EP1003755A1 - Novel transition metal complexes - Google Patents

Novel transition metal complexes

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Publication number
EP1003755A1
EP1003755A1 EP98937653A EP98937653A EP1003755A1 EP 1003755 A1 EP1003755 A1 EP 1003755A1 EP 98937653 A EP98937653 A EP 98937653A EP 98937653 A EP98937653 A EP 98937653A EP 1003755 A1 EP1003755 A1 EP 1003755A1
Authority
EP
European Patent Office
Prior art keywords
transition metal
pentalene
catalyst composition
cyclopentadienyl
composition according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP98937653A
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German (de)
French (fr)
Inventor
Frederick Geoffrey Nethersole Cloke
Julian Stephen Parry
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BP Chemicals Ltd
Original Assignee
BP Chemicals Ltd
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Publication date
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Publication of EP1003755A1 publication Critical patent/EP1003755A1/en
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F17/00—Metallocenes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F110/02—Ethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00—Polymerisation catalysts
    • C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62—Refractory metals or compounds thereof
    • C08F4/64—Titanium, zirconium, hafnium or compounds thereof
    • C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
    • C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F4/00—Polymerisation catalysts
    • C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
    • C08F4/62—Refractory metals or compounds thereof
    • C08F4/64—Titanium, zirconium, hafnium or compounds thereof
    • C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
    • C08F4/65916—Component covered by group C08F4/64 containing a transition metal-carbon bond supported on a carrier, e.g. silica, MgCl2, polymer

Definitions

  • the present invention relates to novel transition metal complexes and in particular to novel transition metal complexes comprising pentalene ligands and to their use as catalyst components for the polymerisation of olefins.
  • metallocene based olefin polymerisation catalysts are now well established. Examples of such catalysts may be found in EP 129368, EP 206794 and EP 260130.
  • the catalyst compositions comprise a metallocene complex for example a bis(cyclopentadienyl) zirconium dichloride together with an activator for example methyl aluminoxane.
  • a metallocene complex for example a bis(cyclopentadienyl) zirconium dichloride together with an activator for example methyl aluminoxane.
  • transition metal complex having a constrained geometry configuration has been used for the polymerisation of olefins. Examples of these complexes may be found in EP 420436 and EP 416815.
  • Such contrained geometry complexes may also be used in the presence of aluminoxanes but may also be used together with boron activators.
  • transition metal complex suitable for use as a catalyst component is described in EP 672672.
  • the complexes described therein comprise cyclooctatetraene ligands and may also be used for the polymerisation of olefins.
  • transition metal complexes comprise at least one cyclopentadienyl ligand together with the transition metal
  • transition metal complexes comprise at least one cyclopentadienyl ligand together with the transition metal
  • a novel class of transition metal complex comprising a pentalene ligand which may be used as a catalyst component for the polymerisation of olefins.
  • M is a Group IVA transition metal (Cotton and Wilkinson 2 n ⁇ Edition)
  • X is an anionic ligand
  • L is a neutral donor eg THF, amine and L, X or Y may be connected to the pentalene ligand,
  • Preferred complexes are those wherein y is 1 , M is zirconium or titanium, X is halogen and Y is cyclopentadienyl.
  • Suitable X ligands include hydride, halogen, alkyl, aryl or oxygen or nitrogen containing ligands.
  • the cyclopentadienyl ligand Y when present may be substituted with alkyl. Alternatively two substituents may be joined together to form a ring eg indenyl.
  • the pentalene ligand When substituted the pentalene ligand is most suitably substituted in the 1,5- position for example with trimethylsilyl groups.
  • X, Y or L group When a X, Y or L group is connected to the pentalene ligand it may be bridged via the group (J 2 Z) n wherein Z is carbon, silicon, germanium or boron and J is hydrogen or hydrocarbyl and n is 1-8.
  • Preferred complexes are:
  • the complexes When used as components of catalyst compositions for the polymerisation of olefins the complexes are used in the presence of a suitable activator.
  • a catalyst composition suitable for the polymerisation of olefins comprising:
  • the preferred activator is an organoaluminium oxy compound for example an aluminoxane.
  • a most preferred activator is methyl aluminoxane.
  • boron activators may also be suitable for use in the catalyst compositions according to the present invention for example boron compounds.
  • Suitable boron activators include tris(pentafluorophenyl) boron or trialkylammonium tetrakis (pentafluorophenyl) borates or N,N-dialkylanilinium tetrakis (pentafluorophenyl) borates.
  • the molar ratio of transition metal to activator is in the range 1 :0.1 to 1 : 10,000 and most preferably in the range 1 : 1 to 1 :2,000.
