GB2377936A - Sterically hindered amine compounds - Google Patents

Sterically hindered amine compounds Download PDF

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Publication number
GB2377936A
GB2377936A GB0211338A GB0211338A GB2377936A GB 2377936 A GB2377936 A GB 2377936A GB 0211338 A GB0211338 A GB 0211338A GB 0211338 A GB0211338 A GB 0211338A GB 2377936 A GB2377936 A GB 2377936A
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Prior art keywords
radicals
formula
hydrogen
tert
butyl
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GB2377936B (en
GB0211338D0 (en
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Dario Lazzari
Graziano Zagnoni
Stephen Mark Andrews
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BASF Schweiz AG
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Ciba Spezialitaetenchemie Holding AG
Ciba SC Holding AG
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477—Six-membered rings
    • C08K5/3492—Triazines
    • C08K5/34926—Triazines also containing heterocyclic groups other than triazine groups
    • 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
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0834—Compounds having one or more O-Si linkage
    • C07F7/0838—Compounds with one or more Si-O-Si sequences
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
    • C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
    • C09K15/30—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing heterocyclic ring with at least one nitrogen atom as ring member

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  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
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  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

A product of the formula (XI) <EMI ID=1.1 HE=64 WI=138 LX=288 LY=593 TI=CF> <PC>in which<BR> the radicals R<SB>31</SB> independently of one another are hydrogen, C<SB>1</SB>-C<SB>8</SB>alkyl or C<SB>1</SB>-C<SB>20</SB>acyl with 5 to 85 % of the radicals R<SB>31</SB> independently of one another being hydrogen or C<SB>1</SB>-C<SB>8</SB>alkyl and the remaining radicals R<SB>31</SB> being C<SB>1</SB>-C<SB>20</SB>acyl, and<BR> n<SB>6</SB> is a number from 2 to 50. The product finds use as a stabilizer of organic materials, in particular synthetic polymers, against the effects of light, heat and oxidation.

Description

Sterically hindered amine compounds The present invention relates to
products containing 1-(C'-C20acyl)-2,2,6,6-tetramethyl-4-
piperidyl groups as well as 2,2,6,6-tetramethyi-4-piperidyl groups the latter of which may optionally be substituted on the piperidyl nitrogen by C,-C alkyl, to the use of these products as light stabilizers, heat stabilizers and oxidation stabilizers for organic materials, particularly synthetic polymers, and to the organic materials thus stabilized.
2,2,6,6-tetramethylpiperidine derivatives are, for example, disclosed in EP-A-209,126, EP-A-849,327, DE-A-2,718,458 (= US-A-4,293,468 and US-A-4, 369,275), DE-A-2,755,340 (= US-A-4,238,613), EP-A-52,579 (= US-A-4,419, 472), EP-A-107,805, DE-A-3,403,116
(= US-A-4,532,279), US-A-4,670,488 and US-A-4,948,88g.
In detail, the present invention relates to a product containing 5to85%, for example 15to85%, 15to80%, 15to75%or5to75%, 15to70%or 20 to 70 %, 15 to 60 %, 20 to 60 %, 30 to 60 %, 25 to 50%, 40 to 60 % or 50 % of a group (A-1-a) and/or (A-1-b) H3C\ CH3
<N-H (A- 1 -a) H3C CH3
V {IN-C1-C8aikyl (A-1-b) H3C CH3
and15to95%,forexample15to85%,20to85%,25to85%or25to95%,30to85% or30to80%, 40to85%,40to30%,40to70%or50to75%,4Cto60%or50%ora group (A-2), H3C CH3
N-Cl-C2,acyl (A-2) Hi< H3C CH3
the total sum of the groups (A-1-a), (A-1-b) and (A-2) being 100 %.
- 2 A product which corresponds to the formula (1) as defined under a), the formula (11) as defined under b), the formula (V) as defined under c), the formula (Vi) as defined under d), the formula (Vu) as defined under e), a reaction product as defined under f), or which corresponds to the formula (IX) as defined under g), the formula (X) as defined under h), the formula (Xl) as defined under i), the formula (Xll) as defined under j), the formula (X111) as defined under k), the formula (XIV) as defined under 1), the formula (XVI) as defined under m), the formula (XVII) as defined under n), the formula (XV111) as defined under o) or the formula (XIX) as defined under p) is preferred.
a) a product mixture of the formula \/ O R] N/ > 0 C-R2 (I)
n1 in which the radicals R. independently of one another are hydrogen, C'C8alkyl or C'-C20acyl with 5 to 8S % of the total sum of the radicals R. independently of one another being hydrogen or C,-Caalkyl and the remaining radicals R. being C,-C20acyl; n, is20r4, if n, is 2, R2 is C -C, 4alkylene or bis{(C,-C20alkyi)oxycarbonyi}C4-C1Oalkanetetrayl, and if n, is 4, R2 is C4-C,Oalkanetetrayl; b) a product mixture of the formula X, /W IN R4 N R5 N R N '? X3
N:N R. N WN NJ:N R. N 'N
X2 X /: N X4 X /4 N XG X7
(11) in which
- 3 R3 and R7 independently of one another are hydrogen or C,-C,2alkyl, R4, R5 and R6 independently of one another are C2-C,0alkylene, and X, Xz, X3, X<, Xs, X6, X7 and Xa independently of one another are a group of the formula (111), H3C CH3
it< R8 Rg ( 1 1 1) H3C CH3
in which R8 is hydrogen, C,-C 2alkyl, Cs-C,2cycloalkyl, C,-C4alkylsubstituted Cs-C'2cycloalkyl, phenyl, -OH- and/or C,-C,Oalkyl-substituted phenyl, C7-Cgphenylalkyl, C7-Cgphenylalkyl which is substituted on the phenyl radical by -OH and/or C,-C,Oalkyi; or a group of the formula (IV), H3C CH3
MAN-R ( I V)
H3C CH3
and the radicals Rg and Rio independently of one another are hydrogen, C C8alkyl or C,-C20acyl with 5 to 85 % of the total sum of the radicals Rg and R,o independently of one another being hydrogen or C,-C8alkyl and the remaining radicals Rg and R,o being C,-C20acyl; c) a product mixture of the formula Xg N X44 (V) N,,N X,O in which Xg, X,O and X,, independently of one another are a group of the formula (111) with 5 to 85 % of the total sum of the radicals Rg and Rio independently of one another being hydrogen or C,-C8alkyl and the remaining radicals Rg and R,o being C,C20acyl;
d) I R, 1: (Vl) 1 R15 R,4 n2 in which Rip, Rut, Ret and Rats independently of one another are hydrogen, C,-C,2alkyl, C5-C,2cycloalkyl, C' -C4alkyl-substituted Cs-C 2cycloalkyl, phenyl, -O H- and/or C -C Oalkyl substituted phenyl, C7-Cgphenylalkyl, C7-Cgphenylalkyl which is substituted on the phenyl radical by -OH and/or C1-C'0aikyl; or a group of the formula (IV), R,2 is C2-C,6alkylene, Cs-C7cycloalkylene or C C4alkylenedi(Cs-C7cycloalkyiene), or the radicals Rip R j2 and R,3, together with the nitrogen atoms to which they are attached, form a 5- to 10-membered heterocyclic ring, or Rat and R,5, together with the nitrogen atom to which they are attached, form a 5- to 10 membered heterocyclic ring, n2 is a number from 2 to 50, and at least one of the radicals Rig, Rat, Rat and Rob is a group of the formula (IV) with 5 to 85 % of the radicals Rio independently of one another being hydrogen or C -C8alkyl and the remaining radicals Rio being C,-C20acyI;
- 5 e) I -0 - (Vu) l H3C I |CH3
H3C N CH3
R18 n3 in which R,6 is C -C,Oalkyl, Cs-C zcycloalkyl, C,-C4alkylsubstituted Cs-C'2cycloalkyl, phenyl or C,-C,Oalkyl-substituted phenyl, R, 7 is C3-C,Oalkylene, the radicals R,8 independently of one another are hydrogen, C,-C8alkyi or C,-C20acyl with 5 to 85 % of the radicals R,8 independently of one another being hydrogen or C,-C8alkyl and the remaining radicals R'8 being C,-C20acyl, and n3 is a number from 2 to 50; f) a product obtainable by reacting a compound, obtained by reaction between a polyamine of the formula (Villa) and cyanuric chloride, with a compound of the formula (Vlilb) or a rr.ixture of the compounds (Vlilb) and (Vlllb*) to give an intermediate H2N (CH2) 4 NH (CH2) n' NH (CH2) NH2 (Vlila) H-N-R 9 (Vlilb), H-N R. 9 (Vjilb*) H3C CH3 H3C < CH3
H3C N CH3 H3C NI CH3
H R20
in which
- 6 n'4, n"4 and n"'4 independently of one another are an integer from 2 to 12, R,g is hydrogen, C,-C'2alkyl, Cs-C,2cycloalkyl, phenyi or C7Cgphenylalkyl, and R20 is C,-C8aikyl, with the proviso that in the mixture of the compounds (Vlllb) and (Vlilb*) at least 15 % of the compound (Vlilb) is present; and subsequent acylation of the groups of the formula (A-1-a) being present in the intermediate \/ IN-H (A- 1 -a) H3C CH3
in a proportion to give a product which contains 15 to 95 % of the groups of the formula (A-2) H3C CH3
N - C,-c20acyl (A-2) H3C CH3
and 5 to 85 % of the groups of the formula (A-1-a) and/or (A-1-b), H3C CH3
IN-C,-Caalky (A-1-b) H3C CH3
relative to the total sum of the groups (A-1-a), (A-1-b) and (Am);
- 7 9) - I CH2 1 23 (IX)
O I O R23 of N 0 R27 121 126
H3C >ACHE R2s H3C N CH3
n5 in which R2, and R26 independently of one another are a direct bond or a group -N(Y4)-CO-Yz cO-N(y3)-, YE and Y3 independently of one another are hydrogen, C -Caalkyl, C5-C,2cycloalkyl, phenyi, C7-Cgphenylalkyl or a group of the formula (IV), Y2 is a direct bond or C,-C4alkylene, the radicals R22 independently of one another are hydrogen, C,-C8alkyi or C'C20acyl, R23, R24, R27 and R28 independently of one another are hydrogen, C,-C30alkyl, Cs-C,2cycloalkyl or phenyl, R2s is hydrogen, C -C30alkyl, CsC,2cycloalkyl, phenyl, C7-Cgphenylalkyl or a group of the formula (IV) with 5 to 85 % of the total sum of the radicals Rio and R22 independently of one another being hydrogen or C -C8alkyl and the remaining radicals Rio and R22 being C,-C20acyl, and nS is a number from to 50; h) a product mixture of the formula
O H3C CH3
11,Y C 0 N R30
/ \ 7<
K: CH C H3C CH3 (X)
W \ H3C CH3
R29 \ am<, C-O ( N-R30
1 1 '7:,
H3C CH3
in which R29 is hydrogen, C,-C 2alkyl or C,-C,2alkoxy, and the radicals R30 independently of one another are hydrogen, C,-C8alkyl or C,-C20acyl with 5 to 85 % of the total sum of the radicals R30 independently of one another being hydrogen or C,-C8alkyl and the remaining radicals R30 being C,-C20acyl; _ _ ICH-CH2 0 _
j) (CH)D-CHf CHZ O (Xl) I H3C |CH3
H3C IN CH3
R31 n 6 in which the radicals R3, independently of one another are hydrogen, C,-C8alkyl or C,-C20acyl with 5 to 85 Ma of the radicals R3. independently of one another being hydrogen or C -C3alkyl and the remaining radicals R3' being C,-C20acyl, and n6 is a number from 2 to 50;
- 9 - j) a product mixture of the formula H3C: 3 1 33 1 3s 0 R33 H CH3 R NOUN C-C NOON-R32 (Xll) i\ 1 /\ H3C CH3 R34 H3C CH3
in which the radicals R32 independently of one another are hydrogen, C,C8alkyi or C,-CzOacyl with 5 to 85 % of the total sum of the radicals R32 independently of one another being hydrogen or C,-C3alkyl and the remaining radicals R32 being C,-C20acyl, the radicals R33 independently of one another are hydrogen, C,-C,2alkyl or C,-C'2acyl, and R34 and R3s independently of one another are C,-C,2alkyl; k) --C-R36 1CH R37 CH-R38 C O-Rut< X R40 0-_ o=l 7=0 H3C CH3 H3C CH3
_ H3C I CH3 H3C R41 n 7 (X111)
in which R36, R37, R38, R39 and R40 independently of one another are a direct bond or C,-C,Oalkylene, the radicals R4, independently of one another are hydrogen, C,-C8alkyl or C -C20acyl with 5 to 85 % of the radicals R4, independently of one another being hydrogen or C,-C8alkyl and the remaining radicals R4, being C,-C20acyl, and n7 is a number from 1 to 50; 1) a product mixture of the formula
- 10 o Xjz\ Xl4 Of N NO X13 in which Xi2, X13 and X,4 independently of one another are a group of the formula (XV) _C 2-f H CH2-A (XV) OH inwhichAisagroupoftheformula(lll)with5to85%ofthetotalSumofthe radicals Rig and Rio independently of one another being hydrogen or C,-C6alkyl and the remaining radicals Rg and R:o being C -C20acyl; m) a product mixture of the formula H3C CH3 R43 1 43 H CH3
R42 N / N R43 N AN R42 (XVI)
>I /\
H3C CH3 H3C CH3
in which the radicals R42 independently of one another are hydrogen; C,-C alkyl or C,-C20acyl with 5 to 85 % of the total sum of the radicals R42 independently of one another being hydrogen or C,-C3alkyl and the remaining radicals R42 being C,-C20acyl the radicals R43 independently of one another are C,-C20acyl (C -C alkoxy)carbonyl (Cs-C 2cycloal koxy) carbonyl (C,-C alkyl)aminocarbonyl (Cs-c 2cycloalkyl)aminocarbonyl (C7Cgphenylalkyl)aminocarbonyl C,-C6alkyl Cs-C,2cycloalkyl which is unsubstituted or substituted by 1 2 or 3 C,-C4alkyl; C3-C6alkenyl C7Cgphenylalkyl which is unsubstituted or substituted on the phenyl by 1 2 or 3 C,-C4alkyl; or -CH2CN and R43 is C2-C22alkylene Cs-C7cycloalkylene C, -C4alkylenedi(C5-C7cycloalkylene) phenylene or phenyienedi(C,-C4alkylene); n) a product mixture of the formula
- 11 H3C CH3 1 l H CH3 R4s R R44 (XVil) H3C CH3 45 H3C CH3
in which the radicals R44 independently of one another are hydrogen, C,C3alkyl or C,-C20acyl with 5 to 85 % of the total sum of the radicals R44 independently of one another being hydrogen or C,-Ceaikyl and the remaining radicals R44 being C,-C20acyl, the radicals R4s independently of one another are hydrogen, C,-C,2alkyl or C -C'2acyl,and R46 is C,-C, Oalkylene; a) a product mixture of the formula H3C CH
N N {IN-R47 (XV111)
H3C)Z 3 N J
R47-N IN,N
O H3C CH3
in which the radicals R47 independently of one another are hydrogen, C,C3alkyl or C -C20acyl with 5 to 85 % of the total sum of the radicals R47 independently of one another being hydrogen or C,-Cealkyl and the remaining radicals R47 being C,-C20acyl; or
- 12 _ p) R4s I Rsl C (XIX) 1=0:=0
l l Rso Rs2 _ n in which R48 and Rs' independently of one another are C C, alkylene, the radicals R49 independently of one another are hydrogen or C,-C,Oalkyl, Rso is C,-C Oalkyl, Rs2 is C,-C,Oalkyl or a group of the formula (IV), and n8 is a number from 3 to 50, with the proviso that at least 50 % of the radicals Rs2 are a group of the formula (IV) with 5 to 85 % of the radicals Rio independently of one another being hydrogen or C -Gaalky! and the remaining radicals Rio being C -C20acyl Examples of alkyl having up to 30 carbon atoms are methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 2-ethylbutyl, n-pentyl, isopentyl, 1-methylpentyl, 1,3-dimethyl-
butyl, n-hexyl, 1-methylhexyl, n-heptyl, isoheptyl, 1,1,3,3tetramethylbutyl, 1-methylheptyl, 3-
methylheptyl, n-octyl, 2-ethylhexyl, 1,1,3-trimethylhexyl, 1,1,3,3tetramethylpentyl, nonyl, decyl, undecyl, 1-methylundecyl, dodecyl, 1,1,3, 3,5,5-hexamethylhexyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyi, octadecyl, eicosyl, docosyl and triacontyl One of the preferred meanings of R23 and R27 is C,-C2salkyi, especially C's-c2saikyl, for example hexadecyl and C,8-C22alkyl. One of the preferred meanings of R2s is C,-C2salkyl, especially octadecyl. One of the preferred meanings of R3 and R, is C,-C4alkyl, especially n-butyl. Examples of C,-C4alkoxy are methoxy, ethoxy, propoxy and butoxy.
Examples of C3-C6alkenyl are allyl, 2-methallyl, butenyl, pentenyl and hexenyl. Allyi is
- 13 preferred. The carbon atom in position 1 is preferably saturated.
Examples of Cs-C 2cycloalkyl are cyclopentyi, cyciohexyl, cycloheptyl, cyclooctyl and cyclododecyl. Cs-Cscycloalkyl, especially cyclohexyl, is preferred.
C,-C4alkyl-substituted Cs-C'2cycloalkyl is for example methylcyclohexyl or dimethylcyclohexyl. -OH- and/or C,-C,Oalkyl-substituted phenyl is for example methylphenyl, dimethylphenyl, trimethylphenyl, tert-butylphenyl or 3,5-di-tert-butyi-4-hydroxyphenyl.
