe 2 ]NiBr 2 (0.010 g, 0.015 mmol) was suspended in cyclopentene (5.0 g, 73.4 mmol). To this was added a 1 M solution of EtAlCI 2 in toluene (0.75 mL, 0.75 mmol). The resulting reaction mixture was stirred at room temperature for 92 h, during which time polycyclopentene precipitated. The reaction was then quenched by addition of -5 mL of methanol under nitrogen. Several drops of concentrated HC1 was then added under air. The product was then filtered off, washed with more methanol followed by acetone, and dried to afford 1.31 g of polycyclopentene as a white powder. DSC of this material showed a broad melting transition centered at approximately 200°C and ending at approximately 250°C; AHf 49 J/g. Thermal gravimetric analysis of this sample showed a weight 255 021 0 6/0 3 ,swl331 I spa.255 Loss starting at -477 0 C; the sample completely decomposed between 477 and 507 0

C.

Example 255 Under nitrogen, [(2,6-i-PrPh) 2 DABMe2)NiBr 2 (0.008 g, 0.015 mmol) was suspended in cyclopentene (5.00 g, 73.4 mmol). To this was added a 1 M solution of EtAlCl 2 in toluene (0.75 mL, 0.75 mmol). A magnetic stirbar was added to the reaction mixture and it was stirred at room temperature; after 92 h at room temperature the reaction mixture could no longer be stirred due to precipitation of polycyclopentene solids. At this point the reaction was then quenched by addition of -5 mL of methanol under nitrogen..

Several drops of concentrated HC1 was then added under air. The product was then filtered off, washed with more methanol followed by acetone, and dried to afford 2.75 g of polycyclopentene as a-white powder. DSC of this material showed a broad melting transition centered at approximately 1900C and ending at approximately 250 0 C; AHf 34 J/g. Thermal gravimetric analysis of this sample showed a weight loss starting at ~480 C; the sample completely decomposed between 480 and 5080C.

Example 256 HBAF (0.776 mmol) was dissolved in 5 ml of A second solution of 0.776 mmol of (2,6-i-PrPh) DABMe 2 in 3 ml of Et20 was added. The reaction turned deep red-brown immediately. After stirring for 2 h the volatiles were removed in vacuo to give the protonated a-diimine salt which was a red crystalline solid.

Example 257

HBF

4 (0.5 mmol) was dissolved in 4 ml of Et20. A second solution of 0.5 mmol of (2,6-i-PrPh) 2 DABMe 2 in 3 ml of Et 2 0 was added. A color change to deep red occurred upon mixing. The reaction was stirred overnight. The volatiles were removed in vacuo to give to give the protonated a-diimine salt which was an orange solid.

-256- D2/0603,sws33 I ,p.2 56 Example 258 HO3SCF3 (0.5 mmol) was dissolved in 4 ml of A second solution of 0.5 mmol of (2,6-i-PrPh) 2 DABMe 2 in 3 ml of Et20 was added. A color change to deep red occurred upon mixing after a few minutes an yelloworange precipitate began to form. The reaction was stirred overnight. The product, believed to be the protonated a-diimine salt, was isolated by filtration rinsed with Et20 and dried in vacuo.

Example 259 HBAF (0.478 mmol) was dissolved in 5 ml of A second solution of 0.776 mmol of PrPh)N=C(CH3))2CH 2 in 3 ml of Et20 was added. The reaction was stirred overnight. Removal of the volatiles in vacuo gave an-off white solid, believed to be the protonated 1,3-diimine salt.

Example 260 HBF4 (0.478 mmol) was dissolved in 5 ml of Et 2 0.

A second solution of 0.478 mmol of PrPh)N=C(CH 3 )]2CH 2 in 3 ml of Et20 was added the reaction turned cloudy with a white precipitate. The reaction was stirred overnight. The white solid, believed to be the protonated 1,3-diimine salt, was isolated by filtration rinsed with Et20 and dried in vacuo.

Example 261 The product of Example 256 (78 mg) was dissolved in 20 ml of toluene. The reaction vessel was charged with 140 kPa (absolute) of ethylene. A solution of mg Ni(COD)2 in 3 ml of toluene was added. Ethylene was added (138 kPa pressure, absolute) and the polymerization was run for 24 h at ambient temperature.

Precipitation with MeOH gave 157 mg of white spongy polyethylene.

257 0 2 1 06/3swI33 spa,257 Examnle22 The product of Example 257 (27 mg) was dissolved in 20 ml of toluene. The reaction vessel was charged with 35 kPa of ethylene. A solution of 10 mg Ni (COD) 2 in 3 ml of toluene was added. Ethylene was added (138 kPa pressure, absolute) and the polymerization was run for 24 h at ambient temperature. Precipitation with MeOH gave 378 mg of sticky white polyethylene.

Example 263 The product of Example 258 (30 mg) was dissolved in 20 ml of toluene. The reaction vessel was charged with 140 kPa (absolute) of ethylene. A solution of mg Ni(COD)2 in 3 ml of toluene was added. Ethylene was added (138 kPa pressure, absolute) and the polymerization was run for 24 h at ambient temperature.

Precipitation with MeOH gave 950 mg of amorphous polyethylene.

ExampleI264 To a burgundy slurry of 1 mmol of VCl 3

"(THF)

3 in ml of THF was added a yellow solution of 1 mmol of (2,6-i-PrPh) 2 DABMe 2 in 4 ml of THF. After 10 minutes of stirring the reaction was a homogenous red solution.

The solution was filtered to remove a few solids, concentrated and then cooled to -30 0 C. The red crystals that formed were isolated by filtration, rinsed with pentane and dried in vacuo. The yield was 185 mg.

Exmpic _2i The product of Example 264 (6 mg) was dissolved in 20 ml of toluene. The resulting solution was placed under 140 kPa (absolute) of ethylene. PMAO solution (0.8 mL, 9.6 wt% Al in toluene) was added and the polymerization Was stirred for 3 h. The reaction was halted by the addition of 10% HCl/MeOH. The precipitated polymer was isolated by filtration, washed with MeOH and'dried in vacuo. The yield was 1.58 g of white polyethylene.

-258 02 /06/03,swIi Jsp,258 Example 266 Lanthanide metal tris-triflates (wherein the lanthanide metals were Y, La, Sm, Er, and Yb), 1 mmol, was slurried in 10 ml of CH2CI 2 A solution of 1 mmol of (2,6-i-PrPh) 2 DABMe 2 in 3 ml of CH2C12 was added and the reaction stirred for 16 h at ambient temperature.

The solution was filtered to give a clear filtrate.

Removal of the solvent in vacuo gave light yellow to orange powders.

Example 267 Each of the-various materials (0.02 mmol) prepared in Example 266 were dissolved in 20 ml of toluene. The resulting solutions were placed under 140 kPa (absolute) of ethylene. MMAO-3A solution (1.0 mL, 6.4 wt% Al in toluene) was added and the polymerizations were stirred for 3 h. The reactions were halted by the addition of 10% HCl/MeOH. The precipitated polymers were isolated by filtration washed with MeOH and dried in vacuo. Polymer yields are shown the following table, Lanthanide Metal Yield (g) Yb 0.117 La 0.139 Sm 0.137 Y 0.139 Er 0.167 Example 268 [(2,6-i-PrPh) 2 DABMe 2 ]Ni-02 (68 mg) was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. PMAO (0.7 mL, 9.6 wt.% Al in toluene) was added and the polymerization was conducted for 16 h. The reaction was halted by the addition of 15 ml of 10% HCl/MeOH solution. The precipitated polymer was isolated by filtration and dried under vacuum to yield 1.67 g of rubbery polyethylene.

0 2 6 /03,sw 1331] spa.259 Example 269 [(2,6-i-PrPh) 2 DABMe 2 ]Ni-0 2 (65 mg) was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. PMAO (0.7 mL, 9.6 wt.% Al in toluene) was added and the polymerization was conducted for 16 h. The reaction was halted by the addition of 15 ml of 10% solution. The precipitated polymer was isolated by filtration and dried under vacuum to yield 1.9 g of rubbery polyethylene.

Example 270 [(2,6-i-PrPh) 2 DABMe 2 ]CrC12'(THF) (15 mg) was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. MMAO-3A (1 mL, 6.4 wt.% Al in toluene) was added and the polymerization was conducted for 3 h. The reaction was halted by the addition of 15 ml of 10% HCl/MeOH solution. The precipitated polymer was isolated by filtration and dried under vacuum to yield 694 mg of polyethylene. DSC (-150 to 2500C at 10 0 C/min) results from the second heating were Tm 129 0 C, AHf 204 J/g.

Example 271 [(2,6-i-PrPh)2DABMe,]CrC13 (14 mg) was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. MMAO-3A (1 mL, 6.4 wt.% Al in toluene) was added and the polymerization was conducted for 3 h. The reaction was halted by the addition of 15 ml of 10% HCI/MeOH solution. -The precipitated polymer was isolated by filtration and dried under vacuum to yield 833 mg of polyethylene. DSC (-150 to 2500C at 10OC/min) results from the second heating were Tm 133 0 C, AHf 211 J/g.

Example 272 [(2,6-i-PrPh) 2 DABMe 2 ]CrCl 2 *(THF) (14 mg) was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. MMAO-3A (1 mL, 6.4 wt.% Al in toluene) was added and the polymerization was conducted for 3 h. The reaction was -260- 0206/03.sw133 I spa.260 halted the addition of 15 ml of 10% HC1/MeDH .olution. The precipitated polymer was isolated by filtration and dried under vacuum to yield 316 mg of polyethylene. DSC results from the second heating were (-150 to 2500°C at 10 0 C/min) Tm 1330°C, *AHf 107 J/g.

Example 273 [(2,6-i-PrPh) 2 DABMe 2 ]CrCl3 (15 mg) was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. MMAO-3A (I mL, 6.4 wt.% Al in toluene) was added and the polymerization was conducted for 3 h. The reaction was halted by the addition of 15 ml of 10% HCl/Me0H solution. The precipitated polymer was isolated by filtration and dried under vacuum to yield 605 mg of polyethylene. DSC (-150 to 2500°C at 10 0 C/min) results from the second heating were Tm 134°C, AHf 157 J/g.

Example 274 A 61 mg sample of {[(2,6-i-PrPh) 2 DABAn]Ni( 3

H

2 CCHCHC1)]BAF was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. PMAO (0.7 mL) was added and the reaction stirred for 16 h. The polymerization was quenched by the addition of 15 ml of 10% HCI/MeOH. The polymer was isolated by filtration, washed with acetone and dried.

The yield was 2.24 g of rubbery polyethylene.

Example 275 A 65 mg sample of [(2,4,6-MePh) 2 DABAn]Ni( 3

H

2 CCHCHC1)]BAF was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. PMAO (0.7 mL) was added and the reaction stirred for 16 h. The polymerization was quenched by the addition of 15 ml of 10% HC/MeOH. The polymer was isolated by filtration, washed with acetone and dried.

The yield was 2.0 g of rubbery polyethylene.

Example 276 A 61 mg sample of {[(2,6-iPrPh)2 DABAn]Ni(7 H2CCHCH2)}Cl was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of 261 02/013.sw 1331 lp., 2 6 1 ethylene. PMAO (0.7 mL) was added and he reaction -:tirred for 16 h. The polymerization was quenched by the addition of 15 ml of 10% HCl/MeOH. The polymer was isolated by filtration, washed with acetone and dried.

The yield was 1.83 g of rubbery polyethylene.

Example 277 A 60 mg sample of {[(2,6-iPrPh) 2 DABMe 2 ]Ni (r 1 3

H

2

CCHCH

2 ))C1 was dissolved in 20 ml of toluene. The reaction vessel was placed under 138 kPa (absolute) of ethylene. PMAO (0.7 mL) was added and the reaction stirred for 16 h. The polymerization was quenched by the addition of 15 ml of 10% HCl/MeOH. The polymer was isolated by filtratpn, washed with acetone and dried.

The yield was 1.14 g of rubbery polyethylene.

Example 278

FN

3 NiBr 2 F N [(2,6-i-PrPh)2DAB(4-F-Ph)2]NiBr 2 In a 250-mL RB flask fitted with pressure equalizing addition funnel, thermometer, magnetic stirrer, and N2 inlet was placed 0.75g (3.0mmol) of 4,4'-difluorobenzil, 13.8mL (80mmol) of 2,6diisopropylaniline (DIPA), and 100mL dry benzene. In the addition funnel was placed 50mL of dry benzene and 2.0mL (3.5g; 18mmol) of titanium tetrachloride. The reaction flask was cooled to 2 0 C with ice and the TiCl 4 solution was added dropwise over 45min, keeping the reaction temperature below 5°C. The ice bath was removed after addition was complete and the mixture was stirred at RT for 72h. The reaction mixture was partitioned between water and ethyl ether, and the ether phase was rotovapped and the concentrated oil was -262- 02/O603.sw331 spa,262 washed with 800mL-1N H to remove the excess iisopropylaniline. The mixture was extracted with 100mL of ether, and the ether layer was washed with water and rotovapped. Addition of 15mL hexane plus 30mL of methanol to the concentrate resulted in the formation of fine yellow crystals which were filtered, methanol-washed, and dried under suction to yield 0.4g of (2,6-i-PrPh)2DAB(4-F-Ph)2, mp: 155-158 0

C.

A 60-mg (0.092-mmol) sample of (2,6-i-PrPh) 2 DAB(4- F-Ph)2 was stirred under nitrogen with 32mg (0.103mmol) of nickel(II) dibromide-dimethoxyethane complex in 20mL of methylene chloride for 66h. The orange-brown solution was rotovapped and held under high vacuum for 2h to yield 86mg of red-brown solids.

The solid product was scraped from the sides of the flask, stirred with 20mL hexane, and.allowed to settle.

The yellow-orange hexane solution was pipetted off and the remaining solid was held under high vacuum to yield 48mg of the orange-brown complex [(2,6-i-PrPh)2DAB(4-F- Ph)2]NiBr 2 Example 279 Ethylene polymerization with [(2,6-i-PrPh)2DAB(4-F- Ph)2]NiBr 2 A 26-mg (0.033-mmol) sample of PrPh) 2DAB (4-F-Ph) 2] NiBr 2 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25mL of dry toluene. Then 0.6mL of polymethylalumoxane was injected, turning the orange-brown solution to a deep green- black solution. The mixture was pressurized immediately with ethylene to 152 kPa (absolute) and stirred at RT for 17h. The reaction soon became warm to the touch; this heat evolution persisted for over an hour and the liquid volume in the Schlenk flask was observed to be slowly increasing. After 17h, the reaction was still dark green-brown, but thicker and significantly increased in volume. The ethylene was vented; the offgas contained about 3% butenes (1butene, t-2-butene, c-2-butene, by GC -263 0 2 0 6/03.swl3311spa,263 Quadrex GSQ Megabc- column; 50-250 0 C at 100 /min). The toluene solution was stirred with 6N HCl/methanol and was separated; the toluene was rotovapped and held under high vacuum to yield 9.53g of low-melting polyethylene wax. There seemed to be significant low-boiling species present, probably lowmw ethylene oligomers, which continued to boil off under high vacuum. 1 H NMR (CDCl 3 60 0 C) of the product showed a CH2:CH 3 ratio of 206:17, which is 57 CH 3 's per 1000 CH2's. There were vinyl peaks at 5-5.8ppm; if the end groups are considered to be vinyls rather than internal olefins, the degree of polymerization was about 34.

Example 280 Synthesis of [(2-CF3Ph)2DABMe 2 ]NiBr 2 C-F3

N

NiBr 2 CF3 [(2-CF 3 Ph) 2DABMe2]NiBr 2 A mixture of 10.2mL (13.ig; 81.2mmol) 2aminobenzotrifluoride and 3.6mL (3.5g; 41mmol) freshlydistilled 2,3-butanedione in 15mL methanol containing 6 drops of 98% formic acid was stirred at 35°C under nitrogen for 8 days. The reaction mixture was rotovapped and the resultant crystalline solids (1.3g) were washed with carbon tetrachloride. The crystals were dissolved in chloroform; the solution was passed through a short alumina column and evaporated to yield of.yellow crystals of the diimine (2- CF3Ph)2DABMe 2 1H NMR analysis (CDC1 3 2.12ppm (s, 6H, CH3); 6.77 2H, ArH, J=9Hz); 7.20 2H, ArH, J=7Hz); 7.53(t, 2H, ArH, J=7Hz); 7.68 2H, ArH, 264 0 20603,swl33 1 spa,264 J=8Hz) Infrared spectrum: 1706, it 1603, 1579, '.319, 1110cm- 1 Mp: 154-156 0

C.

A mixture of 0.207g (0.56mmol) of (2-CF3Ph)2DABMe 2 and 0.202g (0.65mmol) of nickel(II) dibromidedimethoxyethane complex in 13mL of methylene chloride was stirred at RT under nitrogen for 3hr. The redbrown suspension was rotovapped and held under high vacuum to yield 0.3g of [(2-CF 3 Ph)2DABMe2]NiBr 2 complex.

Example 281 Ethylene polymerization with[ (2-CF 3 Ph) 2DABMe2] NiBr 2 A 13-mg (0.022-mmol) sample of

CF

3 Ph) 2 DABMe2]NiBr 2 was placed in a Parr® 600-mL stirred autoclave; 200mL of dry, deaerated hexane (dried over molecular sieves) was added and the hexane was saturated with ethylene by pressurizing to 450 kPa (absolute) ethylene and venting. Then 1.0mL of modified methylalumoxane (1.7M.in heptane; contains about 30% isobutyl groups) was injected into the autoclave with stirring, and the autoclave was stirred for lhr under 690 kPa (absolute) ethylene as the temperature rose from 20 0 C to 61 0 C over the first and then slowly declined to 48 0 C by the end of the run.

The ethylene was vented and 3mL of methanol was injected to stop polymerization; the autoclave contained a white suspension of fine particles of polyethylene; the appearance was like latex paint. The polymer suspension was added to methanol, and the polymer was stirred with MeOH/HC to remove catalyst.

The suspension was filtered and dried in a vacuum oven (75C) to yield 26.8g of fine, white powdery polyethylene Differential scanning calorimetry (150 C/min): Tg -45 0 C; mp 117 0 C (75J/g). GPC (trichlorobenzene, 135°C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn=2,350; Mw=8,640; Mz=24,400; Mw/Mn=3.67. 'A solution of the polymer in chlorobenzene could be cast into a waxy film with little strength.

-265- 02 O0 133 02/06/03,sw l33i r spa.265 Under nitrogen, Ni(COD) 2 (0.017 g, 0.062 mmol) and (2,4,6-MePh) 2 DABAn (0.026 g, 0.062 mmol) were dissolved in 2.00 g of cyclopentene to give a purple solution.

The solution was then exposed to air (oxygen) for several seconds. The resulting dark red-brown solution was then put back under nitrogen, and EtAICl 2 (1 m solution in toluene, 3.0 mL, 3.0 mmol) added. A cranberry-red solution formed instantly. The reaction mixture was stirred at room temperature for 3 days, during which time polycyclopentene precipitated. The reaction was then quenched by the addition of methanol followed by several drops of concentrated HCI. The reaction mixture was filtered, and the product polymer washed with methanol and dried to afford 0.92 g of polycyclopentene as an off-white powder. Thermal gravimetric analysis of this sample showed a weight loss starting at 141OC: the sample lost 18% of its weight between 141 and 470 0 C, and the remaining material decomposed between 470 and 496 0

C.

Example 283 Under a nitrogen atmosphere, Ni(COD) 2 (0.017 g, 0.06 mmol) and the ligand shown below (0.025 g, 0.06 mmol) were dissolved in benzene (5.0 mL). To the resulting solution was added HBAF'(Et 2 0) 2 (0.060 g, 0.06 mmol). The resulting solution was immediately frozen inside a 40 mL shaker tube glass insert. The glass insert was transferred to a shaker tube, and its contents allowed to thaw under an ethylene atmosphere.

The reaction mixture was agitated under 6.9 MPa C 2

H

4 for 18 h at ambient temperature. The final reaction mixture contained polyethylene, which was washed with methanol and dried; yield of polymer 11.0 g.

266 o2oW3,sw1331 Ispa,266 Example 284 The catalyst PrPh) 2DABMe 2 PdCH 2

CH

2

CH

2 C OCH 3 )SbF- (0.025g, 0.03 mmol) and CH 2 =CH(CH2) 6 CoF; (4.74g, 7.52 mmol) were dissolved in 20 mL CH 2 C1 2 in a Schlenk flask in a drybox. The flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. This was stirred at RT under 1 atm of ethylene for 72 hr. Solvent was evaporated to almost dryness. Acetone (70 mL) was added and the mixture was stirred vigorously overnight.

The upper layer was decanted. The resulting yellow solid was washed with 3X15 mL acetone, vacuum dried, and 1.15g of product was obtained. 'H NMR analysis

(CD

2 C1 2 105 methyls per 1000 methylene carbons.

Comparison of the integral of the CH 2 Rf(2.10 ppm) with the integrals of methyls(0.8-1.0 ppm) and methylenes(1.2-1.4 ppm) indicated a comonomer content of 6.9 mol%. The polymer exhibited a glass transition temperature of -55C(13J/g) and a melting point of 57°C by differential scanning calorimetry. Gel permeation chromatography (THF, polystyrene standard): Mw 39,500, Mn 34,400, P/D 1.15.

Example 285 In a 100 mL Schlenk flask, PrPh) 2 DABAn]NiBr 2 (0.012g, 0.017mmol) and

CH,=CH(CH

2 6 CIoF 21 (4.62g, 7.33 mmol) were dissolved in 32 mL of toluene under stirring. This was pressured with 1 atm ethylene and was allowed to stir at 0°C for minutes. MAO (1.7 mL, 8.9 wt% in toluene) was added. This was allowed to vigorously stir at RT for -267- 02/0 /03.swl331 Ispa.267 min. Sixty mL methanol was then added. The white -olid was filtered, followed by 3x30 ml 3:1 methanol/toluene wash, vacuum dried, and 3 .24g of white polymer was obtained. 1H NMR analysis (odichlorobenzene-d 4 ,135 OC): 64 methyls per 1000 methylene carbons. Comparison of the integral of the

CH

2 Rf (2.37ppm) with the integrals of methyls (1.1-1.2 ppm) and methylenes (1.4-1.8 ppm) indicated a comonomer content of 8.7 mol%. Mw 281,157, Mn 68,525, P/D 4.1.

Example 286 In a 100 mL Schlenk flask, PrPh) 2 DABAn]NiBr 2 (0.012g, 0.017mmol) and CH2=CH(CH 2 6 CxoF2, (4.62g, 7.33 mmol) were dissolved in 32 mL of toluene under stirring. This was allowed to stir at 0 °C for 15 minutes. MAO (1.7 mL, 8.9 wt% in toluene) was added. This was allowed to stir at 0°C for 2.5 h and then RT for 3 h. Methanol (200 mL) was then added, followed by 1 mL cone. HC1. The white solid was filtered and washed with methanol, vacuum dried, and 0.79g of white solid polymer was obtained.

By differential scanning calorimetry, Tm 85°C(22J/g).

Example 287 S[(2,6-i-PrPh)2DABMe 2 PdCH 2

CH

2

CH

2 C (O)OCH 3 SbF (0.0205g, 0.024 mmol) and CH 2

=CH(CH

2 4

(CF

2 4 0(CF 2 2 SO2F 7.26 mmol) were dissolved in 18 mL CH 2 C1, in a Schlenk flask in a drybox. The flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. This was stirred at RT under 1 atm of ethylene for 72 hr.

Solvent was evaporated after filtration. The viscous oil was dissolved in 10 mL CH 2 C1 2 followed by addition of 100 mL methanol. The upper layer was decanted. The reverse precipitation was repeated two more time, followed by vacuum drying to yield 3.68g of a light yellow viscous oil. 1H NMR analysis (CDC13): 89 methyls per 1000 methylene carbons. Comparison of the integral of the CHCF 2 (2.02 ppm) with the integrals 268 0 2 /0603.swt331 sp.26 of methyls(0.8-i.0 ppm) and methylenes(1.1-1.4 ppm) 4ndicated a comonomer content of 8.5 mol%. "F NMR (CDC1 3 45.27 ppm, -SO 2 F; -82.56 ppm, -83.66 ppm, 112.82 ppm, -115.34 ppm, -124.45 ppm, -125.85 ppm, CF 2 peaks. The polymer exhibited a glass transition temperature of -57 oC by differential scanning calorimetry. Gel permeation chromatography (THF, polystyrene standard): Mw 120,000, Mn 78,900, P/D 1.54. The turnover numbers for ethylene and the comonomer are 2098 and 195, respectively.

Example 288 In a 100 mL Schlenk flask, PrPh) 2 DABAn]NiBr 2 (0.017g, 0.024 mmol) and CH2=CH(CH 2 )4(CF 2 4 0(CF 2 2

SO

2 F (5.0g, 10 mmol) were dissolved in 25 mL of toluene under stirring. MAO (2.3 mL, 8.9 wt% in toluene) was added. This was allowed to stir at RT for 15 hr. Sixty mL methanol was then added, followed by 1 mL cone. HC1. The upper layer was decanted, residue washed with mL), vacuum dried, and 1.20g of a white viscous oil was obtained. 19F NMR (Hexafluorobenzene, 80 OC): 45.20 ppm, -SO 2 F; -81.99 ppm, -82.97 ppm, -112.00 ppm, 114.36 ppm, -123.60 ppm, -124.88 ppm, CF 2 peaks.

Example 289 In a Schlenk flask, [(2,6-i-PrPh) 2 DABAn]NiBr 2 (0.012g, 0.017mmol) and CH2=CH(CH 2 4

(CF,)

4 0(CF 2 2SO2F (3.26g, 6.77mmol) were dissolved in 35 mL of toluene under stirring. This was pressured with 1 atm ethylene and was allowed to stir at 0°C for 15 minutes. MAO (1.7 mL, 8.9 wt% in toluene) was added. This was allowed to vigorously stir at RT for 45 minutes.

Methanol (140 mL) was then added, followed by addition of 1 mL of conc. HC1. The white solid was filtered, followed by methanol wash, vacuum dried to obtain 2.76g of a white rubbery polymer. 1H NMR analysis (odichlorobenzene-d,, 100 98 methyls per 1000 methylene carbons. Comparison of the integral of the

CH

2

CF

2 (2.02 ppm) with the integrals of methyls (0.8- 269 0 0603..w33 1sp.269 ppm) and methylenes (1.1-1.4 ppm) indicated a remonomer content of 3.5 mol%. 19 F NMR dichlorobenzene-d 45.19 ppm, -SO 2 F; -82.70 ppm, 83.72 ppm, -112.96 ppm, -115.09 ppm, -124.37 ppm, 125.83 ppm, CF 2 peaks. The polymer exhibited Tm of 97 0 C by differential scanning calorimetry. Mw 156,000, Mn 90,000, P/D 1.73.

Example 290 S[ (2,6-i-PrPh) 2 DABMe 2 PdCH 2

CH

2

CH

2 C OCH 3 SbF,6 (0.030g, 0.035 mmol) and CH2=CH(CH2) 4

(CF

2 2

CO

2 Et 11.7 mmol) were dissolved in 20 mL CHC1 in a Schlenk flask in a drybox. The flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. This was stirred at RT under 1 atm of ethylene for 72 h.

Solvent was evaporated. The viscous oil was dissolved in 10 mL acetone, followed by addition of 60 mL methanol. The mixture was centrifuged. The upper layer was decanted. The oil was dissolved in 10 mL acetone followed by addition of 60 mL methanol. The mixture was centrifuged again. The viscous oil was collected, and vacuum dried to obtain 1.50g of a light yellow viscous oil. 1H NMR analysis (CDC13): 67 methyls per 1000 methylene carbons. Comparison of the integral of the CH2CF 2 (2.02 ppm) with the integrals of methyls(0.8-1.0 ppm) and methylenes(1.1-1.4 ppm) indicated a comonomer content of 11 mol%. The polymer exhibited a Tg of -61°C by DSC. GPC (THF, polystyrene standard): Mw 73,800, Mn 50,500, P/D 1.46.

Example 291 In a Schlenk flask, [(2,6-i-PrPh) 2 DABAn]NiBr 2 (0.019g, 0.026 mmol) and CH 2

=CH(CH

2 4

(CF

2 )2CO 2 Et 11.7 mmol) were dissolved in 35 mL of toluene. This was placed under 1 atm of ethylene at 0°C for minutes. MAO (2.6 mL, 8.9 wt% in toluene) was added.

This was allowed to vigorously stir at 0°C for minutes. Methanol (120 mL) was then added, followed by 1 mL cone. HC1. The solid was filtered, washed with -270- o0/003.sw1331 Ispa,270 the CHCF 2 (2.0 ppm) with the integrals of rrmthyls(0.8-1.0 ppm) and methylenes(l.1-1.4 ppm) indicated a comonomer content of 2.9 mol%. The polymer exhibited a Tg of -66 0 C by DSC. GPC (THF, polystyrene standard): Mw 186,000, Mn 90,500, P/D 2.06.

The turnover numbers for ethylene and the comonomer are 6,122 and 183, respectively.

Examples 294-300 All of these Examples were done under 1 atm ethylene with a MA concentration of 1.2M and [(diimine)PdMe(Et 2 O) 'SbF 6 concentration of 0.0022M at RT for 72 hr. Results are shown in the Table below.

Ex. Diimine MA(mol%)* Mn P/D No.

294 6 12,300 1.8 PrPh),DABMe 2 295 (2,6-EtPh) 2 DABMe 2 16 7,430 1.9 296 23 2,840 2.1 MePh) 2 DABMe 2 297 (2,4,6-MePh) 2 DABAn 37 1,390 1.4 298 (2,4,6-MePh)DABH 2 46 1,090 3.1 299 (2-i-PrPh) 2 DABMe 2 17 410 300 (2-MePh) 2DABMe 2 29 320 In the polymer Mn characterized by 1H NMR.

Example 301 [(2,6-EtPh) 2 DABMe 2 PdCH3(Et2O) )'SbFE- (0.0778g, 0.10 mmol) and methyl acrylate (4.78g, 0.056 mol) were dissolved in 40 mL CH 2 C1 2 in a Schlenk flask in a drybox. The flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. This was stirred at RT under 1 atm of ethylene for 72 h. The mixture was filtered through silica gel, solvent was evaporated and then vacuum dried, and 1.92g light of a yellow:viscous oil was obtained. 1H NMR analysis (CDC1 3 69 methyls per 1000 methylene carbons. Comparison of the integral -271 02/0 6 03.sw1331 1spa.27 methanol and hexane, and vacuum dried to yied 1.21g of Swhite rubbery solid. H NMR analysis (TCE-d, 1100C): Comparison of the integral of the CH2CF 2 (2.06 ppm) with the integrals of methyls(0.8-1.0 ppm) and methylenes(1.1-1.4 ppm) indicated a comonomer content of 6.0 mol%. The polymer exhibited a Tg of -460C and Tm's at 40 0 C and 82°C by DSC.

Example 292 In a Schlenk flask, [(2,6-i-PrPh) 2 DABAnJNiBr, (0.022g, 0.030 mmol) and CH 2

=CH(CH

2 4 (CF2) CO 2 Et 13.7 mmol) were dissolved in 30 mL of toluene. This was placed under nitrogen at 0°C for 15 minutes. MAO mL, 8.9 wt% in toluene) was added. This was allowed to stir at 0°C for 2.5 h and then RT for 6 h.

Fifty mL methanol was then added, followed by 1 mL cone. HC1. The mixture was washed with 3x60 mL water.

The organic layer was isolated and dried by using Na 2

SO

4 Evaporation of toluene and addition of hexane resulted in precipitation of an oil. The oil was washed with hexane another two times, and vacuum dried to yield 0.16g of a yellow oil. Mw 35,600, Mn 14,400, P/D 2.47.

Example 293 [(2,6-i-PrPh) 2 DABMe2] PdCH2CH 2

CH

2 C OCH 3 SbF, (0.0848g, 0.1 mmol) and CH 2

=CH(CH

2 )4(CF 2 2 0(CF 2 2

SO

2

F

(11.5g, 0.03 mol) were dissolved in 72 mL CH2C1 2 in a Schlenk flask in a drybox. The flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. This was stirred at RT under 1 atm of ethylene for 72 hr.

The solution was filtered through Celite and then concentrated to 70 mL. Methanol (400 mL) was added under stirring. The upper layer was decanted. The oil was redissolved in 70 mL CH2C1, followed by addition of 350 mL methanol. The viscous oil was collected, vacuum dried and 24.1g of a light yellow viscous oil was obtained. 2H NMR analysis (CDC1 3 113 methyls per 1000 methylene carbons. Comparison of the integral of -272 03,w3 sp2 02/06/03,swl3311spa,272 of the methyl on the ester groups (2.3 ppm) with the integrals of carbon chain methyls(0.8-1.0 ppm) and methylenes(1.l-1.4 ppm) indicated a comonomer content of 16 mol%. The polymer exhibited a Tg of -68 0 C by DSC. GPC (THF, polystyrene standard).: Mw 14,300, Mn 7,430, P/D 1.93.