  • the catalyst compositions according to the present invention may also be used in the supported form.
  • Typical supports include inorganic oxides for example silica, alumina.
  • Other supports include magnesium chloride or polyethylene.
  • the catalyst composition may be prepared by conventional means.
  • novel transition metal complexes according to the present invention may be prepared for example from cyclooctatetraene. Full experimental details of the preparation are given in the accompanying examples.
  • the present invention also provides a process for the production of polyolefins, in particular homopolymers of ethylene and copolymers of ethylene with minor amounts of at least one C3 to CIO, preferably C3 to C8 alpha-olefin.
  • the process comprises contacting the monomer or monomers, optionally in the presence of hydrogen, with the catalyst composition according to the invention at a temperature and pressure sufficient to initiate the polymerisation reaction.
  • the alpha olefin may be propylene, butene-1, hexene-1, 4-methyl pentene-1 and octene-1.
  • the olefin polymerisation catalyst compositions according to the present invention may be used to produce polymers using solution polymerisation, slurry polymerisation or gas phase polymerisation techniques. Methods and apparatus for effecting such polymerisation reactions are well known and described in, for example, Encyclopaedia of Polymer Science and Engineering published by John Wiley and Sons, 1987, Volume 7, pages 480 to 488 and 1988, Volume 12, pages 504 to 541.
  • the catalysts of the present invention are particularly suitable for use in the gas phase.
  • the catalyst according to the present invention can be used in similar amounts and under similar conditions to known olefin polymerisation catalysts.
  • the polymerisation may optionally be carried out in the presence of hydrogen.
  • Hydrogen or other suitable chain transfer agents may be used to control the molecular weight of the produced polyolefin.
  • Ethylene was polymerised in toluene at 10 bar and at room temperature in the presence of an aliquot (20 mg) of [Zr ⁇ C 8 H 4 (Si'Pr 3 -l,5) 2 ⁇ 2 ] prepared in
  • Example 2 and 1000 equivalents of methyl aluminoxane. The reaction proceeded exothermically (up to 50°C) and 2.5 gm polyethylene were produced after 1 hr.
  • Silica (lg, Crosfield ES70, calcined at 700°C under flowing N 2 ) was placed in a Schlenk tube. To this was added a solution of MAO (5.7ml of 1.5M MAO in toluene) and Pentalene(TMS) 2 cyclopentadienyl zirconium chloride (20mg) in toluene (10ml). The slurry was allowed to stand with occassional shaking for 90 minutes at room temperature. The catalyst was dried under vacuum at room temperature. Polymerisations
  • the reagents used in the polymerisations were Ethylene Grade 3.5 (Supplied by Air Products), 1-hexene (Supplied by Aldrich) distilled over sodium/nitrogen, trimethylaluminium (2M in hexanes, Supplied by Aldrich) and triisobutylauminium (1M in hexanes, Supplied by Aldrich).
  • a 3 litre reactor was heated under flowing nitrogen for 1 hour at 77°C before sodium chloride (300g, predried under vacuum, 160°C, >4 hours) was added.
  • Trimethyl aluminium (3ml, 2M in hexanes) was added to the reactor and allowed to scavenge the reactor of poisons for V ⁇ hour. After this period of time the alkyl aluminium was vented from the reactor using 4*4 bar nitrogen purges.
  • the gas phase was composed with 0.1 bar 1-hexene and 8 bar ethylene at 77°C prior to catalyst injection. After the catalyst (0.203g) prepared in Example 5 had been injected, under nitrogen the temperature was adjusted to 80°C. The ratio of hexene to ethylene during the polymerisation was keep constant by monitoring the gas phase composition by mass spectrometer and adjusting the flow rate of 1- hexene as required via a HPLC pump.
  • the polymerisation was allowed to continue for 1 hour before being terminated by purging the reactants from the reactor with nitrogen and reducing the temperature to ⁇ 30°C.
  • the polymer was washed with water to remove the sodium chloride, then with acidified methanol (50ml HC1/2.5L methanol) and finally with water/ethanol (4: 1 v/v).
  • the polymer was dried under vacuum, at 40°C, for 16 hours.
  • a 3 litre reactor was heated under flowing nitrogen for 1 hour at 78°C before sodium chloride (300g, predried under vacuum, 160°C, >4 hours) was added.
  • Trimethyl aluminium (3ml, 2M in hexanes) was added to the reactor and allowed to scavenge the reactor of poisons for 1 ' _ hours. After this period of time the alkyl aluminium was vented from the reactor using 4*4 bar nitrogen purges.