Examples of C7-Cgphenylalkyl are benzyl and phenylethyl.
C7-Cgghenylalkyl which is substituted on the phenyl radical by -OH and/or by alkyl having up to 10 carbon atoms is, for example, methylbenzyl, dimethylbenzyl, trimethylbenzyl, tert-
butylbenzyl or 3, 5-di-tert-butyl-4-hydroxybenzyl.
C,-C20acyi (e.g. C2-C20acyl) is preferably C,-C20alkanoyl or C2C20alkanoyl, C3-C20alkenoyl or benzoyl. Examples are formyl, acetyl, propionyl, butyryl, pentanoyl, hexanoyl, octanoyl, benzoyl, acryloyl and crotonoyl. C, -C,Oacyl (e.g. C2-C,0acyl), in particular C, -C8acyl or C2C8acyl such as C,-C8alkanoyl or C2-C8alkanoyl, C3-C8alkenoyl or benzoyl, especially acetyl, is preferred.
Examples of (C,-C8alkoxy)carbonyl are methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl, pentoxycarbonyl, hexoxycarbonyl, heptoxycarbonyl and octoxycarbonyi. One of the preferred meanings of A is (C,-C2alkoxy)carbonyl.
A particularly preferred example of (Cs-C,2cycloalkoxy)carbonyl is cyclohexoxycarbonyi.
Examples of (C,-C8alkyl)aminocarbonyl are methylaminocarbonyl, ethylaminocarbonyl, propylaminocarbonyl, butylaminocarbonyl, pentylaminocarbonyl, hexylaminocarbonyl, heptylaminocarbonyl and octylaminocarbonyl. (C,-C4alkyl)aminocarbonyl is preferred.
A particularly preferred example of (Cs-C 2cycloalkyl)aminocarbonyl is cyclohexylaminocarbonyl. A particularly preferred example of (C7Cgphenylalkyl)aminocarbonyl is benzylaminocarbonyl.
Examples of alkylene having up to 22 carbon atoms are methylene, ethylene, propylene, trimethylene, tetramethylene, pentamethylene, 2,2dimethyltrimethylene, hexamethylene, trimethylhexamethylene, octamethylene and decamethylene R 2 is preferably hexamethylene, R36 and Rae are preferably methylene, R39 is preferably 2,2-dimethylethylene and R40 1,1-dimethylethyiene.
An example of C4-C Oalkanetetrayl is 1,2,3,4-butanetetrayl.
An example of bis{(C -C20alkyl)oxycarbonyl}C4-C,Oalkanetetrayl is bis{tridecyloxycarbonyl}butanetetrayl. An example of Cs-C7cycloalkylene is cyclohexylene.
An example of C -C4alkylenedi(Cs-C7-cycloalkylene) is methyienedicyclohexylene.
An example of phenylenedi(C -C4alkylene) is phenylenedimethylene.
Where the radicals Rig,, Rig and R,3, together with the nitrogen atoms to which they are attached, form a 5- to 10-membered heterocyclic ring, the resulting ring is for example CH 1 3 1 -\)
rC\ / \ N N-, N N- or -N N / / A 6-membered heterocyclic ring is preferred.
Where the radicals R,4 and Rid, together with the nitrogen atom to which they are attached, form a 5- to 1 O-membered heterocyclic ring, the resulting ring is for example 1 -pyrrolidyl, piperidino, morpholino, 1piperazinyl, 4-methyl-1-piperazinyl, 1-hexahydroazepinyl, 5,5,7-
trimethyl-1-homopiperazinyl or 4,5,5,7-tetramethyl-1-homopiperazinyl. Morpholino is
- 15 particularly preferred.
One of the preferred meanings of R23 and R27 is phenyl.
Y2 and R37 are preferably a direct bond.
One of the preferred meanings of Y. and Y3 is hydrogen.
H:iCH3 H: CH3 A preferred meaning of the group {_<N-ct-ceal is IN-C,C4alky!, in H3C CH3 H3C CH3
H3C CH3
particular IN-CH3.
H3C CH3
n2 is preferably 2-25.
n3 is preferably 2-25, especially 2-20 or 2-10.
n4', n4" and n4"' are preferably 2-4.
Us is preferably 2-25, especially 2-20 or 2-10.
n6 is preferably 2-25, especially 2-20 or 2-10.
n7 is preferably 1-25, especially 1-20 or 1-10.
n3 is preferably 3-25, especially 3-20.
A product which is of interest is one wherein n'is2Or4, if n, is 2, R2 is C2-C,0alkylene or bis{C -C,salkyl}oxycarbonyl, and if nil is 4, R2 is 1,2, 3,4-butanetetrayl; R3 and R7 independently of one another are hydrogen, C'-C4alkyl or C,-C20acyl, R4, Rs and R6 independently of one another are Cz-C6alkylene, and
- 16 R8 is hydrogen, C,-C6alkyl, Cs-C8cycloalkyl, methyl-substituted Cscacycloalkylt phenyl, C -Cgphenylalkyl or a group of the formula (IV); R', , Rat, Ret and Rats independently of one another are hydrogen, C'-csalkyl, Cs-C3cycloalkyl, methyl-substituted Cs-C8cycloalkyl, phenyl, C7Cgphenylalkyl or a group of the formula (IV), or the radicals R,4 and R'5, together with the nitrogen atom to which they are attached, form a 6membered heterocyclic ring, R 2 is C2-C,Oalkylene, and n2 is a number from 2 to 25; Rue is C,-C4alkyl, Cs-C cycloalkyl or phenyl, R,7 is C3C6alkylene, and n3 is a number from 2 to 25; n'4, n"4 and n"'4 independently of one another are an integer from 2 to 4, and Rig is C,C4alkyl; Rig, and R26 independently of one another are a direct bond or a group -N(Y4)-CO-Y2-CO-N(Y3)-,
Y. and Y3 independently of one another are hydrogen or C -C4alkyl, Y2 is a direct bond, R23 and R27 are C,-C2salkyl or phenyl, R24 and R28 are hydrogen or C,-C4alkyl, R2s is C,-C2salkyl or a group of the formula (IV), and nS is a number from 2 to 25; R29 is hydrogen, C,-C4alkyl or C,C4alkoxy; n6 is a number from 2 to 25; the radicals R33 independently of one another are hydrogen or C'-C4alkyi, and the radicals R34 and R3s independently of one another are C,-C4alkyl;
- 17 R36, Rae, R39 and R40 independently of one another are C -C4alkylene, R37 is a direct bond, and n7 is a number from 1 to 25; R43 is C2C6alkylene, cyclohexylene or phenylene; the radicals R4s independently of one another are hydrogen or C1 C4alkyl, and R46 is C2-C6alkylene; and R48 and Ins, independently of one another are C,-C6alkylene, the radicals R49 independently of one another are hydrogen or C -C4alkyl, R50 is C,C4alkyl, R52 is C,-C4alkyl or a group of the formula (IV), and n8 is a number from 3 to 25.
A product which relates to a preferred embodiment is one corresponding a) to a product mixture of the formula H C3 0-C-(CH2)3 C O;CH3 1 (I-a) H3C CH3 H3C CH3
wherein 5 to 85 % of the total sum of the radicals R. are hydrogen or methyl and the remaining radicals R. are C,-C,Oacyl; to a product mixture of the formula H2lC ICH fH fH2 {l-b) C=0 C=0 C=0 C=0
1 1 1 1
H3C CH3 H3C:CH3 H3C >CH3 H3C cH3 H3C I CH3 H3C N CH3 H3C I CH3 H3C I CH3
R. R. R' R.
wherein 5 to 85 % of the total sum of the radicals R. are hydrogen or methyl and
- 18 the remaining radicals R. are C -C,Oacyl; or to a product mixture of the formula H2f f H - f H - fH2 - (l c) Cl≥0 C o I =0 C-o o o o o R' R' R. Rat wherein two of the radicals R* are -COO-C 3H27, and ACHE two of the radicals Ret are a group - <N-Rig with 5 to 85 % of the total H3C CH3
sum of the radicals Rat being hydrogen or methyl and the remaining radicals R. being C,-C,Oacyl; b) to a product mixture of the formula (Ila) Rs AN-. --N (CH2), N C 2Cti2 - (ii a) H3C CH3 l H. H NAN H3C: <CH HgC4N/ N --N-C4Hg H3C IN CH3 H3C <CH3 H3C CH3
R9 H3C N CH3 H3C I CH3
Rg Rg 2 wherein 5 to 85 % of the tote! sum of the radicals Rig are hydrogen or methyl and the remaining radicals Erg are C -C,Oacyl; c) to a product mixture of the formula (V-a)
- 19 H3C CH3 \
Rg N}N /' N / N R (V-a) H3C CH3 C4Hg N N C4Hg H C CH3 N C4Hg H3C CH3
H3C N CH3
Rg wherein 5 to 85 % of the total sum of the radicals Rg are hydrogen or methyl and the remaining radicals Rg are C,-C,Oacyl; d) to the formula (Vl-a), (Vl-b), (Vl-c), (Vl-d) or (Vl-e) _ N (CH2)6 N N\I_ (Vl-a) H3C CH3 H3C <CH3 \
H C N CH H C IN CH3 N-C H.
H3 c>:NiC 3 R,on 2 _ N-(CH2)6 N N\ - (Vl-b) H3C CH3 H3C <CH3 \
H3C IN CH3 H3C I 3 N C-CH2 C-CH3 n 2
- 20 - (CH2) > i (Vl-c) HH33Cc CH3 H3C CH3 n N-(CH2)6 N /N:r _ (Vl-d) H3C CH3 H3C CEl3 \ H3C N CH3 H3C CH3 N-H
R10 Rlo f N _-(CH)- N /N (Vl e) H3C CH3 H3C CH3
H3C Nl CH3 H3C Nl CH3 N-H RIO RIO H C-C-CH
CH3 n 2 wherein 5 to 85 % of the radicals R'o independently of one another are hydrogen or methyl and the remaining radicals R,o are C -C, Oacyl; e) to the formula (Vil-a)
- 21 ICH3 _ Si O-- (Vl l-a) L.. (CH2)3
H3C; CH3
H C N CHAT
- 1 R1.3 n3 wherein 5 to 85 % of the radicals R,a independently of one another are hydrogen or methyl and the remaining radicals R4r3 are C,-C, Oacyl; f) to a product obtainable by reacting a compound, obtained by reaction between a polyamine of the formula (Villa-1) and cyanuric chloride, with a compound of the formula (Vlilb-1) or a mixture of the compounds (Vlllb-1) and (Vlllb*-1) to give an intermediate H2N (CH2)3 NH(CH2)2 NH (CH2)3 NH2 (Vlila-1) H-N C4Hg (Vlllb-1), H-I C4Hg (Vlllb*-1) H3C 1-- CH3 H3C <CH3
H3C INCH3 H3C ICH3
H CH3 with the proviso that in the mixture of the compounds (Vlilb-1) and (Vlllb*-1) at least 15 % of the compound (Vlllb-1) is present; and subsequent acylation of the groups of the formula (A-1-a) being present in the intermediate H3C C H3
-(7<N-H (A-l-a) H3C CH3
- 22 in a proportion to give a product which contains 15 to 95 % of the groups of the formula (A-2-1) H3C CH3
N-C,-C,Oacyl (A-2-1) H3C CH3
and 5 to 85 % of the groups of the formula (A-1-a) and / or (A-1-b-1), H <CH3
N-CH3 (A-1 b-1) H3C CH3
relative to the total sum of the groups (A-1 -a), (A-1 -b-1) and (A-2-1); g) to the formula (IX-a), (IX-b) or (IX-c) H _
H2 7z, (lava) H C: CH3 3 H. C>:: CH3
H3C R22 H3C I CH3
n C, H 7 [,, ( I X b) H3C\ CH3
H3C I CH3
R22 n
- 23 l H I ---To CH C I I CH C (lX-c) o<N:O C H O N>o C16H33 7=0 Ic-o lc o lc=o NH NH
H3C CH3 H3C CH3
H3C IN CH3 H3C I CH3
R22 R10 _ n5 wherein 5 to 85 % of the radicals Rio and R22 independently of one another are hydrogen or methyl and the remaining radicals Rio and R22 are C,-C'Oacyi; h) to a product mixture of the formula (X-a) o H CH3 C-On_ AN-R30 H3CO CH C H3C CH3 (X-a) Hi:< CH3 C-O AN-R30
H3C CH3
wherein 5 to 85 % of the total sum of the radicals R30 are hydrogen or methyl and the remaining radicals R30 are C,-C,Oacyl; i) to the formula (Xl) wherein 5 to 85 % of the radicals R3, independently of one another are hydrogen or methyl and the remaining radicals R3' are C,-C,Oacyl; I) to a product mixture of the formula (Xll-a)
- 24 H3C CH3 H if H3 0 H H CH3 R32 N I ' N - C C-N IN-R32 (Xl l-a) H3C CH3 CH3 H3C CH3
wherein 5 to 85 % of the total sum of the radicals R32 are hydrogen or methyl and the remaining radicals R32 are C,-C Oacyl; k) to the formula (X111-a) ARC-CH2 C H C H-CHz-C-O-CHz-C - /-'-CHz - O-
3- OH H,C, CH
(Xl 11 -a) wherein S to 85 % of the radicals Rip independently of one another are hydrogen or methyl and the remaining radicals R4, are C -C Oacyl; 1) to a product mixture of the formula (XlV-a) H3C CH3 O
R--_ N H-CH Ch-2\ /C / 2 (Xl V-a) HI CH3 _, C N/ Cow, 3 fH2 wherein 5 to 85 % of the total sum of the radicals Rg are hydrogen or methyl and the remaining radicals Rg are C,-C,Oacyl;
- 25 m) to a product mixture of the formula (XVI-a) H3C CH3 R R43* H CH3
R42 - Nit N (CH2)6 N KIN R42 (XVI-a) /\ /\ H3C CH3 H3C CH3
wherein 5 to 85 % of the total sum of the radicals R42 are hydrogen or methyl and the remaining radicals R42 are C'-C Oacyl; and the radicals R43* are C,-C,Oacyl; n) to a product mixture of the formula (XVII-a) H3C CH3 1 l Hi2 CH3 R44 New N-CH2CH2-C-N R44 (XVII-a) H3C CH3 H3C CH3
wherein 5 to 85 % of the total sum of the radicals R44 are hydrogen or methyl and the remaining radicals R44 are C,-C,Oacyl; a) to a product mixture of the formula (XV111) wherein 5 to 85 % of the total sum of the radicals R47 are hydrogen or methyl and the remaining radicals R47 are C C,Oacyl; or p) to the formula (XlX-a) -CH2-of CH2-fH (XlX-a) :=0 I-o f f CH3 Rs2 n wherein the radicals Rs2 independently of one another are ethyl or a group of the formula (IV),
- 26 with the provisos that (1) at least 50 % of the radicals Rs2 are a group of the formula (IV) with R:o being hydrogen, methyl or C -C Oacyl, and the remaining radicals R52 are ethyl and (2) 5 to 85 % of the radicals Rio independently of one another are hydrogen or methyl and the remaining radicals Rio are C'-C,Oacyl A product which relates to a further preferred embodiment is one corresponding a) to a product mixture of the formula (I-a) wherein 20 to 70 TO of the total sum of the radicals R. are hydrogen or methyl and the remaining radicals R. are C -C,Oacyl; to a product mixture of the formula (I-b) wherein 20 to 70 TO of the total sum of the radicals R. are hydrogen or methyl and the remaining radicals R. are C,-C,Oacyl; or to a product mixture of the formula (I-c) wherein 20 to 70 % of the total sum of the radicals R. are hydrogen or methyl and the remaining radicals R. are C,-C,Oacyl; b) to a product mixture of the formula (Il-a) wherein 20 to 70 /O of the total sum of the radicals Rig are hydrogen or methyl and the remaining radicals Rg are C,-C Oacyl; c) to a product mixture of the formula (V-a) wherein 20 to 70 % of the total sum of the radicals Rg are hydrogen or methyl and the remaining radicals Rg are C -C,Oacyl; d) to the formula (Vl-a), (Vl-b), (Vl-c), (Vl-d) or (Vim) wherein 20 to 70 % of the radicals Rio independently of one another are hydrogen or methyl and the remaining radicals Rio are C,-C,Oacyl; e) to the formula (Vll-a) wherein 20 to 70 % of the radicals R,8 independently of one another are hydrogen or methyl and the remaining radicals R,8 are C,-C'Oacyl; f) to a product obtainable by reacting a compound, obtained by reaction between a
- 27 polyamine of the formula (Vlila-1) and cyanuric chloride, with a compound of the formula (Vlilb-1) or a mixture of the compounds (Vlllb-1) and (Vlilb*-1) to give an intermediate with the proviso that in the mixture of the compounds (Vlilb-1) and (Vlllb*-1) at least 30 % of the compound (Vlllb-1) is present; and subsequent acylation of the groups of the formula (A-1-a) being present in the intermediate in a proportion to give a product which contains 30 to 80 % of the groups of the formula (A2-1) and 20 to 70 % of the groups of the formula (A-1-a) and / or (A-1-b1), relative to the total sum of the groups (A-1-a), (A-1-b-1) and (A-2-1) ; g) to the formula (IX-a), (IX-b) or (IX-c) wherein 20 to 70 % of the radicals Rio and R22 independently of one another are hydrogen or methyl and the remaining radicals Rio and R22 are C,-C,Oacyl; h) to a product mixture of the formula (X-a) wherein 20 to 70 % of the total sum of the radicals R30 are hydrogen or methyl and the remaining radicals R30 are C,C,Oacyl; i) to the formula (Xl) wherein 20 to 70 % of the radicals R3, independently of one another are hydrogen or methyl and the remaining radicals Rat are C,-C Oacyl; j) to a product mixture of the formula (Xlla) wherein 20 to 70 % of the total sum of the radicals R32 are hydrogen or methyl and the remaining radicals R32 are C,-C,Oacyl; k) to the formula (Xl11-a) wherein 20 to 70 % of the radicals R4, independently of one another are hydrogen or methyl and the remaining radicals R4, are C,C,Oacyl; I) to a product mixture of the formula (XlV-a) wherein 20 to 70 % of the total sum of the radicals Rg are hydrogen or methyl and the remaining radicals Rg are C,-C'Oacyl; - 28 m) to a product mixture of the formula (XVI-a) wherein 20 to 70 % of
the total sum of the radicals R<2 are hydrogen or methyl and the remaining radicals R4z are C'-C Oacyl; n) to a product mixture of the formula (XVII-a) wherein 20 to 70 % of the total sum of the radicals R44 are hydrogen or methyl and the remaining radicals R44 are C,-C Oacyl; a) to a product mixture of the formula (XV111) wherein 20 to 70 % of the total sum of the radicals R47 are hydrogen or methyl and the remaining radicals Rat are C -C Oacyl; or p) to the formula (XlX-a) wherein 20 to 70 % of the radicals R'o independently of one another are hydrogen or methyl and the remaining radicals Rio are C -C Oacyl.