Example 302 [(2,6-i-PrPh) 2DABMe 2 PdCH 2

CH

2 CH2C OCH 3 )SbFJ- (0.254g, 0.30 mmol) and CH2=CHCO 2

CH

2

(CF

2 6

CF

3 (90.2g, 0.20 mol) were dissolved in 150 mL CH2C12 in a flask in the drybox. The-flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. This was stirred at RT under 1 atm of ethylene for 24 h. The solution was decanted to 1200 mL methanol, resulted formation of oil at the bottom of the flask. The upper layer was decanted, oil dissolved in 150 mL CH 2 Cl1, followed by addition of 1200 mL of methanol. The upper layer was decanted, oil dissolved in 600 mL hexane and filtered through Celite®. Solvent was evaporated, and then vacuum dried, yielding 54.7g of a viscous oil. 'H NMR analysis (CDC1 3 99 methyls per 1000 methylene carbons. Comparison of the integral of the CH 2

CF

2 (4.56 ppm) with the integrals of methyls(0.8-1.0 ppm) and methylenes(1.1-1.4 ppm) indicated a comonomer content of 5.5 mol%. The polymer exhibited a Tg of 49 0 C by DSC. Mw 131,000, Mn 81,800.

Example 303 S[ (2,6-i-PrPh) 2 DABMe 2 PdCH 2

CH

2

CH

2 C OCH3) SbF6 (0.169g, 0.20 mmol) and P-hydroxyethyl acrylate (6.67g, 0.057 mol) were dissolved in 40 mL CH 2 C1 2 in a flask in the drybox. The flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. This was stirred at RT under 1 atm of ethylene for 45 h. Solvent was evaporated. The residue was dissolved in 100 mL hexane, followed by addition of 400 mL methanol. Upon standing overnight, a second upper layer formed and was 273 02I03.sw331 p27 decanted. The.oil was dissolved in 60 mL THF, tolld6wL.

by addition of 300 mL water. The upper layer was decanted. The residue was dissolved in 100 mL 1:1

CH

2 Cl 2 /hexane. This was filtered through Celite®. The solvent was evaporated, vacuum dried and 6.13g of a light yellow oil was obtained. 'H NMR analysis

(CD

2 Cl 2 142 methyls per 1000 methylene carbons.

Comparison of the integral of the CH 2

CO

2 (2.30 ppm) with the integrals of methyls(0.8-1.0 ppm) and methylenes(1.1-1.4 ppm) indicated a comonomer content of 2.6 mol%. Mw 53,100, Mn 37,900, P/D 1.40.

Example 304 [(2,6-i-PrPh) 2 DABMe2]PdCH 2

H

2 2 CC OCH3}ISbF (0.169g, 0.20 mmol) and hydroxypropyl acrylate 7 .52g, 0.058 mol) were dissolved in 40 mL CH 2 Cla in a flask in the drybox. The flask was connected to a Schlenk line and the flask was then briefly evacuated and refilled with ethylene from the Schlenk line. This was stirred at RT under 1 atm of ethylene for 72 h. Solvent was evaporated. Eighty mL methanol was added to dissolve the residue, followed by 250 mL water. The upper layer was decanted. The reverse precipitation was repeated one more time. The oil was isolated, vacuum dried, and l.lg of a light yellow oil was obtained. 'H NMR analysis (CD 2 C1 2 94 methyls per 1000 methylene carbons. Comparison of the integral of the CH 2

CO

2 (2.30 ppm) with the integrals of methyls(0.8-1.0 ppm) and methylenes(l.1-1.4 ppm) indicated a comonomer content of 6.5 mol%. Mw 39,200, Mn 28,400, P/D 1.38.

Example 305 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed into a glass vial in the dry box (0.0141 g, 0.025 mmol). Cyclopentene was added (3.41 g, 2,000 equivalents/Ni). A solution of MMAO (Akzo Nobel MMAO- 3A, modified methylaluminoxane, 25% isobutyl groups in place of methyl groups) was added while stirring (0.75 ml, 1.7 M Al in heptane, 50 equivalents/Ni). Following -274- 02 /06/03.sw 13311 spa,274 additic of the MMAO, the solution was homogeneous.

After stirring for several hours, solid polymer started to precipitate. After stirring for 46 hours, the solution was filtered and the solids were washed several times on the filter with pentane. The polymer was dried in vacuo for 12 hours at room temperature to yield 0.66 g polymer (388 turnovers/Ni). The polymer was pressed at 292 0 C to give a transparent, light gray, tough film. DSC (25 to 300 0 C, 15 0 C/min, second heat): Tg 104 0 C, Tm (onset) 210 0 C, Tm (end) 2851C, Heat of fusion 14 J/g. X-ray powder diffraction shows peaks at d-spacings 5.12, 4.60, 4.20, 3.67, and 2.22.

1H NMR (500 MHz, 155 0 C, d 4 -o-dichlorobenzene, referenced to downfield peak of solvent 7.280 ppm): 0.923 (bs, 1.0 H, -CHCH2CH-); 1.332 (bs, 2.0 H,

CHCH

2 CH2CH-); 1.759 (bs, 4.0 H, -CHCH 2 CH2CH- and

CHICH

2

CH

2 1.947 (bs, 1.0 H, -CHCH 2 The assignments are based upon relative integrals and IH 13 C correlations determined by 2D NMR. This spectrum is consistent with an addition polymer with cis-1,3 enchainment of the cyclopentene.

Example 306 Cyclopentene was polymerized by MePh) 2 DABMe2]PdMeCl and MMAO according to Example 305 to give 0.37 g polymer (217 turnovers/Pd). The polymer was pressed at 250 0 C to give a transparent, light brown, tough film. DSC (25 to 300 0 C, 15 0 C/min, second heat): Tg 84 0 C, Tm(onset) 175 0 C, Tm (end) 255°C, Heat of fusion 14 J/g. 1 H NMR (400 MHz, 120 0 C, d 4 -odichlorobenzene, referenced to downfield peak of solvent 7.280 ppm): 0.90 (bs, 1 H, -CHCH 2 1.32 (bs, 2 H, -CHCH2CH 2 1.72, 1.76 (bs, bs 4 H, CHCH2CHzCH- and -CCHCH 2 CHC-); 1.94 (bs, 1 H, -CHCH2CH- The assignments are based upon relative integrals and 1 H 13 C correlations determined by 2D NMR. This spectrum is consistent with an addition polymer with cis-1,3 enchainment of the cyclopentene.

ExamleP 307 -275- 02/06/03.sw 3311 spa.275 Cyclopentene was polymerized by o- FtPh) 2 DABMe 2 )PdMeCl and MMAO according to Example 305 to give 0.39 g polymer (229 turnovers/Pd). The polymer was pressed at 250 0 C to give a transparent, light brown, tough film. DSC (25 to 3000C, 15 0 C/min, second heat): Tg 880C, Tm(onset) 175°C, Tm (end) 255Oc, Heat of fusion 16 J/g. IH NMR (300 MHz, 120°C, d 4 -odichlorobenzene) is very similar to the spectrum of Example 306.

Example 3Q08 Cyclopentene was polymerized by MePh)2DABMe 2 ]NiBr 2 and MMAO according to Example 305 to give 0.36 g polymer (211 turnovers/Ni). The polymer was pressed at 250°C to give a transparent, colorless, tough film. DSC (25 to 300°C, 15°C/min, second heat): Tg 98°C, Tm(onset) 160°C, Tm (end) 260°C, Heat of fusion 22 J/g. 1H NMR (500 MHz, 120 OC, d 4 -odichlorobenzene) is very similar to the spectrum of Example 306. X-ray powder diffraction shows the same crystalline phase as observed in Example 305.

Example 309 Cyclopentene was polymerized by PrPh) 2 DABMe 2 )PdMeC1 and MMAO according to Example 305 to give 0.73 g of fine powder (429 turnovers/Pd). The polymer was pressed at 2500C to give a transparent, light brown tough film. DSC (25 to 300°C, 15 0 C/min, second heat): Tg 96°C, Tm(onset) 175°C, Tm (end) 250°C, Heat of fusion 14 J/g. 1H NMR (400 MHz, 1200C, d 4 -o-dichlorobenzene) is very similar to the spectrum of Example 306. X-ray powder diffraction shows the same crystalline phase as observed in Example 305.

Example 310 Cyclopentene was polymerized by PrPh) 2 DABMe2]PdCl 2 and MMAO according to Example 305 to give 0.856 g polymer (503 turnovers/Pd). The polymer was pressed at 250"C to give a transparent, light brown, tough film. DSC (25 to 300°C, 15 0 C/min, second heat): Tg 104°C, Tm(onset) 140°C, Tm (end) 245*C, -276 02 /06/03,swl3311spa,276 Heat of fusion 19 1H NMR (400 MHz, 120 0 C, d 4 -o- .ichlorobenzene) is very similar to the spectrum of Example 306.

Example 311 Cyclopentene was polymerized by EtPh) 2 DABMe2NiBr2 and MMAO according to Example 305 to give 0.076 g polymer (45 turnovers/Ni). 1H NMR (400 MHz, 120 0 C, d 4 -o-dichlorobenzene) is very similar to the spectrum of Example 306.

Example 312 Cyclopentene was polymerized by MePh) 2

DABH

2 ]NiBr2 and MMAO according to Example 305 to give 0.66 g polymer (388 turnovers/Ni). The polymer was pressed at 292°C to give a tough film. 1H NMR (400 MHz, 120 0 C, d 4 -o-dichlorobenzene) is very similar to the spectrum of Example 306. A DSC thermal fractionation experiment was done in which a sample was heated to 330°C at 20 0 C/minute followed by stepwise isothermal equilibration at the followed temperatures (times): 280 0 C (6 hours), 270°C (6 hours), 260°C (6 hours), 250 0 C (6 hours), 240 0 C (4 hours), 230°C (4 hours), 220°C (4 hours), 2100C (4 hours), 200°C (3 hours), 190°C (3 hours), 180 0 C (3 hours), 170°C (3 hours), 160 0 C (3 hours), 1500C (3 hours). The DSC of this sample was then recorded from 0°C 330 C at 100 C/min. Tg 98 0 C, Tm (onset) 185°C, Tm (end) 310°C, Heat of fusion 35 J/g.

Example 313 Cyclopentene was polymerized by PhPh) 2 DABMe 2 ]NiBr2 and MMAO according to Example 305 to give 1.24 g polymer (728 turnovers/Ni). The polymer was pressed at 292°C to give a transparent, light gray, brittle film. DSC (25 to 320 0 C, 10 0 C/min, second heat): Tm(onset) 160°C, Tm (end) 285°C, Heat of fusion 33 J/g. 1H NMR (400 MHz, 120 0 C, d 4 -odichlorobenzene) is very similar to the spectrum of Example 306. Several peaks attributed to cyclopentenyl end groups were observed in the range 5.2-5.7 ppm.

-277- 02/0/03.sw133 I spa,277 Integration of-these pea' was used to calculate Mn "130. IR (pressed film, cm-) 3050 (vw, olefinic end group, CH stretch), 1615(vw, olefinic end group, cis- CH=CH- double bond stretch), 1463(vs), 1445(vs), 1362(s), 1332(s), 1306(s), 1253(m),.1128(w), 1041(w), 935(m), 895(w), 882(w), 792(w), 721(w, olefinic end group, cis-CH=CH-, CH bend). GPC (Dissolved in 1,2,4trichlorobenzene at 150 0 C, run at 100°C in tetrachloroethylene, polystyrene calibration): Peak MW 13,900; Mn 10,300; Mw 17,600; Mw/Mn 1.70.

Example 314 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed into a glass vial in the dry box (0.032 g, 0.050 mmol).

Toluene (2.35 ml and cyclopentene (6.81 g, 2,000 equivalents/Ni) were added, followed by C 6 HsNHMe2* B(CsF5)4 (0.04 g, 50 equivalents/Ni). A solution of Et 3 Al was added while stirring ml, 1 M in heptane, equivalents/Ni). After stirring for 46 hours, the solution was filtered and the solids were washed several times on the filter with pentane. The polymer was dried in vacuo for 12 hours at room temperature to yield 0.16 g of fine powder (47 turnovers/Ni). A control experiment with no C 6 HsNHMe2 B(C 6 Fs) 4 gave no polymer.

Example 315 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed into a glass vial in the dry box (0.032 g, 0.050 mmol) Toluene (3.46 ml and cyclopentene (6.81 g, 2,000 equivalents/Ni) were added. A solution of Et 2 AICI was added while stirring (1.39 ml, 1.8 M in toluene, equivalents/Ni). After stirring for 46 hours, the solution was filtered and the solids were washed several times on the filter with pentane. The polymer was dried in vacuo for 12 hours at room temperature to yield 0.53 g of fine powder (156 turnovers/Ni) Example 316 The complex [(2,4,6-MePh) 2 DABMe 2 NiBr 2 was weighed into a glass vial in the dry box (0.0070 g, 0.0130 -278- 0206/03.sw 1331 Ipa,278 mmol) Pentane (2.2 ml and cyclo- tene (10.0 g, 11,300 equivalents/Ni) were added. A solution of EtAlC12 was added while stirring (0.73 ml, 1.0 M in hexanes, 56 equivalents/Ni). After stirring for 192 hours, the solution was filtered and the solids were washed several times on the filter with pentane. The polymer was dried in vacuo for 12 hours at room temperature to yield 2.66 g of fine powder (3010 turnovers/Ni). The polymer was mixed with 200 ml of MeOH in a blender at high speed to produce a fine powder. The solid was collected by filtration and then mixed for 1 hour with 39 ml of a 1:1 mixture of MeOH/concentrated aqueous HC1. The solid was collected by filtration, washed with distilled water, and then washed on the filter 3X with 20 ml of a 2 wt. solution of Irganox® 1010 in acetone. The polymer was dried in vacuo for 12 hours at.room temperature. DSC to 300°C, 10°C/min, controlled cool at 10 0 C/min, second heat): Tg 98°C, Tm(onset) 160°C, Tm (end) 2400C, Heat of fusion 17 J/g. TGA(air, T(onset of loss) 3300C. T(10% loss) 450°C. 13C NMR (500 MHz IH frequency, 3.1 ml of 1,2,4trichlorobenzene, 0.060g Cr(acac) 3 1200C) 30.640 (s, 2C), 38.364 1C), 46.528 2C). This spectrum is consistent with an addition polymer of cyclopentene with cis-l,3-enchainment. A sample of the polymer was melted in a Schlenk tube under a nitrogen atmosphere.

Fibers were drawn from the molten polymer using a stainless steel cannula with a bent tip. A nitrogen purge was maintained during the fiber drawing. The fibers were tough and could be drawn about 2X by pulling against a metal surface heated to 1250C.

Example 317 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed into a glass vial in the dry box (0.0093 g, 0.0146 mmol). Cyclopentene (10.0 g, 10,000 equivalents/Ni) was added. A solution of EtAlC1 2 was added while stirring (0.73 ml, 1.0 M in hexanes, -279- O ,3J p..

2 02/06/03.swl331 lspa.279 equivalen' After stirring for 16T9hours, the -olution was filtered and the solids were washed several times on the filter with pentane. The polymer was dried in vacuo for 12 hours at room temperature to yield 4.66 g of fine powder (4660 turnovers/Ni). The polymer was mixed with 200 ml of MeOH in a blender at high speed to produce a fine powder. The solid was collected by filtration and then mixed for 1 hour with 39 ml of a 1:1 mixture of MeOH/concentrated aqueous HC1. The solid was collected by filtration, washed with distilled water, and then washed on the filter 3X with 20 ml of a 2 wt. solution of Irganox 1010 in acetone. The polymer was dried in vacuo for 12 hours at room temperature. DSC (25 to 350 0 C, 15 0 C/min, second heat): Tg 97 0 C, Tm(onset) 160 0 C, Tm (end) 285 0 C, Heat of fusion 25 J/g. 13 C NMR (500 MHz IH frequency, 3.1 ml of 1, 2 ,4-trichlorobenzene, 0.060g Cr(acac) 3 120 0 30.604 2C), 38.333 1C), 46.492 2C). This spectrum is consistent with an addition polymer of cyclopentene with cis-1,3enchainment. A sample of the polymer was melted in a Schlenk tube under a nitrogen atmosphere. Fibers were drawn from the molten polymer using a stainless steel cannula with a bent tip. A nitrogen purge was maintained during the fiber drawing. The fibers were tough and could be drawn about 2X by pulling against a metal surface heated to 125 GPC (Dissolved in 1,2,4-trichlorobenzene at 150 0 C, run at i00 0 C in tetrachloroethylene, polystyrene calibration): Peak MW 137,000; Mn 73,000; Mw 298,000; Mw/Mn 4.08.

Example 318 The complex {[(2,6-i-PrPh) 2 DABMe 2 ]PdMe(Et20) }SbF-- (0.05 g, 0.060 mmol) was added to 10.0 g of stirring cyclopentene. Solid polymer formed rapidly and precipitated. The polymer was isolated by filtration, washed on the filter 3X with pentane, and dried in vacuo at room temperature to give 1.148 g finely divided powder (282 turnovers/Pd). DSC (25 to 350 0

C,

280 o 02 103,s. 13311spa.280 0 C/min, first heat): Tm(onset) 175 0 C, Tm (end) 0 C, Heat of fusion 16 J/g.

Example 319 The complex PrPh)2DABMe 2 ]PdCH 2

CH

2

CH

2

C(O)OCH

3 )+SbF 6 (0.05 g, 0.059 mmol) was added to 10.0 g of stirring cyclopentene.

The complex is not very soluble in cyclopentene. The amount of solids increased slowly. After 27 days, the solid polymer was isolated by filtration, washed on the filter 3X with pentane, and dried in vacuo at room temperature to give 1.171 g finely divided powder (292 turnovers/Pd). DSC (25 to 350°C, 15°C/min, first heat): Tm(onset) 1700C, Tm (end) 255°C, Heat of fusion 24 J/g.

Example 320 The complex [(2,6-i-PrPh) 2 DABMe 2 ]NiBr 2 was weighed into a glass vial in the dry box (0.025 g, 0.040 mmol).

Cyclopentene (10.0 g, 1,000 equivalents/Ni) was added.

A solution of MMAO was added while stirring (0.802 ml, 2.5 M in heptane, 50 equivalents/Ni). After stirring for 5 minutes, the mixture was rusty brown and still contained some solids. An additional 50 equivalents of MMAO were added and the solution became homogeneous.

After 12 hours, the mixture was filtered and the solids were washed several times on the filter with pentane.

The polymer was dried in vacuo for 12 hours at room temperature to yield 0.238 g of fine powder (87 turnovers/Ni). DSC (25 to 350°C, 15°C/min, second heat): Tm(onset) 1700C, Tm (end) 265°C, Heat of fusion 18 J/g.

Example 321 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed into a glass vial in the dry box (0.0093 g, 0.0146 mmol). Cyclopentene (10.0 g, 10,000 equivalents/Ni) and anhydrous methylene chloride (48.5 ml) were added.

A solution of EtAlC1 2 was added while stirring (2.92 ml, 1.0 M in toluene, 200 equivalents/Ni). After stirring for 163 hours, the solution was filtered and 281 02/06'3.sw,3311 spa.

2 8 the solids were washed several times on the filter with pFntane. The polymer was dried in vacuo for 12 hours at room temperature to yield 1.64 g of fine powder (1640 turnovers/Ni). A DSC thermal fractionation experiment was done according to the.procedure of Example 312. A DSC was then recorded from 0 0 C to 330°C at 10 0 C/min. Tg 92 0 C, Tm (onset) 150 0 C, Tm (end) 250 0 C, Heat of fusion 11.4 J/g.

Example 322 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed into a glass vial in the dry box (0.0093 g, 0.0146 mmol). Cyclopentene (10.0 g, 10,000 equivalents/Ni) was added. A solution of i-BuAlCl 2 was added while stirring (2.92 ml, 1.0 M in toluene, 200 equivalents/Ni). After stirring for 163 hours, the solution was filtered and the solids were washed several times on the filter with pentane. The polymer was dried in vacuo for 12 hours at room temperature to yield 1.99 g of fine powder (1990 turnovers/Ni). The polymer was pressed at 292 0 C to give a transparent, light gray, tough film. A DSC thermal fractionation experiment was done according to the procedure of Example 312. A DSC was then recorded from 0°C to 330 0

C

at 10 OC/min. Tg 103 0 C, Tm (onset) 150 0 C, Tm (end) 290 0 C, Heat of fusion 27 J/g.

Example 323 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed into a glass vial in the dry box (0.0932 g, 0.146 mmol). Cyclopentene (5.0 g, 500 equivalents/Ni) and toluene (6.54 ml) were added. A solution of PMAO (Akzo Nobel Polymethylaluminoxane) was added while stirring (3.16 ml, 2.32 M Al in toluene, 50 equivalents/Ni).

After stirring for 163 hours, the solution was filtered and the solids were washed several times on the filter with pentane. The polymer was dried in vacuo for 12 hours at room temperature to yield 3.64 g of fine powder (364 turnovers/Ni). The polymer was pressed at 292 0 C to give a brown film that seemed tough, but -282 02/06/03,swl3311spa,282 failed along a straight line when it broke. A DSC -hermal fractionation experiment was done according to the procedure of Example 312 was then recorded from 0"C to 330 0 C at 10 0 C/min. Tg 100 0 C, Tm (onset) 150 0

C,

Tm (end) 270 0 C, Heat of fusion 21 J/g.

Example 324 A mixture of 20mg (0.032mmol) of NiBr2[(2,6-i- PrPh)2DABMe2) was magnetically-stirred under nitrogen in a 50-mL Schlenk flask with 15mL of dry, deaerated toluene as 0.6mL of 3M poly(methylalumoxane) was injected via syringe. The mixture became deep blueblack. Then 2.5mL (14mmol). of beta-citronellene, (CH3) 2 C=CHCH2CH2CH(CH3)CH=CH2, was injected and the mixture was immediately pressurized with ethylene at 190 kPa (absolute) and was stirred at 23 0 C for 17h; by the end of 17h, the solution was too thick to stir.

The ethylene was vented and the toluene solution was stirred with 6N HC1 and methanol and was decanted. The polymer was stirred with refluxing methanol for an hour to extract solvent; oven-drying yielded 0.90g of rubbery polyethylene. 1 H NMR (CDC1 3 showed a CH2:CH3 ratio of 83:12, which is 101 CH3's per 1000 CH2's; there were small peaks for the beta-citronellene isopropylidene dimethyls (1.60 and 1.68ppm), as well as a tiny peak for vinyl H (5.0ppm); diene incorporation was estimated at 0.7mol%. Differential scanning calorimetry: -51°C GPC data (trichlorobenzene, 135°C; PE standard): Mn=23,200; Mw=79,200; Mz=154,000; Mw/Mn=3.42.

Example 325 A 15-mg (0.024-mmol) sample of NiBr2[(2,6-i- PrPh)2DABMe2) was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25mL of dry, deaerated toluene and 5mL (27mmol) of dry, deaerated 1,9decadiene. Then 0.6mL of polymethylalumoxane (1.7M MAO in heptane; contains about 30% isobutyl groups) was injected; the tan suspension did not change color. The mixture was pressurized with ethylene to 190 kPa -283 02/06/0.swl331 Jsp.283 (absolute) and was stirred for 1hr; it began to grow r-een-gray and darker in color, so 0.6mL more MAO was added, after which the mixture soon turned deep greenblack. The reaction was stirred for 16hr and the ethylene was then vented; by this time the solution had become thick and unstirrable. The mixture was stirred with refluxing 6N HC1 and methanol, and the polymer was washed with methanol, pressed free of solvent, and dried under high vacuum to yield 1.0g of rubbery polyethylene. The polymer was insoluble in hot dichlorobenzene, demonstrating incorporation of the diene.

Example 326 A 21-mg (0.034-mmol) sample of NiBr 2 PrPh)2DABMe 2 was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25mL of dry, deaerated toluene. Then 0.6mL of 2.9M polymethylalumoxane was injected; the red-brown suspension became deep green.

The mixture was purged with ethylene and then (1.4g; 15mmol) of 2-methyl-l,5-hexadiene was added; the mixture was pressurized with ethylene to 190 kPa and was stirred for 18h; the solution became brown. The ethylene was vented and the toluene solution was stirred with 6N HCI and methanol and was separated; rotary evaporation of the toluene layer yielded, after acetone washing to remove catalyst, 47mg of viscous liquid polymer. 1H NMR (CDCl 3 showed a CH2:CH3 ratio of 82:15, which is 130 CH3's per 1000 CH2's. There were also peaks for the incorporated diene at 1.72ppm (0.5H; Cl3-C=CH2) and 4.68ppm (0.3H; CH3-C=CH2) and no evidence of terminal vinyl (-CH=CH2; 4.95 and 5.80ppm) from unincorporated diene. The level of diene incorporation was about 0.7mol%.

Example 327 A 30-mg (0.049-mmol) sample of NiBr2[(2,6-i- PrPh)2DABMe2] was magnetically stirred under nitrogen in a 50-mL Schlenk flask with 25mL of dry, deaerated toluene. Then 1.0mL of methylalumoxane (1.7M in -284- 02/06/03.5w133 I spa284 heptane; contains- about 30% isobutyl groups) was -njected; the red-brown suspension became deep green.

The mixture was saturated with ethylene and then (0.38g; 3.0mmol) of 2-methyl-2,7-octadiene was added; the mixture was pressurized with ethylene to 190 kEa (absolute).and was stirred for 18h; the solution became brown. The ethylene was vented and the toluene solution was stirred with 6N HC1 and methanol and was separated; rotary evaporation of the toluene yielded, after acetone washing to remove catalyst, 0.15g of viscous liquid polymer. 1H NMR (CDC13) showed a

CH

2 :CH3 ratio of 81.5:13.5, which is 117 CH3's per 1000 CH2's. The level of diene incorporation was about judging from the diene isopropylidene methyls at 1.60 and 1.69ppm.

Examples 328-335 Acrylate Chelate Complexes. The chelate complexes for these examples were generated in situ for NMR studies by the reaction of [(ArN=C(R)- C(R)=NAr)PdMe(OEt2)]BAF with H 2 C=CHC(O)OR' and on a preparative scale by the reaction of NaBAF with (ArN=C(R)-C(R)=NAr)PdMeC1 and H 2 C=CHC(O)OR' (vide infra). In these examples, the following labeling scheme is used to identify the different chelate complexes that were observed and/or isolated.

Assignments of all 1H NMR chelate resonances were confirmed by homonuclear decoupling experiments.

-285- 0 2 /06/03,swi 331 Isp,285 Ar Ar Ar OR'4 RTN\0 R N OR' N O= r RO OAF OoR' R, OAF -O_ Pd OR' BAF Pd BAF Pd BAF Ar Me Me Ar 4x(R') Sx(R') 6x(R') Ar Ar R R R N OR' N (a)H Me NPd BAF Pd BAF Me t-Bu R N R An CH(CF2)CF, SMe

(FOA)

Ar 2,6-CsH 3 BAF B[,5-C4H-(CF) h

J

4 General Procedure for the Synthesis of Chelate Complexes A gastight microliter syringe was used to add 1.1 equiv of H2C=CHC(O)OR' to a mixture of 1 equiv of NaBAF and 1 equiv of [(2,6-i-PrPh) 2

DABR

2 )PdMeC1 suspended in mL of Et20. The sides of the Schlenk flask were rinsed with an additional 25 mL of Et20 and the reaction mixture was stirred for 1-2 days at RT.

Sodium chloride was removed from the reaction mixture via filtration, yielding a clear orange solution. The was removed in vacuo and the product was washed with hexane and dried in vacuo. For R' Me or t-Bu, no further purification was necessary (yields 87%).

Recrystallization lowered the yield of product and did not result in separation of the isomeric mixtures.

For R' -CH2(CF 2 )6CF 3 contamination of the product with unreacted NaBAF was sometimes observed.

Filtration of a CH2C1 2 solution of the product removed the NaBAF. The CH2C1 2 was then removed in vacuo to yield a partially oily product. A brittle foam was obtained by dissolving the product in Et20 and removing the Et20 in vacuo (yields Although isolable, chelate complexes derived from FOA tended to be less stable than those derived from MA or t-BuA and decomposed with time or additional handling.

Spectral Ilata for the BAF Counterion The following 1H and 13 C spectroscopic assignments of the BAF counterion in CD2C1 2 were invariant for different -286 02 /0/03,swI33j Jspa,286 complexes and temperatures and are not repeated in the -pectroscopic data for each of the cationic complexes: (BAF). 1 H NMR (CD2C12) 6 7.74 8, Ho), 7.57 4, Hp); 13 C NMR (CD2C12) 6 162.2 JCB 37.4, Cipso), 135.2 129.3 JCF 31.3, Cm), 125.0 JCF 272.5, CF3), 117.9 (Cp).

Example 328 The above synthesis using PrPh) DABH2]PdMeCl (937 mg, 1.76 mmol), NaBAF (1.56 g, 1.75 mmol), and MA (175 pL, 1.1 equiv) was followed and the reaction mixture was stirred for 12 h. The resulting orange powder (2.44 g, 96.0%) consisted of a mixture of 6a(Me) 5'a(Me) and 5a(Me) according to 1 H NMR spectroscopy. 6a(Me): 1H NMR (CD2C12, 400 MHz, rt) 6 8.31 and 8.26 1 each, 7.5 7.2 6, Haryl), 3.17 3, OMe), 3.14 and 3.11 (septet, 2 each, CHMe2 and C'HMe2), 2.48 2, J 5.8, CH2C(O)), 1.75 2, J 5.8, PdCH2), 1.38, 1.32, 1.25 and 1.22 6 each, J 6.8, CHMeMe' and C'HMeMe'), 0.73 (pentet, 2, J 5.8, PdCH 2 CH2CH2C(O)); 13C NMR (CD2C12, 100 MHz, rt) 6 183.9 167.1 (JCH 181.4, 160.7 (JCH .181.3, 142.9 and 142.4 (Ar, Ar': Cipso), 139.7 and 138.7 (Ar, Ar': Cipso), 129.8 and 129.0 (Ar, Ar': Cp), 124.6 and 124.1 (Ar, Ar': Cm), 55.2 (OMe), 35.9 and 32.3 (PdH2CH2CH2CC(0)), 29.3 and 29.1 (CHMe2, C'HMe2), 23.8 (PdCH2CH2CH2C(O)), 24.5, 23.9, 23.2 and 22.5 (CHMeMe', C'HMeMe'); IR (CH2C12) 1640 cm- 1 1 3 C NMR (CD2C12, 100 MHz, rt) 6 193.2 Anal. Calcd for (C6 3

H

5 7 BF24N202Pd)

C,

52.28; H, 3.97; N, 1.94. Found: C, 52.08; H, 3.75; N, 1.61.

Example 329 The above synthesis using PrPh)2DABMezlPdMeCl (634 mg, 1.13 mmol), NaBAF (1.00 g, 1.13 mmol), and MA (112 ML, 1.1 equiv) was followed.

The reaction mixture was stirred for 2 days and the product was recrystallized from CH2C12 at -30 OC to 287 0 03.sw3311spa,287 give 956 mg of orange crystals 2 crops).. The rrystals consisted of a mixture of 6b(Me) and Sb(Me) according to 1 H NMR spectroscopy. 6b(Me): 1 H NMR (CD2C1 2 400 MHz, rt) a 7.43 7.26 6, Haryl), 3.03 OMe), 2.95 (septet, 2, J 6.79, CHMe2), 2.93 (septet, 2, J 6.83, C"HMe2), 2.39 2, J 5.86, CH2C(O)), 2.22 and 2.20 1.41 2, J 5.74, PdCH2), 1.37, 1.30, 1.25 and 1.21 6 each, J 6.80 6.94, CHMeMe', C'HMeMe'), 0.66 (pentet, 2, J 5.76, PdCH2CH2CH2C(O)); 1 3 C NMR (CD2C12, 100 MHz, rt) 8 183.4 178.7 and 171.6 140.8 and 140.5 (Ar, Ar': Cipso), 138.6 and 138.0 (Ar, Ar': Co), 129.3 and 128.3 (Ar, Ar': Cp), 124.9 and 124.4 (Ar, Ar': Cm), 54.9 (OMe), 35.8 and 30.3 (PdCH2CH 2

CH

2 29.5 and 29.2 (CHIMe2, C'HMe2), 23.7 (PdCH2CH 2

CH

2 23.91, 23.86, 23.20 and 23.14 (CHMeMe', C'HMeMe'), 21.6 and 19.9 IR (CH2C12) 1643 cm- 1 5'b(Me): 1H NMR (CD2C1 2 400 MHz, rt) 3.47 3, OMe), 2.54 1, CHIMeC(O)), 2.19 and 2.18 3 each, 1.02 3, J 7.23, CHMeC(O)); 1 3 C NMR (CD2C12, 100 MHz, rt) 6 194.5 179.2 and 172.2 55.6 (OMe), 44.3 (CMeC(Q)), 28.4 (PdCH 2 21.2 and 19.6 (N=C(Me)- 18.1 (CHMeC(0)). 5b(Me): 1 H NMR (CD2C12, 400 MHz, rt) 5 0.26 3, PdCHMe). Anal. Calcd for (C65H61BF24N202Pd): C, 52.92; H, 4.17; N, 1.90.