  • the gas phase was composed with 0.1 bar 1 -hexene and 8 bar ethylene at 78°C prior to catalyst injection. After the catalyst (0.23g) prepared in Example 6 had been injected, under nitrogen the temperature was adjusted to 80°C. The ratio of hexene to ethylene during the polymerisation was keep constant by monitoring the gas phase composition by mass spectrometer and adjusting the flow rate of 1- hexene as required via a HPLC pump.
  • the polymerisation was allowed to continue for 1 hour before being terminated by purging the reactants from the reactor with nitrogen and reducing the temperature to ⁇ 30°C.
  • the polymer was washed with water to remove the sodium chloride, then with acidified methanol (50ml HC1/2 5L methanol) and finally with water/ethanol (4: 1 v/v).
  • the polymer was dried under vacuum, at 40°C, for 16 hours.
  • a 3 litre reactor was heated under flowing nitrogen for 1 hour at 78°C before sodium chloride (300g, predried under vacuum, 160°C, >4 hours) was added.
  • Trimethyl aluminium (4ml, 2M in hexanes) was added to the reactor and allowed to scavenge the reactor of poisons for lhour. After this period of time the alkyl aluminium was Vented from the reactor using 4*4 bar nitrogen purges.
  • the reactor was cooled to below 30°C and trimethyl aluminium (2ml of 2M in hexanes) was added to the reactor.
  • the reactor was heated to 78°C and the gas phase composed 0.1 bar 1 -hexene and 8 bar ethylene at 78°C prior to catalyst injection.
  • the catalyst (0.173g) prepared in Example 6 had been injected, under nitrogen the temperature was adjusted to 80°C.
  • the ratio of hexene to ethylene during the polymerisation was keep constant by monitoring the gas phase composition by mass spectrometer and adjusting the flow rate of 1 -hexene as required via a HPLC pump.
  • the polymerisation was allowed to continue for 1 hour before being terminated by purging the reactants from the reactor with nitrogen and reducing the temperature to ⁇ 30°C.
  • the polymer was washed with water to remove the sodium chloride, then with acidified methanol (50ml HC1/2.5L methanol) and finally with water/ethanol (4: 1 v/v).
  • the polymer was dried under vacuum, at 40°C, for 16 hours.
  • a 3 litre reactor was heated under flowing nitrogen for 1 hour at 78°C before sodium chloride (300g, predried under vacuum, 160°C, >4 hours) was added.
  • Trimethyl aluminium (4ml, 2M in hexanes) was added to the reactor and allowed to scavenge the reactor of poisons for lhour. After this period of time the alkyl aluminium was vented from the reactor using 4*4 bar nitrogen purges.
  • the reactor was cooled to below 30°C and triisobutyl aluminium (2ml of 1M in hexanes) was added to the reactor.
  • the reactor was heated to 78°C and the gas phase composed 0.1 bar 1 -hexene and 8 bar ethylene at 78°C prior to catalyst injection.
  • the catalyst 0.220g prepared in Example 6 had been injected, under nitrogen the temperature was adjusted to 80°C.
  • the ratio of hexene to ethylene during the polymerisation was keep constant by monitoring the gas phase composition by mass spectrometer and adjusting the flow rate of 1 -hexene as required via a HPLC pump.
  • the polymerisation was allowed to continue for 1 hour before being terminated by purging the reactants from the reactor with nitrogen and reducing the temperature to ⁇ 30°C.
  • the polymer was washed with water to remove the sodium chloride, then with acidified methanol (50ml HC1/2.5L methanol) and finally with water/ethanol (4: 1 v/v).
  • the polymer was dried under vacuum, at 40°C, for 16 hours.
  • the weight of polymer was 7.3g
  • Examples 11-17 were carried out in a 1 litre capacity autoclave using isobutane as the reaction medium.
  • the reactor was heated to 85°C and thoroughly purged with nitrogen (2l/min) for 90 min. The temperature was then reduced to 50°C and the reactor charged with the chosen alkylaluminium scavenger and isobutane (500ml). The mixture was stirred (200rpm) at 75°C for a minimum of 120 min, the temperature was varied to the subsequent polymerisation temperature (T) and 10 bar overpressure of ethylene was then added.
  • the metal complex (see belov ) and MAO were mixed together and then added to the reactor. Ethylene was added to maintain constant reactor pressure for the duration of the run.
  • the metal complexes were (cyclopentadienyl) (1,5 -d i(trimethylsilyl) pentalene) zirconium chloride or the titanium analogue or (pentamethyl cyclopentadienyl) zirconium (l,5-di(trimethylsilyl) pentalene) zirconium chloride.