A product which relates to a particular preferred embodiment is one corresponding a) to a product mixture of the formula (I-a) wherein 15 to 30 % of the total sum of the radicals Rat are hydrogen or methyl and the remaining radicals Rig are C1-C Oacyl; b) to a product mixture of the formula (Il-a) wherein 30 to 50 / of the total sum of the radicals R9 are hydrogen or methyl and the remaining radicals Rg are C -C,Oacyl; d) to the formula (Vl-a) wherein 15 to 85 % of the radicals Rio independently of one another are hydrogen or methyl and the remaining radicals Rio are C -C Oacyl; or to the formula (Vl-b) or (Vl-c) wherein 15 to 60 % of the radicals Rio independently of one another are hydrogen or methyl and the remaining radicals P(,O are C,-C Oacyl; e) to the formula (Vll-a) wherein 15 to 35 % of the radicals R,8 independently of one another are hydrogen or methyl
- 29 and the remaining radicals R,8 are C -C,Oacyl; f) to a product obtainable by reacting a compound, obtained by reaction between a polyamine of the formula (Vlila-1) and cyanuric chloride, with a compound of the formula (Vlllb-1) or a mixture of the compounds (Vlilb-1) and (Vlilb*-1) to give an intermediate with the proviso that in the mixture of the compounds (Vlilb-1) and (Vlllb*-1) at least 50 % of the compound (Vlllb-1) is present; and subsequent acylation of the groups of the formula (A-1-a) being present in the intermediate in a proportion to give a product which contains 50 to 70 % of the groups of the formula (A-2-1) and 30 to 50 % of the groups of the formula (A-1-a) and / or (A-1-b-1), relative to the total sum of the groups (A-1 -a), (A-1 -b-1) and (A-2-1); k) to the formula (Xl11-a) wherein 15 to 30 % of the radicals R4, independently of one another are hydrogen or methyl and the remaining radicals Red are C,-C,Oacyl; or m) to a product mixture of the formula (XVI-a) wherein 30 to 50 /0 of the total sum of the radicals R42 are hydrogen or methyl and the remaining radicals R42 are C,-C Oacyl.
A product wherein the meaning C,-C Oacyl is acetyl is especially preferred.
A product which corresponds to the formula (Vl-a) wherein 40 to 60 %, e.g. 25 to 50 %, of the radicals R'o independently of one another are hydrogen or methyl is also preferred.
A product which corresponds to the formula (Vl-a) wherein 40 to 60 %, e.g. 25 to 50 %, of the radicals Rio are hydrogen and the remaining radicals Rio are acetyl is particularly preferred.
- 30 The products described under a) to p) above can be prepared, for example, by the method indicated below under "Example of a preparation process', using the corresponding 2,2,6,6-
tetramethylpiperidine derivatives (unsubstituted nitrogen in the 2 2 6 6tetramethyl-4-piperid groups) as starting compounds. The 2,2,6,6tetramethylpiperidine derivatives are essentially known (some are commercially available) and can be prepared by known methods, for example as described in US-A-3,640,928, US-A-4,1 08,829, US-A-3,925,376, tJS-A-
4,086,204, EP-A-782,994, EP-A-850,938, US-A-4,331,586, US-A-5,051,458,
US-A-4,477,615 and Chemical Abstracts - CAS No 13650a-96-6, US-A-4,857, 595, DD-A-262,439 (Derwent 89-122983/17, Chemical Abstracts 111:58964u), WO-A-94/12,544 (Derwent 94- 177274/22), GB-A-2,269,819, US-A-4,340,534, EP-A- 172,413, tJS-A-4,52g,760, US-A-5,182,390 (Chemical Abstracts - CAS No. 144923-25-1), US-A-4,976,889, SU-A-768,175 (C)erwent 88-138,751/20), US-A-4,769,457 and DE-A-2,748,36 (C)erwenl 3 517B/1 9).
The 2,2,6,6-tetramethylpiperidine derivative intermediate belonging to item f) above can be prepared in analogy to known methods, for example by reacting a polyamide of the formula (Villa) with cyanuric chloride in a molar,atio of from l:2 to 1:4 in the presence of anhydrous lithium carbonate, sodium carbonate or potassium carbonate in an organic solvent such as 1,2-dichloroethane, toluene, xylene, benzene, dioxane or tertamyl alcohol at a temperature of from -20 C to +10 C, preferably from 10 C to +1 0 C, in particular from 0 C to +10 C, for from 2 to 8 hours and then reacting the resulting product with a 2,2,6,6-tetramethyl-4-
piperidylamine of the formula (Vlllb). The molar ratio of 2,2,6,6tetramethyl- -piperidylamine to the polyamide of the formula (Vlila) which is employed is' for example, from 4:1 to 8:1.
The quantity of 2,2,6,6-tetramethyl-4-piperidylamine can be added in one go or in two or more portions at an interval of a few hours.
The ratio of polyamide of the formula (Villa) to cyanuric chloride to 2,2, 6,6-tetramethyl-4-
piperidylamine of the formula (Vlllb) is preferably from 1:3:5 to 1:3:6 The following example indicates a possible method of preparing the preferred 2,2,6,6-
tetramethylpiperidine derivative intermediate which belongs to item f) above.
Example: 23.6 g (0.128 mol) of cyanuric chloride, 7.43 9 (0.0426 mol) of N,N'-bis[3-
aminopropyl]ethylenediamine and 18 g (0.13 mol) of anhydrous potassium carbonate are
- 31 reacted in 250 ml of 1,2-dichloroethane at 5 C for 3 hours with stirring. The mixture is heated at room temperature for a further 4 hours. 27.2 9 (0.128 mol) of N-(2,2,6,6-tetramethyl-4-
piperidyl)butylamine are added and the mixture obtained is heated at 60 C for 2 hours. A further 18 g (0.13 mol) of anhydrous potassium carbonate are added and the mixture is heated at 60 C for a further 6 hours. The solvent is distilled off under a slight vacuum (200 mbar) and replaced by xylene. 18.2 g (0.085 mol) of N-(2,2,6,6-tetramethyl-4-
piperidyl)butylamine and 5.2 g (0.13 mol) of ground sodium hydroxide are added and the reaction mixture is heated at reflux for 2 hours, and for a further 12 hours, the water produced in the reaction is removed by azeotropic distillation. The mixture is filtered. The solution is washed with water and dried over Na2SO4. The solvent is evaporated off and the residue is dried in vacua (0.1 mbar) at 120-130 C. The desired product is obtained as a colourless resin.
In general, a 2,2,6,6-tetramethylpiperidine derivative intermediate belonging to item f) above can be represented, for example, by a compound of the formula (V111-1), (V111-2) or (Vl11-3). It can also be present as a mixture of these three compounds.
HN (CH2)2 42 N ( 2) 2 42 2 '2 _
N N NiN NiN he' Rlg R'g /Q N 3\ Rlg -N /t N At\ N H3C CH3 H3C <CH3 H3C Oh< CH3 H3C CH3 H3C CH3 H3C Nl CH3 H3C I CH3 H3C IN CH3 H3C IN CH3 H3C Nl CH3 H H H H H _
_ no (Vl11-1)
- 32 HN (CH2) N - _
N 1 N 2-421
N N '9 ( H2)2 42
H3C cCHH3 N 1 N (CHZ) 2- 2N 1 N H N N R s79 N /: N N R s H3C > CH3 H3C CH3 H3C CH3 H3C CH3
H3C N CH3 H3C IN CH3 H3C IN CH3 H3C IN CH3
H H H H
n4 (V1 1 1-2)
r N - - (CHz) 2 12 N >' -N-Rl9 (CH2)2 2 (IH2)2-12 H3C N CH3 19\ ':\ / R,s R 9 R H3C <CH1 hlC C-3 H3C CF 3 H 3C > < Ci-13 H3C N CH3 H3C N CH3 H3C N CH3 h3C N CH3 L H H H H - n (V1 1 1 -3)
A preferred meaning of the formula (V111-1) is HN - (C 2) N (CH2)2 N -(CH2)-NH
N N N N N N
/ N:\ n-HgC4 \ 1 -N 3\ n-H:C4 \ 'N '\ C4H9-n N-C4H9-n N N - C4Hg-n N HIC> <cH3 H3C> CH3 H3C> <CH3 H3C <CH3 H3C. CH3 H3C Nl CH3 H3C IN CH3 H3C N CH3 -3C I CH3 H3C IN CH3 _ H H H H H _ n4 A preferred meaning of the formula (V111-2) is
- 33 HN (CH2) N _
N1N 3 1
N: N C4H9-n (CH2) 2 H3C CH3 N (CH2) N H
H3C,N CH3 N l N n-HgC N 1 N n-H9C4 N /4 N ' N-C4H9-n \ N N $, C4H9 n H3C > ( <CH3 H3C))( CH3 H3C CH3 H3C > < CH3
H3C IN CH3 H3C IN CH3 H3C IN CH3 H3C Nl CH3 _ H H H H r n A preferred meaning of the formula (V111-3) is N (CH2) - N _ _
-1 2 1
N N (CH2)3 (CH2)3
/ N N _ C4Hg-n NH NH H3C n-H9c4 N1N n HgC4\ N 1N C4H9 n H N N-C4H;-n N N H3C)h(CH3 H3C)h<CH3 H3C)h<CH3 H3C CH H3C I CH3 H3C IN CH3 H3C I CH3 H3C IN CH3
H H H H n4 In the above formulae (V111-1) to (V111-3), n4 is preferably 1 to 20, e.g. 2 to 20.
Preferred commercially available starting materials for the preparation of the compounds shown above under items a) to b), d) to g), i) to k) and m) to p) are TINUVIN 770, MARK LA 57, MARK LA 67, CHIMASSORB 905, CHIMASSORB 202O,
CHIMASSORB944, CYASORB UV3346, DASTIB 1082, UVASIL299, UVASORB HA
88, UVINUL5050 H. LICHTSCHUTZSTOFF UV 31, LUCHEM HA-B 1 8, HOSTAVIN N
3O, SUMISORBTM 61, MARKLA 68, UVINUL4050 H. DIACETAM 5, a0UVINUL 4049 and FERRO AM 806.
Particularly preferred starting materials are the products disclosed in EP-A-85O,938, especially the products disclosed therein in EXAMPLES 1 to 7, in particular EXAMPLE 1.
EP-A-850,938 which is equivalent to US Patent Application No. 08/994,977 filed on
- 34 December 1g, 1997 is incorporated herein by reference Further particularly preferred starting materials are the products disclosed in EP-A-782,994, especially the products disclosed therein in EXAMPLES 1 to 12, in particular EXAMPLE 10.
EP-A-782,994 which is equivalent to US Patent Application No. 08 756,225 filed on November 25, 1996 is also incorporated herein by reference.
In more detail, those products essentially known from EP-A-850,9387 which correspond to the following formula (Vl*) may be displayed as starting materials.
N A N R:2 1 N N I Ri2 1 1 A (Vl*) R'4 H3C CH3 i' H3C CH3 | H3C N Cn3 N-R s,C N CH3 j H L R,4 n in which n2 iS a number from 2 to 14, in particular a number from 2 to 6, the radicals R,, Rig, Rig and Rids independently of one another are as defined above, and the radicals A independently of one another are C) -C::acyl, (C,-C8alkoxy)carbonyl, (C5-C.2cycloalkoxy) carbonyl, (C,-C8alkyl)aminocarbonyl, (Cs-c 2cycloalkyl)aminocarbonyl' (C7Cgphenylalkyl)aminocarbonyl, C,-Caalkyl, Cs-C.2cycloalkyl which is unsubstituted or substituted by 1, 2 or 3 C,-C4alkyl; C3-Cfialkenyl, C7Cgphenylalkyl which is unsubstituted or substituted on the phenyl by 1, 2 or 3 C,-C4alkyl; or -CH2CN; in particular C,-C20acyl, especially C,C8acyl.
Various examples of the above chemical meanings are listed further above.
Particularly preferred are those products of the formula (Vl*) which have a narrow, well defined molecular weight distribution.
The polydispersity indicates the molecular-weight distribution of a polymeric compound. In the present application, the polydispersity is the ratio of weight-average (Mw) and number-
average (Mn) molecular weights. A value of Mw/Mn equal to 1 means that the compound is monodispers and has only one molecular weight and no molecular weight distribution. A narrow molecular weight distribution is characterized by a polydispersity close to 1.
- 35 Further, those products essentially known from EP-A-782,994, which correspond to the following formula (Vl**) may be displayed as starting materials.
it's'-N IN R,2-N N: N R,2 N N:N-R I, NO ON l l NON | N<N I, 4 R1i H. C> CH3 R'' H3C; ACHEI-it's' '4 R,4 H R'4 H6 Rl4t (Vl**) wherein n6 is a number from 2 to 14, in particular a number from 2 to 6, R.,, R'2, R,4 and R,5 are as defined above, the radicals R,4' independently of one another have one of the meanings given for Ret, the radicals Pus' independently of one another have one of the meanings given for R,5, and the groups -N(R,4')(R 5') are identical or different.
According to a preferred embodiment, all groups -N(R,4')(R,5') are -N(C,C,2alkyl)2, in particular-N(C4Hg)2 and all goups -N(R,4)(R,5) are H3C CH3
/Y ' N (, N-H.
1 - /<
4 9 H3C CH3
The starting materials of the formula (Vl*) or (Vl**) have preferably a polydispersity of 1 to 1.7, 1 to 1.65, 1 to 1.6, 1 to 1.55, 1 to 1.5,1 to 1.45, 1.1 to 1.7, 1.1 to 1.65, 1.1 to 1.6, 1.1 to 1.55, 1.1 to 1.5, 1.1 to 1.45, 1.2 to 1.7, 1.2 to 1.65, 1.2 to 1.6, 1.2 to 1.55, 1.2 to 1.5, or 1.2 to 1.45. A polydispersity of 1.1 to 1.5 is particularly preferred.
GPC (Gel Permeation Chromatography) is used as an analytical procedure for separating molecules by their difference in size and to obtain molecular weight averages(Mw, Mn) or information on the molecular weight distribution of polymers.
- 36 The technique is well known and described, for instance, in "Modern Size -
Exclusion Liquid Chromatography" by W.W.Yan et al., edited by J.Wiley 8t Sons, N Y., USA, 1979, pages 4-8, 249-283 and 315-340.
The GPC analyses of this application are carried out with a (3PC chromatograph Perkin-Elmer LC 250 equipped with Perkin-Eimer Rl detector LC 30 and with Perkin-Elmer oven LC 101.
Ail the analyses are carried out at 45 C by using three columns PLGEL 3 tom Mixed E 300 mm length x 7.5 mm i.d. (from Polymers Laboratories Ltd. Shropshire, U K) Tetrabydrofurane is used as eluant (flow 0.40 margin) and the samples are dissolved in tetrahydrofurane (2%) (% w/v).
EXAMPLE OF A PREPARATION PROCESS
The products described under a) to q) above can be prepared in analogy to known methods; for example by treating the abovementioned 2,G,6,6tetramethylpiperidine derivative starting materials with an acylating agent such as an acyl chloride, an organic anhydride, a carboxylic acid or a carboxylic ester. A preferred acylating agent is an organic anhydride, in particular acetic anNydride The molar ratio between the 2,2, C,6-tetramethyl-4-piperidyl groups in the starting material and the acylating agent depends on the desired degree of acylation in the final product. In order to acylate 50 % of the original 2,2,6,6-tetrarnethyl-4 piperidyl groups in a compound, preferably 0.6 equivalents of acylating agent are used for one equivalent of 2,2,6,6-tetramethyl-4-piperidyl group to be acylated. The reaction is conveniently carried out in an inert organic solvent, for example toluene, xylene, benzene, n hexane, an ether, tetrahydrofuran, chloroform or dichloromethane. Preferred solvents are xylene and toluene. The temperature is preferably 0 to 140 C, depending on the selected acylating agent. When the acylating agent is an organic anLydride, a temperature of 80 to 1 35 C is preferred.