Found: C, 52.91; 8, 4.09; N, 1.68.

Example 330 The above synthesis was followed using PrPh) 2 DABAn]PdMeCl (744 mg, 1.13 mmol), NaBAF (1.00 g, 1.13 mmol), and MA (112 pL, 1.1 equiv). The reaction mixture was stirred for 2 days and the product was recrystallized from CH2C12.at -30 0 C to give 600 mg 2 crops) of a mixture of 6c(Me) 5"c(Me) and Sc(Me) according to IH NMR spectroscopy. 6c(Me): 1H NMR (CD2C1 2 400 MHz, rt) 6 8.17 1, J 8.37, An: Hp), 8.15 1, J -288- 02/06/03.sw133 I ispa.288 3.49, n' 7.62 7.40 8, An, An': Hm, H'm; Hm, Hp; Ar': H'm, 7.08 1, J 7.19, An:

H

o 6.60 1, J 7.44, An': 3.37 (septet, 2, J 6.79, CHMe2), 3.33 (septet, 2, J 6.86, C'HMe 2 2.55 2, J 5.93, CH2C(O)), 1.79 2, J 5.66, PdCH2), 1.45, 1.42, 1.13 and 1.02 6 each, J 6.79 6.90, CHMeMe', C'HMeMe'), 0.80 (pentet, 2, J 5.82, PdCH2CH2CH2C(O)); 13 C NMR (CD2C1 2 100 MHz, rt) 6 183.5: 175'3 and 168.7 145.9 (An: quaternary 141.3 and 140.5 (Ar, Ar': Cipso), 139.7 and 138.4 (Ar, Ar': Co), 133.3 and 132.6 (An: CH), 131.9 (An: quaternary 129.8, 129.7, 129.6 and 128.5 (Ar, Ar': Cp; An: CH), 126.44 and 125.8 (An: quaternary 126.4 and 125.6 (An: CH), 125.5 and 124.6 (Ar, Ar': Cm), 55.0 (OMe), 35.9 and 31.3 (PdCH2CH2CH2C(O)), 29.7 and 29.4 (CHMe2, C'HMe2), 24.1 (PdCH2CH2CH2C(0)), 24.1, 23.8, 23.32 and 23.27 (CHMeMe', C'HMeMe'); IR (,CH2C1 2 1644 cm- 1 5'c(Me): 1 H NMR (CD2C12, 400 MHz, rt) 6 3.64 3, OMe), 2.70 1, CHMeC(O)); 13

C

NMR (CD2C12, 100 MHz, rt) 6 192.8 1 H NMR (CD2C12, 400 MHz, rt) 6 3.67 3, OMe), 2.46 2, J 6.99, CH2C(O)), 1.72 2, J 7.04, PdCH2). 5c(Me): 1H NMR (CD2C12, 400 MHz, rt) 6 0.44 3, PdCHMe).

Anal. Calcd for (C73H61BF24N202Pd): C, 55.80; H, 3.91; N, 1.78. Found: C, 55.76; H, 3.82; N, 1.62.

Example 331 The above synthesis was followed using PrPh) 2

DABH

2 ]PdMeCl (509 mg, 0.954 mmol), NaBAF (845 mg, 0.953 mmol), and t-BuA (154 pL, 1.1 equiv). The reaction mixture was stirred for 1 day and yielded an orange powder (1.24 g, 87.3%) that was composed of a mixture of 6a(t-Bu) 5'a(t-Bu) and Bu) according to 1 H NMR spectroscopy. 6a(t-Bu): IH NMR (CD2C12, 400 MHz, rt) 6 8.27 and 8.25 7.45 7.20 6, Haryl), 3.20 and 3.11 (septet, 2 each, J 6.9, CHMe2 and C'HMe2), 2.42 (t, 2, J 5.9, CH2C(O)), 1.77 2, J 5.3, PdCH2), 289 02 0 6/03,w13 spa.29 1.39, 1.36, 1.;22 and 1.21 6 each, J 6.7, CHMeMe' And C'HMeMe'), 1.01 9, OCMe 3 0.68 (pentet, 2, j 6.1, PdCH2CH 2

CH

2 1 3 C NMR (CD2C1 2 100.MHz, rt, excluding Ar resonances) 6 182.6 88.8 (OCMe 3 37.8, 33.6 and 23.9 (PdCH2CH2CH 2 29.3 and 29.0 (CHMe2, C'HMe2), 27.8 (OCMe3), 24.8, 24.5, 22.7 and 22.6 (CHMeMe', C'HMeMe'); IR (CH2Cl 2 1615 cm-l 5'a(t-Bu): 1H NMR (CD2C1 2 400 MHz, rt; excluding Ar and i-Pr resonances) 6 8.29 and 8.22 1 each, 2.53 1, J 7.3, C(H) 1.75 1, J 8.9, PdCHH'), 1.53 (dd, 1, J 9.0, 7.0, PdCHH'), 1.16 (OCMe3); 1 3 C NMR (CD2C12, 100 MHz, rt; excluding Ar resonances) 6 194.0 90.6 (OCMe 3 45.9 (CHMeC(O)), 30.0 (PdCH 2 29.4, 29.3, 29.1 and 29.1 (CHMe2, C'HMe2, C"''HMe2, C"''IHMe2), 27.7 (OCMe3), 24.6, 24.4, 23.81, 23.79, 23.3, 23.3, 22.62 and 22.58 (CHMeMe', C'HMeMe, C''HMeMe', C'''HMeMe'), 18.7 (CHMeC(O)); IR (CH2C1 2 1577 cm- 1 Sa(t-Bu): 1H NMR (vide infra); 1 3 C NMR (CD2C12, 100 MHz, rt) S 190.4 166.7 and 160.7 48.1 (CH2C(O)), 35.3 (PdCHMe). Anal. Calcd for (C66H63BF 24

N

2 0 2 Pd): C, 53.22; H, 4.26; N, 1.88.

Found: C, 53.55; H, 4.20; N, 1.59.

Example 332 The above synthesis using t(2,6-i- PrPh) 2 DABMe 2 ]PdMeCl (499 mg, 0.889 mmol), NaBAP (786 mg, 0.887 mmol), and t-BuA (145 pL, 1.1 equiv) was followed. The reaction mixture was stirred for 1 day to yield an orange powder (1.24 g, 91.8%) that consisted of a mixture of 6b(t-Bu) and 5b(t-Bu) according to 1 H NMR spectroscopy. 1 H NMR (CD2C12, 300 MHz, rt; diagnostic resonances only) 6b(t-Bu): 8 2.35 2, J 6.1, CH2C(0)), 0.97 9, 0CMe3), 0.60 (pentet, 2, J 5.7, PdCH2CH2CH2C(O)); 5'b(t-Bu): 6 2.43 1, J 7.2, CHMeC(0)), 1.08 9, OCMe3); Sb(t-Bu)t 6 0.99 9, OCMe3), 0.29 3, J 6.74, PdCHMe); 13 C NMR (CD2C12, -290- 02 3,sw 1sp290 02/6/03,sw311spa,290 MHz, rt; diagnosti resonances only) 6b(t-Bu): b 182.3 88.3 (OCMe3), 37.9 and 31.9 (PdCH2CH2CH2C(O)),. 27.9 (OCMe3), 22.0 and 20.1 5'b(t-Bu): 8 193.8 178.8 and 171.8 90.0 (OCMe3), 45-8 (CHMeC(O)), 28.7 (PdCH2), 21.1 and 19.6 18.6 (CHMeC(O0)); 5b(t-Bu) 190.7 48.4 33.9 (PdCHMe). Anal. Calcd for (C 6 8 H67BF24N202Pd):

C,.

53.82; H, 4.45; N, 1.85. Found: C, 53.62; H, 4.32; N, 1.55.

Example 333 The above synthesis was followed using [(2,6-i-Prph) 2 DABAn]PdMeC1 (503 mg, 0.765 mmol), NaBAF (687 mg, 0.765 mmol), and t-BuA (125 gL, 1.1 equiv). The reaction mixture was stirred for 1 day to yield an orange powder (1.08 g, 87.8%) that consisted of a mixture of Ec(t-Bu) Sc'(t-Bu) and Bu) according to 1 H NMR spectroscopy. 1 NMR (CD2C12, 300 MHz, rt; diagnostic chelate resonances only) Ec(t-Bu): 5 2.48 2, J 6.05, CH 2 1.80 2, PdCH2), 1.07 9, OCMe3), 0.73 (pentet, 2, J 5.87, PdCH 2 CH2CH2C(O)); 5'c(t-Bu): 6 2.57 1, J 6.96, CHMeC(O)), 1.58 (dd, 1, J 8.80, 6.96, PdCRH'), 1.21 9, OCMe3); 5c(t-Bu): 8 0.73 3, PdCHMe); 13 C NMR (CD2C12, 75 MHz, rt; diagnostic chelate resonances only) 6c(t-Bu): 8 181.8 87.9 (OCMe3), 37.4 and 32.2 (PdCH 2 CH2CH2C(0)), 27.4 (OCMe3) 8 193.0 89.5 (OCMe3), 45.5 (CHMeC(O)), 28.5 (PdCH2), 27.2 (OCMe3), 18.1 (CHMeC(O)). Anal. Calcd for (C 7 6H67BF24N202Pd):

C,

56.57; H, 4.19; N, 1.74. Found: C, 56.63; H, 4.06; N, 1.52.

Example 334 The above synthesis using PrPh) 2

DABH

2 ]PdMeCl (601 mg, 1.13 mmol), NaBAF (99 mg, 1.13 mmol), and FOA (337 pL, 1.1 equiv) yielded after 1 day of stirring 1.21 g of 6a(FOA) as a red foam: 1 H NMR (CD2C12, 300 MHz, 0 iC) 8 8.33 and 8.27 -291 ovosw 2 02106/0.1.wi3311 spa1291 1 each, 7.4 7.2 6, Haryl), 3.85 2, JHF 13.05, OCH2(CF 2 )6CF 3 3.13 and 3.08 (septet, 2 each, J 6.9, CHMe2 and C'HMe 2 2.65 (t, 2, J 5.62, CH2C(O)), 1.74 2, J 5.59, PdCH 2 1.36, 1.29, 1.15 and 1.13 6 each,. J 6.73 6.82, CHMeMe', C'HMeMe'), 0.76 (pentet, 2, J 5.44, PdCH2CH2CH2C(0)).

Example 335 The above synthesis using PrPh) 2 DABMe 2 ]PdMeC1 (637 mg, 1.13 mmol), NaBAF (1.00 g, 1.13 mmol), and FOA (339 gL, 1.1 equiv) yielded after 1 day of stirring 1.36 g of 6b(FOA) as a yellow foam: 1 H NMR (CD2C12, 300 MHz, 0 iC) 6 7.5 7.0 (m, 6, Haryl), 3.64 2, JHF 12.72,.OCH2(CF 2 6

CF

3 2.90 and 2.88 (septet, 2, J 6.74, CBMe2 and C'HMe 2 2.56 2, J 5.82, CH2C(O)), 2.32 and 2.22 (N=C(Me)- 1.34, 1.27, 1.23 and 1.19 6 each, J 6.75 6.82, CHMeMe', C'HMeMe'), 0.68 (pentet, 2, J 5.83, PdCH2CH2CH2C(O)).

Examples 336-338 The labeling scheme given in Examples 328-335 is also used here. Spectral data for the BAF counterion is the same as given in Examples 328-335.

Low-Temperature NMR Observation of Methyl Acrylate Olefin Complex Formation and Chelate Formation and Rearrangement. One equivalent of MA was added to an NMR tube containing a 0.0198 M solution of iPrPh) 2DABH 2 ]PdMe(OEt2)] }BAF in CD2C12 (700 uL) at -780 C, and the tube was transferred to the precooled NMR probe. After 14.25 min at -80 0 C, approximately 80% of the ether adduct had been converted to the olefin complex. Two sets of bound olefin resonances were observed in a 86:14 ratio. This observation is consistent with the existence of two different rotamers of the olefin complex. Insertion of MA into the Pd-Me bond occurred with predominantly 2,1 regiochemistry to give the 4-membered chelate 4a(Me) at -80iC (tl/2 The resonances for the major rotamer of the olefin 292- 02/0603.swlM331sp*, 2 9 2 complex disappeared before those of t minor rotamer.

Much slower conversion of 4a(Me) to the chelate Sa(Me) also began at -80 0 C. Upon warming to 0 C, complete and selective formation of occurred in less than 4 h. The 5-membered chelate was relatively stable at temperatures below -50 0 C, however, upon warming to -20 0 C, rearrangement to the 6-membered chelate 6a(Me) was observed. NMR spectral data for the olefin complex, 4a(Me), and Sa(Me) follow. Spectral data for 6a(Me) is identical to that of the isolated chelate complex (see Examples 328-335).

Example 336

J[(

2 ,6-i-PrPh)2DABH2 )Pd(Me)

[H

2 C=CHC(O)OMel

}BAF.

1 H NMR (CD2C12, -80 0 C, 400 MHz) Major Rotamer: 8 8.45 and 8.32 1 each, 7.5 7.1 6,.

Haryl), 5.14 J 15.2, 4.96 (dd, J 14.9, 8.6, 4.63 J 8.5, 3.68 3, OMe), 3.03, 2.90, 2.80 and 2.67 (septet, 1 each, ClMe2, C'RMe2, C"IHMe2, C"'HMe2), 1.5 1.0 (doublets, 24, CHMe2), 0.61 3, PdMe); Minor Rotamer: 5 8.25 and 8.18 1 each, 5.25 1, HH'C=), 4.78 (dd, 1, 4.58 1, HHIC=), 3.63 (OMe).

Example 337 2 ,6-i-PrPh)2

DABH

2 ]Pd [CIEtC(0)OMe]}BAF 4a(Me).

3H NMR (CD2C12, 400 MHz, -60 0 C) 6 8.25 and 8.22 7.5 7.2 6, Haryl), 3.74 3, OMe), 3.55, 3.27, 3.08 and 2.76 1 each, CMe2, C'HMe2, C"HMe2, C"'Me2), 2.62 (dd, J 10.8, 2.9, CHEt), 1.4 1.0 (doublets, 24, CHMe2), 0.79 and -0.49 1 each, CH(CHH'Me)), 0.71 3, J 6.6, CH(CHH'Me)).

Example 338 {[(2,6-i-PrPh). 2

DABH

2 ]Pd[CHMeCH2C(0) OMe]) BAF 1H NMR (CD2C12, 400 MHz, -60iC) 8 8.24 and 8.21 7.4 7.2 6, Haryl), 3.59 3, OMe), 3.47, 3.32, 2.98 and 2.81 (septet, 1 each, CHMe2, C'fMe2, C"IHMe2, C''HMe2), 3.08 (dd, 1, J 18.4, 7.3, CHH'C(0)), 1.74 (pentet, 1, J 6.9, -293 306/003.swI331 spa.293 PdCHMe), 1 1, J 18.6, CHH'C(O)) 1.34 6, J 5.6, C'HMeMe' and C' 'HMeMe'), 1.32 3, J 6.2, CHMeMe'), 1.24 3, J 6.8, C'"HMeMe'), 1.18 6, J 6.8, C'HMeMe' and C''HMeMe'), 1.15 3, J 6.8, C'''HMMe 1.08 3, CHMeMe'), 0.35 3, J 6.9, PdCHMe) 1 3 C NMR (CD2C12, 100 MHz, -80 0 C) 6 190.5 166.1 (JCH 181, 160.7 (JCH 181, 142.8 and 141.6 (Ar, Ar': Cipso), 139.0, 138.6, 138.2 and 137.7 (Ar: Co, Co' and Co, Co'), 128.8 and 128.2 (Ar, Ar': Cp), 124.1, 123.54, 123.48, 123.4 (Ar: Cm, Cm' and Ar': Cm, 55.5 (OMe), 45.1 (CH2C(O)), 35.6 (PdCHMe), 28.8, 28.5, 28.1 and 27.8 (CHMe2, C'HMe2, C"HMe2, C" 'HMe2), 25.6, 24.2, 23.1, 23.0, 22.7, 22.3, 21.9, 21.3, and 21.3 (CHMeMe', C'HMeMe', C'"HMeMe', C'''HMeMe' and PdCHMe).

Example 339-342 The labeling scheme given in Examples 328-335 is also used for Examples 339-342. Spectral data for the BAF counterion is the same as given in Examples 328- 335.

Low-Temperature NMR Observation of t-Butyl Acrylate Olefin Complex Formation and Chelate Formation and Rearrangement. One equiv of t-BuA was added to an NMR tube containing a 0.0323 M solution of PrPh) 2

DABH

2 ]PdMe(OEt2)}BAF in CD2C12 (700 L) at -78 0

C,

and the tube was transferred to the precooled NMR probe. The olefin complex was observed at -80 0 C, and the probe was then warmed to -70C. After 1 h at -700 C, conversion to 5a(t-Bu) and 5'a(t-Bu) was almost complete, with small amounts of the olefin complex and 4a(t-Bu) still present. Conversion of Sa(t-Bu) to 6a(t-Bu) was followed at -10 0 C (tl/2-1 h).

When this experiment was repeated using 5 equiv of t- BuA, conversion to 5a, 5'a and 6a was observed at -800 C. After allowing the solution to stand at rt for days, partial conversion to the unsubstituted membered chelate 5''a(t-Bu) was observed. Spectral data for the olefin complex, 4a(t-Bu), Sa(t-Bu) and 294 02/06/03.swl33r1sp.a294 follow. Spectral data for 5'a(t-Bu) anc.

6a(t-Bu) are identical to that of the isolated chelate complexes (see Examples 328-335).

Example 339 2 ,6-i-PrPh) 2 DABH 2)PdMeH2C=CHC(0)O-t-Bu]

)BAF.

1H NMR (CD2C12, 400 MHz, -801C) 6 8.45 and 8.30 1 each 7.4 7.2 6, Haryl), 5.15 (d, 1, J 15.3, 4.89 (dd, 1, J 14.7, 8.4, 4.61 1, J 7.7, 2.92, 2.90, 2.80 and 2.64 (septets, 1 each, CHMe2, C'HMe2), C"HMe2 and C"'HMe2), 1.31 9, OCMe3), 1.5 0.8 (doublets, 24, CHMe2), 0.60 3, PdMe).

Example 340 1( 2 ,6-i-PrPh) 2DABH 1]Pd[CHEtC(0)O-t-Bu )BAF 4a(t- Bu). 1H NMR (CD2C12, 400 MHz, -70 0 C) 6 8.22 and 8.21 1 each, 2.21 1, J 9.2, PdCHEt), 0.71 3, J 7.9, PdCH(CH2Me)), 0.5 and 0.4 (br m, 1 each, PdCH(CHH'Me)).

Example 341 2 6 i PrPh) 2

DABH

2 Pd[CHMeCH2C(0)O-t-Bul

}BAF

Sa(t-Bu). 1 H NMR (CD2C12, 400 MHz, -40 0 C) 6 8.28 and 8.24 1 each, 7.4 7.2 6, Haryl), 3.44, 3.32, 2.96 and 2.86 (septet, 1 each, CHMe2, C'HMe2, C''HMe2, C" 'HMe2), 2.94 (dd, 1, J 18.6, 7.1, CHH'C(O)), 1.79 (pentet, 1, J 6.7, PdCHMe), 1.62 1, J 18.5, 1.4 (doublets, 24, CHMe2), 1.10 9, OCMe3), 0.22 3, J 6.9, PdCHMe).

Example 342 2 ,6-i-PrPh)2

DABH

2 ]PdCH12CH2C()O-t-Bu}BAF 1 H NMR (CD2C12, 400 MHz, rt) 6 2.40 2, J 7.0, CH2C(O0)), 1.65 2, J 7.0, PdCH2).

Example 343 The labeling scheme given in Examples 328-335 is also used for Example 343. Spectral data for the BAF counterion is the same as given in Examples 328-335.

LTow-Temperature NMR Observation of FOA Chelate Formation and Rearrangement. One equiv of FOA was -295 o os sp 0210"/3.swl 3311 sp,295 added to an NMR tube containing a 0.0285 M solution of S[(2,6-i-PrPh) 2

DABH

2 PdMe(OEt2) }BAF (la) at -78 C in CD2C12 (700 and the tube was briefly shaken at this temperature. A 1 H NMR spectrum at -80 0 C showed that FOA was not dissolved. The sample was allowed to warm slightly as it was shaken again and another spectrum was then acquired at -80 0 C. Approximately equal amounts of 5a(FOA) and 6a(FOA) were observed along with small amounts of the ether adduct la and FOA (an olefin complex was not observed). Rearrangement of Sa(FOA) to 6a(FOA) was observed at -40"C and was complete upon warming to -30 0 C. NMR spectral data for Sa(FOA) follow. Spectral data for 6a(FOA) are.

identical with that of the isolated complex (vide supra).

PrPh) 2 DABH2]Pd[CHMeCH2C(O)OCH2(CF2)6CF3] }BAF 1H NMR (CD2C12, 300 MHz, -40iC) 6 8.23 and 8.22 1 each, 3.47 2, JHF 13.38,

OCH

2 (CF2)6CF3), 3.20 (dd, 1, J 19.25, 7.28, CHH'C(O)), 2.58 (pentet, 1, J 6.99, PdCHMe), 1.77 (d, 1, J 19.81, CHH'C(O)), 0.33 3, J 6.88, PdCHMe).

Spectral data for the BAF counterion is the same as given in Examples 328-335.

Example 344 NMR Observation of PrPh) 2

DABH

2 ]Pd[CHR''CH2CH2C(0)OMe }BAF and PrPh) 2

DABH

2 IPd[CH2CH2C(O)OMe] )BAF. A solution of S[(2,6-i-PrPh) 2

DABH

2 ]PdMe(OEt2)}BAF (21.5 mg, 0.0150 mmol) in 700 pL of CD2C12 was prepared at -78 0

C.

Ethylene (5 equiv) was added via gastight syringe and the tube was shaken briefly to dissolve the ethylene.

Methyl acrylate (5 equiv) was then added to the solution, also via gastight microliter syringe, and the tube was shaken briefly again. The tube was transferred to the NMR probe, which was precooled to 0 C. Resonances consistent with the formation of the ethylene adduct [(2,6-i-PrPh) 2

DABH

2 iPdMe(H2C=CH2) }BAF -296 o2 3, 296 0206f03,sw13311spa,296 were observed. The solution was warmed and ethylene insertion was monitored at -40 to -200C. The consumption of one equiv of methyl acrylate occurred as the last equiv of ethylene disappeared, and resonances consistent with the formation of a substituted 6membered chelate complex PrPh) 2

DABH

2 Pd [CHR' CH2CH2C(O)OMe] }BAF were observed [8.30 and 8.29 3.17 The large upfield shift of the methbxy resonance is particularly diagnostic for formation of .the 6-membered chelate complex in these systems. The substituted 6membered chelate complex was observed at -20°C and initially upon warming to RT. After 2 h at RT, decomposition of the substituted 6-membered chelate complex had begun. After 24 h at RT, an additional equiv of MA had been consumed and triplets at 2.42 and 1.66 ppm, consistent with the formation of the unsubstituted 5-membered chelate complex PrPh) DABH 2 ]Pd[CH2CH2C(O)OMe] }BAF, were observed.

Spectral data for the BAF counterion is the same as given in Examples 328-335.

Example 345 NMR Observation of (t(2,6-i- PrPh) 2 DABMe 2 ]Pd(CHR''CH 2 CH2C(O)OMe] }BAF. The procedure of Example 344 was followed with analogous results, resonances for the formation of a substituted 6membered chelate complex PrPh) 2 DABMe] Pd[CHR''CH 2 CH2C(0)OMe])BAF were observed following complete ethylene consumption [3.03 OMe), 3.12, 2.96, 2.89, 2.83 (septets, CM4e2, C'HMe2, C'"HMe2 and C' 'HMe2), 2.23 and 2.19 Again, the large upfield shift of the methoxy resonance is diagnostic for the formation of the six-membered chelate complex. The observation of four i-propyl methine resonances (vs. two i-propyl methine resonances in the unsubstituted six-membered chelate complex) reflects the asymmetry introduced in the molecule due to the introduction of the substituent on Ca of the -297- 02/03,swl331 Ispa,297 chelate ring and further supports the proposed structure. Spectral data for the BAF counterion is the same as given in Examples 328-335.

Example 346 PrPh) DABH 2 Pd(H2C=CH2) [CH2CH2CH2C(O)OMe] )BAF.

Ethylene was transferred at -78 0 C via gastight microliter syringe to an NMR tube containing a CD2C12 solution of the chelate complex PrPh) DABH 2 ]Pd[CH2CH2CH2C(O)OMe] )BAF. NMR data for the ethylene complex follow; it was observed in equilibrium with the starting chelate complex: 1 HENMR (CD2C12, 300 MHz, 182 0 K) 8 8.30 and 8.29 1 each, N=C(H)- 7.38 7.24 6, Haryl), 3.72 3, OMe), 3.43 (br s, 4, H2C=CH2), 3.10 2, CHMe2), 2.70 (m, 2, 2.20 2, CH2C(O)), 1.25, 1.16, 1.09 and 1.07 6 each, J 7, CHMeMe', C'HMeMe'), 1.20 (PdCH2 (obscured by CHMeMe' peaks, observed by H,H-COSY)), 0.56 2, PdCH 2 CH2CH2C(O)); 1 3 C NMR (CD2C12, 400 MHz, -80°C) 6 178.9 162.7 (JCH 179, 162.5 (JCH 179, 141.3 and 140.5 (Ar, Ar': Cipso), 138.5 and 138.1 (Ar, Ar': Co), 128.5 and 128.3 (Ar, Ar': Cp), 124.1 and 124.0 (Ar, Ar': Co), 122.9 (JCH 159.3, free H2C=CH2), 70.2 (JCH 158.6, bound H2C=CH2), 53.0 (OMe), 36.5, 33.0 and 22.6 (PdCH 2

CH

2 CH2C(O)), 27.8 (CHMe2, C'HMe2), 25.6, 25.3, 22.1 and 21.4 (CHMeMe', C'HMeMe'). Spectral data for the BAF counterion is the same as given in Examples 328-335.

Example 347 PrPh) 2 DABMe 2 Pd(H2C=CH2) [(CH 2 CH2CH2C OMe] }BAF.

Ethylene was transferred at -78 0 C via gastight microliter syringe to an NMR tube containing a.CD 2 C12 solution of the chelate complex PrPh) 2 DABMe2]Pd [CH2CH2CH2C OMe] BAF. NMR data for the ethylene complex follow; even at low temperature and in the presence of a large excess of ethylene, this 298 02//0.swl3311spa,298 complex could only be observed in the presence of at least an equimolar amount of the corresponding sixmembered chelate: 1 HENMR (CD2C12, 300 MHz, 172 0 6 7.35 7.19 6, Haryl), 4.31 (br s, 4, H 2 C=CH2), 3.45 3, OMe), 2.73 2.54 4, CHMe2), 2.38 and 2.22 3 each, 1.64 2, CH2C(O)), 1.02 6, J 6, CHMeMe''). From the available H,H-COSY data, the remaining PdCH 2 CH2CH2C(O)and CHMe-signals could not be unambiguously assigned, due to the presence of the six-membered chelate.

Spectral data fot the BAF counterion is the same as given in Examples 328-335.

Exnamle 348 PrPh) 2 DABAn]Pd(H2C=CH2)

(CH

2

CH

2 CH2C(0)OMe]

}BAF.

Ethylene was transferred at -78 0 C via gastight microliter syringe to an NMR tube containing a CD2C12 solution of the chelate complex PrPh) 2 DABAn])Pd(CH2CH2CH2C(0)OMe)]BAF. NMR data for the ethylene complex follow; it was observed in equilibrium with the starting chelate complex: 1H NMR (CD2C12, 300 MHz, 178 0 8 8.06 and 8.02 J 8, 1 each, An and An': Hp and 7.50 7.38 8, An and An': H', and Hm, Ar: Hm and Hp 6.48 J 7, 2 An and An': Ho and 4.56 (br s, 4, H 2 C=CH2), 3.45 3, OMe), 2.99 and 2.91 2 each, ChMe2 and C'HMe2), 1.77 2, CH2C(0)), 1.29, 1.27, 0.82 and 0.77 J 6 7, 6 each, CHMeMe', C'HMeMe') H,H-COSY reveals that the remaining PdCH2CH2CH2C()-signals- are obscured by the CHMe-signals at 1.2 ppm. Spectral data for the BAF counterion is the same as given in Examples 328-335.

Example 349 PrPh),DABH 2 Pd[CHCH2CH2C(0)OCH2(CF2) 6 CF3 (H 2 C=CH2) }BAF Ethylene (0.78 equiv) was added via gastight microliter syringe to a 0.0105 M solution of the chelate complex PrPh) 2

DABH

2 1Pd[CH2CH2I2C (0)OCH2(CF2)6CF3]}BAF in -299 V02or/3.,ws33 1 spa.299 CD2C12 (700 pL) NMR data for the ethylene complex follow; it was observed in equilibrium with the starting chelate complex: 1H NMR (CD2C12, 300 MHz, 213.0 0 K) 5 8.40 and 8.25 7.5 7.1 6, Haryl), 4.50 2, JHF 13.39, OCH2(CF2) 6

CF

3 4.41 4, H2C=CH2), 2.94 and 2.70 (septet, 2 each, CHMe2, C'HMe2), 1.80 3, CH 2 1.4 (CHMeMe', C'HMeMe', PdCH2CH2CH2C(O)). Spectral data for the BAF counterion is the same as given in Examples 328-335.

Example 350 A 12 mg (0.02 mmol) sample of PrPh) 2 DABAn]NiBr2 was placed in a 25 mL high pressure cell. The reactor was purged with argon. The reactor was cooled to 0°C before 2 mL of a 10 MAO solution in toluene was added under a positive argon purge. The reactor was filled (3/4 full) with liquid C0 2 (4.5 MPa) and a 689 kPa head pressure of ethylene was added by continuous flow. A 6 degree exotherm was observed. A layer of polyethylene formed immediately at the ethylene CO02 interface. After 20 minutes, the cell was vented and the polyethylene removed from the reactor.

The polymer was dried in vacuo for several hours.

Polyethylene (2.05 g) was isolated; Mn 597,000, Mw/Mn 2.29, Tm 128°C. This example demonstrates the applicability of liquid CO02 as a solvent for polymerization in these catalyst systems.

Example 351 A 12 mg (0.02 mmol) sample of PrPh) 2 DABAn]NiBr2 was placed in a 25 mL high pressure cell and the reactor was purged with argon. The reactor was heated to 40°C and 2 mL of a 10 MAO solution in toluene was added. C02 (20.7 MPa) and ethylene (3.5 MPa, continuous flow) was then added to the reactor. Polyethylene began adhering to the sapphire window within minutes. After 20 minutes, the cell was vented and the polyethylene removed from the reactor. The polymer was dried in vacuo for several 300 0 2 /06$O3,swl3311spa,300 hours. Polyethylene (0.95 g) was isolated; Mn 249,000, Mw/Mn 2.69, Tm 113 0 C. This example demonstrates the applicability of supercritical CO2 as a solvent for polymerization in these catalyst systems.

xample 352 A standard solution of [(2,6-i-PrPh)2 DABAn)NiBr2 was prepared as follows: 1,2-difluorobenzene (10 mL) was added to 6.0 mg of t(2,6-i-PrPh)2 DABAn]NiBr2 (8.4 x 10- 6 mol) in a 10 mL volumetric flask. The standard solution was transferred to a Kontes flask and stored under an argon atmosphere.

A 1000 mL Parr® stirred autoclave under an argon atmosphere, was charged with 1 mL of a standard solution of [(2,6-i-PrPh)2DABAn]NiBr2 (8.3x10- 7 mol), and 200 mL of dry, deaerated toluene. The reactor was purged with ethylene before addition of 2 mL of a MAO solution in toluene. The autoclave was rapidly pressurized with ethylene to 1.4 MPa as the internal temperature increased from 25 0 C to 45°C within seconds.

Activation of the internal cooling system returned the reactor temperature to 30°C. After 10 minutes, the ethylene was vented and acetone and water were added to -quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HCI, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 7.0 g (1.8x10 6 TO/h) of polyethylene. Differential scanning calorimetry: Tm 118 0 C (133 Gel permeation chromatography (trichlorobenzene, 1359C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 470,000; Mw 1,008,000; Mw/Mn 2.14. 1 3 C-NMR analysis: total methyls/1000 CH2 methyl ethyl propyl butyl amyl Example 353 A 1000 mL Parr® stirred autoclave under an argon atmosphere, was charged with 1 mL of a standard solution of [(2,6-i-PrPh)2DABAn]NiBr2 (8.3xi0- 7 mol), 301 02/06/03,swl 13311 spa,301 and 200 mL of dry, deaerated toluene. The reactor was purged with ethylene before addition of 2 mL of a MAO solution in toluene. The autoclave was rapidly pressurized with ethylene to 2.8 MPa as the internal temperature increased from 25*C to 48 0 C within seconds.