Abstract

Novel transition metal complexes having pentalene ligands are described. The complexes are suitable for use in the polymerisation of olefins in the presence of suitable activators. Typical complexes are, for example: (I) or (II).

Description

NOVEL TRANSITION METAL COMPLEXES
The present invention relates to novel transition metal complexes and in particular to novel transition metal complexes comprising pentalene ligands and to their use as catalyst components for the polymerisation of olefins.
The use of metallocene based olefin polymerisation catalysts is now well established. Examples of such catalysts may be found in EP 129368, EP 206794 and EP 260130. Typically the catalyst compositions comprise a metallocene complex for example a bis(cyclopentadienyl) zirconium dichloride together with an activator for example methyl aluminoxane. More recently another type of transition metal complex having a constrained geometry configuration has been used for the polymerisation of olefins. Examples of these complexes may be found in EP 420436 and EP 416815. Such contrained geometry complexes may also be used in the presence of aluminoxanes but may also be used together with boron activators.
Another type of transition metal complex suitable for use as a catalyst component is described in EP 672672. The complexes described therein comprise cyclooctatetraene ligands and may also be used for the polymerisation of olefins.
The majority of these transition metal complexes comprise at least one cyclopentadienyl ligand together with the transition metal We have now found a novel class of transition metal complex comprising a pentalene ligand which may be used as a catalyst component for the polymerisation of olefins.
Thus according to the present invention there is provided a novel transition metal complex having the general formula'
LpM
Y Xz
wherein
M is a Group IVA transition metal (Cotton and Wilkinson 2nα Edition)
X is an anionic ligand
Y = cyclopentadienyl
L is a neutral donor eg THF, amine and L, X or Y may be connected to the pentalene ligand,
R is hydrogen, alkyl, aryl, silyl, alkylsilyl or similar and may be the same or different n is 0-6 p = 0 or 1 y = 1 or 2 and when y = 1 , z or x = 0, 1 or 2 when y = 2, z and x = 0.
Preferred complexes are those wherein y is 1 , M is zirconium or titanium, X is halogen and Y is cyclopentadienyl.
Suitable X ligands include hydride, halogen, alkyl, aryl or oxygen or nitrogen containing ligands.
The cyclopentadienyl ligand Y when present may be substituted with alkyl. Alternatively two substituents may be joined together to form a ring eg indenyl.
When substituted the pentalene ligand is most suitably substituted in the 1,5- position for example with trimethylsilyl groups.
Preferred complexes according to the present invention are represented by the formula:
TMS = trimethylsilyl
When a X, Y or L group is connected to the pentalene ligand it may be bridged via the group (J2Z)n wherein Z is carbon, silicon, germanium or boron and J is hydrogen or hydrocarbyl and n is 1-8. Preferred complexes are:
(cyclopentadienyl)[l,5-di(trirnethylsilyl) pentalene] zirconium chloride, (cyclopentadienyl)[l,5-di(trimethylsilyl) pentalene] titanium chloride,
(pentamethylcyclopentadienyl)[l,5-di(trimethylsilyl) pentalene] zirconium chloride, bis [l,5-di(isopropylsilyl)pentalene] zirconium.
When used as components of catalyst compositions for the polymerisation of olefins the complexes are used in the presence of a suitable activator.
Thus according to another aspect of the present invention there is provided a catalyst composition suitable for the polymerisation of olefins comprising:
(a) a transition metal complex as described above, and
(b) an activator. The preferred activator is an organoaluminium oxy compound for example an aluminoxane. A most preferred activator is methyl aluminoxane.
Other activators may also be suitable for use in the catalyst compositions according to the present invention for example boron compounds. Suitable boron activators include tris(pentafluorophenyl) boron or trialkylammonium tetrakis (pentafluorophenyl) borates or N,N-dialkylanilinium tetrakis (pentafluorophenyl) borates.
The molar ratio of transition metal to activator is in the range 1 :0.1 to 1 : 10,000 and most preferably in the range 1 : 1 to 1 :2,000.
The catalyst compositions according to the present invention may also be used in the supported form. Typical supports include inorganic oxides for example silica, alumina. Other supports include magnesium chloride or polyethylene. When supported the catalyst composition may be prepared by conventional means.
The novel transition metal complexes according to the present invention may be prepared for example from cyclooctatetraene. Full experimental details of the preparation are given in the accompanying examples.