* According to a particularly preferred embodiment of the invention, the acylation of the appropriate starting material is carried out using carboxylic acid anhydride, in particular acetic anhydride. Pursuant to this method, as a maximum, only 50 % of the 2,2,6,6
- 37 tetramethyl-4-piperidyl >NH-groups can be acylated since the other 50 % of these >NH-
groups form a salt with the carboxylic acid liberated. After neutralizing with an appropriate base, e.g. NaOH, the corresponding free 2,2,6,6tetramethyl-4-piperidyl groups are obtained from the salt. After isolation, the resultant product can be reacted in a second step with further carboxylic acid anhydride to give a product with a higher acylation degree, which in turn can again be reacted with carboxylic acid anhydride to give a product with an even higher acylation degree and so on. This procedure is illustrated in more detail e.g. in present EXAMPLES 1 B and 2.
Therefore, a preferred embodiment of this invention also relates to a product containing 5 to 85 % of a group (A-1-a) and/or (A-1-b) H3C CH3
<N-H (A- 1 -a) H3C CH3
IN-ct-caalkyl (A-l-b) H3C CH3
and 15 to 95 % of a group (A-2-a), H3C CH3
IN-C,-c20acYi (A-2-a) H3C CH3
the total sum of the groups (A-1-a), (A-1-b) and (A-2-a) being 100 %; obtainable (1) by reacting an appropriate starting material containing two or more groups of the formula (A-1 -a) \ IN-H (A- 1 -a) H3C CH3
- 38 with C2-C40carboxylic acid anhydride in a molar ratio of up to 0.6 equivalent C2-C40carboxylic acid anhydride per 1 equivalent groups of the formula (A-1-a) to obtain an intermediate product which contains groups of the formula (A-2-a) H3C CH3
7<N-C,-C20acyl (A-2-a) H3C CH3
and groups of the formula (A-2-b) H3C CH3
- N-H C,-C2cacyl 0 (A-2-b) H.3C CH3
in a molar ratio of about 1: 1, reacting this intermediate with a base, e. g. an aqueous NaOH solution, to convert the groups of the formula (A-2-b) to groups of the formula (A-1-a), and isolating the resultant product; and (2) optionally repeating step (1) until the desired acylation degree is obtained.
In the above explanations, a preferred meaning of C,-C20acyl is C2C20acyl or C2-C,0acyl or C2-C8acyl and a preferred meaning of C2C40carboxylic acid anhydride is C4-C40carboxylic acid anhydride or C4C20carboxylic acid anKydricie or C4-C,6 carboxylic acid anhydride.
In general, the definition of the terminal groups which saturate the free valences in the products of the formulae (Vl), (Vll), (V111-1), (V111-2), (Vill-3), (IX), (Xl), (X111) and (XIX) depend on the processes used for their preparation. The terminal groups can also be modified after the preparation of the products.
In the products of the formula (Vl), the end group attached to the diamino radical may be for example hydrogen, C,-Cz0acyl, (C -C alkoxy) carbonyl, (Cs-C 2cycloalkoxy)carbonyl, (C,-C alkyl)aminocarbonyl, (Cs-C, 2cycloalkyl)aminocarbonyl,
- 39 (C7-Cgphenylalkyl)aminocarbonyl, C1-C8alkyl, Cs-C1zcycloalkyl which is unsubstituted or substituted by 1, 2 or 3 C,-C4alkyl; C3-C6alkenyl, C7C9phenylalkyl which is unsubstituted or substituted on the phenyl by 1, 2 or 3 C1-C4alkyl; -CH2CN or a group of the formula N it/ NI R15 am/ R,4' N R1s' R14' wherein the radicals R,4' independently of one another have one of the meanings given for R,4, and the radicals Pus' independently of one another have one of the meanings given for R,s The end group attached to the triazinic ring may be for example halogen, e.g. Cl, or a group N Rz N A' 1 1 1 R11 R13
with A' being hydrogen, C1-C20acyl, (C1-C8alkoxy)carbonyl, (C5C12cycloalkoxy)carbonyl, (C, -C8alkyl)aminocarbonyl, (Cs-C1 2cycloalkyl) aminocarbonyl, (C -Cgphenylalkyl)aminocarbonyl, C1-C8alkyl, CsC12cycloalkyl which is unsubstituted or substituted by 1, 2 or 3 C C4alkyl; C3-C6alkenyl, C7-Cgphenylalkyl which is unsubstituted or substituted on the phenyl by 1, 2 or 3 C1-C4alkyl; -CH2CN or a group of the formula N I/ IN Rest R14' Nl R1s' R141 wherein the radicals R,4' independently of one another have one of the meanings given for R,4, and the radicals R'sHndependently of one another have one of the meanings given for R,s When the end group attached to the triazinic ring is halogen, it is advantageous to replace it, for example, by -OH or an amino group when the reaction is complete. Examples of amino groups which may be mentioned are pyrrolidin-1-yl, morpholino, -NH2, -N(C,-C8alkyl)2 and
- 40 -NR(C1-C6alkyl), in which R is hydrogen or a group of the formula (IV).
In the products of the formula (Vll), the terminal group bonded to the silicon atom can, for example, be (R'6)3Si-O- and the end group bonded to the oxygen atom can, for example, be -Si(R,6) -
The products of the formula (Vu) can also exist as cyclic products if n3 is a number from 3 to 10; in other words, the free valences depicted in the structural formula in that case form a direct bond.
In the intermediates of the formula (V111-1), (V111-2) and (V111-3), the terminal group bonded to the triazine radical is, for example, Cl or a group H3C\ ACHE
N N-- H
\9 Hi CH3 and the terminal group bonded to the amino radical is, for example, hydrogen or a group N N n HYC4 \ 1-NL C4FJ9-n H3C CH3 H3C CH3
H3C N CH3 H3C N CH3
H H In the products of the formula (!X), the te!rn!.na! group bonded to the 2,5-dioxopy!ro!idine ring is, for example, hydrogen and the terminal group bonded to the radical -C(R27)(R2)- is, for example,
_ ---
I o r 126 121
R2s H3C I MACHO
H3C N CH
1 3 R22
- 41 In the products of the formula (Xl), the terminal group bonded to the dimethylene radical can, for example, be -OH and the terminal group bonded to the oxygen can, for example, be hydrogen. The terminal groups can also be polyether radicals.
In the products of the formula (Xl11), the terminal group bonded to the carbonyl radical is, for example,
H:<CH3
-0 N R4'
H3C CH3
and the terminal group bonded to the oxygen radical is, for example, H3C CH3
C R36 fH R37 fH-R38 C 0 R41 O=C C=0
1 1 H3C C 3
O O H3C. <:CH3 H3C CH3
H3C N CH3 H3C N CH3
R41 R41
In the products of the formula (XIX), the terminal groups are for example hydrogen.
The products according to this invention are very effective in improving the light, heat and oxidation resistance of organic materials, especially synthetic polymers and copolymers.
Examples of organic materials which can be stabilized are: 1. Polymers of monoolefins and diolefins, for example polypropylene, polyisobutylene, po-
lybut-1-ene, poly-4-methylpent-1-ene, polyisoprene or polybutadiene, as well as polymers of cycloolefins, for instance of cyclopentene or norbornene, polyethylene (which optionally can be crosslinked), for example high density polyethylene (HDPE), high density and high mole-
cular weight polyethylene (HDPE-HMW), high density and ultrahigh molecular weight poly
- 42 ethylene (HDPE-UHMW), medium density polyethylene (MDPE), low density polyethylene (LDPE), linear low density polyethylene (LLDPE), (VLDPE) and (ULDPE).
Polyolefins, i.e. the polymers of monoolefins exemplified in the preceding paragraph, prefe-
rably polyethylene and polypropylene, can be prepared by different, and especially by the following, methods: a) radical polymerization (normally under high pressure and at elevated temperature).
b) catalytic polymerization using a catalyst that normally contains one or more than one metal of groups IVb, Vb, Vlb or Vlil of the Periodic Table. These metals usually have one or more than one ligand, typically oxides, halides, alcoholates, esters, ethers, arnines, alky!s, alkeny!s and/or aryls that may he either a- or -coordinated.
These metal complexes may be in the free form or fixed on substrates, typically on activated magnesium chloride, titanium(l11) chloride, alumina or silicon oxide These catalysts may be soluble or insoluble in the polymerization medium. The catalysts can be used by themselves in the polymerization or further activators may be used, typically metal alkyls, metal hydrides, metal aikyl halides, metal alkyl oxides or metal alkyloxanes, said metals being elements of groups la, lla and/or Illa of the Periodic Table. The activators may be modified conveniently with further ester, ether, amine or silyl ether groups. These catalyst systems are usually termed Phillips, Standard Oil Indiana, Ziegler (-Natta), TNZ ([DuPont), metallocene or single site catalysts (SSC).
2 Mixtures of the polymers mentioned under 1), for example mixtures of polypropylene with polyisobutylene, polypropylene with polyethylene (for example PP/HDPE, PP/LDPE) and mixtures of different types of polyethylene (for example LDPE/HDPE).
3 Copolymers of monoolefins and diolefins with each other or with other vinyl monomers, for example ethylene/propylene copolymers, linear low density polyethylene (LLDPE) and mixtures thereof with low density polyethylene (LOPE), propylene/but-1-ene copolymers, propylene/isobutylene copolymers, ethylene/but-1-ene copolymers, ethylene/hexene copo-
lymers, ethylene/methylpentene copolymers, ethylene/heptene copolymers, ethylene/octane copolymers, propylene/butadiene copolymers, isobutylene/isoprene copolymers, ethy
- 43 lene/alkyl acrylate copolymers, ethylene/alkyl methacrylate copoiymers7 ethylene/vinyl ace-
tate copolymers and their copolymers with carbon monoxide or ethylene/acrylic acid copo-
lymers and their salts (ionomers) as well as terpolymers of ethylene with propylene and a diene such as hexadiene, dicyclopentadiene or ethylidenenorbornene; and mixtures of such copolymers with one another and with polymers mentioned in 1) above, for example polypropylene/ethylenepropylene copolymers, LDPE/ethylene-vinyl acetate copolymers (EVA), LDPE/ethylene-acrylic acid copolymers (EM), LLDPE/EVA, LLDPE/EM and alter-
nating or random polyalkylene/carbon monoxide copolymers and mixtures thereof with other polymers, for example polyamides.
4. Hydrocarbon resins (for example Cs-Cg) including hydrogenated modifications thereof (e.g. tackifiers) and mixtures of polyalkylenes and starch.
5. Polystyrene, poly(p-methylstyrene), poly(a-methylstyrene).
6. Copolymers of styrene or -methylstyrene with dienes or acrylic derivatives, for example styrene/butadiene, styrene/acrylonitrile, styrene/alkyl methacrylate, styrene/butadiene/alkyl acrylate, styrene/butadiene/alkyl methacrylate, styrene/maleic anLydride, styrene/acryloni-
trile/methyl acrylate; mixtures of high impact strength of styrene copolymers and another polymer, for example a polyacrylate, a diene polymer or an ethylene/propylene/diene terpo-
lymer; and block copolymers of styrene such as styrene/butadiene/styrene, styrene/iso-
prene/styrene, styrene/ethylene/butylene/styrene or styrene/ethylene/propylene/ styrene.
7. Graft copolymers of styrene or a-methylstyrene, for example styrene on polybutadiene, styrene on polybutadiene-styrene or polybutadieneacrylonitrile copolymers; styrene and acrylonitrile (or methacrylonitrile) on polybutadiene; styrene, acrylonitrile and methyl meth-
acrylate on polybutadiene; styrene and maleic anhydride on polybutadiene; styrene, acrylo-
nitrile and maleic anhydride or maleimide on polybutadiene; styrene and maleimide on poly-
butadiene; styrene and alkyl acrylates or methacryiates on polybutadiene; styrene and acry-
lonitrile on ethylene/propylene/diene terpolymers; styrene and acrylonitrile on polyalkyl acry-
lates or polyalkyl methacrylates, styrene and acrylonitrile on acrylate/butadiene copolymers, as well as mixtures thereof with the copolymers listed under 6), for example the copolymer mixtures known as ABS, MBS, ASA or AES polymers.
- 44 8. Halogen-containing polymers such as po ychloroprene, chlorinated rubbers, chlorinated and brorninated copolymer of isobutylene-isoprene (halobutyl rubber), chlorinated or sulfo-
chlorinated polyethylene, copolymers of ethylene and chlorinated ethylene, epichlorobydrin homo- and copolymers, especially polymers of halogencontaining vinyl compounds, for example polyvinyl chloride, polyvinylidene chloride, polyvinyl fluoride, polyvinylidene fluoride, as well as copolymers thereof such as vinyl chloride/vinylidene chloride, vinyl chloride/vinyl acetate or vinylidene chloride/vinyl acetate copolymers.
9. Polymers derived from a, unsaturated acids and derivatives thereof such as polyacry-
lates and polymethacrylates; polymethyl methacrylates, polyacrylamides and polyacryloni-
triles, impact-modified with butyl acrylate.
10. Copolymers of the mcnorrcrs mentioned under 9) with each other or with other unsatu-
rated monomers, for example acrylonitrile/ butadiene copolymers, acrylonitrile/alkyl acrylate copolymers, acrylonitrile/alkoxyalkyl acrylate or acrylonitrile/vinyl halide copolymers or acry-
lonitrile/ alkyl methacrylate/butadiene terpolymers.
11. Polymers derived from unsaturated alcohols and amides or the acyl derivatives or ace-
tals thereof, for example polyvinyl alcohol, polyvinyl acetate, polyvinyl stearate, polyvinyl benzoate, polyvinyl maleate, polyvinyl butyral, polyallyl phthalate or polyallyl melamine; as well as their copolymers with olefins mentioned in 1) above.
12. Homopolymers and copolymers of cyclic ethers such as polyalkylene glycols, polyothy-
lene oxide, polypropylene oxide or copolymers thereof with bisgiycidyi ethers.
13. Polyacetals such as poiyoxymethylene and those polyoxymethylenes whichcontain ethylene oxide as a comonomer; polyacetals modified with thermoplastic polyurethanes, acrylates or MBS.
14. Polyphenylene oxides and sulfides, and mixtures of polyphenylene oxides with styrene polymers or polyamides.
- 45 15. Polyurethanes derived from hydroxyl-terminated polyethers, polyesters or polybutadi-
enes on the one hand and aliphatic or aromatic polyisocyanates on the other, as well as precursors thereof.
16. Polyamides and copolyamides derived from diamines and dicarboxylic acids and/or from aminocarboxylic acids or the corresponding lactams, for example polyamide 4, polyamide 6, polyamide 6/6, 6/10, 6/9, 6/12, 4/6, 12/12, polyamide 11, polyamide 12, aromatic polyamides starting from mxylene diamine and adipic acid; polyamides prepared from hexamethylenediamine and isophthalic or/and terephthalic acid and with or without an ela-
stomer as modifier, for example poly-2,4,4,-trimethylhexamethylene terephthalamide or poly-
m-phenylene isophthalamide; and also block copolymers of the aforementioned polyamides with polyolefins, olefin copolymers, ionomers or chemically bonded or grafted elastomers; or with polyethers, e.g. with polyethylene glycol, polypropylene glycol or polytetramethylene glycol; as well as polyamides or copolyamides modified with EF'DM or ABS; and polyamides condensed during processing (RIM polyamide systems).
17. Polyureas, polyimides, polyamide-imides, polyetherimids, polyesterimids, polyhydantoins and polybenzimidazoles.
18. Polyesters derived from dicarboxylic acids and diols and/or from hydroxycarboxylic acids or the corresponding lactones, for example polyethylene terephthalate, polybutylene terephthalate, poly-1,4dimethylolcyclohexane terephthalate and polyhydroxybenzoates, as well as block copolyether esters derived from hydroxyl-terminated polyethers; and also poly-
esters modified with polycarbonates or MBS.
19. Polycarbonates and polyester carbonates.
20. Polysulfones, polyether sulfones and polyether ketones.
21. Crosslinked polymers derived from aldehydes on the one hand and phenols, ureas and melamines on the other hand, such as phenol/formaldehyde resins, urea/formaldehyde re-
sins and melamine/formaldebyde resins.
22. Drying and non-drying alkyd resins.
- 46 23. Unsaturated polyester resins derived from copolyesters of saturated and unsaturated dicarboxylic acids with polyhydric alcohols and vinyl compounds as crosslinking agents, and also halogen-containing modifications thereof of low flammability.
24. Crosslinkable acrylic resins derived from substituted acrylates, for example epoxy acry-
lates, urethane acrylates or polyester acrylates.
25. Alkyd resins, polyester resins and acrylate resins crosslinked with melamine resins, urea resins, isocyanates, isocyanurates, polyisocyanates or epoxy resins.
26. Crosslinked epoxy resins derived from aliphatic, cycloaliphatic, heterocyclic or aromatic g!ycidyl compounds, e r,, products of diglycidyi ethers of bisphenol A and bisphenol F. which are crosslinked with customary hardeners such as anLydrides or amines, with or without acce I e rato rs.
27 Natural polymers such as cellulose, rubber, gelatin and chemically modified nornoloyous derivatives thereof, for example cellulose acetates, cellulose propionates and cellulose butyrates, or the cellulose ethers such as methyl cellulose; as well as rosins and their derivatives. 28. Blends of the aforementioned polymers (polyLlends), for example PP/EPDM, Poly-
amide/EPDM or ABS, PVC/EVA, PVC/ABS, PVC/MBS, PC/ABS, PBTP/ABS, PC/ASA, I4( /l t; I, V:/UPL, F'vCiacryiates, POMitherrnopiasti:; PU, PC/thei-inoplastic PUR, POM/acrylate, POM/MBS, PPO/HIF,S, PPO/PA 6.6 and copolymers, PA;HDPE, F:'A/PP, PA;PPO, PBT/PC/ABS or PBT/PfET/PC.