Activation of the internal cooling system returned the reactor temperature to -30 0 C. After 10 minutes, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene.was recovered from the reactor collected and washed with 6 M HC1, and acetone. The resulting polymer was dried under high vacuum overnight to yield 8.85 g (2.3x10 6 TO/h) of polyethylene. DSC: Tm 122°C. GPC (trichlorobenzene, 135°C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 485,000; Mw 1,042,000; Mw/Mn 2.15. 13 C-NMR analysis: total methyls/1000

CH

2 methyl ethyl propyl butyl amyl Example 354 A 1000 mL Parr® stirred autoclave under an argon atmosphere, was charged with 1 mL of a standard solution of [(2,6-i-PrPh)2DABAn]NiBr2 (8.3x10- 7 mol), and 200 mL of dry, deaerated toluene. The reactor was purged with ethylene before addition of 2 mL of a MAO solution in toluene. The autoclave was rapidly pressurized with ethylene to 4.1 MPa as the internal temperature increased from 250C to 45 0 C within seconds.

Activation of the internal cooling system returned the reactor temperature to -30 0 C. After 10 min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, and acetone. The resulting polymer was dried under high vacuum overnight to yield 7.45 g (1.9x10 6 TO/h) of polyethylene. DSC: Tm 126*C. GPC (trichlorobenzene, 135 0 C, polystyrene reference, results calculated as polyethylene using universal -302- 0 03. spa 02/06o3.swl3311sp302 calibi ion theory): Mn 510,000; Mw 1,109,000; Mw/Mn 2.17. 13 C-NMR analysis: total methyls/1000 CH2 methyl ethyl propyl butyl arnyl Example 355 A 1 mg (1.7x10 6 mool) sample of PrPh) 2 DABH2]NiBr2 was placed in a Parr® 1000 mL stirred autoclave under argon. The autoclave was sealed and 200 mL of dry toluene was added. The reactor was purged with ethylene before addition of mL of a 10% MAO solution in toluene. The autoclave was rapidly pressurized with ethylene to 1.4 MPa as the internal temperature increased from 25°C to 45°C within seconds. Activation of the internal cooling system returned the reactor temperature to -30°C. After min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 14.1 g (1.8x10 6 TO/h) of polyethylene. DSC: Tm 126°C (151 GPC (trichlorobenzene, 135°C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 32,000; Mw 89,000; Mw/Mn 2.75.

Rxample 356 A 1 mg (1.7x10- 6 mol) sample of PrPh) 2 DABH2]NiBr2 was placed in a Parr® 1000 mL stirred autoclave under argon. The autoclave was sealed and 200 mL of dry toluene was added. The reactor was purged with ethylene before addition of mL of a 10% MAO solution in toluene. The autoclave was rapidly pressurized with ethylene to 2.1 MPa as the internal temperature increased from 25°C to 50°C within seconds. Activation of the internal cooling system returned the reactor temperature to -30*C. After min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was -303- 02/06103.sw I 311 spa.303 recovered from the reactor collected and w ,hed with c M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 16.1 g (2x10 6 TO/h) of polyethylene. DSC: Tm 1290C (175 GPC (trichlorobenzene, 1350C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 40,000; Mw 89,000; Mw/Mn 2.22.

Example 357 A 1.2 mg (1.9x10 6 mol) sample of PrPh) 2 DABMe2]NiBr2 was placed in a Parr® 1000 mL stirred autoclave under argon. The autoclave was sealed and 200 mL of dry toluene was added. The reactor was purged with ethylene before addition of mL of a 10% MAO solution in toluene. The autoclave was rapidly pressurized with ethylene to 1.4 MPa as the internal temperature increased from 24°C to 31°C within seconds. Activation of the internal cooling system returned the reactor temperature to -25°C. After 12 min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 8 g (9x10 TO/h) of polyethylene. DSC: Broad melt beginning approximately 0°C with a maximum at 810C (25 GPC (trichlorobenzene, 135 polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 468,000; Mw 1,300,000; Mw/Mn 2.81. 1 3 C-NMR analysis: total methyls/1000 CH2 methyl ethyl propyl butyl amyl Example 358 A 1.2 mg (1.9x10 6 mol) sample of PrPh) 2 DABMe2]NiBr2 was placed in a Parr® 1000 mL stirred autoclave under argon. The autoclave was sealed and 200 mL of dry toluene was added. The reactor was purged with ethylene before addition of 304 0 2 /06/03,sw1331 spa.34 mL of a 10% MAO solotic in toluene. The autoclave was rapidly pressurized with ethylene to 2.8 MPa as the internal temperature increased from 24°C to 34*C within seconds. After 12 min, the ethylene was vented and acetone and water were added to quench the reaction.

Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, H20, and acetone.

The resulting polymer was dried under high vacuum overnight to yield 6.5 g (6x10 5 TO/h) of polyethylene.

DSC: Broad melt beginning approximately 60 0 C with a maximum at 109 0 C (80 GPC (trichlorobenzene, 135° C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 616,000; Mw 1,500,000; Mw/Mn 2.52. 13

C-NMR

analysis: total methyls/1000 CH2 methyl ethyl propyl butyl amyl Example 359 A 1.2 mg (1.9x10 6 mol) sample of prPh) 2 DABMe2]NiBr2 was placed in a Parr® 1000 mL stirred autoclave under argon. The autoclave was sealed and 200 mL of dry toluene was added. The reactor was purged with ethylene before addition of mL of a 10% MAO solution in toluene. The autoclave was rapidly pressurized with ethylene to 4.1 MPa. After 12 min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 7.2 g (7x10 TO/h) of polyethylene. GPC (trichlorobenzene, 135iC, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 800,000; Mw 1,900,000; Mw/Mn 2.43. 1 3

C-NMR

analysis: total methyls/1000 CH2 methyl ethyl'(1.7), propyl butyl amyl -305- 02/06/03,swj]31 lspa.305 A 1.5 mg (2.4xl0- 6 me sample of PrPh)2DABMe2]NiBr 2 and 200 mL of dry toluene was added to a Parr® 1000 mL stirred autoclave under an argon atmosphere. The reactor was heated to 50 0 °C and purged with ethylene before addition of 3.0.mL of a 7% MMAO solution in heptane. The autoclave was rapidly pressurized with ethylene to 690 kPa. After 10 min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 6.25 g (6x10 5 TO/h) of polyethylene. DSC: Broad melt beginning approximately -25°C with a maximum at Tg -36*C. GPC (trichlorobenzene, 135iC, polystyrene.

reference, results calculated as polyethylene using universal calibration theory): Mn 260,000; Mw 736,000; Mw/Mn 2.83.

Example 361 A 1.5 mg (2.4xI0- 6 mol) sample of PrPh)2DABMe2)NiBr2 and 200 mL of dry toluene was added to a Parr® 1000 mL stirred autoclave under an argon atmosphere. The reactor was heated to 65 0 C and purged with ethylene before addition of 3.0 mL of a 7% MMAO solution in heptane. The autoclave was rapidly pressurized with ethylene to 690 kPa. After 10 min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 7.6 g (7x10 TO/h) of polyethylene. DSC: Broad melt beginning approximately -50*C with a maximum at 24*C. GPC (trichlorobenzene, 135°C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 176,000; Mw 438,000; Mw/Mn 2.49.

Example 362 -306 02/06/03.sw33 I sp..,1D6 A 1.5 mg (2.4x10 6 mol) sample of PrPh) 2 DABMe2]NiBr2 and 200 mL of dry toluene was added to a Parr® 1000 mL stirred autoclave under an argon atmosphere. The reactor was heated to 80 0 C and purged with ethylene before addition of 3.0 mL of a 7% MMAO solution in heptane. The autoclave was rapidly pressurized with ethylene to 690 kPa. After 10 min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 1.0 g (0.9x10 5 TO/h) of polyethylene. DSC: Broad melt beginning approximately -50 0 C with a maximum at -12°C.

GPC (trichlorobenzene, 135*C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 153,000; Mw 273,000; Mw/Mn 1.79.

Example 363 A 1.5 mg (2.4x10- 6 mol) sample of PrPh) 2 DABMe2]NiBr2 and 200.mL of dry toluene was added to a Parr® 1000 mL stirred autoclave under an argon atmosphere. The reactor was heated to 80°C and purged with ethylene before addition of 3.0 mL of a 7% MMAO solution in heptane. The autoclave was rapidly pressurized with ethylene to 2.1 MPa. After 10 min, the ethylene was vented and acetone and water were added to quench the reaction. Solid polyethylene was recovered from the reactor collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 1.05 g (0.9x10 5 TO/h) of polyethylene. DSC: Broad melt beginning approximately -25°C with a maximum at 36 0

C.

Example 364 A standard solution of [(2,6-i-PrPh)2DABAn]NiBr2 was prepared as follows: 1,2-difluorobenzene (10 mL) was added to 6.0 mg of [(2,6-i-PrPh) 2 DABAn]NiBr2 (8.4x10- 6 mol) in a 10 mL volumetric flask. The 03/06/03,swl3311ipa,307 standard solution was transferred to a Kontes flask and stored under an argon atmosphere.

A 250 mL Schlenk flask was charged with 1 mL of a standard solution of [(2,6-i-PrPh)2DABAn]NiBr2 (8.3x10- 7 mol), and 100 mL of dry, deaerated-toluene. The flask was cooled to -20°C in a dry ice isopropanol bath and filled with ethylene (100 kPa, absolute) before addition of 1.5 mL of a 10% MAO solution in toluene.

After 30 min, acetone and water were added to quench the reaction. Solid polyethylene was recovered from the flask collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 0.8 g (7x10 4 TO/h) of polyethylene. GPC (trichlorobenzene, 135°C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 519,000; Mw 768,000; Mw/Mn 1.48.

Example 365 A 250 mL Schlenk flask was charged with 20 mg of [(2,6-i-PrPh)2 DABMe2]NiBr2 (3.2xl0- 5 mol), and 75 mL of dry, deaerated toluene. The flask was cooled to 0 C filled with propylene (100 kPa absolute) before addition of 1.5 mL of a 10% MAO solution in toluene.

After 30 min, acetone and water were added to quench the reaction. Solid polypropylene was recovered from the flask and washed with 6 M HC1, H20, and acetone.

The resulting polymer was dried under high vacuum overnight to yield 0.15 g polypropylene. DSC: Tg -31 OC. GPC (trichlorobenzene, 135°

C

polystyrene reference): Mn 25,000; Mw 37,000; Mw/Mn 1.47.

Example 366 Cyclopentene (16 AL, 10 eq) was added to a suspension of [(2,6-i-PrPh)2DABAn]NiBr2 (12 mg, 1.6x10mol) in 50 mL of dry toluene. A 10% MAO solution (1.5 mL) in toluene was added and the homogenous mixture stirred for 2 h at 25°C. After 2 h, the flask was filled with ethylene (100 kPa, absolute) and the reaction stirred for 15 min. Acetone and water were 308 03/06103,swl331 added to quench the polymerization and precipitate the_ polymer. Solid polyethylene was recovered from the flask collected and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 3.6 g (32,000 TO/h) polyethylene. GPC: (trichlorobenzene, 135C, polystyrene reference, results calculated as polyethylene using universal calibration theory): Mn 87,000; Mw 189,000; Mw/Mn 2.16. A control experiment was run under identical conditions to that described above except no cyclopentene was added to stabilize the activated nickel complex. Polyethylene (380 mg, 3500 TO/h) was isolated. This example demonstrates the applicability of the Ni agostic cation as a potential soluble stable initiator for the polymerization of ethylene and other olefin monomers.

Example 367 1-Hexene (3 mL, 6 vol was added to a suspension of [(2,6-i-PrPh)2DABAn]NiBr2 (12 mg, 1.6x10- 5 mol) in 50 mL of dry toluene. The flask was cooled to -20 0 C in a dry ice isopropanol bath and 1.5 mL of a 10% MAO solution in toluene was added. After stirring the reaction for 1.5 h, acetone and water were added to quench the polymerization and precipitate the polymer.

Solid poly(l-hexene) was recovered from the flask collected and washed with 6 M HCI, H20, and acetone.

The resulting polymer was dried under high vacuum overnight to yield 200 mg poly(l-hexene).

GPC

(trichlorobenzene, 135°C, polystyrene reference): Mn 44,000; Mw 48,000; Mw/Mn 1.09.

Example 368 1-Hexene (2.5 mL, 6 vol was added to a suspension of [(2,6-i-PrPh)2DABAn]NiBr2 (6 mg, 8.3x10- 6 mol) in 50 mL of dry toluene. The flask was cooled to -100C in a dry ice isopropanol bath and 1.5 mL of a 7% MMAO solution in heptane was added. After stirring the reaction for 1 h, acetone and water were added to quench the polymerization and precipitate the polymer.

-309- 0 3 /06/03sw1331 spa.309 Solid poly(l-hexene) was recovered from the flask and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 250 mg poly(l-hexene). GPC (dichloromethane, polystyrene reference): Mn 51,000; Mw 54,000; Mw/Mn 1.06.

Example 369 Propylene (1 atm) was added to a Schlenk flask charged with a suspension of [(2,6-i-PrPh)2DABAn]NiBr 2 (12 mg, 1.7x10 5 mol) in 50 mL of dry toluene after cooling the mixture to -15 0 C in a dry ice isopropanol bath. A 7% MMAO solution in heptane was added. After stirring the reaction for 30 min, acetone and water were added to quench the polymerization and precipitate the polymer. Solid polypropylene was recovered from the flask and washed with 6 M HCl, H20, and acetone.

The resulting polymer was dried under high vacuum overnight to yield 800 mg polypropylene. GPC (dichloromethane, polystyrene reference): Mn 84,000; Mw 96,000; Mw/Mn 1.14 Example 370 Propylene (100 kPa, absolute) was added to a Schlenk flask charged with a suspension of PrPh) 2 DABAn]NiBr2 (12 mg, 1.7x10- 5 mol) in 50 mL of dry toluene. After cooling the mixture to -15iC in a dry ice isopropanol bath, a 7% MMAO solution in heptane was added. After stirring the reaction for 30 min, 5 mL of dry l-hexene was added and the propylene removed in vacuo. The polymerization was allowed to stir for an additional 30 min before acetone and water were added to quench the polymerization and precipitate the polymer. Solid polypropylene-b-poly(l-hexene) was recovered from the flask and washed with 6 M HC1, and acetone. The resulting polymer was dried under high vacuum overnight to yield 1.8 g polypropylene-bpoly(l-hexene). GPC (dichloromethane, polystyrene reference): Mn 142,000; Mw 165,000; Mw/Mn 1.16.

1 H-NMR analysis: indicates the presence of both a -310- 03/6/03.swl331Ispa.10 polypropylene and poly(l-hexene) block. TH-NMR also suggests that the DP of the propylene block is substantially higher than the DP of the 1-hexene block.

DSC analysis: Tg -18 0 C corresponding to the polypropylene block. No other transitions were observed.

Example 371 1-Octadecene (4 mL, 8 vol was added to a suspension of [(2,6-i-PrPh)2DABAn]NiBr 2 (12 mg, 1.6x10- 5 mol) in 50 mL of dry toluene. The flask was cooled to -10 0 C in a dry ice isopropanol bath and 2 mL of a 7% MMAO solution in heptane was added. After stirring the reaction for 1 h, acetone and water were added to quench the polymerization and precipitate the polymer.

Solid poly(l-octadecene) was recovered from the flask collected and washed with 6 M HCI, H 2 0, and acetone.

The resulting polymer was-dried under high vacuum overnight to yield 200 mg poly(l-octadecene).

GPC

(trichlorobenzene, 135°C, polystyrene reference): Mn 19,300; Mw 22,700; Mw/Mn 1.16. DSC: Tm 37°C.

1 H-NMR (CDC1 3 analysis 47 branches/1000 C (theoretical 56 branches/1000 C).

Example 372 A 12-mg (.022 mmol) sample of ((para-Me- Ph)2DABMe2]NiBr 2 was placed in'a Parr® 1000 mL stirred autoclave under an argon atmosphere. with 200 mL of dry toluene (reactor temperature was 65C) The reactor was purged with ethylene and 1.5 nL (100 eq) of a MAO solution in toluene was added to the suspension.

The autoclave was rapidly pressprized to 5.5 MPa and the reaction was stirred for 60 min. A 15°C exotherm was observed. The oligomerization was quenched upon addition of acetone and water. The solvent was removed in vacuo resulting in 20 g of ethylene oligomers. 1

H-

NMR (CDCl3) analysis 83% a-olefin.

Example 373 A 12-mg (.022 mmol) sample of [Ph2DABAn]NiBr 2 was placed in a Parr® 1000 mL stirred autoclave under an -311- 0306/03,swI331Ispa.31 argon atmosphere with 200 mL of dry toluene (reactor temperature was 550C). The reactor was purged with ethylene and 2 mL (100 eq) of a 7% MMAO solution in heptane was added to the suspension. The autoclave was rapidly pressurized to 5.5 MPa and the reaction was stirred for 60 minutes. A 180C exotherm was observed.

The oligomerization was quenched upon addition of acetone and water. The solvent was removed in vacuo resulting in 26 g (corrected for loss of C4, Cg, and Cg during work-up) of ethylene oligomers. 1H-NMR (CDC1 3 and GC analysis: Distribution: C4-C18, C4 C 6 21%, Cg 22%, C 1 0 17%, C12 16%, C14 13%, C 1 6 C18 trace; 90% a-olefin.

Example 374 A 12-mg (.022 mmol) sample of [Ph2DABAn]NiBr 2 was placed in a Parr® 1000 mL stirred autoclave under an argon atmosphere with 200 mL of dry toluene (reactor temperature was 450C). The reactor was purged with ethylene and 2 mL (100 eq) of a 7% MMAO solution in heptane was added to the suspension. The autoclave was rapidly pressurized to 5.5 MPa and the reaction was stirred for 60 min. The oligomerization was quenched upon addition of acetone and water. The solvent was removed in vacuo resulting in 32 g (corrected for loss of C4, C6, and C8 during work-up) of ethylene oligomers. 1 H-NMR (CDC13) and GC analysis: Distribution: C4-C20, C4 C6 19%, CS 19%, 15%, C12 14%, C14 11%, C16 C18 4%, 92% a-olefin.

Example 375 A 12-mg (.022 mmol) sample of [(Ph)DABAn]NiBr 2 was placed in a 1000 mL stirred autoclave under an argon atmosphere with 200 mL of deaerated toluene (reactor temperature was 25C). The reactor was purged with ethylene and 2 mL (100 eq) of a 10% MAO solution in toluene was added to the suspension. The autoclave was rapidly pressurized to 2.1 MPa and the reaction was stirred for 30 min. A 200C exotherm was observed. The -312- 0 3/06/03,swI3311 sp,312 oligomerization was quenched upon addition of acetone and water. The solvent was removed in vacuo resulting in 16.1g of a fluid/waxy mixture (50,000 TO/h based on isolated oligomer). 1H-NMR (CDC13) analysis 80% aolefin. Distribution of isolated oligomers by GC analysis: Cio 20%, C 12 28%, C 14 23%, C 16

C

18 10%, C 20 All C 4

C

6

C

8 and some C 0 o was lost during work-up.

Example 376 A 12-mg (.022 mmol) sample of [(Ph)DABAn]NiBr 2 was placed in a 1000-mL stirred autoclave under an argon atmosphere with 200 mL of deaerated toluene (reactor temperature was 25 0 The reactor was purged with ethylene and 2 mL (100 eq) of a 10% MAO solution in toluene was added to the suspension. The autoclave was rapidly pressurized to 4.1 MPa and the reaction was stirred for 60 minutes. A 20 0 C exotherm was observed.

The oligomerization was quenched upon addition of acetone and water. The solvent was removed in vacuo resulting in 28.3g of crude product (50,000 TO/h based on isolated oligomer). Trace Al was removed by an aqueous/organic work-up of the crude mixture. 1

H-NMR

(CDC13) analysis 85% a-olefin. Distribution of isolated oligomers by GC analysis: Cio 13%, C 12 30%, C 14 26%, C 16 18%, C18 10%, C 20 All C 4

C

6

C

8 and some C 1 o was lost during work -up.

Example 377 A 12-mg (.022 mmol) sample of [(Ph)DABAn]NiBr2 was placed in a 1000 mL stirred autoclave under an argon atmosphere with 200 mL of deaerated toluene (reactor temperature was 25 0 The reactor was purged with ethylene and 2 mL (100 eq) of a 10% MAO.solution in toluene was added to the suspension. The autoclave was rapidly pressurized to 6.7 MPa and the reaction was stirred for 60 min. A 150C exotherm was observed. The oligomerization was quenched upon addition of acetone and water. The solvent was removed in vacuo resulting in 21.6g of crude product (40,000 TO/h based on -313- 0 3 03,w3 03/06/03,sw]3311isp.313 isolated oligomer). 1 H-NMR (CDC13) analysis-93% aolefin. Distribution of isolated oligomers by GC analysis: Clo 13%, C 12 27%, C 14 26%, C 16 18%,

C

18 12%, C 20 All C 4

C

6 Ce and some Clo was lost during work-up.

Example 378 A 12-mg (.022 mmol) sample of [Ph 2 DABAn]NiBr 2 was placed in a 1000 mL stirred autoclave under an argon atmosphere with 200 mL of dry toluene (reactor temperature was 50°C). The reactor was purged with ethylene and 2 mL (100 eq) of a 10% MAO solution in toluene was added to the suspension. The autoclave was rapidly pressurized to 5.5 MPa and the reaction was stirred for 60 minutes. A 15°C exotherm was observed.

The oligomerization was quenched upon addition of acetone and water. The solvent was removed in vacuo resulting in 22.3g of crude product (40,000 TO/h based on isolated oligomer). 1 H-NMR (CDC1 3 analysis 92% aolefin. Distribution of isolated oligomers by GC analysis: Cio 10%, C 12 28%, C 14 25%, Cie 19%, Cle 12%, C 20 All C 4

C

6

C

8 and some C 1 o was lost during work-up.

Examples 379-393 General Procedure for Copolymerizations Experiments at Ambient Pressure: A Schlenk flask containing the catalyst precursor was cooled to 78 0 C, evacuated, and placed under an ethylene atmosphere. In subsequent additions, methylene chloride and the acrylate were added to the cold flask via syringe. The solution was allowed to warm to room temperature and stirred with a magnetic stir bar.

After the specified reaction time, the reaction mixture was added to -600 mL of methanol in order to precipitate the polymer. Next, the methanol was decanted off of the polymer, which was then dissolved.

in -600 mL of-Et20 or petroleum ether. (For copolymerizations with FOA, a second precipitation of the polymer solution into methanol was often necessary 314 03 6 /03 w3, 3311spa,314 in order L remove all of the acrylate from the polymer.) The solution was filtered though a plug of Celite® and/or neutral alumina, the solvent was removed, and the polymer was dried in vacuo for several days. The copolymers were isolated as clear, freeflowing or viscous oils. The copolymers were often darkened by traces of palladium black, which proved difficult to remove in some cases. Polymers with high FOA incorporation were white, presumably due to phase separation of the fluorinated and hydrocarbon segments.

Experiments at Elevated Pressure: Reactions were carried out in a mechanically stirred 300 mL Parr reactor, equipped with an electric heating mantle controlled by a thermocouple dipping into the reaction mixture. A solution of 0.1 mmol of catalyst precursor in methylene chloride, containing the functionalized comonomer (5-50 mL, total volume of the liquid phase: 100 mL), was transferred via cannula to the reactor under a nitrogen atmosphere. After repeatedly flushing with ethylene or propylene, constant pressure was applied by continuously feeding the gaseous olefin and the contents of the reactor were vigorously stirred.

After the specified reaction time, the gas was vented.

Volatiles were removed from the reaction mixture in vacuo, and the polymer was dried under vacuum overnight. In representative runs, the volatile fraction was analyzed by GC for low-molecular-weight products. Residual monomers (tBuA, FOA) or homooligomers of the functionalized comonomer (MVK) were removed by precipitating the polymer from methylene chloride solution with methanol. This procedure did not.significantly alter the polymer composition.

Copolymer Spectral Data. In addition to the signals of the methyl, methylene and methine groups originating from ethylene or propylene, the 1H and 13

C

NMR spectra of the copolymers exhibit characteristic resonances due to the functionalized comonomer. The -315 03/6/03,sw13311 spa 3 IR-spectra display the carbonyl band c: the functionalgroups originating from the comonomer.

Ethylene-MA Copolymer: 11 NMR (CDC1 3 400 MHz) 6 3.64 OCH3), 2.28 J 7, CH2C(O)), 1.58 (m,

CH

2 CH2C(0)); 1 3 C NMR (C6D6, 100 MHz) 6 176 50.9 (OCH3); IR (film): 1744 cm-1 Ethylene-FOA Copolymer: 1 H NMR (CDC13, 400 MHz) 6 4.58 JHF 14, OCH2(CF2)6CF3), 2.40 J 7, CH2C(O)), 1.64 CH2CH2C(0)); 1 3 C NMR (CDC1 3 100 MHz) 6 172.1 59.3 JCF 27, OCH2(CF 2 6

CF

3 IR (film): 1767 cm- 1 Ethylene-tBuA Copolymer: 1 H NMR (CDC13, 300 MHz) 8 2.18 J 7, CH2C(O)), 1.55 CH2CH2C(O)), 1.42 OCMe3); 13C NMR (CDC13, 62 MHz) 6 173.4 IR (film): 1734 cm- 1

(CO).

Ethylene-MVh Copolymer: 1 H NMR (CDC1 3 250 MHz) 6 2.39 J 7, CH2C(O0)), 2.11 C(O)CH 3 1.5 (m, CH2CH2C 1 3 C NMR (CDC13, 62 4Hz) 8 209 IR (film): 1722 cm- 1 Propylene-MA Copolymer: 1 H NMR (CDC13, 250 MHz) 6 3.64 OCH3), 2.3 CH2C(0)); 13 C NMR (CDC13, 62 MHz) 8 174.5 51.4 (OCH3); IR (film): 1747 cm- 1 Propylene-FOA Copolymer: 1 H NMR (CDC1 3 250 MHz) .6 4.57 JHF 14, OCH2(CF2)6CF3), 2.39 CH2C(O)); 1 3 C NMR (CDC13, 62 MHz) 6 172.2 59.3 JCF 27, OCH2(CF2)6CF3); IR (film): 1767 cm- 1 Results of the various polymerization are given in the Table below.

316- 031 6W03.sw1331Ias316 Ex. react. results polymer monomers cone. mass comon.- TONe Mn f Pix. cat. e camon. piatvni pouymer incorp. eh re. I omon. x Iu 31 M I m 379 6b E MA 0.6 M 2 22.2 1.0% 7710 78 88 1.8 380 6b E MA 2.9 M 2 4.3 6.1% 1296 84 26 1.6 381 6b E MA 5.8 M 2 1.8 12.1% 455 63 11 1.6 382 6b E MA 5.B M 6 11.2 4.0% 3560 148 42 1.8 383 6a E MA 5.8 M 6 1.2 5.0% 355 19 0.39 384 6b E MA 5.8 M 6 1.2 4.7% 364 18 10 1.8 385 6b E tBuA 3.4 M 6 2.9 0.7% 956 7 25 1.6 386 Gb E tBuA 0.4 M 1 1.9 0.4% 665 3 6 1.8 387 la E FOA 0.6 M 1 1.5 0.3% 506 2 3 1.6 388 lb E FOA 0.6 M 1 27.5 0.6% 9928 55 106 3.1 399 6b E FOA 1.8 1 9.5 0.9% 2962 27 95 2.7 390 6b E MVK 3.0 M 6 1.8 1.3% 626 8 7 391 6b E 6 10.3 37127 384 3.1 392 6b P MA 0.6 M 6 5.0 1.1% 1179 13 37 1.8 393 6b P FOA 1.8 M 2 1.0 5.6% 145 9 18 1.8 do.1 mmol catalyst (Ex. 391: 0.01 mmol); solvent: CH 2 C1 2 (total volume CH 2 C1 2 and comonomer: 100 mL; Ex.

387 388: 60 mL) temperaturei 35 OC (Ex. 386-389 391 reaction time: 18.5 h (Ex. 386-388: 24 h; Ex.

389, 37 bcomplexes 6: {[(2,6-i-PrPh) 2DABR 2 JPd.[CH 2

CF

2

CH

2 C(O)OMe]J)BAF R Me Complexes 1:{[(2,6-i-PrPh) 2

DABR

2 Pd(Me)(OEt2)WBAF; R H R Me CEthylene propylene meth yl acrylate tert-butyl acrylate (tBuA), H 2 C=CHC(0)OCH 2 (CF2)6CF 3 (FOA), methyl vinyl ketone (MVK). dIn mol eTurnover number moles of substrate converted per mole of catalyst. t Determined by GPC vs.

polystyrene standards; 9determined by 1 H NMR spectroscopy of the non-volatile product fraction; -0.5 g of volatile products formed additionally; hBranching: Ethylene Copolymers: -100 methyl groups/1000 carbon atoms (Tg's: 77 -67 OC); Propylene Copolymers: -210 methyl groups/1000 carbon atoms..

Example 394 (30 mL) was added to a round bdttom flask containing 445 mg (1.10 mmol) of (2,6-i-PrPh)2DABMe 2 and 316 mg (1.15 mmol) of Ni(COD) 2 Methyl acrylate (100 pL) was then added to the flask via microliter syringe. The resulting blue solution was stirred for several hours before the Et20 was removed in vacuo.

The compound was then dissolved in petroleum ether and the resulting solution was filtered and then cooled to -35"C in the drybox freezer. Purple single crystals of I(2,6-i-PrPh) 2 DABMe 2 ]Ni[H2C=CHCO(OMe)] were isolated: 1 H NMR (CD 2 C1 2 300 MHz, -40 0 C) 8 7.4 7.2 6, Haryl), 3.74 (br septet, 1, CHMe2), 3.09 (septet, 1, J 6.75, C'HMe2), 2.93 (septet, 1, J 6.75, C''"HMe 2 2.85 3, OMe), 2.37 (br septet, 1, C'''HMe 2 2.10 (dd, 1, J 13.49, 8.10, H2C=CHC(O)OMe), 1.66 (dd, 1, J 13.49, 4.05, HH'C=CHC(O)OMe), 1.41 3, J 6.75, CHMeMe'), 1.35 (dd, 1, J 8.10, 4.05, HH'C=CHC()OMe), 1.26 3, J 8.10, C"HMeMe'), 1.24 3, J 8.09, C'HMeMe'), 1.13 3, J 6.75, C'HMeMe'), 1.09 1.03 (doublets, 12, CHMeMe', C"HMeMe', C'''HMeMe'), 0.79 and 0.62 3 each, 1 3 C NMR

(CD

2 Cl 2 300 MHz, -20 oC) 8 174.2 (C(O)OMe), 166.6 and 165.5 147.9 and 146.8 (Ar, Ar': Cipso), S139.5, 139.0, 138.2 and 137.7 (Ar: Co, C'o and Ar': Co, 125.6 and 125.4 (Ar, Ar': Cp), 123.5, 123.4,.

123.3 and 123.0 (Ar: C, C'm and Ar': Cm, 49.9 and 39.8 (H2C=CHC()OMe), 28.8, 28.5, 28.4.and 28.3 (CHMe2, C'HMe2, C''"HMe2, C"''HMe2), 26.1 (H2C=CHC(O)OMe), 24.3, 23.8, 23.6, 23.4, 23.0, 22.9, 22.7 and 22.7 (CHMeMe', C'HMeMe', C''HMeMe', C"''HMeMe'), 20.21 and 20.16 Example 395 In a nitrogen-filled drybox, 289 mg (0.525 mmol) of [(2,6-i-PrPh) 2 DABMe 2 Ni(H 2 C=CHCO(OMe))] and 532 mg (0.525 mmol) of H(OEt 2 2 BAF were placed together in a round bottom flask. The flask was cooled in the -35 0

C

freezer before adding 20 mL of cold (-35 0 C) Et 2 to it.