The present invention also provides a process for the production of polyolefins, in particular homopolymers of ethylene and copolymers of ethylene with minor amounts of at least one C3 to CIO, preferably C3 to C8 alpha-olefin. The process comprises contacting the monomer or monomers, optionally in the presence of hydrogen, with the catalyst composition according to the invention at a temperature and pressure sufficient to initiate the polymerisation reaction.
Suitably the alpha olefin may be propylene, butene-1, hexene-1, 4-methyl pentene-1 and octene-1.
The olefin polymerisation catalyst compositions according to the present invention may be used to produce polymers using solution polymerisation, slurry polymerisation or gas phase polymerisation techniques. Methods and apparatus for effecting such polymerisation reactions are well known and described in, for example, Encyclopaedia of Polymer Science and Engineering published by John Wiley and Sons, 1987, Volume 7, pages 480 to 488 and 1988, Volume 12, pages 504 to 541. The catalysts of the present invention are particularly suitable for use in the gas phase. The catalyst according to the present invention can be used in similar amounts and under similar conditions to known olefin polymerisation catalysts.
The polymerisation may optionally be carried out in the presence of hydrogen. Hydrogen or other suitable chain transfer agents may be used to control the molecular weight of the produced polyolefin.
The present invention will now be further illustrated by reference to the following examples. Example 1 Synthesis of K,rCκH4f Si'Pr^-l.S^l
(a) Cyclooctatetraene (11.3 gm, 0.108 mol) in a slow stream (1.5 cm3 min"1 at STP) of dinitrogen was passed through a quartz tube at 615 ± 1°C under a controlled dynamic vacuum of 1.0 ± 0.05 mbar over a period of 24 hours in a FVP apparatus; the resultant mixture of dihydropentalenes was collected in a trap at - 78°C. The latter was then dissolved in precooled (-78°C) hexane (100 cm3) and dimethyl ether (DME) (23 cm3, 0.22 mol) added, followed by LiBu" (2.5M in hexanes, 88 cm3, 0.22 mol) dropwise with stirring, which resulted in the precipitation of white [Li(DME)]2[C8H6]. After warm up to room temperature, the latter was isolated by filtration on a frit, washed with hexane (3 x 50 cm3), and dried under vacuum. Yield 27.8 gm, 87% based on cyclooctatetraene.
(b) To a stirred solution of [Li(DME)]2[C8H6] (2.95 gm, 10 mmol) in THF (100 cm3) at -78°C was added tri(isopropylsilyl) triflate (6.12 gm, 20 mmol) dropwise; the mixture was then allowed to warm to 0°C and the solvent removed in vacuo at this temperature. The resultant white solids were extracted with pentane (3 x 100 cm3), filtered and the pale yellow filtrates concentrated and cooled to -40°C to afford white crystals of [C8H6SiiPr3-l,5)2], These were collected and washed with pentene (2 x 10 cιτr) at -78°C. Total yield (two crops) 3.2 gm, 77%.
(c) To a stirred, solid mixture of [CgH6(Si'Pr3-l ,5)2] (2.08 gm, 5 mmol) and [KMe] (0.54 gm, 10 mmol) in a -78°C bath was added diethyl ether, precooled to -
78°C, and the mixture allowed to warm to room temperature overnight. The orange solution was then filtered from small amounts of insoluble material and evaporated to dryness in vacuo to afford off-white K2[C8H (Si'Pr3-l,5)2] in essentially quantitative yield. Example 2
ZrCl4 and K2[C H4(Si'Pr3-l,5)2] prepared in Example 1 were reacted in Et2O overnight and then pumped to dryness followed by extraction with pentane, filtered, concentrated and cooled to -40°C to give orange crystals. Mass spectroscopy indicated [Zr{C8H4(Si'Pr -l,5)2}2]; and nmr indicated a mixture of isomers. Example 3 Polymerisation
Ethylene was polymerised in toluene at 10 bar and at room temperature in the presence of an aliquot (20 mg) of [Zr{C8H4(Si'Pr3-l,5)2}2] prepared in
Example 2 and 1000 equivalents of methyl aluminoxane. The reaction proceeded exothermically (up to 50°C) and 2.5 gm polyethylene were produced after 1 hr.
Example 4
Preparation of complexes used in Examples 5-17 (a) Cp*Zr(pent")Cl
Li2pent" (0.70g, 2.69 mmol) was added to Cp*ZrCl3 (0.895g, 2.69 mmol) suspended in cold toluene (40ml, -80 degC). The mixture was allowed to warm up to room temperature and then stirred overnight. The solvent was removed in vacuo and the residue extracted with pentane (100 + 30 ml). Concentration of the resulting clear yellow solution and standing overnight resulted in yellow prisms of the product which were isolated by decantation and washed (2 times 10 ml cold pentane (-40 deg C)) and dried in vacuo. Yield 0.41 g, 30%
(b) CpZr(pent")Cl was prepared in a similar way using CpZrC as a starting material.