29. Naturally occurring and synthetic organic materials which are pure monomeric com-
pounds or mixtures of such compounds, for example mineral oils, animal and vegetable fats, oil and waxes, or oils, fats and waxes based on synthetic esters (e.g pUthalates, adipates, phosphates or trimellitates) and also mixtures of synthetic esters with mineral oils in any weight ratios, typica ly those used as spinning compositions, as well as aqueous emulsions of such materials
- 47 30. Aqueous emulsions of natural or synthetic rubber, e.g. natural latex or latices of carbo-
xylated styrene/butadiene copolymers.
The invention thus also relates to a composition comprising an organic material susceptible to degradation induced by light, heat or oxidation and at least one product according to this invention. The organic material is preferably a synthetic polymer, more particularly one selected from the aforementioned groups. Polyolefins, in particular polyethylene and polypropylene, are preferred. Polycarbonate such as listed in item 19 above, and blends of polycarbonate, such as listed in item 28 above are also preferred.
An organic material of interest is further a thermoplastic polyolefin, PP/EPDM, black pigmented PC-PBT blend, PVDC, PET, PET, PVC or ASAIPVC.
Blends of polycarbonate with various styrenic polymers represent a growing family of materials for automotive usage. In particular blends of polycarbonate / acrylonitrile-
butadiene-styrene and polycarbonate / acrylonitrile-styrene-acrylate are experiencing significant growth for automotive interior and exterior construction respectively. These materials offer an attractive combination of properties conferred by both components -
improved notch sensitivity and high impact strength, lower melt viscosity and processing temperatures compared to pure polycarbonate. The light stabilization of pigmented polycarbonate / styrenic blends is a complex issue due to several factors, including the composition of the polymer blend components, and the selection and concentration of light and heat stable pigments. For instance, acrylonitrile-butadiene-styrene can be prepared by mass, emulsion, or hybrid technologies each of which carries over varying levels of emulsifiers, coagulants and stabilizers into the final polymer blend. The acrylonitrile-styrene-
acrylate and acrylonitrile-butadiene-styrene terpolymers are multiphase materials of various compositions. The type of rubber and rubber content of such styrenic polymers can influence the gloss, color, impact and heat aging properties as the polymer (blend) undergoes weathering. An impediment to even further growth of the pigmented or molded-in-color grades, is the difficulty in providing adequate light stabilization for a broad color palette. Copious
- 48 information exists on the photodegradation and stabilization of the individual polycarbonate and styrenic polymers, yet limited information exists on the photodegradation of their blends.
The light stabilization of poiycarbonate blends is more complex than simply using the standard stabilizer systems for each polymer component in the blend.
Acceptable stabilizers for use in blends of polycarbonate should exhibit minimal detrimental interaction with the polymers during high temperature extrusion or molding. Melt rheology is a rapid method to assess the stability of a polymer in the melt state and thus to relate the interaction of any additives to changes in apparent melt viscosity and ultimately the molecular weight of the polymer. When melt rheology is conducted at a single, constant shear rate, a decrease in apparent melt viscosity over time can indicate that polymer degradation and molecular weight reduction is occurring.
The products according to this invention exhibit a significantly lower effect on polymer melt viscosity ratio than other sterically hindered amides. Furtner, they show only minima interaction with the polymer blend in the molten state. The products according to this invention also improve color protection and retention of high impact strength, in particular in various pigmented polycarbonate / acrylonitrile-butadienestyrene blends.
A further embodiment of this invention is a method for stabilizing an organic material against degradation induced by light, heat or oxidation, which comprises incorporating into said organic material at least one product according to this invention.
The products according to taxis inver tion cart be used in vai-ious Hropoitic,' s degcndir 9 on the nature of the material to be stabilized, on the end use and on the presence of other additives. In general, it is appropriate to use, for example, 0.01 to 5 TO by weight of the products of this invention, relative to the weight of the material to be stabilized, preferably 0.05 to 2 %, in particular 0.05 to 1 %.
The products of this invention can be added, for example, to the polymeric materials before, during or after the polymerization or crosslinking of the said materials. Furthermore, they can
- 49 be incorporated in the polymeric materials in the pure form or encapsulated in waxes, oils or polymers. In general, the products of this invention can be incorporated in the polymeric materials by various processes, such as dry mixing in the form of powder, or wet mixing in the form of solutions or suspensions or also in the form of a masterbatch which contains the products of this invention in a concentration of 2.5 to 25 % by weight; in such operations, the polymer can be used in the form of powder, granules, solutions, suspensions or in the form of latices.
The materials stabilized with the products of this invention can be used for the production of mouldings, films, tapes, monofilaments, fibres, surface coatings and the like.
If desired, other conventional additives for synthetic polymers, such as antioxidants, UV absorbers, nickel stabilizers, pigments, fillers, plasticizers, corrosion inhibitors and metal deactivators, can be added to the organic materials containing the products of this invention.
Particular examples of said conventional additives are: 1. Antioxidants 1. 1. Alkylated monoQhenols, for example 2,6-di-tert-butyl-4-methylphenol, 2- tert-butyl-4,6-di-
methylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butyl-4-nbutylphenol, 2,6-di-tert-bu-
tyl-4-isobutylphenol, 2,6-dicyclopentyl-4-methylphenol, 2-(ccmethylcyclohexyl)-4,6-dimethyl-
phenol, 2,6-dioctadecyl-4-methylphenol, 2,4,6-tricyclohexylphenol, 2,6-ditert-butyl-4-
methoxymethylphenol, nonylphenols which are linear or branched in the side chains, for example, 2,6-di-nonyl-4-methylphenol, 2,4-dimethyl-6-(1'methylundec-1'-yl)phenol, 2,4-di-
methyl-6-(1'-methylheptadec-1'-yl)phenol, 2,4-dimethyl-6-(1'-methyltridec1'-yl)phenol and mixtures thereof.
1.2. Alkylthiomethylphenols, for example 2,4-dioctylthiomethyl-6-tertbutylphenol, 2,4-dioc-
tylthiomethyl-6-methylphenol, 2,4-dioctyithiomethyl-6-ethylphenol, 2,6-didodecylthiomethyl-
4-nonyiphenol.
- 50 1.3. Hvdroquinones and alkylated hydroquinones, for example 2,6-ditert-butyl-4-methoxy-
phenol, 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amylLydroquinone, 2,6diphenyl-4-octade-
cyloxyphenol, 2,6-di-tert-butylhydroquinone, 2,5-di-tert-butyl-4hydroxyanisole, 3,5-di-tert-
butyl-4-hydroxyanisoTe, 3,5-di-tert-butyl-4-hydroxyphenyl stearate, bis(3,5-di-tert-butyl-4-
hydroxyphenyl) adipate.
1.4. Tocopherols, for example cr-tocopherol, -tocopherol,:-tocopherol, 6tocopherol and mixtures thereof (Vitamin E).
1.5. Hvdroxvlated thiodiphenyl ethers, for example 2,2'-thiobis(6-tertbutyl-4-methylphenol), 2,2'-thichis(4-octylphenol), 4,4'-thiobis(6-tertbutyl-3-methylphenol), 4,4'-thiobis(6-tert-butyl-
2-methylphenol), 4,4'-thichis-(3,6-di-sec-amylphenol), 4,4'-bis(2,6dimethyl-4-hydroxyphe-
ny!)disu!fide 1.6. A!kvlidenebisphenols, for example 2,2'-methy!?nebis(6tcrt-buty!-4-methylphenol), 2 2'-
methy!enebis(6-tert-butyl-4-ethylptleno!), 2,2'- methy!enebis 4-methy!-6( -methy!cyc!ohexyl)-
pheno!], 2,2'-methy!encUis(4-methy! 6-cyc!ohexylpheno!), 2,':.'methy!enebis( -r.ony!-4-me-
hy!pher o!), 2,2'-methy!enebis(4,f3-di-tert butylphenol), 2,2'-ctty!idenebis(4,6-di-tert-buty!-
pheno!), 2,2'-ethy!idenebis(6-tert-buty!-4-isobutylpheno!), 2,2'methylenebis[ -( -methy!b n-
zy!)-4-nony!pheno!1, 2,2'-methy!enebis[6-(c1-,cx-dimethylbenzy!)-4nonylpheno!], 4,4'-mothy lenebis(2,6-di-tert-butylphenol), 4,4'-methy!erebis(6-tert-buty!-2-methy!phenol), 1,1-bis(5 tert-butyl-4-hydroxy-2methylpheny!)butane, 2,6-bis(3-tert-butyl-5-methyl--2-hydroxyb nzy!)-4-
methy!phenol, 1,1,3-tris(5-tert-buty!-4-hydroxy-2-methylphenyl)butano, 1, 1-bis(5-tert-buty!-4-
hydroxy-2-methy!-pheny!)-3-n-dodecy!mercaptobutane, ethy!ono glyco! bisL3, 3-bis( 3-tert buty!-4'-hydroxyphenyl)butyrate], bis(3-tert-buty!-4hydroxy-5-methy!-phenyl)dicyclopentadi-
enc, bis[2-(3'-tert-butyl- -hydroxy-5'-methy!benzyl)-6-tert-buty!-4methylphenyl]terephtha!ato, l,1-bis-(3,5-dimethyl-2-hydroxypheny!)butane, 2,2-bis-(3,5-di--tert-butyl-4-hydroxyphe-
nyl)propane, 2,2-bis-(5-tert-butyl--4-hydroxy2-methy!pheny!)-4-ndodecylmercaptobutano, 1,1,5,5-tetra-(5-tert-butyl-4-hydroxy-2methylpheny!)pentane. 1.7. O-, N- and S-benzvi compounds, for example 3,5, 3',5'-tetra-tert-butyl-4,4'-dihydroxydi-
benzyl ether, octadecyl-4-hydroxy-3,S-dimethylbenzylmercaptoacetate, tridecyl-4-hydroxy-
3,5-di-tert-butylbenzylmercaptoacetate, tris(3,5-di-tert-butyl-4hydroxybenzyl)amine, bis(4
- 51 te rt-butyl-3-hydroxy-2, 6-dimethylbenzyl)dithioterephthalate, bis (3,5-di-tert-butyl-4-hydroxy-
benzyl)su If ice, isooctyl-3,5-di-tert-butyl-4-hydroxybenzylm ercaptoacetate.
1.8. Hydroxvbenzylated malonates, for example dioctadecyl-2,2-bis-(3,5-ditert-butyl-2-hy-
droxybenzyl)-malonate, di-octadecyl-2-(3-tert-butyl-4-hyd roxy-5-m ethylbenzyl)-malonate, di-
dodecylmercaptoethyl-2,2-bis-(3,5-di-tert-butyl-4-hydroxybenzyl)malonate, bis[4-(1,1,3,3-te-
tram ethylbutyl)ph enyl]-2,2-bis(3,5-di-tert-butyl-4-hydroxybenzyl) malonate.
1.9. Aromatic hvdroxybenzvl compounds, for example 1,3,5-tris-(3,5-ditert-butyl-4-hydroxy-
benzyl)-2,4,6-trimethylbenzene, 1,4-bis(3,5-di-tert-butyl-4-hydroxybenzyl) -2,3,5,6-tetrame-
thylbenzene, 2,4, 6-tris(3,5-di-te rt-butyl-4-hydroxybenzyl) phenol.
1.10. Triazine Compounds, for example 2,4-bis(octylmercapto)-6-(3,5-ditert-butyl-4-hy-
d roxyanilino)- 1,3,5-triazine, 2-octylmercapto-4,6-bis(3,5-di-tert-butyl4-hydroxyaniiino)- 1,3,5-
triazine, 2-octylmercapto-4,6-bis(3,5-di-tert-butyl-4-hydroxyphenoxy)-1,3, 5-triazine, 2,4,6-
tris(3, 5-di-tert-butyl-4-hydroxyphenoxy)- 1,2,3-triazine, 1, 3,5-tris-(3, 5-di-tert-butyl-4-hydroxy-
benzyl)isocyanurate, 1,3,5-tris(4-tert-butyl-3-hydroxy-2,6-dimethylbenZyl) iSOCyanurate} 2,4,6-
tris(3,5-di-tert-butyl-4-hydroxyphenylethyl)-1,3,5-triazine, 1,3,5-tris(3, 5-di-tert-butyl-4-
hydroxyphenylpropionyl)-hexabydro-1,3,5-triazine, 1,3,5-tris(3,5dicyclohexyl-4-hydroxyben-
zyl)isocyanurate. 1.11. Benzylphosphonates, for example dimethyl-2,5-ditert-butyl-4-hydroxybenzylphospho-
nate, diethyl-3,5-di-tert-butyl-4-hydroxybenzylphosphonate, dioctadecyl3, 5-di-tert-butyl-4-hy-
droxybenzylphosphonate, dioctadecyl-5-tert-butyl-4-hydroxy-3methylbenzylphosphonate, the calcium salt of the monoethyl ester of 3,5di-tert-butyl-4-hydroxybenzylphosphonic acid.
A,, for example 4-hydroxylauranilide, 4-hydroxystearanilide, octyl N-
(3 5-di-tert-butyl-4-hydroxyphenyl)carbamate.
1.13. Esters of t3-(3,5-di-tert-butyl-4-hvdroxYPhenyl)QroPionic acid with mono- or polyLydric alcohols, e.g. with methanol, ethanol, n-octanol, ioctanol, octadecanol, 1,6-hexanediol, 1,9-
nonanediol, ethylene glycol, 1,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethy-
lene glycol, triethylene gIycol, pentaerythritol, tris(hydroxyethyl) isocyanurate, N,N'-bis(hy
- 52 droxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylol-
propane, 4-hydroxymethyl-1-phospha-2,6,7-trioxabicyclo[2.2 2]octane 1 14 Esters of 6-(5-tert-butyl-4-hvdroxv-3-methylphenyl)propionic acid with mono- or poly-
hydric alcohols, e g with methanol, ethanol, n-octanol, i-octanol, octadecanol, 1,6-hexane-
diol, 1,9-nonanediol, ethylene glycol, 1,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl) isocyanurate, N,N'-
bis(hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trirnethylhexanediol, trimetnylolpropane, 4-hydroxymethyl-1-phospha-2,G,7trioxabiCyclo[2 2 2]octanc 1 15 Este.rs of R-(3 5-dicyclohexyl-4hydroxyphenVl)Dro o-n-ic acid witt- mono- or polynydric alcohols, e g with metncinol, ethanol, octar- ol, octaciecanol, 1,6-hexanedir l, 1,9nonanediol, etnyiene giyc.:l, i,2-F uopanodiol, r:F- erity glyc,; hiodiethyier,e 9iycG, ' ct',y enc 5IYCG\' trietnylenc, c lycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N'-bis(hydroxyetnyl)ox-
a nice, 3-thiaundecanol, 3-thiapentadec r ol, trimethylhexanedic>l, trime thylulprou:anc, 4 -hy-
drc>xymetnyl-1-ph:;pha-2,r 7-trioxc t icyclQ'2 2 2joctane 1 16 Exterx C: 3,5-di-;ert:utyl-4-t,vcroxy;:nenvl acetic aciri with monc- 0!- POIYnY6r;C C1IC'O hors, e g with methanol, etnanol, octano, octacir.canol, 1,6hexane idol, 1,9-nonanediol, ethylene glycol 1,2-pro anediol, ne::p entvl glycol, thiodiethyl: ne glycol, diethylen:-: c lycol, trietnylene qlycol, pen aerJthritol, tris(hydroxyettlyl)i-,or.yariurate, N,N'bix(hyciroxyethyl)ox-
amide, 3-thiaundecanol, 3-ttr iapentadec.c r ol, trimetnylhexanediol, trirT eti ylolpr-opane, 4-tny-
droxymethyl-l-prc spha-2 6,7-trioxabicyclo[2 2loctane 1 17 Amides_o' g 3. 5-di-tert-butv-4-tr vdroxyrhenviNpropion c acid e g N,N'-bix(3,5di-tert-
butyl--A,-tlydroxyptlenylpropionyl)hexamethylGnediamide, N,N'-bis(3,5 di-tert-h:tyl-- -hydroxy-
phenylpropionyl)trjmethylene djamjUe, N,N'-bix(3,5 di-tert-butyl-4hydroxypt enylpropi<'nyl)-
hydrazide, N,N'-bis[2-(3-[3,5-di-tert-butyl-4-hydroxyptlenyl]propionylc xy)cttlylloxamide (Naugard' XL-1 supplied by Uniroyal) 1 18 Ascorbic acid (vitamin C) 1 19 Aminic antioxidants, for example N,N'-di-isopropyl-p-phenylenediamine, N,N'-di-sec-
butyl-p-phenylenediamine, N,N'-bis(1,4 dimethylpentyl)-p-phenylenediamine, N,N'-bis(1
- 53 ethyl-3-methylpentyl)-p-phenylenediamine, N,N7-bis(1-methylheptyl)-pphenylenediamine, N,N'-dicyclohexyl-p-phenylenediamine, N. N'-diphenyl-pphenylenediamine, N. N'-bis(2-naph-
thyl)-p-phenylenediamine, N-isopropyl-N'-phenyl-p-phenylenediamine' N-(1, 3-dimethylbutyl)-
N'-phenyl-p-phenylenediamine, N-(l-methyiheptyl)-N'-phenyl-pphenylenediamine, N-cyclo-
hexyl-N'-phenyl-p-phenlenediamine, 4-(p-toluenesulfamoyl)diphenylamine, N, N'-dimethyl-
N,N'-di-sec-butyl-p-phenylenediamine, diphenylamine, N-allyldiphenylamine, 4-isopropoxy-
diphenylamine, N-phenyl-l-napUthylamine, N-(4-tert-octylphenyl)-1naphthylamine, N-phe-
nyl-2-napUthylamine, octylated diphenylamine. for example p7p'-di-tertoctyldiphenylamine, 4-
n-butylaminophenol, 4-butyrylaminophenol, 4-nonanoylaminophenol, 4dodecanoylamino-
phenol, 4-octadecanoylaminophenol, bis(4-methoxyphenyl)amine, 2,6-di-tertbutyl-4-dime-
thylaminomethylphenol, 2,4'-diaminodiphenylmethane, 4,4'diaminodiphenyimethane, N,N,N',N'-tetramethyl-4,4' diaminodiphenylmethane, 1,2-bis[(2-methylphenyl)amino]ethane, 1,2-bis(phenylamino)propane, (otolyl)biguanide, bis[4-(1',3'-dimethylbutyl)phenyl]amine, tert-
octylated N-phenyl-1-napUthylamine, a mixture of mono- and dialkylated tert-butyl/tert-
octyldiphenylamines, a mixture of mono- and dialkylated nonyldiphenylamines, a mixture of mono- and dialkylated dodecyldiphenylamines. a mixture of mono- and dialkylated isopro-
pyl!isohexyldiphenylamines, a mixture of mono- und dialkylated tertbutyldiphenylamines, 2,3-dihydro-3,3-djmethyl-4H-l,4-benzothiazine, phenothiazine, a mixture of mono- und dial-
kylated tert-butyl/tert-octylphenothiazines, a mixture of mono- und dialkylated tert-octyl-phe-
nothiazines, N-allylphenothiazin, N,N,N',N'-tetraphenyl-1,4-diaminobut-2ene, N,N-bis-
(2,2,6,6-tetramethyj-piperid-4-yl-hexamethylenediamine, bis(2,2,6,6tetramethylpiperid-4-yl)-
sebacate, 2,2,6,6-tetramethylpiperidin-4-one, 2,2,6,6tetramethylpiperidin-4-ol.