318 /03/06 ,swl331spa,318 The reaction mixture was then allowed t- warm to room temperature as it was stirred for 2 h. The solution was then filtered and the solvent was removed in vacuo to yield 594 mg of the 4-membered chelate, [(2,6-i-PrPh) 2 DABMe2]Ni[CHMeC(O)OMe] )BAF, as a burnt orange powder: 1 H NMR (CD2C12, 300 MHz, rt) 6 7.72 (s, 8, BAF: Ho), 7.56 4,'BAF: Hp), 7.5 7.2 6, Haryl) 3.52 3, OMe), 3.21 1, J 6.75, CHMeC(O)OMe), 3.45, 3.24, 3.02 and 3.02 (septet, 1 each, CHMe2, C'HMe2, C''HMe2 and C'''HMe2), 2.11 and 2.00 3 each, 1.55, 1.50, 1.47, 1.33, 1.28, 1.24, 1.23 and 1.17 3 each, CHMeMe', C'HMeMe', C''HMeMe' and HMeMe'), -0.63 3, J 6.75, CHMeC(O)OMe); 1 3 C NMR (CD2C12, 300 MHz, rt) 6 178.2, 177.0 and 174.1 (C(O)OMe, 162.2 (q, JCB 49.7, BAF: Cipso), 141.2 and 139.8 (Ar, Ar': Cipso), 139.4, 138.89, 138.79 and 138.40 (Ar, Ar': Co, 135.2 (BAF: Co), 130.0 and 129.6 (Ar, Ar': Cp, 129.3 BAF: Cm), 125.6, 125.2, 125.0 and 124.7 (Ar, Ar': Cm, 125.0 JCF 272.5, BAF: CF 3 117.9 (BAF: Cp), 53.6 (OMe), 30.3, 30.0, 29.9 and 29.8 (CHMe2, C'HMe2, C"HMe2, C 'HMe2), 24.5, 24.1, 24.0, 23.7, 23.33, 23.26, 23.1 and 23.1 (CHMeMe', C'HMeMe', C''HMeMe', C' "'HMeMe'), 20.6 and 19.5 6.9 (CHMeC(O)OMe).

Examples 396-400 Polymerization of ethylene by PrPh)2DABMe2]Ni[CHMeC(0)OMe] BAF. This compound was used to catalyze the polymerization of polyethylene at temperatures between RT to 80 0 C. Addition of a Lewis acid often resulted in improved yields of polymer.

General Polymerization Procedure for Examples 396- 400. In the drybox, a glass insert was loaded with {[(2,6-i-PrPh) 2 DABMe2]Ni[CHMeC(O)OMe]}BAF. In addition, 2 equiv of a Lewis acid (when used) was added to the insert.' The insert was cooled to -35 0 C in a drybox freezer, 5 mL of deuterated solvent was added to the cold insert, and the insert was then capped and 319- 03/ 06 /3.w3311 spa.319 sealed. Outside of the drybox, the cold tube was placed under 6.9 MPa of ethylene and allowed to warm to RT or 80°C as it was shaken mechanically for 18 h. An aliquot of the solution was used to acquire a 1 H NMR spectrum. The remaining portion was added to -20 mL of MeOH in order to precipitate the polymer. The polyethylene was isolated and dried under vacuum.

Example 396 Polymerization Conditions: PrPh) 2 DABMe2]Ni[CHMeC(0)OMe]}BAF (84.8 mg, 0.06 mmol); No Lewis Acid; C6D6; RT. No polymer was isolated and polymer formation was not observed in the 1H NMR spectrum.

Example 397 Polymerization Conditions: PrPh),DABMe,]Ni[CHMeC(0)OMe]}BAF (84.8 mg, 0.06 mmol); 2 Equiv BPh 3 C6D6, RT. Solid white polyethylene (0.91 g) was isolated.

Example 398 Polymerization Conditions: PrPh) 2 DABMea]Ni[CHMeC(0)OMe]}BAF (84.8 mg, 0.06 mmol); 2 Equiv B[3,5-trifluoromethylphenyl]3; CED6, RT.

Solid white polyethylene (0.89 g) was isolated.

Example 399 Polymerization Conditions: PrPh)2DABMe2]Ni [CHMeC(O)OMe] BAF; 2 Equiv BPh3; C6D6, 0 C. Polyethylene (4.3 g) was isolated as a spongy solid.

Example 400 Polymerization Conditions: PrPh) 2 DABMe 2 ]Ni[CHMeC(O)OMe]}BAF (84.8 mg, 0.06 mmol); No Lewis Acid; CDC13, 80 0 C. Polyethylene (2.7 g) was isolated as a spongy solid.

Example 401 An NMR tube was loaded with PrPh) 2 DABH2]NiMe(OEt 2 ))BAF. The tube was capped with a septum, the septum was wrapped with Parafilm®, and the tube was cooled to -78 0 C. CD2C1 2 (700 uL) and one -320 0 3/06/03.sw3311 sp,320 equiv of methyl acrylate were added to the cold tube in subsequent additions via gastight microliter syringe.

The tube was transferred to the cold NMR probe.

Insertion of methyl acrylate and formation of the 4membered chelate complex, prPh) 2

DABH

2 )Ni[CHEtC(O)OMe]}BAF, was complete at 1H NMR (CD2C12, 400 MHz, -10 0 C) 6 8.23 and 8.03 1 each, 7.72 8, BAF: Ho), 7.55 (s, 4, BAF: Hp), 7.5 7.2 6, Haryl), 3.69, 3.51, 3.34 and 3.04 (septet, 1 each, CfHMe 2 C'HMe 2 C' 'HMe 2 and C' 'HMe 2 3.58 3, OMe), 1.48, 1.46, 1.46, 1.45, 1.30, 1.27, 1.193 and 1.189 3 each, J 6.5 7.3, CHMeMe', C'HMeMe', C''HMeMe' and C' 'HMeMe'), 0.79 and -0.52 1 each, CH(CHH'CH3), 0.68 3, J 6.9,

CH(CH

2 CH3), (CHEt signal was not assigned due to overlap with other protons).

Example 402 A solution of the 4-membered chelate complex 2 ,6-i-PrPh)DABH 2 ]Ni[CHEtC(

O

)OMe]}BAF was allowed to stand at RT for 1 day. During this time, conversion to the 6-membered chelate complex, PrPh) 2

DABH

2 ]Ni [CH 2

CH

2

CH

2 C(0)OMe]} BAF, was complete: 1H NMR (CD2C12, 400 MHz, rt) 6 8.47 and 8.01 1 each, 7.72 8, BAF: Ho), 7.56 4, BAF: Hp), 7.5 7.0 6, Haryl), 3.61 3, OMe), 3.45 and 3.09 (septet, 2 each, CHMe 2 and C'HMe 2 2.25 2, J 7.3, CH 2 1.61 (pentet, 2, J 7.3, NiCH 2

CH

2

CH

2 1.50, 1.50, 1.46, and 1.30 6 each, J 6.8 6.9, CHMeMe', C'HMeMe'), 0.92 2, J 7.4, NiCH 2 Examples 403-407 These Examples illustrate the formation of metallacycles of the formula shown on the right side of the equation, and the use of these metallacycles as polymerization catalysts.

321 03/06/03.sw13311sp.a32 M O BPh' CH M OPh' R NOE

-C-

4 R N OEt 2 A/ M Ni, Pd: R H, Me BPh'- B[3,.5-CH 3 (CF3)2J 4 (R H, Me, An; M Ni, Pd) In the absence of olefin, the ether-stabilized catalyst derivatives were observed to decompose in

CD

2 C1 2 solution with loss of methane. For the catalyst derivative where M Pd and R H, methane loss was accompanied by clean and selective formation of the metallacycle resulting from C-H activation of one of the aryl i-propyl substituents. This metallacycle could be isolated, although not cleanly, as its instability and high solubility prevented recrystallization. Also it could be converted to another metallacycle in which the diethyl ether ligand is replaced by an olefin ligand, especially ethylene.

Example 403 A 700 pL CD 2 C1 2 solution of PrPh)2DABH 2 3PdMe(OEt 2 )}BAF (68.4 mg) was allowed to stand at room temperature for several hours and then at 0 C overnight. Such highly concentrated solutions of the resulting metallacycle wherein R is H and M is Pd were stable for hours at room temperature, enabling 1

H

and 13C NMR spectra to be acquired: 1H NMR (CD2C1 2 400 MHz, 41 oC) 8 8.17 2, 7.75 (s, 8, BAF: Ho), 7.58 4, BAF: Hp), 7.5 7.0 6, Haryl), 3.48 4, J 6.88, O(CH2CH 3 2 3.26 (septet, 1, J 6.49, CHMe 2 3.08 (septet, 1, J 6.86, C'BMe2), 2.94 (septet, J 6.65, C''HMe2), 2.70 (dd, 1, J 6.67, 0.90, CHMeCHH'Pd), 2.43 (dd, 1, J 7.12, 4.28, CHMeCHH'Pd), 2.23 (br m, 1, CHMeCH2Pd), 322- 03/06'3.swl331tspi,322 1.54 3, J 6.86, CHMeCH2Pd), 1.43 3, J 6.7, C"HMeMe'), 1.40 3, J 7.12, CHMeMe'), 1.37 3, J 6.95, C'HMeMe'), 1.27 6, J 6.79, C'HMeMe', C''HMeMe'), 1.12 3, J 6.54, CHMeMe'), 1.23 (br m, 6, O(CH2CH3)2), 0.21 (CH4); 1 3 C NMR (CD2C12, 400 MHz, 41 OC) 6 162.5 (JCH 181.5, 162.3 JBC 49.8, BAF: Cipso), 161.2 (JCH 178.4, 145.8 and 144.5 (Ar, Ar': Cipso), 141.6, 140.7, 140.3 and 138.8 (Ar, Ar': Cipso), 135.3 (BAF: Co), 131.6 and 129.8 (Ar, Ar': Cp), 129.4 JCF 29.9, BAF: CF3), 128.1, 127.6, 125.2 and 124.5 (Ar, Ar': Co, C o 125.1 (BAF: CF3), 118.0 (BAF: Cp), 72 (br, O(CH 2 CH3)2), 43.2 (CHMeCH2Pd), 40.5 (CHMeCH2Pd), 29.5,. 29.1 and 28.8 (CHMe2, C'HMe2, C"'HMe2), 26.2 25.3, 25.2, 25.1, 24.5 23.3 and 22.1 (CHMeMe', C'HMeMe', C"HMeMe', CHMeCH2Pd), 15.5 (br, O(CH2CH3)2), -14.8 (CH4).

Example 404 Addition of ethylene to a CD2C12 solution of the compound prepared in Example 403 resulted in loss of ether and formation of the corresponding ethylene adduct (spectral data: see Example 405.) Warming of the ethylene adduct in the presence of excess ethylene resulted in branched polymer formation: 1.3 ppm (CH2)n, 0.9 ppm (CH3). For the ethylene polymerization initiated by this metallacycle, rates of initiation were significantly slower than rates of propagation.

Example 405 The metallacycle of Example 403 wherein the diethyl ether ligand was replaced by an ethylene ligand was stable enough so that NMR spectra could be obtained. 1 H NMR (CD2C12, 400 MHz, -61 6 8.25 and 8.23 7.74 8, BAF: Ho), 7.55 (s, 4, BAF: Hp), 7.55 7.16 6, Haryl), 4.67 2, HH'C=CHH'), 4.40 2, HH'C=CHH'), 2.95 (septet, 1, J 6.30, CHMe2), 2.80 (septet, 2, J 6.36, C'HMe2 and C"'HMe2), 2.53 (br m, 1, CHMeCH2Pd), 2.43 1, J 8.16, CHMeCHH'Pd), 1.73 (dd, 1, J 8.16, 2.84, CHMeCHH'Pd), 1.45 and 1.19 3 each, J 6.79 6.40, -323 03/06/03,sw13311 spa,323 CHMeMe'), 1.42 3, J 7.05, CHMeCH 2 Pd), 1.30, 1.30-, 1.19 and 0.99 3 each, J 6.40 6.65, C'HMeMe' and C''HMeMe'); 13 C NMR (CD2C1 2 400 MHz, -61 oC) 6 162.7 (JCH 179.7, N=CH), 162.1 (JCH 180.9, 161.6 JCB 49.7, BAF: Cipso), 144.7, i41.7, 141.2, 139.2, 137.5 and 137.1 (Ar, Ar': Cipso, Co, 134.6 (BAF: Co), 131.0 and 129.0 (Ar, Ar': Cp), 128.6 (q, BAF: Cm), 124.4 JCF 272.5, BAF: CF3), 124.6 and 124.0 (Ar, Ar': Cm), 117.4 (BAF: Cp), 92.3 (JCH 162.4, H2C=CH2), 45.1 (CH2Pd), 41.1 (CHMeCH 2 Pd), 28.9, 28.5 and 28.2 (CHMe2, C'HMe 2 C"HMe 2 26.1, 25.6, 25.1, 24.9, 24.6, 22.9 and 21.4 (CHMeMe', C'HMeMe', C''HMeMe', CHMeCH 2 Pd).

Example 406 In a nitrogen-filled drybox, 30 mL of THF was added to a flask containing (2,6-i-PrPh) 2 DABAn (1.87 g, 3.72 mmol) and Ni(COD) 2 (1.02 g, 3.72 mmol). The resulting purple solution was stirred for several hours before removing the solvent in vacuo. The product was dissolved in a minimum amount of pentane and the resulting solution was filtered and then placed in the drybox freezer (-35 0 C) to recrystallize. Purple crystals of (2,6-i-PrPh) 2 DABAn]Ni (COD) were isolated (1.33 g, 53.5%, first crop). 1 H NMR (CD2C1 2 300 MHz, rt) 6 7.77 2, J 8.06, Haryl), 7.44 2, J 7.52, Haryl), 7.33 2, J 7.70, Haryl), 6.89 2, J 7.70, Haryl), 6.13 2, J 6.13, Haryl) 3.93 (br s, 4, COD: 3.48 (septet, 4, J 6.87, CHMe2), 2.54 (br m, 4, COD: 1.51 4, COD: 1.37 12, J 6.60, CHMeMe'), 0.77 12, J 6.60, CHMeMe'); 13 C NMR (CD2C1 2 75.5 MHz, rt) 8 151.7, 151.6, 138.5, 137.1, 133.0, 132.1, 128.8, 125.6, 123.8, 123.7, 119.0 (Caryl), 88.7 (COD: 29.9 (COD: 28.0, 25.1 and 23.8 (CHMeMe').

Example 407 In the drybox, a glass insert was loaded with 35.2 mg (0.0527 mmol) of [(2,6-i-PrPh) 2 DABAn]Ni(COD) and 55.2 mg (0.0545 mmol) of H(OEt2)2BAF. The insert was 324 03/06/03.rsw 33 lsp.324 cooled to -35CC in the drybox freezer, 5 mL of CDC13 was added to the cold insert, and the insert was then capped and sealed. Outside of the drybox, the cold tube was placed under 6.9 MPa of ethylene and allowed to warm to rt as it was shaken mechanically for 18 h.

An aliquot of the solution was used to acquire a 1H NMR spectrum. The remaining portion was added to -20 mL of MeOH in order to precipitate the polymer. The polyethylene (6.1 g) was isolated and dried under vacuum.

Examples 408-412 (acac)NiEt(PPh3) was synthesized according to published procedures (Cotton, F. Frenz, B. A.; Hunter, D. L. J. Am. Chem. Soc. 1974, 96, 4820-4825).

nGeneral Polymerization Procedure for Examples 408- A12. In the drybox, a glass insert was loaded with 26.9 mg (0.06 mmol) of (acac)NiEt(PPh3), 53.2 mg (0.06 mmol) of NaBAF, and 0.06 mmol of an a-diimine ligand.

In addition, 2 equiv of a phosphine scavenger such as BPh 3 or CuCl was sometimes added. The insert was cooled to -35°C in the drybox freezer, 5 mL of C6D6 was added to the cold insert, and the insert was then papped and sealed. Outside of the drybox, the cold tube was placed under 6.9 MPa of ethylene and allowed to warm to RT as it was shaken mechanically for 18 h.

An aliquot of the solution was used to acquire a 1 H NMR spectrum. The remaining portion was added to -20 mL of MeOH in order to precipitate the polymer. The polyethylene was isolated and dried under vacuum.

Example 408 The a-diimine was (2,6-i-PrPh) 2 DABMe 2 Solid white polyethylene (1.6 g) was isolated.

Example 409 The a-diimine was (2,6-i-PrPh) 2 DABMe 2 and 29.1 mg of BPh 3 was also added. Solid white polyethylene g) was isolated.

325 o03/003,Jsw 13311sa.325 Example 410 The a-diimine was (2,6-i-PrPh) 2 DABMe 2 and 11.9 of CuCl was also added. Solid white polyethylene (0.8 g) was isolated.

Example 411 The a-diimine was (2,6-i-PrPh) 2 DABAn. Solid white polyethylene (0.2 g) was isolated.

Example 412 The a-diimine was (2,6-i-PrPh) 2 DABAn, and 29.1 mg of BPh 3 was also added. Solid white polyethylene (14.7 g) was isolated.

Examples 413-420 The following synthetic methods and polymerization procedures were used to synthesize and test the polymerization activity of the functionalized a-diimine ligands of these Examples.

Synthetic Method A. One equiv of glyoxal or the diketone was dissolved in methanol. Two equiv of the functionalized aniline was added to the solution along with -1 mL of formic acid. The solution was stirred until a precipitate formed. The precipitate was collected on a frit and washed with methanol. The product was then dissolved in dichloromethane and the resulting solution was stirred overnight over sodium sulfate. The solution was filtered and the solvent was removed in vacuo to yield the functionalized a-diimine.

Synthetic Method B. One equiv of glyoxal or the diketone was dissolved in dichloromethane and two equiv of the functionalized aniline was added to the solution. The reaction mixture was stirred over sodium sulfate week). The solution was filtered and the solvent was removed in vacuo. The product was washed or recrystallized from petroleum ether and then dried in vacuo.

-326 03/06/03,swl331tspa326 Nickel Polymerization Procedure. In the drybox, a-.

glass insert was loaded with one equiv each of Ni(COD)2, H(OEt 2 )2BAF, and the a-diimine ligand. The insert was cooled to -35 0 C in the drybox freezer, 5 mL of CD 6 was added to the cold insert, and the insert was then capped and sealed. Outside of the drybox, the cold tube was placed under 6.9 MPa of ethylene and allowed to warm to RT as it was shaken mechanically for- 18 h. An aliquot of the solution was used to acquire a 1H NMR spectrum. The remaining portion was added to mL of MeOH in order to precipitate the polymer.

The polyethylene was isolated and dried under vacuum.

Palladium Polymerization Procedure. In the drybox, a glass insert was loaded with one equiv each of [CODPdMe(NCMe)]BAF and the a-diimine ligand. The insert was cooled to -35 0 C in the drybox freezer, 5 mL of C6D6 was added to the cold insert, and the insert was then capped and sealed. Outside of the drybox, the cold tube was placed under 6.9 MPa of ethylene and allowed to warm to RT as it was shaken mechanically for 18 h. An aliquot of the solution was used to acquire a 1 H NMR spectrum. The remaining portion was added to mL of MeOH in order to precipitate the polymer.

The polyethylene was isolated and dried under vacuum.

Examle'413 a-Diimine was (2-hydroxyethylPh) DABMe 2 Synthetic Method B: 1 H NMR (CDC13, 300 MHz, rt) 6 7.28 7.20 4, Haryl), 7.12 2, J 7.52, Haryl), 6.67 2, J 7.67, Haryl), 3.74 4, J 6.79, CH20H), 3.11 (br s, 2, OH), 2.76 4, J 6.79, CH2CH20H), 2.16 6, 13C NMR (CDC13, 75 MHz, rt) 6 168.2 149.0 (Ar: Cipso), 128.4 (Ar: Co), 130.4, 127.1, 124.6 and 118.2 (Ar: Cm, Cp, Cm', 62.9 (CH20H), 35.3 (CH2CH20H), 15.8 Nickel Polymerization Procedure: (0.02 mmol scale) Seventy mg of polyethylene was isolated. 1

H

327 03/0603,sw1331 lsp.327 NMR spectrum (CGD6) shows the production of 1- and 2butenes along with smaller amounts of higher olefins.

Palladium Polymerization Procedure: (0.06 mmol scale) No polymer was isolated, however, the 1 H NMR spectrum shows peaks consistent with'the formation of branched polyethylene: 1.3 ppm (CH2)n, 0.9 ppm (CH 3 of branches). Broad a-olefinic resonances are observed in the baseline.

Example 414 a-Diimine is (2,6-Et-3,5-chloroPh) 2 DABMe 2 Synthetic Method-A: 1H NMR (CDC1 3 300 MHz, rt) 6 7.19 1, Haryl), 2.64 (sextet, 4, J 7.19, CHH'CH 3 2.36 (sextet, 4, J 7.11, CHH'CH 3 2.10 6, 1.05 12, J 7.52, CH2CH 3 13

C

NMR (CDC13, 75 MHz, rt) 8 168.8 149.3 (Ar: Cipso), 132.3 and 127.4 (Ar: Co and Cm), 124.7 (Ar: Cp), 22.5 (CH 2

CH

3 16.8 12.1 (CH2CH3).

Nickel Polymerization Procedure: (0.06 mmol scale) Solid white polyethylene (14.6 g) was isolated.

Palladium Polymerization Procedure: (0.06 mmol scale) Polyethylene (0.06 g) was isolated as an oil.

1 H NMR spectrum (C6D 6 shows branched polyethylene along with some internal olefinic end groups.

Palladium Polymerization Procedure: {0.03 mmol scale; Isolated [(2,6-Et-3,5chloroPh) 2 DABMe 2 PdMe (NCMe) BAF was used.

Polyethylene (2.42 g) was isolated as an oil.

Example 415 a-Diimine is (2,6-Et-3-chloroPh) DABMe 2 Synthetic Method A: 1 H NMR .(CDC1 3 300 MHz, rt) 8 7.10 2, J 8.43, Haryl), 7.04 2, J 8.07, Haryl), 2.65 (m, 2, CHH'CH3), 2.49 2, CHH'CH3), 2.30 4, C'HH'C'H3), 2.08 6, 1.15 and 1.07 6 each, 7.52, CH2CH 3 and C'H2C'H3); 13 C NMR (CDC13, 75 MHz, rt) 8 168.4 148.5 (Ar: Cipso), 132.0, 129.1 and 128.6 (Ar: Co, Co', Cm), 126.9 -328- 0310 6103,sw133 1spk328 and 124.3 (Ar: Cm' and Cp), 24.4 and 22.6 (CH2CH3 and

C'H

2 C'H3), 16.5 13.4 and 12.4 (CH2CH3 and C'H2C'H3).

Palladium Polymerization Procedure: {0.03 mmol scale; Isolated [(2,6-Et-3chloroPh) 2 DABMe 2 MePdMe(NCMe)]BAF was used.) Polyethylene g) was isolated as an amorphous solid.

Example 416 a-Diimine is (2,6-bromo-4-MePh) DABMe 2 Synthetic Method A: 1H NMR (CDC13, 300 MHz, rt) 6 7.40 4, Haryl), 2.32 6, Ar: Me), 2.14 6, N=C(Me)- 1 3 C NMR (CDC13, 75 MHz, rt) 6 171.5 (N=C- 144.9 (Ar: Cipso), 135.7 (Ar: Cp), 132.4 (Ar: Cm), 112.3 (Ar: Co), 20.2 and 16.9 (N=C(Me)-C(Me) =N and Ar: Me) Nickel Polymerization Procedure: (0.02 mmol scale) Solid white polyethylene (5.9 g) was isolated.

1H NMR spectrum (C6D6) shows a significant amount of branched polymer along with internal olefinic end groups.

Palladium Polymerization Procedure: (0.06 mmol scale) Polyethylene (0.38 g) was isolated as an oil.

1H NMR spectrum (C6D6) shows a significant amount of branched polymer along with internal olefinic end groups.

Example 417 a-Diimine is (2,6-Me-4-bromoPh) 2 DABH2. Synthetic Method A: 1H NMR (CDC13, 300 MHz, rt) 6 8.07 2, N=CH-CH=N), 7.24 4, Haryl), 2.15 12, Ar: Me); 1 3 C NMR (CDC13, 300 MHz, rt) 6 163.6 148.7 (Ar: Cipso), 131.0 and 128.7 (Ar: Co and Cm), 117.7 (Ar: Cp), 18.1 (Ar: Me).

Nickel Polymerization Procedure: (0.06 mmol scale) Solid white polyethylene (9.5 g) was isolated.

Palladium Polymerization Procedure: (0.06 mmol scale) No polymer was isolated, however, the 1 H NMR spectrum (C6D6) shows the production of a- and internal olefins (butenes and higher olefins). A small -3293/06/03,swl331 sp329 resonance exists at 1.3 ppm and is cons stent with theresonance for (CH2)n.

Example 418 a-Diimine is (2,6-Me-4-bromoPh) 2 DABMe 2 Synthetic Method A: 1 H NMR (CDC13, 300 MHz, rt) 6 7.22 4, Haryl), 2.02 6, 2.00 12, Ar: Me); 1 3 C NMR (CDC1 3 75 MHz, rt) 6 168.5 147.3 (Ar: Cipso), 130.6 (Ar: Cm), 126.9 (Ar: Co), 115.9 (Ar: Cp), 17.6 (Ar: Me), 15.9 Nickel Polymerization Procedure: (0.06 mmol scale) Solid white polyethylene (14.9 g) was isolated.

Palladium Polymerization Procedure: (0.06 mmol scale) Polyethylene (1.3 g) was isolated as an oil.

The 1H NMR spectrum (C6D6) shows resonances consistent with the formation of branched polymer. Resonances consistent with olefinic end groups are observed in the baseline.

Palladium Polymerization Procedure: {0.03 mmol scale; Isolated[(2,6-Me-4bromoPh) 2 DABMe 2 )PdMe(NCMe)]BAF was used.} Polyethylene (3.97 g) was isolated as a mixture of a soft white solid and an amorphous oil. 1 H NMR spectrum (C 6

D

6 shows branched polyethylene.

Example 419 a-Diimine is (2-Me-6-chloroPh) 2 DABMe 2 Nickel Polymerization Procedure: (0.02 mmol scale) Solid white polyethylene (220 mg) was isolated.

In addition, the 1H NMR spectrum (C 6

D

6 shows the production of 1- and 2-butenes.

-330- 03 1 06 /03,swl33 i p330 Palladium Polymeriz. aion Procedure: (0.03 mmol scale; Isolated [(2-Me-6chloroPh) 2 DABMe 2 ]PdMe(NCMe)]SbF 6 was used.) Polyethylene (3.39 g) was isolated as an oil. The 1H NMR spectrum (C 6

D

6 shows the production of branched polyethylene; internal olefin end groups are also present.

Example 420 (2,6-t-BuPh) 2

DABAN

This compound was made by a procedure similar to that of Example 25. Two g (9.74 mmol) of butylaniline and 0.88 g (4.8 mmol) of acenaphthenequinone were partially dissolved in 50 mL of methanol. Attempted crystallization from ether and from CH2C12 yielded an orange/yellow powder (1.75 g, 66%--not optimized). 1 H NMR (CDC13, 250 MHz) 6 7.85 2H, J 8.1 Hz, BIAN: Hp), 7.44 2H, J 8.4 Hz, Ar: Hm), 7.33 (dd, 2H, J 8.4, 7.3 Hz, BIAN: Hm), 7.20 (dd, 2H, J 8.1, 2.2 Hz, Ar: Hp), 6.99 2H, J 2.2 Hz, Ar: Ho), 6.86 2H, J 7.0 Hz, BIAN: Ho), 1.37, 1.27 18H each, C(CH3)3).

Example 421 A 100mg sample of PrPh)2DABMe2]PdCH 2 CH2CH2C(O)OCH3)}BAF- in a Schlenk flask was dissolved in CH2C12 (4ml) and cyclopentene (8ml) added. The flask was flushed well with a ethylene in N2 mix and the solution stirred with a slow flow of the gas mixture passing through the flask.

After 15 hours the product had solidified into a single mass of yellow/brown polymer. The reaction was quenched with MeOH and the polymer broken into pieces and washed with MeOH. Yield 2.0g. DSC: Tm 165 0

C

(32J/g). Integration of the 1 H-NMR spectrum indicated 83 mole% cyclopentene.

Example 422 A 37mg sample of [(2,4,6-MePh)2DABAn]NiBr2 in cyclopentene (5ml) was placed in a Schlenk flask under an atmosphere of ethylene. Modified MAO (l.lml, 7.2wt% -331- 03/063,swl331,i,33 Al) was added and the reaction allowed to run for 16 hours after which time the product had solidified into a mass of green polymer. The reaction was quenched by addition of MeOH/10%HC1 and the polymer was crushed and washed well with MeOH and finally a 2t Irganox/acetone solution. Yield 3.6g.

Example 423 A 30mg sample of ((2,6-i-PrPh)2DABMe2]NiBr 2 was slurried in toluene (2ml) and norbornene PMAO (iml, 9.6wt% Al) was added. The solution immediately turned deep blue/black and in less than a minute became extremely viscous. The reaction was quenched after hours by addition of MeOH/10%HCl causing the polymer to precipitate. The solid was filtered, washed well with MeOH and finally with a 2% Irganox® 1010 in acetone solution. The polymer was cut into pieces and dried.

Yield 0.8g 1H-NMR (ODCB, 120 0 1.0-2.5 ppm complex multiplet confirms that the product is an addition polymer. The absence of olefinic peaks precludes the existence of ROMP product and indicates that the polymer is not of extremely low molecular weight.

Example 424 A 32mg sample of ((2,6-i-PrPh)2DABMe 2 ]CoCl 2 was slurried in toluene (2ml) and norbornene PMAO 9.6wt% Al) was added. The solution immediately turned deep purple and within a few minutes became extremely viscous and difficult to stir. The reaction was quenched after 4 hours by addition of MeOH/10%HC1 causing the polymer to precipitate. The solid was filtered, washed well with MeOH and finally with a 2% Irganox in acetone solution. The polymer was dried overnight at 110OC under vacuum. Yield 2.1g It was possible to further purify the product by dissolving in cyclohexane and reprecipitating with MeOH. IH-NMR (TCE, 120 0 1.0-2.5 ppm complex multiplet.

332 030 ,sw133 sp,2 03/0903,swl33Fisps.332 Example 4 2 A 33mg sample of ((2,4,6-MePh) 2 DABAn)CoC12 was slurried in toluene (2ml) and norbornene

PMAO

9.6wt% Al) was added. The solution immediately turned deep blue and within a few minutes the viscosity began to increase. The reaction was quenched after 4 hours by addition of MeOH/10%HCI causing the polymer to precipitate. The solid was filtered, washed well with MeOH and finally with a 2% Irganox® 1010 in acetone solution. The polymer was dried overnight at 1100 under vacuum. Yield 0.8g It was possible to further purify the product by dissolving in cyclohexane and reprecipitating with MeOH. 1H-NMR (TCE, 120 0

C):

1.0-2.5 ppm complex multiplet.

Example 426 .A 23mg sample of [(2,4,6-MePh)2 DABH2]PdMeCl was slurried in toluene (2ml) and norbornene

PMAO

(l.OmL, 9.6wt% Al) was added. Solids immediately formed and after a few seconds stirring stopped. The reaction was quenched after 2 hours by addition of The solid was filtered, crushed and washed well with MeOH and finally with a 2% Irganox® 1010 in acetone solution. Yield 2.5g Example 427 A 16mg sample of [(2,4,6-MePh)2 DABH2)NiBr2 was slurried in dicyclopentadiene MMAO (1.2ml, 7.2wt% Al) was added. Solution immediately turned deep red/purple and started to foam. The reaction was quenched after 16 hours by addition of MeOH/10%HC1 which precipitated the polymer. The solid was filtered and washed well with MeOH and finally with a 2% Irganox® 1010 in acetone solution. Yield 0.25g.

Example 428 A 20mg sample of [(2,4,6-MePh)2 DABH2]PdMeCl was slurried in toluene (2ml) and ethylidene norbornene (2 ml). PMAO (l.OmL, 9.6wt% Al) was added. The solution turned a pale orange and after an hour the viscosity had increased. After 14 hours the mixture had 3 0 3 /06/ 03 ,sw 33 11sp,333 solidifed into a gel and stirring had stbppe'd. The reaction was quenched by addition of MeOH/10%HC1. The solid was filtered, crushed and washed well with MeOH and finally with a 2% Irganox® 1010 in acetone solution. Yield 0.7g Example 429 NiI2 (0.26g) was placed in THF (10ml) and (2,6-i- PrPh) 2 DABMe2 (340mg) was added. The resulting mixturewas stirred for 2 days after which the THF was removed and pentane added. The red/brown solid was isolated by filtration and washed several times with pentane.

Yield 0.53g A portion of the product (9 mg) in toluene in a Schlenk flask was placed under an atmosphere of ethylene (140 kPa [absolute]) and 0.25 ml PMAO solution Al) was added. The solution turned dark green and, after several hours at room temperature, became viscous. After 16 hours the reaction was quenched with HCI which precipitated the polymer. The polymer (1.25g) was collected by filtration, washed well with MeOH and dried under reduced pressure. iH NMR indicated -133 methyl per 1000 methylene.

Example 430 CoI2 (286mg) was dissolved in THF (10ml) and (2,6iPrPh)2DABMe2 (370mg) was added. The resulting mixture was stirred for 3 days after which the THF was removed and pentane added. The brown solid was isolated by filtration and washed several times with pentane.