(c) CpTi(pent")Cl
Cp2TiC12 (0.41g, 1.65 mmol) was mixed with Zn dust (0.107g, 1.65 mmol) and THF (30 ml) added. The solution was stirred for 3 hr, during which time it turned dark green. This was cooled (-80 deg C) and K2pent" (0.53g, 1.65 mmol) added dropwise as a solution in THF (30 ml). The mixture was allowed to warm up to room temperature and stirred overnight to give a purple solution. The solvent was removed in vacuo and the product extracted with pentane. The resulting purple oil was sublimed (80 deg 1 * 10-5 mbar). The oil was dissolved in pentane and 1 equiv of , C1CH2CH2C1 added. The solution immediately turned deep red and was stirred overnight. The solvent was removed in vacuo and the resulting material sublimed (130 deg 1 *10-5 mbar) to yield CpTi(pent")Cl as a red oil. Yield 0.26g, 0.66 mmol 40%. NB. Cp* = (pentamethyl)cyclopentadienyl; pent" = l,5-di(trimethylsilyl) pentalene. Example 5
Pentalene(TMS)2cyclopentadienyl titanium chloride co-impregnated with
MAO on ES70X silica
Silica (0.477g, Crosfield ES70, calcined at 700°C under flowing N2) was placed in a Schlenk tube. To this was added a solution of MAO (2.3ml of 1.78M MAO in toluene) and Pentalene(TMS)2cyclopentadienyl zirconium chloride (8.5mg). The slurry was allowed to stand with occassional shaking for 90 minutes at room temperature. The catalyst was dried under vacuum at room temperature. Example 6 Pentalene(TMS)?cvclopentadienyl zirconium chloride co-impregnated with MAO on ES70X silica
Silica (lg, Crosfield ES70, calcined at 700°C under flowing N2) was placed in a Schlenk tube. To this was added a solution of MAO (5.7ml of 1.5M MAO in toluene) and Pentalene(TMS)2cyclopentadienyl zirconium chloride (20mg) in toluene (10ml). The slurry was allowed to stand with occassional shaking for 90 minutes at room temperature. The catalyst was dried under vacuum at room temperature. Polymerisations
The reagents used in the polymerisations were Ethylene Grade 3.5 (Supplied by Air Products), 1-hexene (Supplied by Aldrich) distilled over sodium/nitrogen, trimethylaluminium (2M in hexanes, Supplied by Aldrich) and triisobutylauminium (1M in hexanes, Supplied by Aldrich).
Example 7
Pentalene(TMS)2Cyclopentadienyl titanium chloride co-impregnated with MAO on ES70X silica Gas Phase, Copolymerisation
A 3 litre reactor was heated under flowing nitrogen for 1 hour at 77°C before sodium chloride (300g, predried under vacuum, 160°C, >4 hours) was added. Trimethyl aluminium (3ml, 2M in hexanes) was added to the reactor and allowed to scavenge the reactor of poisons for Vτ hour. After this period of time the alkyl aluminium was vented from the reactor using 4*4 bar nitrogen purges.
The gas phase was composed with 0.1 bar 1-hexene and 8 bar ethylene at 77°C prior to catalyst injection. After the catalyst (0.203g) prepared in Example 5 had been injected, under nitrogen the temperature was adjusted to 80°C. The ratio of hexene to ethylene during the polymerisation was keep constant by monitoring the gas phase composition by mass spectrometer and adjusting the flow rate of 1- hexene as required via a HPLC pump.
The polymerisation was allowed to continue for 1 hour before being terminated by purging the reactants from the reactor with nitrogen and reducing the temperature to < 30°C. The polymer was washed with water to remove the sodium chloride, then with acidified methanol (50ml HC1/2.5L methanol) and finally with water/ethanol (4: 1 v/v). The polymer was dried under vacuum, at 40°C, for 16 hours.
The weight of polymer was 0.6g Example 8 Pentalene(TMS)?cvclopentadienyl zirconium chloride co-impregnated with MAO on ES70X silicaGas Phase, Copolymerisation
A 3 litre reactor was heated under flowing nitrogen for 1 hour at 78°C before sodium chloride (300g, predried under vacuum, 160°C, >4 hours) was added. Trimethyl aluminium (3ml, 2M in hexanes) was added to the reactor and allowed to scavenge the reactor of poisons for 1 ' _ hours. After this period of time the alkyl aluminium was vented from the reactor using 4*4 bar nitrogen purges.