2. UV absorbers and linht stabilisers 2.1. 2-(2'-Hvdroxyphenyl) benzotriazoles, for example 2-(2'-hydroxy-5'-methylphenyl)-benzo-
triazole, 2-(3',5'-di-tert-butyl-2'-hydroxyphenyl)benzotriazole, 2-(5'tert-butyl-2'-hydroxyphe-
nyl)benzotriazole, 2-(23-hydroxy-5 -(l l'3 3-tetramethylbutyl)phenyl) benzOtriazole' 2-(3',5'-di-
tert-butyl-25-hydroxyphenyl)-s-chloro-benzotriazole! 2-(3'-tert-butyl- 2'hydroxy-5'-methylphe-
nyl)-5-chloro-benzotriazole, 2-(3'-sec-butyl-5'-tert-butyl-2'hydroxyphenyl)benzotriazole, 2-(2'-
hydroxy-4'-octyloxyphenyl)benzotriazole, 2-(3',5'-di-tert-amyl-2'hydroxyphenyl)benzotriazole, 2-(3',5'-bis-(ct, -dimethylbenzyl)-2'hydroxyphenyl)benzotriazole, 2-(3'-tert-butyl-2'-hydroxy-
5'-(2-octylOxycarbonylethyl)phenyl)-5-chloro-benzotriazole, 2-(3'-tertbutyl-5'-[2-(2-
ethylhexyloxy)-carbonylethyl]-2'-hydroxyphenyl)-5-chloro-benzotriazole, 2(3'-tert-butyl-2'-hy
- 54 droxy-5'-(2-methOxyCarbonylethyl)phenyl)-5-chloro-benzotria;tole, 2(3'-tert-butyl-2'-hydroxy-
5'-(2-methoxycarbonylethyl)phenyl)benzotriazole, 2-(3'-tert-butyl-2'hydroxy-5'-(2-octyloxy-
carbonylethyl)phenyl)benzotriazole, 2-(3'-tert-butyl-5'-[2-(2ethylhexyloxy)carbonylethyl]-2'-
hydroxyphenyl) b en zotriazol e, 2 (3'-dodecyl-2'-hydroxy-5'-m ethylphenyl)benzotriazole, 2-(3'-
tert-butyl-27-hydroxy-5 -(2-isooctyloxycarbonylethyl)phenylbenzotriazole, 2,2-methylene-bis-
[4-(1,1,3,3-tetramethylbutyl)-6-benzotriazole-2-ylphenol]; the transesterification product of 2-
[3'-tert-butyl-5-(2-methOxyCarbonylethyl)-2'-hydroxyphenyll-2HbenzOtriazole with polyethy lene glycol 300; R-CH2CH?--COO-CH2CH., where R = 3-tert-butyl-4-hydroxy-5'-2H benzotriazol-2-ylphenyl, 2-[2'-hydroxy3'-(ct,ct-dimethylbenzyl)-5'-(1,1,3,3-tetramethylbutyl) phenyl] benzotriazole; 2-[2'-hydroxy-3'-(1,1,3,3-tetramethylbutyl) 5!-(c',cxdimethylbenzyl) phenyi]benzotriazole. 2.2. 2-HvdroxvUenzophenones, forexample the 4-hydroxy, 4-n,ethoxy, 4-oc.tylc xy, 4-decy!-
oxy 4-dodecyloxy, 4-t er zyloxy! 4,''.4'-trihydroxy and 2'-hydroxy--'., :3'-dimethoxy dor-ivatives.
3. tsters_of substituted ar,ci unsut_S,i Cited benzoic ac d.s, as for oxarnple '.-tertbutyl-:henyl salicylate, phenyl salicylate, cctylF hery: salicylate, dit,er- zoyl resorciroi bix(4-ter;--LutylLcn-
zoyl) resorcinoi, benzoyl resorcinol, ?, -d,-tert-butylpRenyl 3,5-di-te l butyl--4-llydroxybenzo <ire hexadecyi:3,5-di-ter,-butyl 4-hyd roxyLenzoate, oc. adccyl 3, -cii-tert-butyl- '-hydroxy-
benzo.--J;e, 2-meth- yl-4,6-di-tert-butylphenyl 3,5 di-ter'-butyl-4hydroxybenzoatc.
9 A.,4Nr,r\,,l t,:, fix! r x lknp!r methyl f- y rl: -l>.,3-ciipil:!lylac, yl te, isooctvl r: -cy r::,,f, clil tr e-
nylacrylate, methyl cI-carbomethoxycinnar, ate, methyl x-cyano:-r,lethylF,-r-netnoxy cinn -
matc, butyl r;-cyano-13-methyl-p methoxy-cinnarnate, methyl cxcarbomethoxy-F:-methoxycir\-
namate and N-(13-carL ornethoxy-l3-cyanovinyl)-2 methylir,cioline 2.. Nickel compounds, for example nickel complexes of 2,2'-tt io-bis-[4--(1,1, 3,3-tc trame-
thylbutyl)phenol], such as the 1:1 or 1:2 complex, witr or without additicnal ligands such as n-butylamine, triethanolamine or Ncyclohexyldiethanolamine, nickel dibutyldithiocarbamatc, nickel salts of the monoalkyl esters, e.g. the methyl or ethyl ester, of 4-hydroxy-3,5-ditert-
butylbenzylphosphonic acid, nickel complexes of ketoximes, e.g. of 2hydroxy-4-methylphe-
nyl undecylketoxime, nickel complexes of 1-phenyl-4-lauroyi-5hydroxypyrazole, with or without additional ligands.
- 55 2.6. Sterically hindered amines, for example bis(2 2 6 6-tetramethyl4-piperidyl)sebacate, bis(2,2,6,6-tetramethyl-4-piperidyl)succinate, bis(1,2,2,6,6-pentamethyl-4-piperidyl)sebacate, bis(1-octyloxy-2,2,6,6tetramethyl-4-piperidyl)sebacate, bis(1,2,2,6,6-pentamethyl-4-pi-
peridyl) n-butyl-3 5-di-tert-butyl-4-hydroxybenzylmalonate, the condensate of 1-(2-hydroxy-
ethyl)-2,2,676-tetramethyl-4-hydroxypiperidine and succinic acid, linear or cyclic condensates of N. N'-bis (2,2, 6, 6-tetramethyl-4-piperidyl) hexamethylenediam ine and 4-tert-octylamino-2,6-
dich loro- 1,3,5-triazi no, tris(2,2, 6,6-tetram ethyl-4-piperidyl) nitrilotriacetate, tetrakis(2,2, 6, 6-
tetramethyl-4-piperidyl)-1,2,3,4-butane-tetracarboxylate, 1,1'-(1,2ethanediyl)-bis(3,3,5,5-
tetramethylpiperazinone), 4-benzoyl-2,2,6,6-tetramethylpiperidine, 4stearyloxy-2,2,6,6-
tetramethylpiperidine, bis(l,2,2,6,6-pentamethylpiperidyl)-2-n-butyl-2-(2hydroxy-3,5-di-tert-
butylbenzyl)malonate, 3-n-octyl-7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5] decan-2,4-dione, bis(1-octyloxy-2,2,6,6-tetramethylpiperidyl)sebacate, bis(1-octyloxy-2,2,6,6-tetrame-
thylpiperidyl)succinate, linear or cyclic condensates of N,N'-bis-(2,2,6, 6-tetramethyl-4-piperi-
dyl)hexamethylenediamine and 4-morpholino-2,6-dichloro-1,3,5-triazine, the condensate of 2-chloro-4,6-bis(4-n-butylamino-2,2,6,6tetramethylpiperidyl)-1,3,5-triazine and 1,2-bis(3-
* aminopropylamino)ethane, the condensate of 2-chloro-4,6-di-(4-nbutylamino-1,2,2,6,6-pen-
tamethylpiperidyl)-1,3,5-triazine and 1,2-bis-(3-aminopropylamino)ethane, 8-acetyl-3-dode-
cyl-7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione, 3-dodecyl1-(2,2,6,6-tetrame-
thyl-4-piperidyl)pyrrolidin-2,5-dione, 3-dodecyl-1-(1,2,2,6,6-pentamethyl4-piperidyl)pyrroli-
dine-2,5-dione, a mixture of 4-hexadecyloxy- and 4-stearyloxy-2,2,6,6tetramethylpiperidine, a condensation product of N,N'-bis(2,2,6,6tetramethyl-4-piperidyl)hexamethylenediamine and 4-cyclohexylamino-2,6dichloro-1,3,5-triazine, a condensation product of 1,2-bis(3-ami-
nopropylamino)ethane and 2,4,6-trichloro-1,3,5-triazine as well as 4butylamino-2,2,6,6-te-
tramethylpiperidine (CAS Reg. No. [136504-96-6]), N-(2,2,6,6-tetramethyl4-piperidyl)-n-do-
decylsuccinimid, N-(1,2,2,6,6-pentamethyl-4-piperidyl)-ndodecylsuccinirnid, 2-undecyl-
7,7,9,9-tetramethyl-1-oxa-3,8-diaza-4-oxo-spiro[4,5]decane, a reaction product of 7,7,9,9-
tetramethyl-2-cycioundecyl-1-oxa-3,8-diaza-4-oxospiro [4,5]decane und epichlorobydrin, 1,1-
bis(1,2,2,6,6-pentamethyl-4-piperidyloxycarbonyl)-2-(4-methoxyphenyl) ethene, N,Ni-bis-
formyl-N,N'-bis(2,2,6,6-tetramethyl-4-piperidyl)hexamethylenediamine, diester of 4-methoxy-
methylene-malonic acid with 1,2,2,6,6-pentamethyl-4-hydroxypiperidine, poly[methylpropyl-3-
oxy-4-(2 2 6 6-tetramethyl-4-piperidyl)]siloxane' reaction product of maleic acid anhydride-cc-
olefin-copolymer with 2,2,6,6-tetramethyl-4-aminopiperidine or 1,2,2,6,6pentamethyl-4-
aminopiperidine.
- 56 2.7. Oxamides, for example 4,4'-dioctyloxyoxanilide, 2,2'diethoxyoxanilide, 2,2'-dioctyloxy-
5,5'-di-tert-butoxanilide, 2,2'-didodecyloxy-5,5'-di-tert-butoxanilide, 2ethoxy-2'-ethyloxanilide, N,N'-bis(3-dimethylaminopropyl)oxamide, 2ethoxy-5-tert-butyl-2'-ethoxanilide and its mixture with 2-ethoxy-2'ethyl-5,4'-di-tert-butoxanilide, mixtures of o- and p-methoxydisubstituted oxanilides and mixtures of o- and p-ethoxy-disubstituted oxanilides.
2.8. 2-(2-HvdroxyDhenvi)-1 3 5-triazines, for example 2,4,6-tris(2hydroxy-4-octyloxyphenyl)-
1,3,5-triazine, 2-(2-nydroxy-4-octyloxyphenyl)-4 6-bis(2 4-dimCthylphenyl) -17315-triazine, 2-
(2,4-diNyciroxyphenyl)-4,6-bi5(2,4-dimethylphenyl)-1,3,5-triazine, 2,abis(2-hydroxy-4-pro-
pyloxypRcnyl)-6-(2,4-dimethylphenyl)- 1,3,5-triazine, 2-(2- hydroxy- octyloxyphenyl)-4,6-bis-
(4-methylphenyl)-1,3,r,-triazine, 2-(2-hydroxy-4-dc decyloxyphenyl)-4,6bis(2,4-dirncti-1ylphe-
nyl)-1,J,5-triazine, 2-( -hyc:iroxy-4-tridec yioxyg: oryiJ-4, -b,s(2, 4 ciTr, c.t,ylp,hc,,yl) -1,3,5 t,, azine, 2-[2-hydroxy-4-(2-nydroxy-3butyloxy-propoxy)pUcnyll-4,6-bis(2,4-dimethyl)-1,3,5 tri-
azinc, 2-[2-hyd! xy-4 (2-hydEc xy-3-octy!oxy-propyicxy),,nenylj-4,6-bis(2,4-ciimCthyl)-1,.3,6-
triazine' 2-LlT-(dodecy!c xy/tridccyloxy' '-hydroxypropCxJ)-''-hydroxy phenyl]-4,6-bis(2,4-cii-
mcthylpheryl)-1 3,5-triazinc,)-[2--hydroxy-i'.-(2-hydroxy-3-dodecyloxy-c ropCxy)phenyll-4,6 bis(?,4-dimethylphenyl)-1 3,. -lriazine, 2-(2-nydr-oxy 4-h xyloxy)pl Qnyl-4,6-diphe nyl-1 3,.: lriazine, 2-(2--hyc',-oxy-4-methoxyphenyl)-4,6-diphenyl-1,3.5-trkizine, 2,4,6-trisL2 hydroxy-4-(3 butoxy-2-hydroxy-propoxy)phenyl: 1,3,5-triazine, 2 (';-hyciroxyphenyl)- (4-methoxypherlyl) 6-F;:erlyl-1,3,5 tr-ia ine, 2-(2- yd c xy-a-L3-(2-cti ylr: xy! l-c xy) 2-llydroxyF:ropyloxy]F;r: >r 4,6-bis(2,4-dimetnylphenyl)1,3,.,-triazine. 3. Metal dr activat s, for example N,N'-diphr nyloxarnido. N-salicylal-l l'-saiicyloyl hydrazine, N,N'-bis(saiicyloyl) hydrazinc, N,N,-bis(3,5-di tert-butyl-4-hydroxypher ylpropionyl) hydrazine, 3-salicyloylamino-1,2,4-triazole, bis(benzylidene)oxalyl diWydrazide, oxanilide, isophthaloyl dibydrazide, sebacoyl bisphenylLydrazide. N,N'--diacetyladiroyl diRydrazidc, N,N'-bis(salic.yl-
oyl)oxalyl diLydrazide, N,N7-bis(salicyloyl)thiopropionyl diLydrazide.
4 Phot: , for example triphenyl phosphite, diphenyl alkyl phosphites, phenyl dialkyl phosphites, tris(nonylphenyl) phosphite, trilauryl phosphite, trioctadecyl phos-
phite, distearyl pentaerythritol diphosphite, tris(2,4-di-tertbutylphenyl) phosphite, diisodecyl pentaerythrjtoj diphosphite, bis(2,4di-tert-butylphenyl) pentaerythritol diphosphite, bis(2,6-di-
tert-butyl-4-methylphenyl)-pentaerythritol diphosphite, diisodecyloxypentaerythritol di
- 57 phosphite, bis(2 4-di-tert-butyl-6-methylphenyl)pentaerythritol diphosphite, bis(2,4,6-tris(tert-
butylphenyl)pentaerythritol diphosphite, tristearyl sorbitol triphosphite, tetrakis(2,4-di-tert-bu-
tylphenyl) 4,4'-biphenylene diphosphonite, 6-isooctyloxy-2,4,8,10-tetratert-butyl-12H-di-
benz[d,g]-1,3,2-dioxaphosphocin, 6-fluoro-2,4,8,10-tetra-tert-butyl-12methyl-dibenz[dig]-
1,3,2-dioxaphosphocin, bis(2 4-di-tert-butyl-6-methylphenyl) methyl phosphite, bis(2,4-di-tert-
butyl-6-methylphenyl) ethyl phosphite, 2,2',2"-nitrilo[triethyltris(3,3', 5,b'-tetra-tert-butyl-1, 1'-
biphenyl-2,2'-diyl)phosphite], 2-ethylhexyl(3,3',5,5'-tetra-tert-butyl-1, 1 '-biphenyl-2,2'-di-
yl)phosphite. 5. Hydroxylamines, for example, N. N-dibenzylhydroxylam ine, N. N-diethylhydroxylamine, N,N-dioctylhydroxylamine, N,NdilaurylLydroxylamine, N,N-ditetradecylhydroxylamine, N,N-
diLexedecylLydroxylam ine, N. N-dioctadecylhyd roxylam ine, N-h exadecylN-octadecylLy-
droxylam ine, N-heptadecyl-N-octadecylhydroxylam ine, N. N-dial kyl hydroxylam ine derived from hydrogenated tallow amine.