Yield 0.29g 1H NMR (THF-d 8 1.0-1.4 24H, CH-CH3), 2.06 6H, N=C-CH3), 2.6-2.8 4H, C-CH-

(CH

3 2 7.0-7.3 6H, aromatic). This data is consistent with the formula: [(2,6-iPrPh)2DABMe2)Col2 A portion of the above product (14mg, 0.02mmol) in toluene (25mL) in a Schlenk flask was placed under an atmosphere of ethylene (140 kPa [absolute]) and 0.4 ml PMAO solution'(9.6% Al) was added. The solution turned purple and, after several hours at room temperature, became viscous. After 18 hours the reaction was 334 03 06 /03.sw331sp,334 quenched with MeOH/10% HC1 which precipitated the polymer. The polymer (634mg) was collected by filtration, washed well with MeOH and dried under reduced pressure. 1 H NMR indicated 100 methyl per 1000 methylene. DSC: Tg -45 0

C.

Example 431 Solid n-cyclooctenyl-l,5-cyclooctadienecobalt

(I)

(17mg, 0.06mmol) (prepared according to: Gosser L., Inorg. Synth., 17, 112-15, 1977) and solid (2,6iPrPh) 2 DABMe2 (24mg, 0.06mmol) were placed in a Schlenk flask and toluene (25mL) added. An ethylene atmosphere was admitted (34 kPa gauge) and the solution stirred for 5 minutes. The final color was brown/green. 0.8 ml PMAO solution Al) was added. After 18 hours the reaction was quenched with MeOH/10% HC1 which precipitated the polymer. The polymer (190mg) was collected by filtration, washed well with MeOH and dried under reduced pressure. 1H NMR indicated methyl per 1000 methylene. DSC: Tg -45 0

C.

Example 432 [(2,6-iPrPh)2 DABMe2]CoCl2 (619mg) was slurried in (5ml) and cooled to -25 0 C. Me2Mg (63mg in was added and the solution stirred for minutes. Et20 was removed under reduced pressure and the resulting bright purple solid was dissolved in pentane, filtered to remove MgC12 and the volume reduced to 5 ml. The solution was cooled to -25oC for 2 days and the resulting purple crystals isolated by filtration. Yield 420mg Crystal structure determination confirmed that the product was iPrPh) 2 DABMe2]CoMe2.

[(2,6-iPrPh)2 DABMe2]CoMe2 (34mg) in toluene in a Schlenk flask was placed under an atmosphere of ethylene (140 kPa [absolute]) and after stirring for 2 hours, 0.6 ml PMAO solution Al) was added. The solution remained dark purple and, after several hours at room temperature, became viscous. After 48 hours the reaction was quenched with MeOH/10% HC1 which -335- 03/06/O3,sw1331 Isp,335 precipitated the polymer. The polymer (0.838g) was collected by filtration, washed well with MeOH and dried under reduced pressure. Branching- (H-NMR): 115 methyl per 1000 methylene. DSC: Tg -45 0

C.

Example 43 [(2,6-iPrPh)2DABMe2]CoMe 2 (30mg) was dissolved in benzene (10ml in a shaker tube) and the solution frozen. Montmorillionite K-10 (Aldrich Chemical Co., Milwaukee, WI, U.S.A.)(200mg, conditioned.at 140 0 C for 48hrs under vacuum) suspended in benzene (10ml) was added on top of-the frozen layer and frozen as well.

The solution was thawed under an ethylene atmosphere (6.9 MPa) and shaken at that pressure for 18 hours.

MeOH was added to the resulting polymer which was then isolated by filtration, washed well with MeOH and dried under reduced pressure. Yield 7.5g crystalline polyethylene. Branching 1 H-NMR): 18 Methyl per 1000 methylene.

Example 434 [(2,6-iPrPh)2DABMe 2 ]CoMe 2 (15mg) was dissolved in benzene (10ml in a shaker tube) and the solution frozen. Montmorillionite K-10 (100mg, conditioned at 600 0 C for 48hrs under vacuum) suspended in benzene was added on top of the frozen layer and frozen as well. The solution was thawed under an ethylene atmosphere (6.9 MPa) and shaken at that pressure for 18 hours. MeOH was added to the resulting polymer which was then isolated by filtration, washed well with MeOH and dried under reduced pressure. Yield 3g polyethylene. Branching 1 H NMR): 11 Methyl per 1000 methylene.

Example 435 [(2,6-iPrPh)2DABMe 2 ]CoMe2 (15mg) was dissolved in benzene (10ml in a shaker tube) and the solution frozen. Tris(pentaflorophenyl)boron (25mg) dissolved in benzene (10ml) was added on top of the frozen layer and frozen as well. The solution was thawed under an ethylene atmosphere (6.9 MPa) and shaken at that -336- 03/ 10 603,swl3311sp336 pressure for 18 hours. MeOH was added to the resulting polymer which was then isolated by filtration, washed well with MeOH and dried under reduced pressure. Yield 105mg polyethylene. Branching 1 H NMR): 60 Methyl per 1000 methylene.

Example 436 [(2,6-iPrPh)2DABMe2]CoMe2 (15mg) was dissolved in benzene (10ml in a shaker tube) and the solution frozen. HBAF'2Et20 (30mg) slurried in benzene was added on top of the frozen layer and frozen as well. The solution was thawed under an ethylene atmosphere (6.9 MPa) and shaken at that pressure for 18 hours. MeOH was added to the resulting polymer which was then isolated by filtration, washed well with MeOH and dried under reduced pressure. Yield 3.8g polyethylene. Branching 1 H NMR): 21 Methyl per 1000 methylene.

Example 437 CoC12 (102mg) was placed in acetonitrile and AgBF4 (306mg) added. The solution was stirred for 30 minutes after which the white AgC1 was filtered off. (2,6-i- PrPh) 2 DABMe2 (318mg) was added and the solution stirred overnight. The acetonitrile was removed under reduced pressure and pentane added. The orange product was isolated by filtration and washed and dried. 1

H-NMR

(THF-d8): 1.1-1.4 C-CH-CH3, 24H), 1.8 (CH 3

CN,

6H), 2.2 (N=C-CH3, 6H), 2.7 C-CH-CH3, 4H), 7.0-7.2 C=CH, 6H). The spectrum is consistent with the molecular formula: iPrPh)2DABMe2)Co(CH3CN)2] (BF4)2 A portion of the product (43mg) in toluene in a Schlenk flask was placed under an atmosphere of ethylene (35 kPa gauge) and 0.8 ml PMAO solution (9.6% Al) was added. The solution turned dark purple After 18 hours the reaction was quenched with MeOH/10% HC1 which precipitated the polymer. The polymer (0.310g) was collected by filtration, washed well with MeOH and 337 o31o3,sw33 1s 3 (U/06103,swl35311337 dried under reduced pressure. Branching 1 H NMR): 72-- Methyl per 1000 methylene.

Example 438 Solid Co(II) [(CH 3 2 CHC(0)0-] 2 (17mg, 0.0 7 3mmol) and solid (2,6-iPrPh) 2 DABMe 2 (32mg, '0.079mmol) were placed in a Schlenk flask and toluene (25mL) added. An ethylene atmosphere was admitted (140 kPa [absolute]) and 3.0 ml PMAO solution Al) was added. After i8 hours the reaction was quenched with MeOH/10% HC1 which precipitated the polymer. The polymer (57mg) was collected by filtration, washed well with MeOH and dried under reduced pressure. 1H NMR indicated 32 methyl per 1000 methylene.

Example 439 The complex [(2,6-EtPh) 2 DABMe 2 ]PdMe(NCMe) )+SbF, 6 was weighed (50 mg, 0.067 mmol) into a 100 mL roundbottom flask inside a dry box. Cyclopentene (20 mL, 3400 equivalents per Pd; unpurified) and dichloromethane (20 mL) were added to the flask, and stirred under a nitrogen atmosphere to give a homogeneous solution. A precipitate had formed after 2 days. After 7 days, the solvent was evaporated and the solids were dried in a vacuum oven to give 0.39 g polymer (86 turnovers/Pd). A sample of the polymer was washed several times with petroleum ether and ether, then dried in a vacuum oven. The polymer was pressed at 290°C into a transparent, gray-brown, tough film.

DSC (0 to 300 0 C, 10°C/min, first heat): Tg 120°C, Tm (onset to end) 179 to 232°C, heat of fusion 18 J/g.

1H NMR (400 MHz, 120°C, ortho-dichlorobenzene-d 4 referenced to solvent peak at 7.280 0.905 (bs, 1H, cis -CH-CH 2 1.321 (bs, 2H, cis -CH-CH2-CH 2 1.724 and 1.764 (overlapping bs, 4H, trans -CH- CH2-CH 2 -CH- and -CH-CH2-CH 2 1.941 (bs, 1H, trans CH-CH2-CH-). The 1H NMR assignments are based upon 2D NMR correlation of the 1H and 13C NMR chemical shifts, and are consistent with a poly(cis-1,3-cyclopentylene) repeat unit.

-338-

O

3 .03/.s133s,33S Example 440 The complex ([(2,6-iPrPh) 2 DABAn)PdMe(OEt 2 }SbF 6

D

was weighed (50 mg, 0.054 mmol) into a 100 mL roundbottom flask inside a dry box. Cyclopentene (20 mL, 4200 equivalents per Pd; unpurified) and dichloromethane (20 mL) were added to the flask, and stirred under a nitrogen atmosphere to give a homogeneous solution. A precipitate had formed after 3 days. After 6 days, the solvents were evaporated and the solids were dried in a vacuum oven to give 0.20 g polymer (55 turnovers/Pd). A sample of the polymer was washed several times with petroleum ether and ether, then dried in a vacuum oven. DSC (0 to 300 0 C, 100 C/min, first heat): Tg 42 0 C, Tm (onset to end) 183 to 242 0 C, heat of fusion 18 J/g. 1 H NMR (400 MHz, CDC1 3 referenced to solvent peak at 7.240 ppm): 0.75 (bm, 1H, cis -CH-CH 2 1.20 (bs, 2H, cis -CH-

CH

2

-CH

2 1.59 and 1.68 (overlapping bs, 4H, trans

-CH-CH

2 -CH2-CH- and -CH-C 2

-CH-CH

2 1.83 (bs, 1H, trans -CH-CH2-CH-). The 1 H NMR assignments are based upon 2D NMR correlation of the IH and 13C NMR chemical shifts, and are consistent with a poly(cis-1,3cyclopentylene) repeat unit.

Example 441 The complex [(2,6-iPrPh) 2 DABMe2]PdMeCl was added (28 mg, 0.050 mmol) to a glass vial containing cyclopentene (3.40 g, 1000 equivalents per Pd; distilled twice from Na) inside a dry box. A solution of MMAO in heptane (1.47 mL, 1.7 M Al, 50 equivalents per Pd) was added with stirring to give a homogeneous solution. A precipitate began to form immediately.

After 2 days, the solids were collected by vacuum filtration, washed several times on the.filter with petroleum ether and ether, then dried in a vacuum oven to give 0.254 g polymer (75 turnovers/Pd). The polymer was pressed at 250°C into a transparent, gray-brown, tough film. DSC (0 to 300 0 C, 10 0 C/min, first heat): Tg 114 0 C, Tm (onset to end) 193 to 240°C, heat of 339- 03 1 /0 6 3,swI33 I sp,339 fusion 14 J/g. GPC (Dissolved in 1,2,4trichlorobenzene at 150 0 C, run in tetrachloroethylene at 100 0 C, polystyrene calibration): peak MW 154,000, Mn 70,200, Mw 171,000, M,/Mn 2.43.

Example 442 The complex iPrPh) 2 DABMe2]PdCH2CH 2

CH

2 C(O)OCH3)} SbF 6 D was weighed (42 mg, 0.050 mmol) into a glass vial inside a dry box.

Cyclopentene (3.40 g, 1000 equivalents per Pd; distilled twice from Na) and dichloromethane (4.4 mL) were added with stirring to give a homogeneous solution. After 1 day, the solids were collected by vacuum filtration, washed several times on the filter with petroleum ether and ether, then dried in a vacuum oven to give 1.605 g polymer (471 turnovers/Pd). The polymer was pressed at 250 0 C into a transparent, graybrown, tough film. TGA (25 to 600 0 C, nitrogen): Td (onset to end) 473 to 499, 97.06 weight loss. TGA (25 to 600 OC, 10 oC/min, air): Td 350*C, 5 weight loss. DSC (0 to 300 OC, 10 0 C/min, second heat): Tg 94 0 C, Tm (onset to end) 191 to 242 OC, heat of fusion 14 J/g. GPC (Dissolved in 1,2,4trichlorobenzene at 150 0 C, run in tetrachloroethylene at 100 OC, polystyrene calibration): peak MW 152,000, Mn 76,000, M, 136,000, MW/Mn 1.79.

Example 443 The complex [(2,6-iPrPh) 2 DABMe2]PdCI 2 was weighed (29 mg, 0.050 mmol) into a glass vial inside a dry box.

Cyclopentene was added (6.81 g, 2000 equivalents per Pd; distilled from polyphosphoric acid), and the vial was cooled to A solution of MMAO in heptane (1.00 mL, 1.7 M Al, 34 equivalents per Pd) was added with stirring to give a homogeneous solution. After 1 day, a copious precipitate had formed. After 2 days, the solids were collected by vacuum filtration, washed several times on the filter with ether and cyclohexane, then dried in a vacuum oven to give 1.774 g polymer (520 turnovers/Pd). The polymer was coated with 5000 340- 031 603.swI.33 Isp.340 ppm Irganox® 1010 by evaporating an acetone slurry and drying in a vacuum oven. The polymer was pressed at 290 0 C into a transparent, gray-brown, tough film. DSC to 330 0 C, 10°C/min, second heat): Tg 105 0 C, Tm (onset to end) 163 to 244°C, heat of fusion 21 J/g.

Example 444 The complex [(2,6-iPrPh)2DABMe 2 ]PdCl 2 was weighed (29 mg, 0.050 mmol) into a glass vial inside a dry box.- Cyclopentene was added (6.81 g, 2000 equivalents per Pd; distilled from polyphosphoric acid), and the vial was cooled to <01C. A solution of EtAlC12 in hexane (1.7 mL, 1.0 M, 34 equivalents per Pd) was added with stirring to give a homogeneous solution. After 4 days, the solids were collected by vacuum filtration, washed several times on the filter with ether and cyclohexane, then dried in a vacuum oven to give 1.427 g polymer (419 turnovers/Pd). The polymer was coated with 5000 ppm Irganox® 1010 by evaporating an acetone slurry and drying in a vacuum oven. The polymer was pressed at 290°C into a transparent, gray-brown, tough film. DSC to 330 0 C, 10OC/min, second heat): Tg 103 0 C, Tm (onset to end) 153 to 256°C, heat of fusion 23 J/g.

Example 445 The complex [(2,6-iPrPh) 2 DABMeZ]PdCl2 was weighed (29 mg, 0.050 mmol) into a glass vial inside a dry box.

Cyclopentene was added (6.81 g, 2000 equivalents per Pd; distilled from polyphosphoric acid), and the vial was cooled to A solution of EtAlCl 2 &Et 2 AICl in toluene (1.9 mL, 0.91 M, 68 equivalents Al per Pd) was added with stirring to give a homogeneous solution.

After 4 days, the solids were collected by vacuum filtration, washed several times on the filter with ether and cyclohexane, then dried in a vacuum oven to give 1.460 g polymer (429 turnovers/Pd). The polymer was coated with 5000 ppm Irganox® 1010 by evaporating an acetone slurry and drying in a vacuum oven. The polymer was pressed at 290 0 °C into a transparent, graybrown, tough film. DSC (25 to 330°C, 10 0 C/min, second 341 o03 0 6 /3,swl33llspa,341 heat): T9 101 0 C, Tm (onset to end) 161 to 258 0

C,

heat of fusion 22 J/g.

Example 446 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed (32 mg, 0.050 mmol) into a glass vial inside a dry box.

Cyclopentene was added (6.81 g, 2000 equivalents per Ni; treated with 5 A molecular sieves, and distilled from Na and Ph3CH), and the vial was cooled to

A

solution of EtAlCl 2 AEt 2 AlCl in toluene (1.9 mL, 0.91 M, 68 equivalents Al per Ni) was added with stirring to give a homogeneous solution. After 5 days, the solids were collected by vacuum filtration, washed several times on the filter with ether and cyclohexane, and dried in a vacuum oven to give 2.421 g polymer (711 turnovers/Ni). The polymer was coated with 5000 ppm Irganox® 1010 by evaporating an acetone slurry and drying in a vacuum oven. The polymer was pressed at 290 0 C into a transparent, brown, tough film. DSC to 330 0 C, 10OC/min, second heat): T 9 103°C, Tm (onset to end) 178 to 272°C, heat of fusion 22 J/g.

Example 447 The complex 2 ,4,6-MePh)2DABAn]NiBr 2 was weighed (128 mg, 0.202 mmol) into a glass bottle inside a dry box. Cyclopentene was added (27.1 g, 2000 equivalents per Ni; treated with polyphosphoric acid, and distilled from Na). A solution of EtAIC12 in hexane (6.8 mL, M, 34 equivalents Al per Ni) was added with stirring to give a homogeneous solution. After 1 day, additional cyclopentene was added (58 g, 6200 total equivalents per Ni) to the bottle containing a heavy slurry. After days, the solids were slurried with ether, collected by vacuum filtration, washed several times with ether and cyclohexane on the filter, and dried in a vacuum oven to give 36.584 g polymer (2660 turnovers/Ni). The polymer was washed with 50:50 aqueous HCl/MeOH, followed by several washings with 50:50 H 2 0/MeOH, and dried in a vacuum oven. A fine powder sample was obtained using a 60 mesh screen, and coated with 5000 342 03/06/03,swI3311 Ispa,342 ppm Irga. 1010 by evaporating an acetone slurry and drying in a vacuum oven. The fine powder was pressed at 290°C into a transparent, pale brown, tough film.

TGA (25 to 700°C, 10 0 C/min, nitrogen) Ta (onset to end) 478 to 510°C, 99.28 k weight loss. DSC (25 to 330 0 C, 10°C/min, second heat): T S 101°C, Tm (onset to end) 174 to 279°C, heat of fusion 25 J/g. DSC (330 to 25°C, 10 °C/min, first cool): Tc (onset to end) 247 to 142°C, heat of fusion 28 J/g; T. (peak) 223°C. DSC isothermal crystallizations were performed by heating samples to 330°C followed by rapid cooling to the specified temperatures, and measuring the exotherm half-times (min): 200 210 220 225 230 240 245 DSC thermal fractionation was performed by heating a sample to 330°C followed by stepwise isothermal equilibration at the specified temperatures, and times 290 280 270 260 250 240 230 220 210 200 190 180 170 160 150 140 130 120 110 DSC (25 to 330°C, thermal fractionation sample): Tg 100°C; Tn,, °C (heat of fusion, J/g) 128 139 146 156 166 176 187 197 207 216 226 237 248 258 269 279 283 total heat of fusion 34.6 J/g. DMA (-100 to 200°C, 1, 2, 3, 5, 10 Hz; pressed film): modulus (-100 2500 MPa, y relaxation -67 to -70°C (activation energy 11 kcal/mol), modulus (25°C) 1600 MPa, a relaxation 109 to 110°C (activation energy 139 kcal/mol).

RxaMpei 448 The complex [(2,4,6-MePh) 2 DABAnlNiBr 2 was weighed (32 mg, 0.050 mmol) into a glass bottle inside a dry box. Cyclopentene was added (34.1 g, 10,000 equivalents per Ni; high-purity synthetic material distilled from Na), and the vial was cooled to A 343- o3/06/03,swl 3 3311 sp.,343 solution of MMAO in heptane (2.7 mL, 1. 5 M Al, 100 equivalents Al per Ni) was added with stirring to give a homogeneous solution. After 3 days, a copious precipitate had formed. After 7 days, the reaction was quenched with 20 mL MeOH and 2 mL acetylacetone. The solids were washed several times with 3 mL aqueous HC1 in 30 mL MeOH by decanting the free liquids. The solids were collected by vacuum filtration, washed several times on the filter with methanol, and dried in a vacuum oven to give 14.365 g polymer (4200 turnovers/Ni). The polymer was coated with 5000 ppm Irganox® 1010 by evaporating an acetone slurry and drying in a vacuum oven. The polymer was pressed at 290°C into a transparent, colorless, tough film. DSC (0 to 320°C, 20°C/min, second heat) Tg 95°C, Tm (onset to end) 175 to 287 0 C, heat of fusion 20 J/g.

Example 449 The complex [(2,4,6-MePh) 2 DABAn]NiBr 2 was weighed (32 mg, 0.050 mmol) into a glass bottle inside a dry box. Cyclopentene was added (34.1 g, 10,000 equivalents per Ni; high-purity synthetic material distilled from Na), and the vial was cooled to A solution of EtAlCl 2 dEt 2 AlCl in toluene (2.8 mL, 0.91 M, 100 equivalents Al per Ni) was added with stirring to give a homogeneous solution. After 3 days, a precipitate had formed. After 7 days, the reaction was quenched with 20 mL MeOH and 2 mL acetylacetone. The solids were washed several times with 3 mL aqueous HC1 in 30 mL MeOH by decanting the free liquids. The solids were collected by vacuum filtration, washed several times on the filter with methanol, and dried in a vacuum oven to give 7.254 g polymer (2113 turnovers/Ni). The polymer was coated with 5000 ppm Irganox" .1010 by evaporating an acetone slurry and drying in a vacuum oven. The polymer was pressed at 290°C into a transparent, colorless, tough film. DSC (0 to 320 0 C, 20°C/min, second heat) Tg 94°C, Tm (onset to end) 189 to 274°C, heat of fusion 18 J/g.

344 03/06/03,swl331 Ips344 Bis(benzonitrile)palladium dichloride (0.385 g, 1.00 mmol) and (2,6-iPrPh) 2 DABMe 2 (0.405 g, 1.00 mmol) were weighed into a glass vial inside a dry box.

Dichloromethane (8 mL) was added to give a dark orange solution. Upon standing, the solution gradually lightened in color. Cyclohexane was added to precipitate an orange solid. The solids were collected by vacuum filtration, washed several times with cyclohexane, and dried under vacuum to give 0.463 g of the complex [(2,6-iPrPh)2 DABMe 2 ]PdC12. 'H NMR (300 MHz, CD 2 C12, referenced to solvent peak at 5.32 ppm): 1.19 12H, CH3-CHAr-CH 3 1.45 12H, CH3- CHAr-CH3), 2.07 6H, (CH 3 3.07 4H,

(CH

3 2 -CH-Ar), 7.27 4H, meta ArH), 7.38 2H, para ArH).

Example 4I51 A sample of polycyclopentene prepared in a similar fashion to Example 317 gave a transparent, brown, tough film when pressed at 2900C. DSC (25 to 330°C, second heat): T 9 98°C, Tm (onset to end) 174 to 284 heat of fusion 26 J/g. A 5 g sample that was molded at 280oC into a test specimen suitable for an apparatus that measures the response to changes in pressure, volume and temperature, and the data output was used to calculate the following physical properties. Specific gravity, g/cm 3 at temperature 1.033 1.010 (110°C), 0.887 (280), 0.853 (350). Bulk compression modulus, MPa, at temperature 3500 2300 (110), 1500 (170) The coefficient of linear thermal expansion was 0.00009 OCDI between 30 and 1100C.

Example 452 A solution of {[(2,6-i-PrPh)2DABMe2] PdCH 2

CH

2

CH

2 C(O)OCH3}+SbF6- (1.703 g) in 1.5 L CH2C12 was transferred under nitrogen to a nitrogen purged 1 gallon Hastalloy® autoclave. The autoclave was charged with 300 g of propylene and stirred for 24 h 345 0 3 /06/03,swl331lspa,345 while maintaining the tmperature at 25 0 C. The pressure was then vented. The polymer product was floating on the solvent. Most of the solvent was removed in vacuo, and the polymer was dissolved in minimal CHC1 3 and then reprecipitated by addition of excess acetone. The polymer was dried in vacuo at 60 0

°C

for three days to give 271 g of green rubber.

Quantitative 1 3 C NMR analysis, branching per i000 CH 2 Total methyls (365), Butyl and end of chains

CHCH

2

CH(CH

3 2 -(CH 2 )nCH(CH 3 2 nr2 Based on the total methyls, the fraction of 1, 3 -enchainment is 38%. Analysis of backbone carbons (per 1000 CH 2 6 (138), 84/7 (1.36).

Listed below are the 13 C NMR data upon which the above analysis is based.

Freq ppm 47.1728 46.7692 46.3285 45.8719 45.4684 45.2719 44.4754 39.1923 38.2791 38.1304 37.9074 37.6631 37.2809 35.5074 34.865 34.5889 34.2915 33.2455 32.9747 30.6013 30.134 30.0066 29.7518 29.3217 28-2013 27.9783 27.5376 27.373 27.1659 27.0438 13C NMR data TCB, 120C, 0.05M CrAcAc Intensity 14.6401 9.89618 13.3791 7.94399 11.1421 7.80142 7.11855 29.1488 14.2142 18.7602 14.9366 15.0761 39.5816 8.29039 9.75536 14.9541 24.0579 9.86797 19.2516 52.6926 55.0735 y 25.1831 7 144.066 6+ 12.2121 3B 4 51.5842 39.5566 33.189 35.5457 47.0796 42.1247 -346- 0 3 /6/03,swl331 isp,346 25.6315 21.6632 terminal i. hine of XXVIII 23.3589 15.3063 Methyl of XXVIII and XXIX, 2B 4 2BS+, 2EOC 23.0722 18.4837 Methyl of XXVIII and XXIX, 2B4, 2EOC 22.5306 77.0243 Methyl of XXVIII and XXIX, 2B 4 2EOC- 21.1129 7.78367 20.5554 26.9634 IB1 20.4386 30.3105

IB

1 20.0085 22.478

IB

1 19.743 46.6467 IB1 13.8812 9,03898 1B4+, 1EOC Example 453 A 250 mL Schlenk flask was charged with 10 mg of 2 ,6-i-PrPh)2DABH2]NiBr2 (1.7x10-5 mol), and 75 mL of dry toluene. The flask was cooled to 0 C and filled with propylene (1 atm) before addition of 1.5 mL of a MAO solution in toluene. After 45 min, acetone and water were added to quench the reaction. Solid polypropylene was recovered from the flask and washed with 6 M HC1, H20, and acetone. The resulting polymer was dried under high vacuum overnight to yield 1.2 g (2300 TO/h) polypropylene. Differential scanning calorimetry Tg -19 0 C. GPC (trichlorobenzene, 1350 polystyrene reference): Mn 32,500; Mw 60,600; Mw/Mn 1.86. Quantitative 13 C NMR analysis, branching per 1000 CH2: Total methyls (813), Based on the total methyls, the fraction of 1,3-enchainment is 7%.

Analysis of backbone carbons (per 1000 CH2): 8 6+/y Listed below are the 13 C NMR data upon which the above analysis is based.

13 C NMR data TCB, 120C, 0.05M CrAcAc Freq ppm Intensity 47.194 18.27 46.9922 21.3352 46.8276 35.7365 40.2011 27.2778 45.4153 8.55108 43.5356 2.71929 42.925 3.37998 -347- 03/6/ 0 3,sw13311 sp,347 41.5551 2.63256 38.826 3.03899 38.4012 10.2858 38.0561 8.50185 37.626 7.10732 37.4879 6.55335 37.2755 9.-25058 36.1021 4.48005 35.3057 14.5319 34.4986 11.1193 33.219 9.43548 32.9375 4.94953 .32.242 3.16177 30.8349 24.1766 30.5217 19.8151 30.0916 3.70031 28.1111 144 27.5217 13.9133 27.1394 3.83857 24.5005 6.94946 21.0439 5.25857 20.5342 40.8641 20.0191 60.4325 19.8758 63.0429 16.9236 6.47935 16.3926 5.92056 14.9006 10.6275 14.513 3.39891 Example 454 Preparation of (2-t-BuPh)2DABAn. A Schlenk tube was charged with 2-t-butylaniline (3.00 mL, 19.2 mmol) and acenaphthenequinone (1.71 g, 9.39 mmol). The reagents were partially dissolved in 50 mL of methanol (acenaphthenequinone was not completely soluble) and 1- 2 mL of formic acid was added. An orange solid formed and was collected via filtration after stirring overnight. The solid was crystallized from CH 2 C12 (3.51 g, 1H NMR (CDCl 3 250 MHz) 6 7.85 (d, 2H, J 8.C Hz, BIAn: Hp), 7.52 2H, Ar: Hm), 7.35 (dd, 2H, J 8.0, 7.3 Hz, BIAn: Hm), 7.21 4H, Ar: Hm and Hp), 6.92 2H, Ar: Ho), 6.81 2H, J 6.9 Hz, BIAn: Ho), 1.38 18H, C(CH 3 3 Example 455 Preparation of (2,5-t-BuPh)2DABAn. A Schlenk tube was charged with 2 ,5-di-t-butylaniline (2.00 g, 9.74 mmol) and acenaphthenequinone (0.88 g, 4.8 mmol). The 348 03/06 13 w331 lsp34 reagents were partially dissolved in 50 mL of methano (acenaphthenequinone was not completely soluble) and 1- 2 mL of formic acid was added. A solid was collected via filtration after stirring overnight. Attempted crystallization from ether and from CH2C12 yielded an orange/yellow powder (1.75 g, 66%. 1H NMR (CDC1 3 250 MHz) 6 7.85 2H, J 8.1 Hz, BIAn: Hp), 7.44 2H, J 8.4 Hz, Ar: Hm), 7.33 (dd, 2H, J 8.4, 7.3 Hz, BIAn: Hm), 7.20 (dd, 2H, J 8.1, 2.2 Hz, Ar: Hp), 6.99 2H, J 2.2 Hz, Ar: Ho), 6.86 2H, J 7.0 Hz, BIAn: Ho), 1.37, 1.27 18H each, C(CH3)3).

Example 456 Preparation of [(2-t-BuPh)2DABAn]NiBr2. A Schlenk tube was charged with 0.202 g (0.454 mmol) of (2-t- BuPh) 2 DABAn, which was then dissolved in 15 mL of CH2C12. This solution was cannulated onto a suspension of (DME)NiBr2 (0.135 g, 0.437 mmol) in 10 mL of CH2C12.

The reaction mixture was allowed to stir overnight resulting in a deep red solution. The solution was filtered and the solvent evaporated under vacuum. The residue was washed with ether (2x10 mL) and an orange/rust solid was isolated and dried under vacuum (0.18g, 62%).

Example 457 Preparation of [(2,5-t-BuPh) 2 DABAn]NiBr2. A Schlenk tube was charged with 0.559 g (1.00 mmol) of (2,5-t-BuPh)2DABAn, 0.310 g (1.00 mmol) of (DME)NiBr2 and 35 mL of CH2C12. The reaction mixture was allowed to stir overnight. The solution was filtered and the solvent evaporated under vacuum. The residue was washed with ether and resulted in an orange solid which was dried under vacuum (0.64 g, 83%).

Example 458 Preparation of highly chain-straightened polypropylene with a low Tg. The complex [(2-t-BuPh) 2 DABAn]NiBr2 (0.0133g, 2.0x10- 5 mol) was placed into a flame-dried 250 mL Schlenk flask which was then evacuated and backfilled with propylene, Freshly distilled toluene (100 -349- 006/03,swl331 Is,349 mL) was added via syringe and the resulting solution was stirred in a water bath at room temperature. Polymerization was initiated by addition of methylaluminoxane (MAO; mL 10% soln in toluene) and a propylene atmosphere was maintained throughout the course of the reaction. The reaction mixture was stirred for two hours at constant temperature followed by quenching with 6M HC1. Polymer was precipitated from the resulting solution with acetone, collected, washed with water and acetone, and dried under vacuum. Yield 1.41 g. DSC: T, -53.6 0 C, Tm -20.4 0 C (apparent Tm is a small shoulder on the Tg). quantitative 3 C NMR analysis, branching per 1000 CH 2 Total methyls (226), 2Butyl and end of chains CHCH 2

CH(CH

3 2

(CH

2 )nCH(CH3) 2 n>2 (12.1).

Based on the total methyls, the fraction of 1,3-enchainment is 53%. Analysis of backbone carbons (per 1000 CH 2 6 (254), 8+/y (1.96).

Example 459 Preparation of highly chained-straightened polypropylene with a low Tg. The complex [(2,5-t-BuPh) 2 DABAn]NiBr 2 (0.0155g, 2.0x10 5 mol) was placed into a flamedried 250 mL Schlenk flask which was then evacuated and back-filled with propylene.

Freshly distilled toluene (100 mL) was added via syringe and the resulting solution was stirred in a water bath at room temperature. Polymerization was initiated by addition of mL of a 10% MAO solution in toluene, and a propylene atmosphere was maintained throughout the course of the reaction. The reaction mixture was stirred for two hours at constant temperature followed by quenching with 6M HCI. Polymer was precipitated from the resulting solution with acetone, collected, washed with water and acetone, and dried under vacuum. Yield 0.75 g. DSC: Tg -53.0 0 C, Tm none observed. Quantitative 1 3

C

NMR analysis, branching per 1000 CH2: Total methyls (307), Butyl and end of chains

-CHCH

2

CH(CH

3 2

-(CH

2

)CH(CH

3 2 n.2 Based on the total metals, the fraction of 1,3-enchainment is 43%.