The gas phase was composed with 0.1 bar 1 -hexene and 8 bar ethylene at 78°C prior to catalyst injection. After the catalyst (0.23g) prepared in Example 6 had been injected, under nitrogen the temperature was adjusted to 80°C. The ratio of hexene to ethylene during the polymerisation was keep constant by monitoring the gas phase composition by mass spectrometer and adjusting the flow rate of 1- hexene as required via a HPLC pump.
The polymerisation was allowed to continue for 1 hour before being terminated by purging the reactants from the reactor with nitrogen and reducing the temperature to < 30°C. The polymer was washed with water to remove the sodium chloride, then with acidified methanol (50ml HC1/2 5L methanol) and finally with water/ethanol (4: 1 v/v). The polymer was dried under vacuum, at 40°C, for 16 hours.
The weight of polymer was 9.4g Example 9
Pentalene(TMS ?cyclopentadienyl zirconium chloride co-impregnated with MAO on ES70X silica Gas Phase, Copolymerisation
A 3 litre reactor was heated under flowing nitrogen for 1 hour at 78°C before sodium chloride (300g, predried under vacuum, 160°C, >4 hours) was added. Trimethyl aluminium (4ml, 2M in hexanes) was added to the reactor and allowed to scavenge the reactor of poisons for lhour. After this period of time the alkyl aluminium was Vented from the reactor using 4*4 bar nitrogen purges.
The reactor was cooled to below 30°C and trimethyl aluminium (2ml of 2M in hexanes) was added to the reactor. The reactor was heated to 78°C and the gas phase composed 0.1 bar 1 -hexene and 8 bar ethylene at 78°C prior to catalyst injection. After the catalyst (0.173g) prepared in Example 6 had been injected, under nitrogen the temperature was adjusted to 80°C. The ratio of hexene to ethylene during the polymerisation was keep constant by monitoring the gas phase composition by mass spectrometer and adjusting the flow rate of 1 -hexene as required via a HPLC pump.
The polymerisation was allowed to continue for 1 hour before being terminated by purging the reactants from the reactor with nitrogen and reducing the temperature to < 30°C. The polymer was washed with water to remove the sodium chloride, then with acidified methanol (50ml HC1/2.5L methanol) and finally with water/ethanol (4: 1 v/v). The polymer was dried under vacuum, at 40°C, for 16 hours.
The weight of polymer was 6.2g Example 10 Pentalene(ΥMSV2cyclopentadienyl zirconium chloride co-impregnated with MAO on ES70X silica Gas Phase, Copolymerisation, TiBA present
A 3 litre reactor was heated under flowing nitrogen for 1 hour at 78°C before sodium chloride (300g, predried under vacuum, 160°C, >4 hours) was added. Trimethyl aluminium (4ml, 2M in hexanes) was added to the reactor and allowed to scavenge the reactor of poisons for lhour. After this period of time the alkyl aluminium was vented from the reactor using 4*4 bar nitrogen purges.
The reactor was cooled to below 30°C and triisobutyl aluminium (2ml of 1M in hexanes) was added to the reactor. The reactor was heated to 78°C and the gas phase composed 0.1 bar 1 -hexene and 8 bar ethylene at 78°C prior to catalyst injection. After the catalyst (0.220g) prepared in Example 6 had been injected, under nitrogen the temperature was adjusted to 80°C. The ratio of hexene to ethylene during the polymerisation was keep constant by monitoring the gas phase composition by mass spectrometer and adjusting the flow rate of 1 -hexene as required via a HPLC pump.
The polymerisation was allowed to continue for 1 hour before being terminated by purging the reactants from the reactor with nitrogen and reducing the temperature to < 30°C. The polymer was washed with water to remove the sodium chloride, then with acidified methanol (50ml HC1/2.5L methanol) and finally with water/ethanol (4: 1 v/v). The polymer was dried under vacuum, at 40°C, for 16 hours. The weight of polymer was 7.3g
Examples 11-17 Polymerisations
Examples 11-17 were carried out in a 1 litre capacity autoclave using isobutane as the reaction medium. The reactor was heated to 85°C and thoroughly purged with nitrogen (2l/min) for 90 min. The temperature was then reduced to 50°C and the reactor charged with the chosen alkylaluminium scavenger and isobutane (500ml). The mixture was stirred (200rpm) at 75°C for a minimum of 120 min, the temperature was varied to the subsequent polymerisation temperature (T) and 10 bar overpressure of ethylene was then added. The metal complex (see belov ) and MAO were mixed together and then added to the reactor. Ethylene was added to maintain constant reactor pressure for the duration of the run. The run was terminated by rapidly venting the reactor and cooling to 20°C. Solid polymer product was washed with methanolic hydrogen chloride, rinsed with aqueous ethanol and dried (50°C, in vacuo, 16h). Details of the complexes and ds used are given in Table 1.