6. Nitrones, for example, N-benzyl-alpha-phenyl-nitrone, N-ethyl-alphamethyl-nitrone, N-oc-
tyl-alpha-heptyl-ritrone, N-lauryl-alpha-undecyl-nitrone, N-tetradecylalpha-tridcyl-nitrone, N-
hexadecyl-alpha-pentadecyl-nitrone, N-octadecyl-alpha-heptadecyl-nitrone, N-hexadecyl-
alpha-heptadecyl-nitrone, N-ocatadecyl-alpha-pentadecyl-nitrone, Nheptadecyl-alpha-hep-
tadecyl-nitrone, N-octadecyl-alpha-hexadecyl-nitrone, nitrone derived from N,N-dialkylhy-
droxylamine derived from hydrogenated tallow amine.
7 Thiosynerqists, for example, dilauryl thiodipropionate or distearyl thiodipropionate.
8. Peroxide scavenners, for example esters of Q-thiodipropionic acid, for example the lauryl, stearyl, myristyl or tridecyl esters, mercaptobenzimidazole or the zinc salt of 2-mercapto-
benzimidazole, zinc dibutyldithiocarbamate, dioctadecyl disulfide, pentaerythritol tetrakis( 3-
dodecylmercapto)propionate 9. Polyamide stab lisers, for example, copper salts in combination with iodides and/or phos-
phorus compounds and salts of divalent manganese.
10. Basic co-stabilisers, for example, melamine, polyvinylpyrrolidone, dicyandiamide, triallyl cyanurate, urea derivatives, hydrazine derivatives, amines, polyamides, polyurethanes, alkali
- 58 metal salts and alkaline earth metal salts of higher fatty acids for example calcium stearate, zinc stearate, magnesium behenate, magnesium stearate, sodium ricinoleate and potassium palmitate, antimony pyrocatecholate or sink pyrocatecholate 11. Nucleating agents, for example, inorganic substances such as talcum, metal oxides such as titanium dioxide or magnesium oxide, phosphates, carbonates or sulfates of, preferably, alkaline earth motels; organic compounds such as mono- or polycarboxylic acids and the salts thereof, e.g. 4-tert-butylbenzaic acid, adipic acid, dipnenylacetic acid, sodium succinate or sodium benzoate; polymeric compounds such as ionic copolymers (ionomers) 12 Fillers and roinforcinc agents, for example, calcium carbonate, silicates, glass fibres, glass bulbs, asbestos, talc, kaolin, mica, barium sulfate, metal oxides and hydroxides, c r-
bon black, graphite, wood flour and flours or fibers of otr- cr natural prociucts, syntt eiic fibers 13 Other adapt ens, for example, pla.; ticisers, iubr-icant, emulsifiers, pigments, rheology additives, catalysts, flow-control agents, optical br-icnter- ers, fl rr cproofir,g agents, antistatic assents and blowing agents.
A. Benzofura,lone=., an i indolinones, for example those discloser) in U. S. 4,325,86.3; U.S. 4,333,?44; U.S. 5,175,312; U.S. 5,216,052; U.S. 5,252, 643; DE-A-4'313611
DE-A-4316622; DE-A-4316876; EFF: -A-0589839 or ELP-A-0591102 or 3-[ -(2acetoxyethoxy)-
phenyl]-5,7-di-tert-butyl-benzofuran-2-one, 5,7-di-tert-butyi-3-[4-(2stearoyloxyethoxy)pne nyl]benzofuran-?-one, 3,3'-bi jr5,7-di-tcrt-butyl-3(4- 2- ydroxyethoxy]phenyl)bcynzOfuran-2 ones, 517-di-tc.rt-butyl- -(4tnoxypher- yl)benzofurar-2-one, 3 ( -acetoxy-3,5-dimetnyiphe nyl)-5 7-ditert-butyl-benzofuran-2-one 3-(3,5-dime hyl-4-pivaloyloxyphenyl) 5,7-ditert-butyl benzofuran-2-one, 3-(3,4-dimethylpherlyl)-5,7-di-tert-butylbenzofuran-2-one, 3-(?,3-cii methylphenyl)-o,7-di-tert-butyl-benzofuran-?one The weight ratio of the compounds of this invention to the conventional additives may be 1:0.5 to 1:5 The products according to this invention are preferably used in combination with a pigment and/or an UV absorber.
- 59 The products of the invention can also be used as stabilizers, especially as light stabilizers, for almost all materials known in the art of photographic reproduction and other reproduction techniques as e g. described in Research Disclosure 1990, 31429 (pages 474 to 480).
The invention is illustrated in more detail by the following Examples. All percentages are by weight, unless otherwise indicated.
In the structural formulae of the following examples, n2', no' end n7' indicate that there are repetitive units in the molecules and the products obtained are not uniform. In the following examples, the acylation degree is determined as described below.
DETERMINATION OF THE ACYLATION DEGREE
The analytical determinations are carried out by titration, in a non aqueous environment, using perchloric acid in isopropanol as reagent and a mixture (1:1) of chloroform and acetonitrile as solvent.
Two different measurements are needed to get the result: in the first one, the starting material (oligomer carrying only free NH groups in the piperidyl moieties) is titrated, obtaining a number (A) index of the amount of free NH groups in the compound; the second titration is performed on the final acylated product and gives the number (B) index of the residual free NH groups after the acylation reaction.
The "% acylation degree" is calculated as (100 - Bx100/A).
EXAMPLE 1:
A) Preparation of the intermediate of the formula
- 60 o H3C-C-N (CH,)6-N, N N (CH2)6-N -C-CH3
H3C j J< CH3 H3CJ It CH3 H C-N H3C CH3 H3C CH H3C NCH3 H3C NCH3 1 H3C N CH3 H3C N CH3
H H H3C >A)< CH3 H
H3C N CH3
H n2' A solution of 37 1 g (0.175 moles) of N-(2,2,6,6-tetramethyl-4piperidinyl)-n-butylamine in 30 ml of water is slowly added at 0 C to a solution of 32.2 g (0.175 moles) of cyanuric chloride in 250 ml of xylene, keeping the temperature during the addition and for further 1 hour. After 2 hours at room temperature, tne mixture is cooled to O'C ard an aqueous solution of 7.3 q (0.1: moles) of sodium hydroxide in 25 w- l of water is acded.
After 1/2 hour at OCC and further 2 hour-e at room temperature. the aqueous solution is separaR:d off and 34.6 g (Q.() 37 r oles) of N.N'bisL2,2,6,6-.etramethyl-4-pic cridirlyl]-1,6-
hexanediamine are added.
Ti- c mixture is heated to 50 C for 1 hour ar,d 2:i.2 y (0.175 rr,oles) <:f ground potassium cart::onate are adcied and heated to 60"C f::r:; hours.
A't=. vilsh y vvit, v;ate,, t'i. o,ya, i: g>'>asP is C nCPntE gt{'C-l, n6P! v<- r-n nt 60 -70 -C/10 mbar, t eing 1 5 ml of xylene recovered.
69 g (0.175 moles) of N,N'-bis[2,2,6,6-tetramethyl-4 piperidinyl4-1,6hexanediamine are acided and the mixture is heateci to 150 C for 2 hours, cooled again and 7g (0.175 moles) of ground sodium hydroxide are added.
The mixture is heated to 140 C for further 4 hours, being the residual water of reaction eliminated off azeotropically, and for further 4 hours at 1 600C.
After cooling to 60 C, the mixture is diluted with 130 ml of xylene, filtered and washed three times with 50 ml of ethylene glycol.
- 61 After concentrating under vacuum at 60 C/10 mbar, 7.5 g (0.073 moles) of acetic anLydride are added. After 1/2 hour at room temperature, the mixture is heated to 130 C for 5 hours.
After cooling to room temperature, 20.2 9 (0.146 moles) of ground potassium carbonate are added and the mixture is heated to 1 30 C for 2 hours.
Then, the mixture is cooled to 50 C, filtered and concentrated under vacuum at 140 C/1 mbar.
A solid with a melting range of 128 -134 C is obtained after drying.
Mn (by GPC) = 2712 g/mole Mw/Mn = 1.41 B) Preparation of the product of the formula 0 c, H,C-C-N-(CH2)6 1 _, N. N-(CH2)6 1 -C-CH,
H3C Jim, CH3 H3C ' CH3 H9C4-N H3C JO CH3 H3C JO CH3 H3C N CH3 H3C N CH3 l H3C I CH3 H3C I CH3 Rto Rlo H3C CH3 R4o Rlo H3C I CH3
wherein 45 to 55 % of the radicals R,o are acetyl and the remaining radicals Rat are hydrogen. 150 g (1.47 mol) of acetic anhydride are added to a solution of 290 g of the intermediate described under A), dissolved in 400 ml of toluene. The solution is heated to reflux for eight hours. Then, the solution is cooled to 60 C and 13.1 g of NaOH in 500 ml of water are slowly added. The mixture is left under stirring for additional 5 hours. After cooling to room temperature, the organic layer is separated, washed three times with 100 ml of water, dried over sodium sulfate and concentrated under vacuum. The desired product is obtained as a white powder with a melting range of 127 - 1 37 C.
- 62 Mn (by GPC) = 2500 g/mole Mw/Mn = 1.33 EXAMPLE 2: Preparation of the product of the formula 3wc-c-N (CLl,)6-N - - N (C31.)6 N _ C-- CH3 H3C CH 3 3-!3C '1,, C-3 H ( -N 3C, 3 3 1 CH 3
H3C N C-13 -3C t, CH3, 1 r- 3c N CH3 H3C N CH3 R H.- ', U. Vi3 r R 0 3c N ( -, f) rl,' wherein 70 to 8() '/:, of tL- e radicals R are acetyl anci tretnainir3g radicals R o are r ydroger3 40 9 of acetic anRydride are added to a solution of l z.: 3 of tnc intet-mediate of _XAMPLE l B) in 200 rr l of tcluer3G Tr e soiu ion is heatcd to reflux for 6 t ours. Then, thc solution is cooled to room ter pGr-atur and a solution of 48 9 of NaOF3 in 200 ml of water is added. The mixture is neated to 70"C and allowoci to reac.t for additional 6 hours The oryanic phase is separated off, washec three times wi.r 1(30 ml of water, dried over sodiun-
sulfate and evaporated. n icr vacuum. The dosired product is obtained as a white pOW6Gr with a rr3clting range of 132- -188 C Mn (by GPC) = 2650 g/mole Mw/Mn = 1.29 EXAMPLE 3: Preparation of the compound of the formula
- 63 0 0
H3C-C-N (CH2)6-N-N-N N (CH2)6 N -C-CH3
H. 3 C H. 3 C H. H 9C,- TIC C H H 3C J C H
R1o R1o H3C CH3 R,o R,o H3C I CH3
Rlo n2.
wherein 55-65 % of the radicals R,o are acetyl and the remaining radicals Rio are methyl.
70 g of the compound of EXAMPLE 1 B are dissolved in an aqueous solution of 15.5 9 (0.34 mol) of formic acid in 100 ml of water. Then, 15 g (0.5 mol) of paraformaldehyde are added and the aqueous solution is heated under reflex for 16 hours. After cooling to room temperature, 100 ml of xylene are added. After stirring for 2 hours, 15.5 g (0.39 mol) of NaOH in 100 ml of water are added. Subsequently, the organic phase is separated off, washed twice with water and dried over sodium sulfate. After filtration, the organic phase is evaporated under vacuum. The desired product is obtained as a white powder with a melting range of 134 -139 C.
EXAMPLE 4: Preparation of the compound of the formula H3C-C-N (CH2)6 N N (CH2)6 N -C-CH,
H TIC: C H. 3 H 3C H. C,-Nl H 3 C H. H C C H. R,o R,o H3C CH3 Rio R,o H3C IN CH3
- Rto _ n2' wherein 15-25 % of the radicals R'o are acetyl and the remaining radicals Rio are hydrogen.
Following the procedure reported in EXAMPLE 1 B and using the appropriate amount of reagents (6.5 9 of acetic anhydride for 51.5 g of the compound of EXAMPLE 1A) the desired compound is obtained as a white powder with a melting range of 125 -1 33 C.
- 64 EXAMPLE 5: Preparation of the compound of the formula C4H3 H9C,
N N (CH2 5 N <. N. N (CH2 6 Nl <' N N H,C> < CH3 H3C, CH H,C) CH3 F43C > n N N | C Hg H3C N CH3 H3C N CH3 H,C N CH3 H C N CH l N-CIH.3 HgC4 -N R,3 R!O H9CA-N C,H, [13C> J< CFI, C,H
H,C N CH3
R,O wherein 55-65 /O of the radicals R o are acetyl and the remaining radicals R o are hydrogon.
Following the procedure reported in EXAMPLE 1 B. using the commercial proc uct PCI-dIMASSORB 2020 as starting material and thc right amount of reagents (155 g of acetic anLydride for 300 C of ';>Ci 31MASSORB 2020) the desire i compounci is obtainf d as a white powder with a melting range of 126 -135 '(.
EXAMPLE 6 PrGoaration of the compounc of the form:la C4F 3 I j; N --f; - . --- (CkI2), -- N - l -- N _ CH7),,.N 1 N, | N N 1 t N N - /1\ | rl N > l | |!11 >:,,, GH, HlC CH3 1' H,C.L, Ci'l H3C >l CH, | WI,C, C H., H,!1 H3C C H c 1 ctl. -{ r. N r.H \] - C! 3 9 F1,, _, ! O --
_. ' '3
1 1 (. 49 f 1 H3! 3 ct 3 C,H, H,C N CH3
P o wherein 75-85 /c of the radicals R o are acetyl and the remaining radicals R'o are hydrogen.
Following the procedure reported in EXAMPLE 1 B. using the product of EXAMPLE 5 as starting material and the right amount of reagents (77.8 9 of acetic anLydride for 150 9 of the product of EXAMPLE 5) the desired compound is obtained as a white powder with a melting range of 131 -138 C.
- 65 EXAMPLE 7:
A) Preparation of the intermediate of the formula: O O
H3C-C-N (CH3)6 NN N N (CH,)6 N--C CH3
H3C CH3 H3C < CH3 H3C CH3 H3C CH3
H3C N CH3 H3C I CH3 H-N H3C N CH3 H3C N CH3
H H H3C-IC-CH3 H H
ICH2 H3C-C-CH3
CH3 _ n7, Following the procedure reported in EXAMPLE 1A, using the commercial product CHIMASSORB 944 as starting material and the right amount of reagents (50 g of acetic anLydride for 400 g of CHIMASSORB 944) the desired intermediate is obtained with a melting range of 120 -1 25 C.
B) Preparation of the compound of the formula: 0 0
F13C C- I (CH2)6 N I N N (CH2)6 N -C-CH3
H3C. CH3 H3C J CH3 H3C CH3 H3C CH3
H3C N CH3 H3C I CH3 H-N H3C N CH3 H3C N CH3
R,o Rlo H3C-f-CH3 Rlo Rlo CH2 H3C-C-C H3
CH3 n2, wherein 45-55 % of the radicals R'o are acetyl and the remaining radicals R o are hydrogen.
Following the procedure reported in EXAMPLE 1 B. using the intermediate of EXAMPLE 7A as starting material and the right amount of reagents (175 g of acetic anKydride for 340 g of
- 66 the compound of EXAMPLE 7A) the desired compound is obtained as a white powder with a melting range of 12 1 -1 27 C.
EXAMPLE 8: Preparation of the compound of the formula: o HsC C N (CH,)6 N Off' N (CH2)6-N -C-CTTj H3C -1CH3 H3C> <CH3 N H3C C 43 H3C CH3
H3C N CH3 H3C I CH3 H3C N C 43 H3C N CH3
R.,Rio R,3 R.o _ n2' wherein 50-60 /O of the radicals R'o are acetyl and the remaining radicals Rio are hydrogen.
Following the procedure reported in EXAMPLE 1 B. using the commercial product CYASORB UV 3346 as starting material and the right amount of reagents (93.4 9 of acetic anLydride for 1 Go 9 of CYASORB UV 334) the desired compour- d is obtained as a white powde r with a m eltinq range of 122 '-1 3 "C.
EXAMPLE 9: Preparation of the compound of the formula o T1(--C -- N (CH.)N - _ N:__--- N -- - (C6-)6N--- C -CHIT
Kl3C 1 C 43 1 C I CH3 AN il3C -l 1- CH H C J1 CH3 3 1 3 H3C 11 CH3 J 43( N CE13 H3CN CH3
R R10 L R 3 Fllo _ rift wherein 70--80 % of tire radicals Rio are acetyl and the rennaining radicals Rio are hydrogen.
Following the procedure reported in EXAMPLE 1 B. using the compound of EXAMPLE 8 as starting material and the right amount of reagents (41.5 g of acetic anRydride for 80 g of the compound of EXAMPLE 8) the desired compound is obtained as a yellow powder with a m elting range of 135 -1 43 C.
- 67 EXAMPLE 10: Preparation of the compound of the formula _ -- Ti Go (:H2)3
H3C,CH3
H3C 7 CH3
R,8 _ n3, wherein 70-80 % of the radicals Rue are acetyl and the remaining radicals R,8 are hydrogen.
Following the procedure reported in EXAMPLE 1 B. using the commercial product UVASIL 299 as starting material and the right amount of reagents (21.6 g of acetic anhydride for 38 g of UVASIL 299) the desired compound is obtained as an orange oil.