Example 460 Preparation of highly chain-straightened poly-l-hexene with a high Tm. A flamedried 250 mL Schlenk flask under a nitrogen atmosphere was charged with 40 mL of freshly distilled toluene, 0.0133 g of -350- 0 3 /0603,sw1331 tsp.,350 BuPh) 2 DABAn]NiBr 2 (2.0x10- 5 mol), 5.0 mL of 1-hexene, and 55 mL more toluene (100 mL total volume of liquid) Polymerization was initiated by addition of 2.0 mL of MAO (10% solution in toluene). The reaction mixture was stirred for 11.5 hours at room temperature followed by quenching with 6M HCI. Polymer was precipitated from the resulting solution with acetone, collected via filtration, washed with water and acetone, and dried under vacuum. Yield 1.84 g. DSC: Tg -44.8 0 C, Tm 46.0 C.

Example 461 Preparation of highly chain-straightened poly-lhexene with a high Tm. A flame-dried 250 mL Schlenk flask under a nitrogen atmosphere was charged with mL of freshly distilled toluene, 0.0155g of BuPh)2DABAn]NiBr 2 (2.0x10- 5 mol), 5.0 mL of 1-hexene, and 55 mL more toluene (100 mL total volume of liquid).

Polymerization was initiated by addition of 2.0 mL of MAO (10% solution in toluene). The reaction mixture was stirred for 11.5 hours at room temperature followed by quenching with 6M HC1. Polymer was precipitated from the resulting solution with acetone, collected via filtration, washed with water and acetone, and dried under vacuum. Yield 1.07 g. DSC: Tg -54.7°C, Tm 12.5 C.

Example 462 Preparation of [(2-t-BuPh)2DABAn]PdMe 2 from cyclooctadiene)PdMe2. The Pd(II) precursor cyclooctadiene)PdMe2 ((COD)PdMe 2 was prepared according reported procedures (Rudler-Chauvin, M.; Rudler, H. J. Organomet. Chem., 1977, 134, 115.) and was handled using Schlenk techniques at temperatures of C or below. A flame-dried Schlenk tube was charged with 0.056 g (0.229 mmol) of (COD)PdMe 2 and cooled to 40 C in a dry ice/isopropanol bath. The solid was dissolved in 10 mL of ether, and the diimine (2-t- BuPh)2DABAn (0.106 g, 0.238 mmol) was cannulated onto the stirring solution as a slurry in 15 mL of ether.

351 03 0 6 03 .swI33 Isp.351 The reaction was warmed to 0 C and stirring was continued for two hours. The reaction flask was stored at -30 C for several days and resulted in the formation of a green precipitate which was isolated via filtration. The supernatant was pumped dry under high vacuum and also resulted in a green solid. Both solids were determined to be [(2-t-BuPh) 2 DABAn]PdMe2 by 1 H NMR spectroscopy. Isolated yield 0.083 g (0.143 mmol, 62.4%).

Example 463 Preparation of [(2,5-t-BuPh)2 DABAn]PdMe2 from (1,5-cyclooctadiene)PdMe2. The Pd(II) precursor cyclooctadiene)PdMe2 ((COD)PdMe2) was prepared according reported procedures (Rudler-Chauvin,

M.;

Rudler, H. J. Organomet. Chem., 1977, 134, 115.) and was handled using Schlenk techniques at temperatures of 0 C or below. A flame-dried Schlenk tube was charged with 0.102 g (0.417 mmol) of (COD)PdMe2 and cooled to 0 C in a dry ice/isopropanol bath. The solid was dissolved in 10 mL of ether, and the diimine BuPh) 2 DABAn (0.234 g, 0.420 mmol) was cannulated onto the stirring solution as a slurry in 40 mL of ether.

The reaction was warmed to 0 C and stirring was continued for four hours. The reaction flask was stored at -30 0 C overnight. The resulting dark green solution was filtered and the solvent was pulled off under high vacuum to give a dark green powder.

Analysis by 1H NMR spectroscopy showed the solid to be consistent with the desired product, BuPh) 2 DABAn]PdMe2. Yield 0.256 g (0.370 mmol, 88.7%) Examp e 464 In a dry box, polymer from Example 469 (0.57 g), THF (10.10 g) and acetic anhydride (0.65 g) were placed in a 20 mL vial equipped with a stirring bar. After one hour at room temperature, the vial was removed from the dry box and the polymerization terminated by the addition of THF, water and ether. The organic phase 352- 03/DW03.sw1311 isp352 was separated, washed with water dried over anhydrous sodium sulfate, concentrated at reduced pressure and then dried under vacuum, affording 4.44 g of polymer. GPC analysis (PS STD.): Mn 17600, Mw 26000, PD 1.48.

Example 465i Preparation of CH 2 =CH (CH2) 2 CHICH2 (CF 2 2 0CF 2

CF

2 SO2F A mixture of 72 g of hexadiene, 127.8 g of

ICF

2

CF

2 0CF 2

CF

2

SO

2 F, 7.0 g of Cu powder and 180 mL of hexane was stirred at 90°C overnight. Solids were removed by filtration and washed with hexane. After removal of volatiles, residue was distilled to give 115.3 g of product, bp 80°C/210 Pa. 19 F NMR: +45 J Hz, IF), -82.7 (mn, 2F), -88.1 (dt, J 42.5 Hz, J 12.6 Hz, IF), -88.7 (dt, J 45.5 Hz, J 12.6 Hz, IF), -112.7 2F), -115.9 (ddd, J 2662.2 Hz, J 30.0 Hz, J 8.2 Hz, IF), -118.9 (ddd, J 262.2 Hz, J 26.8 Hz, J 7.4 Hz, IF).

Example 4Z66 Preparation of CH2=CH (0CH2)4 (CF 2 20CF 2

CF

2

SO

2

F

To a stirred solution of 100 g of

CH

2

=CH(CH

2 2

CHICH

2

(CF

2 2 0CF 2

CF

2

SO

2 F and 200 mL of ether was added 63 g of Bu 3 SnH at room temperature. After the addition was complete, the reaction mixture was refluxed for 4 hours and then cooled with ice water.

Excess of Bu 3 SnH was destroyed by addition of iodine.

After being diluted with 200 mL of ether, the reaction mixture was treated with a solution of 25 g of KF in 200 mL of water for 30 min. The solids were removed by filtration through a funnel with silica gel and washed with ether. The ether layer was separated and washed with water, aqueous NaCI solution and dried over MgSO 4 After removal of the ether, residue was.distilled to give 54.7 g of product, bp 72°C/1.3 kPa, and 12.2 g of starting material.

9F NMR: +45 IF), -82.7 2F), -88.0 (m, 2F) -112.6 2F), -118.6 J 18.4 Hz, 2F) 353 0 3 6 /03,sw3311sp,353 Example 467 Preparation of CH 2 =CH (CH2 4

(CF

2 4

OCF

2

CF

2

SO

2

F

A mixture of 24 g of hexadiene, 53 g of

I(CF

2 4

OCF

2

CF

2

SO

2 F, 3.0 g of Cu powder and 60 mL of hexane was stirred at 70°C overnight. Solids were removed by filtration and washed with hexane. After removal of volatiles, residue was distilled to give 115.3 g of adduct, CH 2

=CH(CH

2 2

CHICH

2

(CF

2 4

OCF

2

CF

2

SO

2 F, bp- 74°C/9 Pa. 9 FNMR: +45.5 IF), -82.4 2F), -83.5 2F), -112.2 (dm, J 270 Hz, IF), -112.6 2F), 115.2 (dm, J 2-70 Hz, IF), -124.3 2F), -125.5 (m, 2F).

To stirred solution of 47 g of CH1 2

=CH(CH

2 2

CHICH

2

(CF

2 4

OCF

2

CF

2

SO

2 F and 150 mL of ether was added 27 g of Bu 3 SnH at room temperature. After the addition was complete, the reaction mixture was stirred overnight. Excess of Bu 3 SnH was destroyed by addition of iodine. After being diluted with 150 mL of ether, the reaction mixture was treated with a solution of g of KF in 100 mL of water for 30 min. The solids were removed by filtration through a funnel with silica gel and washed with ether. The ether layer was separated and washed with water, aqueous NaCI solution and dried over MgSO4. After removal of the ether, residue was distilled to give 24.7 g of product, bp 103°C/1.3 kPa.

1F NMR: +45.4 IF), -82.4 2F), -83.5 2F), .112.6 J 2.6 Hz, 2F), -115.1 J 15 Hz, 2F), 124.3 2F), -125.7 J 14 Hz, 2F). HRMS: calcd for C 12 HIiF 13 SO3: 482.0221. Found: 482.0266.

Example 468 Hydrolysis of Copolymer Copolymer containing 8.5 molt of comonomer (1.5 g) was dissolved in 30 mL of THF at room temperature. KOH g) in 5 mL of ethanol and 3 mL of water was added and the resulting mixture was stirred at room temperature for six hours. After removal of the solvent, residue was treated with diluted HCl for hours and then filtered to give solids which were -354- 04O06/03,sw1331 I spa,34 washed with water, HCi and dried under full vacuum at for two days to give 1.4 g solid.

Example 469Q Hydrolysis of Copolymer A mixture of 10.6 g of copolymer5.0 g of KOH, 2 mL of water, 30 mL of ethanol and 30 mL of THF was stirred at room temperature overnight and at 60 to for 5 hours. After removal of a half of solvents, residue Was treated with Conc. HCl to give rubbery material, which was poured into a blender and blended with water for 30 min. Filtration gave solids, which were washed with conc. HCI, and water and dried under vacuum at 60°C overnight to give 8.7 g of dark rubbery material. 19F NMR(THF): -82.8 (br, 2F), -88.5 (br, 2F), -118.3 (br, 2F), -118.5 (br, 2F).

Example 470 Hydrolysis of Homopolymer A solution of 2.0 g of KOH in 25 mL of ethanol and 2 mL of waster was added to a flask with 3.0 g of homopolymer. The resulting heterogeneous mixture was stirred at room temperature overnight and heated to for 2hours. After removal of one-half of liquid, the reaction mixture treated with 40 mL of conc. HCl Sfor 30 min. Filtration gave white solids which were washed with conc. HCl, and distilled water and dried under vacuum at 60-70°C for 24 hours to give 2.9 g of white powder.

Example 471 1-Octadecene (8 mL, 8 vol was added to a suspension of [(2,6-i-PrPh) 2 DABAn]NiBr 2 (12 mg, 1.7x10mol) in 100 mL of dry toluene. The flask was cooled to -I°C using an Endocal® refrigerated circulating bath and 2.5 mL of a 7% MMAO solution in heptane was added.

After stirring the reaction for 40 min, the flask was filled with propylene (1 atm) and stirred for minutes. The propylene was removed in vacuo and the reaction allowed to continue for an additional 40 min.

Acetone and water were added to quench the -355- 03/06/03,swl33 I spM,355 polymei. :ation and precipitate the polymer. The resulting triblock polymer was dried under high vacuum overnight to yield 650 mg of a rubbery solid. GPC (trichlorobenzene, 135 polystyrene reference): Mn 60,100; Mw 65,500; Mw/Mn 1.09. DSC'analysis: Two melt transitions were observed. Tm 8 0 C (32 Tm 37 0 C (6.5 1 H-NMR analysis (CDC13): signals attributable to repeat units of propylene and 1octadecene were observed.

Example 472 Preparation of (2-i-Pr-6-MePh)2DABAn A Schlenk tube was charged with 2-isopropyl-6methylaniline (5.00 mL, 30.5 mmol) and acenaphthenequinone (2.64 g, 14.5 mmol). The reagents were partially dissolved in 50 mL of methanol (acenaphthenequinone was not completely soluble) and 1- 2 mL of formic acid was added. An orange/yellow solid was collected via filtration after stirring overnight, and was washed with methanol and dried under vacuum.

Example 473 Preparation of (2-i-Pr-6-MePh)2DABMe2 A Schlenk tube was charged with 2-isopropyl-6methylaniline (5.00 mL, 30.5 mmol) and 2,3-butanedione (1.31 mL, 14.9 mmol). Methanol (5 mL) and one drop of concentrated HC1 were added and the mixture was heated' to reflux with stirring for 30 minutes. The methanol and remaining dione were removed under vacuum to give a dark, oily residue. The oil was chromatographed on a silica gel column using 10% ethyl acetate: 90% hexane as the eluent. The fractions containing the pure .diimine were combined and concentrated. The remaining solvents were removed under vacuum to give a pale yellow powder (0.9217 g, 17.75 Example 474 Preparation of [(2-i-Pr-6-MePh) 2 DABAn]NiBr2 Under inert conditions, a flame-dried Schlenk tube was charged with 0.50 g (1.13 mmol) of (2-i-Pr-6- MePh)2DABAn, 0.34 g (1.10 mmol) of (DME)NiBr2 and 25 mL -356- 03/0603.sw1331 Isp.356 of CH2C12. The reaction mixture'was allc ed to stir overnight. The solution was filtered and the solvent removed under vacuum. The residue was washed with ether (4 x 10 mL) to give an orange/yellow powder which was dried under vacuum overnight (0.68 g, 94%).

Exampl 475 Preparation of [(2-i-Pr-6-MePh)2DABMe 2 ]NiBr 2 Under inert conditions, a flame-dried Schlenk tubewas charged with 0.3040 g (0.8722 mmol) of 2 -i-Pr-6- MePh)2DABMe2, 0.2640 g (0.8533 mmol) of (DME)NiBr 2 and mL of CH2C1 2 The reaction mixture was allowed to stir overnight. A solid was collected via filtration and washed with ether (2 x 10 mL). Upon sitting, more solid precipitated from the supernatant. This precipitate was isolated via filtration, washed with ether, and combined with the originally isolated product. The combined yellow/orange solids were dried under vacuum overnight (0.68 g, 94%).

Example 476 Under a nitrogen atmosphere, the complex [(2-i-Pr- 6-MePh)2DABAn]NiBr 2 (0.0099 g, 1.5xl0- 5 mol) was placed into a flame-dried 250 mL Schlenk flask which was then evacuated and back-filled with propylene. Freshly distilled toluene (100 mL) was added via syringe and the resulting solution was stirred for five minutes at room temperature. Polymerization was initiated with addition of methylaluminoxane (MAO; 1.5 mL 10% solution in toluene) and a propylene atmosphere was maintained throughout the course of the reaction. The reaction was stirred for two hours at constant temperature, at which point the polymerization was by quenched with 6M HCI. Polymer was precipitated from the resulting solution with acetone, washed with water and acetone, and dried under vacuum. Yield 3.09 g. DSC: Tg 31.2°C. GPC: Mn 142,000; Mw 260,000; Mw/Mn 1.83.

-357- 03/06/03,sw13311spa.357 -ample 477 Under a nitrogen atmosphere, the complex [(2-i-Pr- 6-MePh)2 DABMe2]NiBr2 (0.0094 g, 1.5x10- 5 mol) was placed into a flame-dried 250 mL Schlenk flask which was then evacuated and back-filled with propylene.

Freshly distilled toluene (100 mL) was added via syringe and the resulting solution was stirred for five min at room temperature. Polymerization was initiated with addition of methylaluminoxane (MAO; 1.5 mL solution in toluene) and a propylene atmosphere was maintained throughout the course of the reaction. The reaction was stirred for two hours at constant temperature, at which point the polymerization was by quenched with 6M HC1. Polymer was precipitated from the resulting solution with acetone, washed with water and acetone, and dried under vacuum. Yield 1.09 g.

DSC: Tg -36.1 C. GPC: Mn 95,300; Mw 141,000; Mw/Mn 1.48.

Example 478 Under a nitrogen atmosphere, a flame-dried 250 mL Schlenk flask was charged with 40 mL of freshly distilled toluene, 0.0133 g (2.0x10- 5 mol) of [(2-i-Pr- 6-MePh)2 DABAn]NiBr2, 10.0 mL of 1-hexene, and 50 mL more toluene (100 mL total volume of liquid). The mixture was stirred in a room temperature water bath for 10 minutes and polymerization was initiated with addition of 2.0 mL of MAO (10% solution in toluene).

The reaction mixture was stirred for one hour at room temperature and was quenched with 6M HC1. Polymer was precipitated from the resulting solution with acetone, collected via filtration, washed with water and acetone, and dried under vacuum. Yield 3.23 g. DSC: Tg -58.0 C, Tm -16.50C.

Example 479 Under a nitrogen atmosphere, a flame-dried 250 mL Schlenk flask was charged with 40 mL of freshly distilled toluene, 0.0125 g (2.0x10- 5 mol) of [(2-i-Pr- 6-MePh) 2 DABMe2]NiBr2, 10.0 mL of 1-hexene, and 50 mL 35 0 3 10 6 /03.sw 33 more toluene (100 mL totZ L volume of liquid). Th'e! mixture was stirred in a room temperature water bath for 10 min and polymerization was initiated with addition of 2.0 mL of MAO (10% solution in toluene).

The reaction mixture was stirred for'22 h at room temperature and was quenched with 6M HC1. Polymer was precipitated from the resulting solution with acetone, collected via filtration, washed with water and acetone, and dried under vacuum. Yield 2.10 g. DSC: Tg -56.4°C, Tm 0.2°C.

Example 4i Under a nitrogen atmosphere, a flame-dried 250 mL Schlenk flask was charged with 40 mL of freshly distilled toluene, 0.0133 g (2.0x10- 5 mol) of BuPh)2DABAn]NiBr 2 10.0 mL of 1-hexene, and 50 mL more toluene (100 mL total volume of liquid). The mixture was stirred in an isopropanol bath maintained at approximately -10 to -12iC, and polymerization was initiated with addition of 2.5 mL of MMAO (7.2% solution in heptane). The reaction mixture was stirred for two hours at constant temperature and was quenched with acetone/water/6M HC1. The mixture was added to acetone to precipitate the polymer. After settling overnight the polymer was collected via filtration, washed with water and acetone, and dried under vacuum.

Yield 0.35 g. DSC: (two broad melt transitions observed) Tm(1) 34.3°C, Tm(2) 66.4°C. Based on the H NMR spectrum, the polymer contains 41 methyl branches/1000 carbons (theoretical 55.5 Me/1000 C), indicating a high degree of chain straightening.

Example tAa Under a nitrogen atmosphere, a flame-dried 250 mL Schlenk flask was charged with 25 mL of freshly distilled toluene, 0.0133 g (2.0xi0- 5 mol) of t(2-t- BuPh)2DABAn]NiBr 2 63 mL more toluene, and 12.0 mL of 1-octadecene (100 mL total volume of liquid). The flask was cooled to -10°C in a C02/isopropanol bath and stirred at this temperature for several minutes. The 359 031

W

03 ,sw13311i.pa.359 0 temperature was maintained at approximau ly -10 C throughout the reaction by continually adding dry ice as needed. Polymerization of 1-octadecene was initiated with addition of 2.5 mL of MMAO (7.2% solution in heptane). At 2 h, 10 min the reaction flask was twice evacuated and back-filled with propylene. The polymerization was stirred under one atmosphere of propylene for 20 min. The propylene was removed by repeatedly evacuating the flask and backfilling with argon until propylene evolution from the solution was no longer apparent. The polymerization was allowed to continue stirring in the presence of the remaining 1-octadecene until a total elapsed time of five hours was reached. The reaction was quenched with acetone/water/6M HC1. Polymer was precipitated in methanol/acetone, collected via filtration, washed with water and acetone, and dried under vacuum. Yield C O 1.03 g. DSC: Tg 8.0 C, Tm 53.3 C. GPC: Mn 55,500; Mw 68,600; Mw/Mn 1.24. It is believed a block copolymer was formed.

Example 482 Preparation of [(2-t-BuPh)2DABAn]PdMe(Et2O)BAF- Under inert conditions, a flame-dried Schlenk tube was charged with 0.1978 g (3.404xl0- 4 mol) of BuPh)2DABAn]PdMe2 and 0.3451 g (3.408xl0 4 mol) of H+(Et 2 0) 2 BAF-. The Schlenk tube was cooled to -78 C and 10 mL of ether was added. The Schlenk tube was transferred to an ice water bath and the reaction was stirred until the solids were dissolved and the color of the solution became deep red. The ether was then removed under vacuum to give a red, glassy solid that was crushed into a powder (yield was quantitative).

Example 483 Preparation of [(2,5-t-BuPh)2DABAn]PdMe(Et20)BAF- Following the procedure of Example 482, a red solid with the 'structure BuPh)2DABAn)PdMe(Et20)BAF~ was obtained (quantitative yield).

-360- 0 3 0 6 /03,sw1331 Isp,360 Example 4A4 Preparation of [(2-t-BuPh)2DABMe 2 ]PdMe(NCMe)BAF- Under inert conditions, a flame-dried Schlenk tube was charged with 0.1002 g (0.378 mmol) of (COD)PdMeCl and 0.3348 g (0.378 mmol) of NaBAF. 'The Schlenk tube was cooled to -30 0 C and 25 mL of CH2C1 2 and 0.10 mL of NCMe were added via syringe. The reaction was stirred for two h at -20 to -30 C. The resulting colorless solution was filtered into another cooled Schlenk tube, 20 mL of hexane was added, and the solvents were removed under vacuum to give a white powder [isolated (COD)PdMe(NCMe)BAF-]. This cationic precursor was combined with 0.138 g (0.396 mmol) of (2-t-BuPh) 2 DABMe 2 in 50 mL of NCMe. The reaction mixture was stirred overnight at room temperature. The solution was filtered and extracted with hexane (3 x 10 mL), and the solvents were removed under vacuum. The resulting yellow oil was dissolved in CH2C12/hexane and the solvents were removed under vacuum to give a glassy solid that was crushed into a powder. Two isomers were observed in solution by 1 H NMR spectroscopy. These two isomers arise from the coordination of the unsymmetrically substituted ligand in either the cis or trans fashion in regard to the t-butyl groups relative to the square plane of the complex.

Example 485 Polymerization of ethylene with BuPh)2DABAn]PdMe(Et20)BAF- A flame-dried 250 mL Schlenk flask was charged with 0.1505 g (1.001xl0 4 mol) of BuPh)2DABAn]PdMe(Et20)BAF- in the glove box. The flask was twice evacuated and back-filled with ethylene and then cooled to -60°C. The solid was dissolved in 100 mL of CH2Cl2 and the flask was allowed to warm to room temperature with stirring under an atmosphere of ethylene. After stirring for 23 h the polymerization was quenched with methanol. The solvent was removed under reduced pressure and the polymer was dissolved in 361- 03/06/03.w331 spa,361 petroleum ether and filtered through silica gel. The filtrate was concentrated and the remaining solvent was removed under vacuum to give a clear, colorless, viscous liquid. Yield 0.2824 g. 1 H NMR analysis: 125 Me/1000 CH2.

A flame-dried 250 mL Schlenk flask was charged with 0.1621 g (1.003x10 4 mol) of BuPh) 2 DASAn]PdMe(Et2O)BAF- in the glove box. The flask was twice evacuated and back-filled with ethylene and then cooled to -60 0 C. The solid was dissolved in 100 mL of CH2C12 and the flask was allowed to warm to room temperature with stirring under an atmosphere of ethylene. After stirring for 23 h the polymerization was quenched with methanol. The solvent was removed under reduced pressure and the polymer was dissolved in petroleum ether and filtered through silica gel. The filtrate was concentrated and the remaining solvent was removed under vacuum to give a clear, colorless, viscous liquid. Yield 0.2809 g. IH NMR analysis: 136 Me/1000 CH 2 Example 487 A flame-dried 250 mL Schlenk flask was charged with 0.1384 g (1.007x10 4 mol) of BuPh)2DABMe2]PdMe(NCMe)BAF- in the glove box. The flask was twice evacuated and back-filled with ethylene and then cooled to -60 0 C. The solid was dissolved in 100 mL of CH2C12 and the flask was allowed to warm to room temperature with stirring under an atmosphere of ethylene. After stirring for 23 h the polymerization was quenched with methanol. The solvent was removed under reduced pressure and the polymer was dissolved in petroleum ether-and filtered through silica gel. The filtrate was concentrated and the remaining solvent was removed under vacuum to give a clear, colorless, viscous liquid. Yield 2.40 g. IH NMR analysis: 123 Me/1000 CH 2 3 6 2 03 A I3,sw 33 11 ,M 362 Example 48R Under inert conditions, a Schlenk tube was charged with 0.0142 g (1.02x10 5 mol) of BuPh)2DABAn]PdMe(Et20)BAF-. The Schlenk tube was cooled to -78 0 C and the solid was dissolved in 30 mL of CH2C12. A 300 mL autoclave was charged with 70 mL of CH2C12 under an ethylene atmosphere. The cold catalyst solution was quickly transferred via cannula into the Parr® reactor and the reactor was pressurized to 172 kPa (absolute). The polymerization was stirred for h and the ethylene pressure was released. The red/orange solution was transferred and the solvent was removed under vacuum. A small amount of polyethylene remained after drying under vacuum overnight. Yield 0.17 g. 1 H NMR analysis: 120 Me/1000 CH 2 Example 489 Following the procedure described in Example 488, 1.68 g of polyethylene was produced using 0.0140 g (1.02x10 s mol) of [(2-t-BuPh)2DABMe2]PdMe(NCMe)BAF-.

Yield 1.68 g. IH NMR analysis: 114 Me/1000 CH 2 Example 490 Under nitrogen, Ni(COD)2 (0.017 g, 0.062 mmol) and (2,4,6-MePh) 2 DABAn (0.026 g, 0.062 mmol) were dissolved in 2.00 g of cyclopentene to give a purple solution.

The solution was then exposed to air for several seconds. The resulting dark red-brown solution was then put back under nitrogen, and EtAlCl 2 (1 M solution in toluene, 3.0 mL, 3.0 mmol) was added. A cranberryred solution formed instantly. The reaction mixture was stirred at room temperature for 3 days, during which time polycyclopentene precipitated. The reaction was then quenched by the addition of methanol followed by several drops of concentrated HC1. The reaction mixture was filtered, and the product polymer washed with methanol and dried to afford 0.92 g of polycyclopentene as an off-white powder. Thermal gravimetric analysis of this sample showed a weight loss starting at 141°C: the sample lost 18% of its 363 o 3 0 6 3 ,swl33Ilspa.363 weight between 141 and 470 0 C, and the remaining material decomposed between 470 and 496°C.

Example 491 Under a nitrogen atmosphere, Ni(COD) 2 (0.017 g, 0.06 mmol) and MeC(=N-2,6-C6H 3 -iPr 2 )CH=C(NH-C6H3-iPr2)Me (0.025 g, 0.06 mmol) were dissolved in benzene mL). To the resulting solution was added HBAF'(Et20) 2 (0.060 g, 0.06 mmol). The resulting solution was immediately frozen inside a 40 mL shaker tube glass insert. The glass insert was transferred to a shaker tube, and its contents allowed to thaw under an ethylene atmosphere. The reaction mixture was agitated under 6.9 MPa C2H4- for 40 h at ambient temperature.

The final reaction mixture contained polyethylene, which was washed with methanol and dried; yield of polymer 1.37 g. Branching per 1000 CH 2 's was determined by 13C NMR (C 6

D

3 C1 3 Total methyls (10.2), Methyl Ethyl Propyl Butyl Am and end of chains Bu and end of chains Example 492 Under a nitrogen atmosphere, Ni(COD) 2 (0.017 g, 0.06 mmol) and the ligand shown below (0.025 g, 0.06 mmol) were dissolved in benzene (5.0 mL). To the resulting solution was added HBAF'(Et20)2 (0.060 g, 0.06 mmol). The resulting solution was immediately frozen inside a 40 mL shaker tube glass insert. The glass insert was transferred to a shaker tube, and its contents allowed to thaw under an ethylene atmosphere.

The reaction mixture was agitated under 6.9 MPa C 2

H

4 for 18 h at ambient temperature. The final reaction mixture contained polyethylene, which was washed with methanol and dried; yield of polymer 11.0 g.

H H N N 364 0oJ"3owoJ,13311 spa.364 Example 493 {(2.6-i-PrPh) 2 DABMelPd -CHEtPh) BAF In a nitrogen-filled drybox, 25 mL of Et20 was added to a flask containing rPh) DABMel PdMeCl (402 mg, 0.716 mmol) and NaBAF (633 mg, 0.714 mmol) to yield an orange solution. Styrene (110 AL, 0.960 mmol, 1.35 equiv) was dissolved in -10 mL of Et20 and the resulting solution was added to the reaction mixture, which was then stirred for 3 h. Next, the solution was filtered and the solvent was removed in vacuo: The resulting orange powder (0.93 g, 87%) was washed with hexane and dried in vacuo. 1 H NMR (CD 2 C1 2 300 MHz, rt) 5 7.76 8, BAF: Ho), 7.59 4, BAF: Hp), 7.46 7.17 9, Haryl), 6.29 1, J 7.33, Haryl), 5.65 1, J 6.59, Haryi), 3.33, 3.13, 2.37 and 1.93 (septet, 1 each, J 6.97 6.72, CHMe 2 C'IMe 2 Me 2 C" Me 2 3.17 (dd, 1, J 11.36, 3.66, CHEtPh), 2.22 and 2.17 3 each, 1.52, 1.45, 1.26, 1.26, 1.19, 1.15, 0.94 and 0.73 3 each, J 6.97 6.59, CHMeMe', C'HMeMe', C''HMeMe', C'"'HMeMe'), 0.88 3, J 0.88, CH(CH 2

CH

3 1.13 and -0.06 1 each, CH(CHH'CH 3 13 C NMR (CD 2 C1 2 MHz, rt) 6 176.6 and 174.0 162.2 JCB 49.3, BAF: Cipso), 142.8 and 142.4 (Ar, Ar': Cipso), 138.2, 137.3, 137.1, and 136.9 (Ar, Ar': Co), 135.2 (BAF: Co,Co'), 134.6 and 132.2 (Ph: Co, Cm, or Cp)), 129.4 (BAF: Cm), 129.0 and 128.5 (Ar, Ar': Cp), 125.1, 125.1, 124.9 and 124.7 (Ar, Ar': Cm), 125.1 JCF 272.5, BAF: CF 3 120.2 (Ph: Cipso) and 120.0 (Ph: Co,

C

m or Cp), 117.9 (BAF: Cp), 103.0 and 88.6 (Ph: Co' and 69.1(CHEtPh), 29.9, 29.7, 29.12 and 29.09 (CHMe 2 C'HMe 2 C"HMe 2 C' 'HMe 2 24.4, 24.3, 23.5, 23.4, 23.1, 23.0, 22.9,.and 22.7 (CHMeMe', C'HMeMe', C''HMeMe', C'-'HMeMe'), 20.8, 20.65, and 20.61 CH(CH2CH 3 13.1 (CH(CH 2 CH3)Ph).

365 03 /06/03.sw331 lspa,365 Example 494 If (2.6-i-PrPh)ZDABH1 Pd(n4-CHEt -t-Bu)1)BAF t-Butylstyrene (230 pL, 1.26 mmol, 1.10 equiv) was added via microliter syringe to a mixture of U.2.6-i- PrPhE 2 DfAB2IPdMeC1 (611 mg, 1.15 mmol) and NaBAF (1.01 g, 1.14 mmol) dissolved in 25 mL of Et 2 O. An additional 25 mL of Et20 was added to the reaction mixture, which was then stirred for -12 h. The resulting deep red solution was filtered, and the solvent was removed in vacuo to yield a sticky red solid. The solid was washed with 150 mL of hexane and the product was dried in vacuo. A dull orange powder (1.59 g, 91.7%) was obtained: 1 H NMR (CD 2 C1 2 400 MHz, rt) 8 8.34 and 8.16 1 each, 7.72 8, BAF: Ho), 7.56 4, BAF: Hp), 7.5 7.1 8, Hayl), 6.88 (dd, 1, J 7.1, 1.9, Haryl), 6.11 (dd, 1, J 7.3, 2.0, Haryl), 3.49, 3.37, 2.64 and 2.44 (septet, 1 each, J 6.6 6.9, ClMe 2 C'RMe 2 C"HMe 2 and C'''IMe 2 3.24 (dd, 1, 3 11.3, 4.1, CHEt(4-CsH 4 -t- 1.52, 1.48, 1.24, 1.24, 1.19, 1.18, 1.0 and 0.70 3 each, J 6.8 6.9, CHMeMe', C'HMeMe', C"'HMeMe', and C"'IIHMeMe'), 1.42 and 0.25 1 each,

CH(CHH'CH

3 (4-CsH 4 0.98 9, t-Bu), 0.87 (t, 3, J 7.4, CH(CH 2

CH

3 (4-C 6 H4-t-Bu); 13 C NMR (CD 2 C1 2 100 MHIz, rt) 8 165.0 (JaH 165, 163.3 (JH 165, 162.2 JC 49.9, BAF: Cipso), 157.0 (CsH 4 -t-Bu: Cp), 144.9 and 144.6 (Ar, Ar': Cipso), 139.0, 138.4, 138.2 and 137.4 (Ar, Ar': Co, CO), 135.2 (BAF: Co), 133.3, 129.8, 129.6 and 129.2 (Ar, Ar': Cp;

C

6

H

4 -t-Bu: Co, 129.3 BAF: Cs), 125.0 JCF= 272, BAF: CF 3 124.7, 124.64, 124.55, and 124.3 (Ar, Ar': Cm, 117.9 (BAF: 119.1, 116.4 and 94.9 (CgH 4 -t-Bu: Cm', Cipso, 68.5 (CHEt), 36.2 (CMe 3 30.2 (CMe3), 30.1, 29.9, 28.80 and 28.77 (CHMe 2 C'HMe 2 C''HMe 2 and C'"'HMe 2 25.0, 24.8, 24.1, 22.8, 22.7, 22.45, 22.36, and 22.1 (CHMeMe', C'HMeMe', C'HMeMe' and C"''HMeMe'), 21.7 (C4(CH 2

CH

3 13.2

(CH(CH

2 CHb)). Anal. Calcd for (C 71 H6,BF2 4

N

2 Pd): C, -366- 0 3 10 6 3.Sw33 Ispa366 56.05; H, 4.44; N, 1.84. Found: C, 56.24; H, 4.22; N; 1.59.

Example 495 I ((2.6-i-PrPh) 2 DABMePd 3 -CHEtC 6 F) }BAF A solution of H 2

C=CHC

6

F

5 (138 mg, 0.712 mmol) in mL of Et20 was added to a mixture of I12.6-i- PrPhj 2 DABMealPdMeCl (401 mg, 0.713 mmol) and NaBAF (635 mg, 0.716 mmol) dissolved in 25 mL of Et 2 0. After being stirred for 2 h, the reaction mixture was filtered and the solvent was removed in vacuo. An orange powder (937 mg, 83.0%) was obtained.