The metal complexes were (cyclopentadienyl) (1,5 -d i(trimethylsilyl) pentalene) zirconium chloride or the titanium analogue or (pentamethyl cyclopentadienyl) zirconium (l,5-di(trimethylsilyl) pentalene) zirconium chloride.
TABLE 1
i
The comonomer incorporation (Example 15) xvas determined by 13C-NMR with 3.1Butyl branches per 1000 Carbon atoms.
Cp* = (pentamcthvl) cyclopentadienyl
** = I-hcxene
Mn = molecular weight
PD = polydispersity

Claims

Claims:
1. A transition metal complex having the general formula:
LpM
Yx Xz
wherein
M is a Group IVA transition metal (Cotton and Wilkinson 2 ,nnd╬▒ Edition)
X is an anionic ligand Y = cyclopentadienyl
L is a neutral donor eg THF, amine and L, X or Y may be connected to the pentalene ligand,
R is hydrogen, alkyl, aryl, silyl, alkylsilyl or similar and may be the same or different n is 0-6 p = 0 or 1 y = 1 or 2 and when y = 1, z or x = 0, 1 or 2 when y = 2, z and x = 0.
2. A complex according to claim 1 wherein y is 1, M is zirconium or titanium, X is halogen and Y is cyclopentadienyl.
3. A complex according to claim 1 chosen from the group (cyclopentadienyl)[l,5-di(trimethylsilyl) pentalene] zirconium chloride, (cyclopentadienyl)[l,5-di(trimethylsilyl) pentalene] titanium chloride, (pentamethylcyclopentadienyl)[l,5-di(trimethylsilyl) pentalene] zirconium chloride, or bis [l,5-di(isopropylsilyl)pentalene] zirconium.
4. A catalyst composition suitable for the polymerisation of olefins comprising:
(a) a transition metal complex having the formula:
LpM
Yx Xz
wherein
M is a Group IVA transition metal (Cotton and Wilkinson 2nnd╬▒ Edition)
X is an anionic ligand
Y = cyclopentadienyl
L is a neutral donor eg THF, amine and L, X or Y may be connected to the pentalene ligand,
R is hydrogen, alkyl, aryl, silyl, alkylsilyl or similar and may be the same or different n is 0-6 p = 0 or 1 y == 1 or 2 and when y = 1, z or x = 0, 1 or 2 when y = 2, z and x = 0, and
(b) an activator.
5. A catalyst composition according to claim 4 wherein the activator is an aluminoxane.
6. A catalyst composition according to claim 4 wherein the activator is tris(pentaflurophenyl) boron, a trialkylammonium tetrakis(pentafluorophenyl) borate or a N,N-dialkylanilinium tetrakis (pentafluorophenyl) borate.
7. A catalyst composition according to claim 6 wherein the molar ratio of transition metal to activator is in the range 1 :0.1 to 1 : 10,000.
8. A catalyst composition according to claim 7 wherein the molar ratio of transition metal to activator is in the range 1 : 1 to 1 :2,000.
9. A catalyst composition according to claims 4-8 also comprising a support.
10. A catalyst composition according to claim 9 wherein the support is silica.
11. A process for preparing homopolymer of ethylene or copolymers of ethylene and alpha-olefins comprising performing the polymerisation in the presence of a catalyst composition according to claims 4-10.
12. A process according to claim 1 1 carried out in the gas phase.
EP98937653A 1997-08-07 1998-08-04 Novel transition metal complexes Withdrawn EP1003755A1 (en)

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GB201517648D0 (en) 2015-10-06 2015-11-18 Scg Chemicals Co Ltd Catalysts
GB201608384D0 (en) 2016-05-12 2016-06-29 Scg Chemicals Co Ltd Unsymmetrical metallocene catalysts and uses thereof

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DE19522105A1 (en) * 1995-06-19 1997-01-02 Hoechst Ag Stereorigid metallocene compound
DE19642432A1 (en) * 1996-10-15 1998-04-16 Hoechst Ag New stereo-rigid metallocene comprising transition metal complex with cyclo-pentadienyl-4,5-tetra:hydro-pentalene ligand system

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