EXAMPLE 1 1:
Following the procedure reported in EXAMPLE 1 B. using the commercial product UVASORB HA 88 which contains groups of the formula (A-1-a) H3C CH3
IN-H (A- 1 -a) H3C CH3
as starting material and the right amount of reagents (80 g of acetic anhydride for 62 g of UVASORB HA 88) the desired compound wherein 55-65 % of the groups (A-1-a) are acetylated is obtained as a yellow powder with a melting range of 126 -131 C.
EXAMPLE 12: Preparation of the compound of the formula
- 68 C --C H.-C h H-C H z C -O CHAT C C-C H.: O H3C CH3 H3C CH3
H3C I CH3 H3C CH3 _ n7l wherein 75 85'',h of the radicals Rug are acetyl and the remaining radicals R4, are hydrogen.
Following the procedure reported in EXAMPLE 1 B and using the commercial product MARK LA 68 as starting material and the right amount of reagents (30 9 of acetic anRydridc for 40 g of MARK LA 68) the desired compound is obtained as a pale brown powder with a melting range of 32^-97''C.
EX MPLE 13: Preparation of the product mixture of the formula HO CRI3 l No N;,N. N ( C H.) --- N.-C H 2 C H.-
H C CH3 NOON H N- \N
N C 19 nil::1 H3C ' -,<CH isCt he'"'- N , _r H. H3C N CtI3 H3C ACHE H3( 1 F 43 R9 H3C N CH3 H3C I CH3
Rg Rg 2 wherein 55-65 /O of the radicals Rg are acetyl and the rernaininy radicals Rg are hydrogen Following the procedure reported in EXAMPLE 1 B. using the commercial product CHIMASSORB 905 as starting material and the right amount of reagents (207 9 of acetic anhydride for 350 9 of CHIMASSORB 905) the desired product is obtained as a yellow powder with a melting range of 122 -1 26 C.
- 69 EXAMPLE 14. Preparation of the product mixture of the formula Rg N N // I (CH2)3 N - -. - CHzCH2 3 C4H9 N N
H C CH HgC4 N N. N C4Hg H3C I CH3 H3C CH3 H3C CH3
R9 H3C I CH3 H3C I CH3
R9 R9 2
wherein 55-65 % of the radicals Rg are acetyl and the remaining radicals Rg are methyl.
Following the procedure described in EXAMPLE 3 and using the compound of EXAMPLE 13 as starting material the desired product is obtained as a yellow powder with a melting range of 132 -1360C EXAMPLE 15: Preparation of the product mixture of the formula H3COC - N (CH2)5 N - COCH3
H3C CHa H3C CH3 H3C N CH3 H3C N CH3
R42 R42
wherein 55-65 % of the radicals R42 are acetyl and the remaining radicals R42 are hydrogen.
Following the procedure reported in EXAMPLE 1 B and using N,N'-bis{2,2,6, 6-
tetramethypiperidin-4-yl}hexane-1 6-diamine as starting material and the right amount of reagents (112 9 of acetic anhydride for 42 9 of N,N'bis(2,2,6,6-tetramethylpiperidin-4-
yl}hexane-1,6-diamine) the desired product is obtained as a white powder with a melting range of 134 -138 C.
EXAMPLE 16: Preparation of the product mixture of the formula H3C CH3 H3C CH3
>I R ' o_C (CH2)8 C-OWN R H3C CH3 H3C CH3
wherein 75-85 % of the radicals R. are acetyl and the remaining radicals Rat are hydrogen.
Following the procedure reported in EXAMPLE 1 B and using TINUVIN 770 as starting material and the right amount of reagents (63 9 of acetic anhydride for 100 9 of TINUVIN 770) the desired product is obtained as a pale yellow oil.
OH NMR (300 MHz. CDCI:) Pam: 5.1 (m, 2H); 2.2 (m, 4H); 2.1 (s, 5H); -1.9 (m, 411); 1.6 (m, 4H); 1.4 ( s, 12H); 1.3 (s, 12H); 1.2 (m, 8H); 1.0 (t, AH).
EXAMPLE!-1. Stabilization of a gray pigmented polycarbonate/acrylonitrile butadiene-styrene (PC/ABS) blend.
A commercial PC/ABS blend ( Cycoioy MC 8002) pigmented with 1 /O by weight of Gray 9779 from Uniform Color Company is stabilized by addition of 1 / by weight of 2-(2'-hydroxy-3',5'-bis(1",1 "-dimethylbenzyl)phenyl) benzotriazole and 0.5% by weight of the compound indicated in Table I- I A sample containing only the 1% by weight of the benzotriazole stabilizer and an unstabilized sample - both containing 1 % by weight of gray pigment - servo as comparison.
Izod bars (2.5"L x 0.5"W x 0 1 25"W) are prepared by injection molding on a TROY 30 machine, barrel temperature 246 - 268 C, die temperature 268 C. Accelerated weathering is performed using an 'Atlas Ci65A Woather-O- meter (XAW), operating in 'Dry XAW" mode (ASTM G26-90, method C) After regular intervals, the color change AE according to DIN 6174 is determined. The results are listed in Table l-1.
Table l-1:
I rradiation time: 1 249.8 hours 750 hours
Stabilizer AE AE __ None 2.4 7.8 Benzotriazole stabilizer*) 1.3 5.5 Compound of EXAMPLE 1 B 0.4 2.4 - Compound of EXAMPLE 2 0.5 3.1 *) 2-(2'hydroxy-3l,5 -bis(1,,1 -dimethylbenzyl)phenyl)benzotriazole The PC/ABS samples stabilized according to this invention show an excellent color stability.
EXAMPLE 1-2: Stabilization of a blue pigmented polycarbonate/acrylonitrile-butadiene-styrene (PC/ABS) blend.
Samples are prepared from a commercial PC/ABS blend (@Cycoloy MC 8002) as described in EXAMPLE 1-1 except that 1% by weight of Clue 1 20A from Uniform Color Company is used as pigment and is stabilized by addition of 0.75% by weight of 2-(2'-hydroxy-3',5'-
bis(1",1"-dimethylbenzyl)phenyl)benzotriazole and 0.5% by weight of the compound indicated in Table i-2. A sample containing only the 0.75% by weight of the benzatriazole stabilizer and an unstabilized sample - both containing 1 % by weight of blue pigment - serve as comparison. Weathering and assessment is carried out as described in EXAMPLE 1-1.
The results are shown in Table 1-2.
Table l-2:
_ _ Irradiation time: 249.6 hours 749.3 hours 999.8 hours Stabilizer AE AE AE None 3.6 9.7 12.4 Benzotriazole stabilizer*) 2.6 9.7 12.9 Compound of EXAMPLE 1 B 0.5 3.8 6.1 *) 2-(2'-hydroxy-3,,st-bis(1,,1 dimethylbenzyl)phenyl)benzotriazole The PC/ABS samples stabilized according to this invention show an excellent color stability, particularly at prolonged exposure intervals.
- 72 EXAMPLE 1-3: Stabilization of a white pigmented polycarbonate/acrylonitrile-butadien e-styre ne ( PC/ABS) blend.
A commercially available white pigmented (TiO2) PC/ABS blend (@Cycoloy MC 8002-822; Polymerland Inc.) is stabilized by addition of 1 % by weight of tris{2,4-di-tert-
butylphenyl}phosphite, 0.75 % by weight of 2-(2'-hydroxy-3',5'-bis(1",1"-
dimethylbenzyl)phenyl)benzotriazole and 0.5 Q/O by weight of the compound indicated in Table 1-3.
The extrusion is carried out on a Leistritz 18 mm corotating, intermeshing twin screw extruder (general temperature profile (throat to die in C): 220, 240, 245, 245, 245, 245, 245; extrudate temperature: 256- 258 C). The polymer is predried in vacuo to < 50 ppm moisture.
Izod bars (2.5"L x 0.5''W x 0.125"W) are prepared by injection molding on a DEWY 50 machine (set temperatures = 268 C, 268'C, 271 C; nozzle = 271 279 C; injection pressure = 49.2 at: holding pressure = 49.2 at; back pressure = 3.44 at).
Accelerated weathering is performed using an Atlas Ci-65 Weather-O-meter (Xenon-Arc Weather-O-meter) operated per ASTM G26-90 method C (black panel temperature: SAC; irradiance: 0.35 W/rn2; inner and outer filters: borosilicate).
The results are listed in Table 1--3.
able i -;3 _ Irradiation time: 24g.8 hours 750 hours Stabilizer AE AE _ _
I I\lone 3.8 12.6 Compound of EXAMPLE 1B I 1.1 6.6 _ _ Compound of EXAMPLE 3 1.0 6 1 _, , Compound of EXAMPLE 4 1.1 6.S Compound of EXAMPLE 5 1: 6.8 Compound of EXAMPLE 8 1.3 6.9 Compound of EXAMPLE 10 1.1 6.6
- 73 Compound of EXAMPLE 11 1.1 6.4 Compound of EXAMPLE 13 1.0 6.6 _. ... Compound of EXAMPLE 14 1.0 6.4 Compound of EXAMPLE 16 1.0 5.7 The PC/ABS samples stabilized according to this invention show an excellent color stability.
EXAMPLE 11-1: Stabilization of polyethylene films, treated or untreated with pesticides.
The stabilizers indicated in Table 11-1 are mixed with low density polyethylene (LDPE) pellets (:Riblene FF 29 supplied by ENICHEM, Milano, Italy; melt flow index at 1 90 C and 2.16 kg: 0.62 9/10 min) in a turbo mixer.
The mixture is extruded at a maximum temperature of 200 C in a Berstorff single-screw extruder and the granules so obtained are compression molded in a Pasadena press for 3 min at 170 C. Films of about 150 Am thickness containing 0.3 % of the stabilizer are obtained. Pressmolded films for pesticide treatment are kept inside a dryer for 24 hours at 30 C, in presence of the vapors emitted by 2 liter of an aqueous solution containing 50 % of PAPAS (@Baslini S.p.A., Treviglio, Bergamo, Italy), which, in turn, is an aqueous solution of 382 9 per liter of metam-sodium having the formula CH3-NH-CS-SNa.
Non-treated films are mounted in metal frames while treated films are put into quartz tubes.
Frames and tubes are exposed in an Atlas Ci 65 Xenon Arc Weather-O-meter at 63 C black panel temperature, continues dry cycle, according to ASTM G 26-96. During the exposure, the performance is periodically evaluated measuring the carbonyl increment by means of a Fourier Transform Infrared (FT-IR) Spectrophotometer. The results are summarized in Table 11-1.
Table 11-1:
Pesticide treated; time Non treated; time Stabilizer (hours) to carbonyl (hours) to carbonyl increment = 0.2 increment = 0.1
- 74 Without c 250< 500 _ 0.3 % of the compound of EXAMPLE 1 B 2703190 0. 3 % of the compound of EXAMPLE 2 2954250 (High values indicate a good stabilization.) EXAMPLE 11-2: Stabilization of polypropylene fibres 0 25 % of the stabilizer listed in Table 11-2 is mixed with polypropylene powder ( Moplen FL F20 supplied by Montell, Ferrara, Italy; melt flow index at 230 C and 2 16 Kg: 12 2 g/min) in a turbo mixer together with 0 1 % of tris(2,4-di-t-butylphenyl) phosphite, 0 1 % of calcium monoethyl 3, 5-di-t-butyl-4-hydroxybenzyl-phosphonate, 0 1 % of calcium stearate and 0. 25 % of titanium dioxide ("FOR means "A by weight relative to The Wet OT the polypropylene',).
T he mixture is extruded at a maximum temperature of 230 C in a Berstorif single-screw extruder and the granules so obtained are converted into multifilaments at a maximum temperature of 260 C by fiber spinning in a Leonard apparatus (120/12 deniers).
Multifilaments for teetering are exposed in a forced circulating air oven for 20 min at 120 C.
Non treated and tentered multifilaments are exposed in an Atlas Ci 65 Xenon Arc Weather-
O-meter at 63 C black panel temperature, continues dry cycle, according to ASTM G 26-96.
Curing the exposure, the performance is periodically evaluated measuring the retained tensile strength by an Instron dynamometer. The results are indicated in Table 11-2.
Table 1_-2. Stabilizer % retained tensile strength it_, tel quel tentered _ I Without
50 after 200 hours 50 after 150 Pours , 4 Compound of EXAMPLE 1 B 72 after 1450 hours 1 72 after 1450 hours I (High values indicate a good stabilization.) EXAMPLE 11-3: Stabilization of polypropylene multifilaments and polypropylene plaques Polypropylene multifilaments are prepared as described in EXAMPLE 11-2.
- 75 Injection molded plaques of 1 mm thickness are prepared, starting by adding to polypropylene powder (@Moplen S SE supplied by Montell, Ferrara, Italy; melt flow index at 230 C and 2.16 Kg: 2.0 g/min), 0.1 % of the stabilizer listed in Table 11-3, 0.1 % of tris(2,4-di-
tert-butylphenyl) phosphite, 0.5 % of octadecyl-3-(3,5-di-tert-butyl-4-
hydroxyphenyl)propionate and 0.1 % of calcium stearate, and mixing the components in a turbo mixer ("%" means "% by weight relative to the weight of the polypropylene"). The mixture is extruded at a maximum temperature of 230 C in a Berstorff single-screw extruder and the granules so obtained are converted into plaques 1 mm thick by injection molding in a Negri-Bossi press at a maximum temperature of 220 C.
The multifilaments and the plaques so obtained are exposed in a forced circulating air oven at 120 C and 135 C, respectively.
Evaluations are periodically made until breakage occurs. For multifilaments this event corresponds to falling down of a weight that had been hung to each fiber formulation; for plaques the evaluation is made by bending it with a specific device.
The results are summarized in Table 11-3.
Table il-3
Hours to breakage Hours to breakage Stabilizer of multifilaments at of plaques at 1 20 C 1 35 C
without 120 790 Compound of EXAMPLE 1 B- 1150 1320 (High values indicate a good stabilization.)

Claims (12)

- 76 Claims:
1. A product of the formula (Xl) - I H CH2-O-
/ H.; I H2 (Xl) R. no b in which the radicals Rat independently of one another are hydrogen, C -C3alkyl or C -C70acyl with 5 to 85 % of the radicals Rat independently of one another being hydrogen or C -C8alkyl and the remaining radicals Rat being C,-C20acyl and n6 is a number from 2 to 50.
2. A product according to claim 1 wherein n6 is a number from 2 to 25.
3. A product according to claim 1 wherein 5 to 85 % of the radicals R3, independently of one another are hydrogen or methyl and the remaining radicals R3, are C -C Oacyl.
4. A product according to claim 3 wherein 20 to 70 % of the radicals R3' independently of one another are hydrogen or methyl and the remaining radicals R3' are C,-C,Oacyl.
5. A product according to claim 3 wherein the meaning C,-C,Oacyl is acetyl.
- 77
6. A composition containing an organic material susceptible to degradation induced by light, heat or oxidation and a product according to claim 1.
7. A composition according to claim 6 wherein the organic material is a synthetic polymer.
8. A composition according to claim 6 wherein the organic material is a polyolefin.
9. A composition according to claim 6 wherein the organic material is a polycarbonate or a polycarbonate/graft copolymer blend.
10. A composition according to claim 9, which additionally contains a pigment.
11. A composition according to claim 9, which additionally contains an UV absorber
12. A method for stabilizing an organic material against degradation induced by light, heat or oxidation, which comprises incorporating into said organic material a product according to claim 1.
GB0211338A 1998-12-14 1999-12-10 Sterically hindered amine compounds Expired - Fee Related GB2377936B (en)

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GB0211340A Expired - Fee Related GB2377937B (en) 1998-12-14 1999-12-10 Sterically hindered amine compounds
GB0211335A Expired - Fee Related GB2377935B (en) 1998-12-14 1999-12-10 Sterically hindered amine compounds
GB0211330A Expired - Fee Related GB2377709B (en) 1998-12-14 1999-12-10 Sterically hindered amine compounds
GB0211338A Expired - Fee Related GB2377936B (en) 1998-12-14 1999-12-10 Sterically hindered amine compounds
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GB0211340A Expired - Fee Related GB2377937B (en) 1998-12-14 1999-12-10 Sterically hindered amine compounds
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EP0052579B1 (en) * 1980-11-17 1984-11-14 Ciba-Geigy Ag Stabilisers against photo degradation
FR2642764B1 (en) * 1989-02-03 1993-05-28 Rhone Poulenc Chimie NOVEL PIPERIDINYL FUNCTIONAL COMPOUNDS AND THEIR APPLICATION IN THE PHOTOSTABILIZATION OF POLYMERS
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EP1078929A2 (en) * 1999-08-18 2001-02-28 Clariant Finance (BVI) Limited Sterically hindered amines

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GB2377705B (en) 2003-06-18
GB2377705A (en) 2003-01-22
GB2377936B (en) 2003-06-18
GB2377704B (en) 2003-06-18
GB2377709A (en) 2003-01-22
GB0211333D0 (en) 2002-06-26
GB0211330D0 (en) 2002-06-26
GB2377709B (en) 2003-06-18
GB2377703A (en) 2003-01-22
GB0211335D0 (en) 2002-06-26
GB0211338D0 (en) 2002-06-26
GB2377703B (en) 2003-06-18
GB2377935B (en) 2003-06-18
GB0211341D0 (en) 2002-06-26
GB0211340D0 (en) 2002-06-26
GB2377937A (en) 2003-01-29
GB2377937B (en) 2003-06-18
GB0211332D0 (en) 2002-06-26
GB2377935A (en) 2003-01-29
GB2377704A (en) 2003-01-22

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