Example 496 (2.6-i-PrPh) 2

DABH

2 LNi [3-CHEt(4-C 6

H

4 -t-Bu) ]}BAF In the drybox, f 2.6-i-PrPh) 2 DABMe 2 lNiMe(OEt 2

BAF

(22.4 mg, 0.0161 mmol) was placed in an NMR tube. The tube was sealed with a septum and Parafilm®, removed from the drybox, and cooled to -78 0 C. CD 2 Cl 2 (700 pL) and H 2 C=CH(4-C 6

H

4 -t-Bu) (15 L, 5.10 equiv) were then added via gastight microliter syringe to the cold tube in sequential additions. The septum was sealed with a small amount of grease and more Parafilm, the tube was shaken briefly and then transferred to the cold (-78 0

C)

NMR probe. Insertion of t-butylstyrene was observed at -78C and was complete upon warming to -50°C to yield the n-benzyl complex: 1 H NMR (CD 2 C12, 400 MHz, -50;C) 6 8.43 and 8.18 1 each, 7.76 8, BAF: Ho), 7.58 4, BAF: Hp), 7.5 7.1 8, Haryl) 6.80 1, J 7.3, Haryl), 6.15 1, J 7.7, Haryl), 3.72, 3.18, 2.68 and 2.50 (septet, 1 each, J 6.5 6.7, CHMe 2 C'HMe 2 C''HMe 2 and C HMe 2 2.56 (dd, 1, J 11.5, 3.9, CHEt), 1.6 0.8 (CHMeMe', C'HMeMe', C''HMeMe', C ''HMeMe', and CH(CHH'CH 3 0.94 9, CMe 3 0.72 3, J 7.3, CH(CH 2

CH

3 -0.04 1, CH(CHH'CH3)).

367 0/ 00 3 .wv 133 1, sp 3 67 Examples 497-515 General procedure for the Synthesis of 5-Allyl Tyne Nickel compounds A mixture of one equiv. of the appropriate adiimine, one equiv of NaBAF, and 0.5 egjuiv of ((allyl)Ni(P-X)]2 (X Cl or Br) was dissolved in Et 2

O.

The reaction mixture was stirred for -2 h before being filtered. The solvent was removed in vacuc to yield the desired product, generally as a red or purple powder. (The [(allyl)Ni precursors were synthesized according to the procedures published in the following reference: Wilke, Bogdanovic,

B.;

Hardt, Heimbach, Keim, Kroner,

M.;

Qberkirch, Tanaka, steinrucke, Walter,

D.;

Zimmerman, H. Angew. Chem. Int. Ed. Engl. 1966, 151-164.) The following compounds were synthesized according to the above general procedure.

Pxample 497 (t(2,4,6-MePh) 2 DABMe 2 Ni (l 3 -C315) }BAF Exaplne 498 f(26-i-Prhl DA Me Ni (11 3 -CHs)}BAF Example !199 r PrPh7pABMazWi (1 1 3

-H

2 CCHCHM8)

)BAF

Exampie .{fiz2.6-i-PrL z DABtiNi (qi-H 2 CCHCHPh)

}BAF

Example Ia1 L -i -BprZbhLDAB1a'ZjNi (r 1 3

-H

2 CCHCMe 2

}BAF

Example 502 Wi=(2,r BbIDABAflINi (T1 3

-C

3

H

5

}BAF

Example 503 wz2.6z -biz-ABBANiNi (1-H 2 CCHCHh) }BAF Examnle 504 6 i prpUDABAjNi -q 3 -H2CCHC~h))BA Rxample JlL..6-i-ErPb.LQABADINi 1 3-H 2 CCHCMe 2

}BAF

IFxanMIC 506 2 ,4,6-MePh) 2 DABAn1Ni(fl 3 H2CCHMe)

BAF

-368- 03ID6/03sw331 Isp369 Example 5a7 [(2,4,6-MePh) 2 DABAn] Ni (T 3 -u 2 CcHCHph) }BAP Example [(2,4,6-MePh) 2 DABAnJNi(n 3

-C

3 5

IBAF

Example 509 (2,4 3 6-MePh) 2 DABAnINI1Q3-H 2 CCHCMe 2

)BAF

ExamIe {T(2,-i-PrPh)UDABAnl Ni(n13 H 2 CC(COOMe)CH 2

)BAF

Example 511 2 4, 6 -MePh) 2 DAEAnJ Ni (T13 H 2 CC (COOMe) CH 2

)BAF

Example 512 f 2 A-i-PrPh 2 DABAfNi(1 3

H

2 CCHCH(COOEt)]BAp Examle 513 4, 6 -Me Ph) 2 DABAn] Ni (t3 -H2CCHCx (COOEt) }BAF Example 514 tLr (2L6-i -x.2hX 2 DABAnI1 Ni (v1 3

-H

2 CCHCHC1) )BAF Example ([(2,4,6-NePh) 2 DABAn]Ni (1 3

-H

2 CCHCHC1) AF Examples 516-537 Polymerizations catalyzed by nickel and palladium t-benzyl initiators and by nickel allyl initiators are illustrated in the following Table containing Examples 516-537. The initiation of polymerizations catalyzed by nickel allyl initiators where the allyl ligand was substituted with functional groups, such as chloro or ester groups, was often aided by the addition of a Lewis acid.

-369- 03t6/03swa133J Isp.,369 Example JCompound j Conditions Results i-PrPh)2 DABMe2JPd(T1 3 CI-EtPh)} BAF [(2,6-i.PrPh) 2 DABMc2)Pd&ij- CHEtPh)) BAF ([(2,6-i-PrPh) 2 DABH2Pd(11 3 -CHEt(4-

C

6 H4-I-Bu)))

BAF

j[(2,6.i-PrPh) 2 DABMe2Pd(1 3 I(2,6-i-PTPh) 2 DABMc2]Pd(1l 3 CHEtC6FS)) BAF ([(2,4,6-MePh) 2 DABAIINiO1j 3

H

2 CCHCMC2))

BAF

([(2,6-i-PrPh)2DABM2Ni(1 3 H2CCI-CMC2)} BAF t(2,4.6-MePh) 2 DABMC2JNiQQj-

)BAF

R2.4,6-MePh)2DABAflJNi(TO3-

C

3

H

5

))BAF

1[(2,4,6-MePh) 2 DABAfl]Ni(TO-.

H

2 CCHCHPh) )BAF 0.067 mmol Crnpd; 25 0 C; 1 atm E; 2 days; CH 2

CI

2 0.027 mmol Cmpd; 25 0

C;

6.9 MPa E; 1Sh; C 6 D6 0.016 mmol Cmpd; 25 0

C;

6.9 MPa E; 18 h; C6D6 0.063 mmol Cmpd; 25 0 C; I atm E; 5 days; CH 2 CI2 0.044 mmol Crnpd; 25 *C; 6.9 MPa E; 18 h;C6D36 0.049 mrnol Cmpd; 25 0

C;

6.9 MNa E; 18 h; C6D36 0.034 minol Cmpd; 25 'C; 6.9 MPa. E; 18 h; C6D36 0.047 mmol Crnpd; 80 0

C;

6.9 MPa E; 18 h; C6D6 0.034 mmol -Cmpd; 80 OC; 6.9 MPa E; 18 C6D6 0.026 mmol Cmpd; 80 0

C;

6,9 MPa E; l8b; C6D36 <0.5 g PE (270 TO) 8.2 g PE (11,000

TO)

1.5 g PE (3,300 TO) 4.6 g PE (2,600 TO) 6.4 g PE (5,200 TO) 1.5 g PE 100 TO) 35 mgPE (37 TO) 20 mg PE (15 TO) 260 mg PE (270 TO).

141 mg PE (190 TO)

.L

I R2,6-i-PrPb)2DABAfl]Ni(i&3

H

2 CCHCI-Ph))

BAF

0.040 mmol Cmpd; 80 6.9 MPa E; 18 h; C6D6 992 mg PE (880 TO) -370- 370 -03/06O3swl 1331a4s370 527 528 529 530 531 532 j(2,6-i-PrPh)2 DABAIJN i()3

H

2 CCHCH4Me)j BAF t(2,6-i-PrPh)2DABMC2INi(n

H

2 CCHCMC2)) BAF [(2,6-i-PrPh)2DABAn]Ni(1 3

C

3 H5)} BAF ([(2,4.6-MePh)2DABAnNi(1 3

H

2 CCHCHC1)) BAF ([(2,6-i-PrPh)2DABAn]Ni(Q-3

I-

2

CCHCHCI)}BAF

{U(2,4.6-MePh)2DABAn)N i(ln 3 H2CCHCHCIM BAF j(2,4,6-MePh)2DABAn]Ni(-q 3 H2CCHCI-CI)) BAF ([(2,6-i-PTPh)2DABAnNiO1j 3 H2CCHCH(COOEt)} BAF ((2.6-i-PrPh)2DABAnINiOQ-3

H

2 CCHCHCi)) BAF 0.043 mmol Cmpd; 80 'C; 6.9 MPa 18 h; C 6

D

6 0.044 mm6I Cmpd; 80 0

C;

6.9 MPa E; 18 h; C6D6 0.042 mmol Cmpd; 80 0 C;1 6.9 MPa E, 18 h; C 6 6 0.043 mrnol Cmpd; 25 0

C,

6.9 MPa E; 18 h; C 6

D

6 0.042 mmol Cmpd; 25 GC; 6.9 MPa E; 18 h; C 6 6 0.020 mmol Cmp&, 0.04 mmol B(C6F5) 3 25 0

C;

6.9 MNa E; 18 h; CDCI3 0.020 mmol Cmpd; 0.04 mmol BPh3; 25 0

C;

6.9 MPa E; 18 hi; CDCI3 0.020 mum! Cmpd; 0.04 mmol BPh3; 25 0

C;

6.9 MPa E; 18 h; CDC], 0.020 mmol Cmpd; 0.04 minol BPh3; 80 'C; 6.9 MPa E; 18 h; C6D6 23 mg PE (19 TO) 54 mg PE (44 TO) 15 mg PE- (13 TO) 94 mg PE (78 TO) 8 mg PE (7 TO) 7.8 g PE (14,000

TO)

8.4 g PE (15,000

TO)

4.7 g PE (8,400 TO) 6.8 g PE (12,000

TO)

I. I ([(2,6-i-PTPh)2DABAnNiO1j 3 f! 2 CCHCHIIC)) BAF 0.020 mmol Cmpd; 10 mg montmnorillonice; 80 0 C; 6.9 MEPa E; 18 h;QCD6 326 mg PE (580 TO) -371 31 03 0 6/03.swI3j I Ispa.371 Where the terms "comprise", "comprises", "comprised" or "comprising" are used in this specification, they are to be interpreted as specifying the presence of the stated features, integers, steps or components referred to, but not to preclude the presence or addition of one or more other feature, integer, step, component or group thereof.

372 06/06.3,swl33 11sp doc,372

Claims (49)

1. A process for the polymerization of olefins, comprising, contacting, at a temperature of-100°C to 200 0 C, a transition metal complex of a bidentate ligand selected from the group consisting of: R2 R3 I N R4 N ,(CR 3 2 )n R 29 R4N I LK# N=CR 4 (XXX) (VIII) (xxII) (XXXII) with an olefin wherein: said olefin is selected from the group consisting of ethylene, an olefin of the formula R 7 CH=CH 2 or R' 7 CH=CHR' 7 cyclobutene, cyclopentene, norborene, or a substituted norbornene; said transition metal is selected from the group consisting of Ti, Zr, Sc, V, Cr, a rare earth metal, Fe, Co, Ni or Pd; R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; 10/01/06,ck1331 janl0.claims,373 -373- R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring; R 44 is hydrocarbyl or substituted hydrocarbyl, and R 28 is hydrogen, hydrocarbyl or substituted hydrocarbyl or R 44 and R 28 taken together form a ring; R 45 is hydrocarbyl or substituted hydrocarbyl, and R 29 is hydrogen, substituted hydrocarbyl or hydrocarbyl, or R 45 and R 29 taken together form a ring; each R 30 is independently hydrogen, substituted hydrocarbyl or hydrocarbyl, or two of R 30 taken together form a ring; R 20 and R 23 are independently hydrocarbyl or substituted hydrocarbyl; R 2 1 and R 22 are each in independently hydrogen, hydrocarbyl or substituted hydrocarbyl; each R 17 is independently hydrocarbyl or substituted hydrocarbyl provided that any olefinic bond in said olefin is separated from any other olefinic bond or aromatic ring by a quaternary carbon atom or at least two saturated carbon atoms; and provided that: when said bidentate ligand is (XXX) M is not Pd; when M is Pd a diene is not present; and said transition metal also has bonded to it a ligand that may be displaced by said olefin or add to said olefin; when norbornene or substituted norbornene is used no other olefin is present.

2. The process of claim 1, characterized in that the transition metal complex is of the formula 31/01/06,atl331 .claim pg,2 -374- R3 I N M Q)y M R4 -N (S)z I R 5 (XI) wherein: M is Ti, Zr, Sc, V, Cr, a rare earth metal, Co, Fe, Ni or Pd in the m oxidation state; y+z=m R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring; each Q is independently alkyl, hydride, chloride, iodide, or bromide; and each S is independently alkyl, hydride, chloride, iodide, or bromide.

3. The process of claim 2, characterized in that: M is Ni and m is 2; M is Pd and m is 2; M is Fe and m is 2; M is Co and m is 2; M is Zr and m is 4; M is Sc and m is 3; M is Cr and m is 2 or 3; or M is V and m is 3.

4. The process of claim 3, characterized in that: M is Ti(IV), Q and S are chloride, and y and z are both 2; M is Zr(IV), Q and S are chloride, and y and z are both 2; M is Sc(III), Q and S are chloride, y is 1 and z is 2; 05/01/06,atl331 .claims,375 -375- M is Cr(III), Q and S are chloride, y is 1 and z is 2; M is Cr(II), Q and S are chloride, y is 1 and z is 1; or M is V(III), Q and S are chloride, y is 1 and z is 2.

5. The process of claim 3, characterized in that M is Ni(II), y is 1 and z is 1; M is Pd(II), y is 1 and z is 1; M is Co(II), y is 1 and z is 1; M is Fe(II), y is 1 and z is 1.

6. The process of claim 5, characterized in that M is Ni(II), or M is Pd(II).

7. The process of claim 6, characterized in that the transition metal complex is of the formula R52 R 3 N Q R4 N S R53 (XXXVI) wherein: R 52 is substituted phenyl; and R 53 is phenyl or substituted phenyl; and groups in the 2 and 6 positions of R 52 have a difference in E 3 of 0.15 or more.

8. The process of claim 7, characterized in that groups in the 2 and 6 positions of R 53 have a difference in Es of 0.15 or more. 05/01/06,at13311 .claims,376 -376-

9. The process of claim 6, characterized in that the transition metal complex is of the formula (XXXXI) R 2 Me is methyl. The process of claim 1, characterized in that the transition metal complex is of the formula (II) or (III) R2 R 3 Pd R41 M R 5 X- (II) RR R(XXX R 4 N Z Rs X- (III) 1 wherein: R 2 and R 5 are each independently hydrogen, hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two hydrcarbon atoms bouyl; and to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substitutedthyl. The process of claim 1, chtaken together are hydrocarbylen that the or substion metal hydrocarbylenex is of to form a carbocyclic ring; R 3 N Z I P R5 X 10 wherein:33.claims,377 R 2 and R77- 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring; 05/01/06,at 13311 .claims,377 -377- T' is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, R' 5 or R 5 Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound is less than about 6; X is a weakly coordinating anion; and R 1 5 is hydrocarbyl not containing olefinic or acetylenic bonds; provided that in (II) when R 3 and R 4 taken together are hydrocarbylene to form a carbocyclic ring, Z is not an organic nitrile.

11. The process of claim 10, characterized in that R 3 and R 4 are each independently phenyl or substituted phenyl.

12. The process of claim 11, characterized in that the transition metal complex is of the formula (III); R 3 and R 4 are each independently hydrogen or hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene to form a ring; T' is methyl; and Z is R 6 2 0, wherein each R 6 is independently alkyl.

13. The process of claim 10, characterized in that X is BAF, SbF 6 PF 6 or BF 4

14. The process of claim 10, characterized in that the transition metal complex is of the formula and each of R 2 R 3 R 4 R 5 Z, and X are as follows: R 2 R 3 R 4 R 5 T' Z X 2,6-i-PrPh Me Me 2,6-i-PrPh Me OEt 2 BAF 2,6-i-PrPh H H 2,6-i-PrPh Me OEt 2 BAF 2,6-MePh H H 2,6-MePh Me OEt 2 BAF 2,6-MePh Me Me 2,6-MePh Me OEt 2 BAF 2,6-i-PrPh Me Me 2,6-i-PrPh Me OEt 2 SbF 6 05/01/06,at13311.claims,378 -378- 2,6-i-PrPh 2,6-i-PrPh 2,6-i-PrPh 2,4,6-MePh 2,6-i-PrPh 2,6-i-PrPh Ph 2,6-EtPh 2,6-EtPh 2-t-BuPh 1 -Np Ph 2 CH 2-PhPh Ph Ph Ph Ph 2 CH Ph 2 CH 2,6-i-PrPh 2,6-i-PrPh 2,6-i-PrPh 2,4,6-MePh 2,6-i-PrPh 2,6-i-PrPh Ph 2,6-EtPh 2,6-EtPh 2-t-BuPh 1 -Np Ph 2 CH 2-PhPh Ph Ph Ph Ph 2 CH Ph 2 CH OEt 2 OEt 2 OEt 2 OEt 2 OEt 2 NCMe NCMe NCMe NCMe NCMe NCMe NCMe NCMe NCMe NCMe NCMe NCMe SMe 2 BF 4 PF 6 SbF 6 SbF 6 SbF 6 SbF 6 SbF 6 BAF SbF 6 SbF 6 SbF 6 SbF 6 SbF 6 BAF SbF 6 BAF SbF 6 SbF 6 a CMe 2 CH 2 CMe 2 The process of claim complex is of the formula 1, characterized in that the transition metal (IV) wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and W 4 are each independently hydrogen, hydrocarbyl, substituted 051Oi/06,at 133 1 1.claims,379 -379- hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; M is Ni(II) or Pd(II); each R' 6 is independently hydrogen or alkyl containing 1 to 10 carbon atoms; nis 1, 2, or 3; X- is a weakly coordinating anion; and R 8 is hydrocarbyl.

16. The process of claim 15, characterized in that R 3 and R 4 are each independently hydrogen or hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene to form a ring; and X is BAF, SbF 6 PF 6 or BF 4

17. The process of claim 1, characterized in that the transition metal complex is of the formula R 2 R 2 R 3 T 1 R I Pd- E- PdN R4 N TI/ \N R 15 R 4 R 5 RS X( (V) wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; E is halogen or -OR 8 R 1 8 is hydrocarbyl not containing olefinic or acetylenic bonds; T 1 is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, R' 5 or RISOC(O)-; R 1 5 is hydrocarbyl not containing olefinic or acetylenic bonds; and X' is a weakly coordinating anion. 05/01/06,atl3311.claims,380 -380-

18. The process of claim 1, characterized in that the transition metal complex is of the formula R2 R 3 I R 4 N 11 PT X R4 R HC X- R (VI) wherein: M is Ni(II) or Pd(II); R 2 and R 5 are hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; each R" 1 is independently hydrogen, alkyl or (CH 2 )mCO 2 R'; T 3 is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, or -CH 2 CH 2 CH 2 CO 2 R; P is a divalent group containing one or more repeat units derived from the polymerization of one or more of ethylene, an olefin of the formula R' 7 CH=CH 2 or R'CH=CHR' 7 cyclobutene, cyclopentene, substituted norbornene, or norbornene and, when M is Pd(II), optionally one or more of: a compound of the formula CH 2 =CH(CH 2 )mCO 2 R 1 CO, or a vinyl ketone; R 8 is hydrocarbyl; m is 0 or an integer from 1 to 16; R' is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to carbon atoms; and X- is a weakly coordinating anion. 05/01/06,at1331 .claims,381 -381-

19. The process of claim 1, characterized in that the transition metal complex is of the formula R2 R 3 I T2 N\ T SPd R4 X Rs R (VII) wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; T 2 is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, hydrocarbyl substituted with keto or ester groups but not containing olefinic or acetylenic bonds, or R 15 is hydrocarbyl not containing olefinic or acetylenic bonds; and X is a weakly coordinating anion. The process of claim 1, characterized in that the transition metal complex is of the formula R 2 R 3 I N (Q H M-C-R R4 N H-C-R" R 5 PT 3 (XVI) ()a wherein: M is Zr, Ti, Sc, V, Cr, a rare earth metal, Fe, Co, Ni or Pd of oxidation state m; R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, 05/01/06,atl331 l.claims,382 -382- provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; T 3 is hydrogen, hydrocarbyl not containing olefinic or acetylenic bonds, or -CH 2 CH 2 CH 2 CO 2 R 8 P is a divalent group containing one or more repeat units derived from the polymerization of one or more monomers selected from the group consisting of ethylene, an olefin of the formula R 7 CH=CH 2 or R 7 CH=CHR 7 cyclopentene, cyclobutene, substituted norbornene, and norbornene, and optionally, when M is Pd(II), one or more of: a compound of the formula CH 2 =CH(CH 2 )mCO 2 R 1 CO, or a vinyl ketone; Q is a monovalent anion; R 8 is hydrocarbyl; a is 1 or 2; y+a+ 1 =m; each R 17 is independently hydrocarbyl or substituted hydrocarbyl provided that any olefinic bond in said olefin is separated from any other olefinic bond or aromatic ring by a quaternary carbon atom or at least two saturated carbon atoms; R' is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to carbon atoms; m is 0 or an integer of 1 to 16; and X is a weakly coordinating anion.

21. The process of claim 1, characterized in that the transition metal complex is of the formula 05/01/06,atl331 .claims,383 -383- R2 R 3 IN S4: M CHR 14 R I R 14 HC X- R (IX) wherein: M is Ni(II) or Pd(II); R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; each R 14 is independently hydrogen, alkyl or -(CH 2 )mCO 2 R'; R 1 is hydrogen, or hydrocarbyl or substituted hydrocarbyl containing 1 to carbon atoms; T 4 is alkyl, -Ro 6 C(O)OR 8 R 15 or R 5 is hydrocarbyl not containing olefinic or acetylenic bonds; R 60 is alkylene not containing olefinic or acetylenic bonds; R 8 is hydrocarbyl; and X is a weakly coordinating anion; provided that when R 1 4 is (CH 2 )mCO 2 or T 4 is not alkyl, M is Pd(II).

22. The process of claim 1, characterized in that the transition metal complex is of the formula R 2 M- A R R X XXXVII wherein: M is Ni(II) or Pd(II); 05/01/06,atl3311.claims,384 -384- A is a an-allyl or r7-benzyl group; R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; and CN X is a weakly coordinating anion. c 10 23. The process of claim 1, characterized in that the transition metal complex is of the formula RR R 3 I w R I (XXXVIII) wherein: R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; R 54 is hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound directly to the imino nitrogen atom has at least two carbon atoms bound to it; each R 55 is independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or a functional group; W is alkylene or substituted alkylene containing 2 or more carbon atoms; Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur, or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound (measured in water) is less than about 6, or an olefin of the formula R 7 CH=CHR' 7 each R 17 is independently hydrogen, saturated hydrocarbyl or substituted 05/01/06,atl331 .claims,385 -385- saturated hydrocarbyl; and X is a weakly coordinating anion; provided that when M is Ni, W is alkylene and each R 1 7 is independently hydrogen or saturated hydrocarbyl.

24. The process of claim 1, characterized in that the transition metal complex is of the formula R 2 R 3 SNi- I R (OMe (XXXXfl) wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; and R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring. The process of claim 1, characterized in that the transition metal complex is of the formula R 2 8 (CR3o )n R29 R =N N=C (S)z (XVII) wherein: M is Ti, Zr, V, Cr, a rare earth metal, Co, Fe, Sc, Pd, or Ni, of oxidation state 05/01/06,at1331 I.claims,386 -386- R 44 is hydrocarbyl or substituted hydrocarbyl, and R 28 is hydrogen, substituted hydrocarbyl or hydrocarbyl, or R 44 and R 28 taken together form a ring; R 45 is hydrocarbyl or substituted hydrocarbyl, and R 29 is hydrogen, substituted hydrocarbyl or hydrocarbyl, or R 45 and R 29 taken together form a ring; each R 30 is independently hydrogen, substituted hydrocarbyl or hydrocarbyl, or two of R 30 taken together form a ring; n is 2 or 3; y and z are positive integers; y+z=m Q is alkyl, hydride, chloride, iodide, or bromide; and S is alkyl, hydride, chloride, iodide, or bromide.

26. The process of any one of claims 1 to 25, supported on a heterogenous support.

27. The process of any one of claims 1 to 25, characterized in that said process is adapted for the polymerization of ethylene.

28. The process of any one of claims 10 to 18 or 20 to 23, characterized in that X is part of a heterogeneous support.

29. A compound of the formula (XXXVI) as set forth in any one of claims 7 or 8. A compound of the formula (XXXXI) as set forth in claim 9.

31. A compound of the formula (II) as set forth in any one of claims 10 or 11 and 13 or 14.

32. A compound of the formula (III) as set forth in any one of claims to 12. 05/01/06,atl3311.claims,387 -387-

33. A compound of the formula (IV) as set forth in any one of claims or 16.

34. A compound of the formula as set forth in claim 17. A compound of the formula (VI) as set forth in claim 18.

36. A compound of the formula (VII) as set forth in claim 19.

37. A compound of the formula (XVI) as set forth in claim

38. A compound of the formula (IX) as set forth in claim 21.

39. A compound of the formula (XXXVII) as set forth in claim 22. A compound of the formula (XXXVIII) as set forth in claim 23.

41. A compound of the formula (XXXXIII) as set forth in claim 24.

42. A compound of the formula (XVII) as set forth in claim

43. A process for preparing a compound of the formula (II) as set forth in claim 31, comprising the step of contacting, at a temperature of about -40 0 C to about +60 0 C, a compound of the formula [(r 4 -1,5-COD)PdT'Z]+X" and a diimine of the formula R2 R3 I yN R 4 N (VIII) wherein: 05/01/06,atl331 l.claims,388 -388- \O CC) COD is Z is R' 0 CN; and R io is hydrocarbyl not containing olefinic or acetylenic bonds.

44. The process as recited in claim 43, characterized in that said process is carried out in a solvent of the formula R1'CN, wherein R 1 0 is hydrocarbyl not containing olefinic or acetylenic bonds. A process for the production of a compound of the formula (XXXVIII) as set forth in claim 40, comprising the step of heating a compound of the formula (XXXIX) at a temperature of about -30°C to about +100 0 C for a sufficient time to produce (XXXVIII), and wherein: R 56 is alkyl containing 2 to 30 carbon atoms; and T 5 is alkyl.

46. A process for preparing a compound of the formula (XXXXI) as set forth in claim 30, comprising the step of contacting, at a temperature of about -800C to about +20 0 C, a compound of the formula (r1 4 -1,5-COD) PdMe 2 and a diimine of the formula 05/01/06,atl331 .claims,389 -389- IND R2 N R3 I (VIII) wherein COD is

47. The process of any one of claims 1 to 28, substantially as hereinbefore described with reference to any one of the examples.

48. A compound of any one of claims 29 to 42, substantially as hereinbefore described with reference to any one of the examples.

49. The process of any one of claims 43 to 46, substantially as hereinbefore described with reference to any one of the examples. A compound whenever prepared by the process of any one of claims 43 to 46 or claim 49.

51. A process for the formation of linear a-olefins, comprising the step of contacting, at a temperature of about -100 0 C to about +200, ethylene with a process adapted for the oligomerization of ethylene to one or more a-olefins, characterized in that the process comprises a transition metal complex of the formula (XXXI) (XXXI) wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl; R 3 and R 4 are each independently hydrogen, substituted hydrocarbyl, 05/01/06,atl3311.claims,390 -390- \O S hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted Shydrocarbylene to form a ring; and Q and S are each independently chlorine, bromine, iodine or alkyl; and the process further comprises a compound W, which is a neutral Lewis acid capable of abstracting X- to form WX, provided that the anion formed is a weakly coordinating anion, or a cationic Lewis or Bronsted acid whose counterion is a weakly coordinating anion; CN wherein an a-olefin containing 4 to 40 carbon atoms is produced. 10 52. The process of claim 51, characterized in that said compound W is an alkyl aluminum compound.

53. The process of claim 52, characterized in that said compound W is R 9 3 A1, R 9 2 A1CI, R 9 A1C1 2 R 9 A10 or R 9 3 A1 2 C 3 wherein R 9 is alkyl containing 1 to 25 carbon atoms.

54. The process of claim 53, characterized in that R 9 contains 1 to 4 carbon atoms.

55. A process for the formation of linear a-olefins, comprising the step of contacting, at a temperature of about -100 0 C to about +200, ethylene with a process adapted for the oligomerization of ethylene to one or more a-olefins, characterized in that the process comprises a transition metal complex of the formula (III) or (XXXIV) R2 1+ R 3 7 N Z I 05/01/06,at1331 1.claims,391 -391- N\ x- R2 (XXXIV) wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl; R 3 and R 4 are each independently hydrogen, substituted hydrocarbyl, hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a ring; T 1 is hydrogen or n-alkyl containing up to 38 carbon atoms; Z is a neutral Lewis base wherein the donating atom is nitrogen, sulfur, or oxygen, provided that if the donating atom is nitrogen then the pKa of the conjugate acid of that compound (measured in water) is less than about 6; U is n-alkyl containing up to 38 carbon atoms; and X is a noncoordinating anion; and wherein an a-olefin containing 4 to 40 carbon atoms is produced.

56. A process for the formation of linear a-olefins, comprising the step of contacting, at a temperature of about -100 0 C to about +200 0 C, ethylene with a process adapted for the oligomerization of ethylene to one or more a-olefins, characterized in that the process comprises a Ni{II} complex of a ligand of the formula (VIII) R2 R3 I R4 N R (VIII) 05/01/06,atl3311.claims,392 -392- wherein: R 2 and R 5 are each independently hydrocarbyl or substituted hydrocarbyl, provided that the carbon atom bound to the imino nitrogen atom has at least two carbon atoms bound to it; R 3 and R 4 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl, or R 3 and R 4 taken together are hydrocarbylene or substituted hydrocarbylene to form a carbocyclic ring; and wherein an a-olefin containing 4 to 40 carbon atoms is produced.

57. The process of any one of claims 51 to 56, characterized in that R 3 and R 4 are hydrogen, methyl or 1,8-naphthylylene.

58. R 5 are phenyl. The process of any one of claims 51 to 57, characterized in that R 2 and

59. The process of any one of claims 51 to 58, characterized in that a partial pressure of said ethylene is about atmospheric pressure to about 275 MPa. The process of any one of claims 51 to 59, substantially as hereinbefore described with reference to any one of the examples.

61. The linear a-olefin whenever formed by the process of any one of claims 51 to DATED this 3 rd day of January, 2006 E.I. DU PONT DE NEMOURS AND COMPANY and UNIVERSITY OF NORTH CAROLINA CHAPEL HILL By their Patent Attorneys: CALLINAN LAWRIE 05/01/06,at1331 .claims,393 -393-