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US5143992A Expired / Lapsed US ⏱️ 0.0 years remaining

Methathesis polymerizable adducts of a divinylcyclohydrocarbon and cyclopentadiene

Assignee: Shell USA Inc
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Filing: 1991-07-12
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Granted: 1992-09-01
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Expires: 2011-07-12
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Abstract

Abstract An improved thermoset polymer having good mechanical properties and no detectable dicyclopentadiene odor is obtained by the ring-opening polymerization of a novel mixture of adducts comprising divinyl cyclohydrocarbon compound, such as 3,5-divinylcyclopentene and cyclopentadiene, optionally with added cycloolefinic compound, such as dicyclopentadiene, at polymerization conditions in the presence of an olefin metathesis catalyst.

Inventors

  • 👤 Donald R. Kelsey

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 11:19
CPC Classifications
C; C08; C08G; C08G61/00; C08G61/02; C08G61/04; C08G61/06; C08G61/08

Claims Analysis

Total Claims: 30
Claim 1
Independent Claim 84 words
A process for the polymerization under ring-opening polymerization conditions of a mixture comprising a major proportion of (1) adducts of a divinyl cyclohydrocarbon compound of up to 20 carbon atoms containing two vinyl groups as substituents on carbon atoms at least one carbon atom apart on an aliphatic ring system of from 5 to 10 carbon atoms and of 1 ring or 2 fused rings and cyclopentadiene, and (2) cyclopentadiene oligomers in the presence of an olefin methathesis catalyst system and, optionally, added dicyclopentadiene.
Claim 2
Dependent Claim 84 words
A process for the polymerization under ring-opening polymerization conditions of a mixture comprising a major proportion of (1) adducts of a divinyl cyclohydrocarbon compound of up to 20 carbon atoms containing two vinyl groups as substituents on carbon atoms at least one carbon atom apart on an aliphatic ring system of from 5 to 10 carbon atoms and of 1 ring or 2 fused rings and cyclopentadiene, and (2) cyclopentadiene oligomers in the presence of an olefin methathesis catalyst system and, optionally, added dicyclopentadiene.
Claim 3
Dependent Claim 79 words
The process of claim 1 wherein the divinyl cyclohydrocarbon compound is of the formula ##STR5## wherein z is 0 or 1 and A individually is hydrogen, alkyl of from 1 to 4 carbon atoms inclusive, or the two A groups taken together form a second valence bond between the two carbon atoms to which they are attached or a divalent linking group of from 3 to 4 carbon atoms in the bridge and up to 1 carbon-carbon double bond.
Claim 4
Dependent Claim 21 words
The process of claim 2 wherein the catalyst system comprises a di(alkylphenoxy)tungsten halide, a triorganotin compound and, optionally, a boron halide.
Claim 5
Dependent Claim 59 words
The process of claim 3 wherein the tungsten halide is of the formula ##STR6## wherein R independently is alkyl of up to 10 carbon atoms inclusive, R' independently is hydrogen or R, R" independently is hydrogen or R, X is halo, x is 2 or 4 and y is 0 or 1 with the sum of x+2y being 4.
Claim 6
Dependent Claim 23 words
The process of claim 4 wherein the triorganotin halide is a trialkyltin halide wherein each alkyl independently has up to 10 carbon atoms.
Claim 7
Dependent Claim 11 words
The process of claim 5 wherein the divinyl cyclohydrocarbon is 1,3-divinylcyclopentane.
Claim 8
Dependent Claim 11 words
The process of claim 5 wherein the divinyl cyclohydrocarbon is 3,5-divinylcyclopentene.
Claim 9
Dependent Claim 10 words
The process of claim 5 wherein the divinylcyclohydrocarbon is 2,4-divinylbicyclo[3.3.0]oct-6-ene.
Claim 10
Dependent Claim 22 words
The process of claim 7 wherein the polymerization is carried out at a temperature from about 25° C. to about 200° C.
Claim 11
Dependent Claim 17 words
The process of claim 9 wherein the polymerization mixture contains at least about 60% total of adducts.
Claim 12
Dependent Claim 22 words
The process of claim 10 wherein the molar ratio of tungsten halide to tin hydride is from about 1:1 to about 1:15.
Claim 13
Dependent Claim 33 words
The process of claim 11 wherein X is chloro or bromo, R is alkyl of from 3 to 6 carbon atoms branched on the α-carbon atom, R' is R and R" is hydrogen.
Claim 14
Dependent Claim 28 words
The process of claim 12 wherein the tin hydride is a trialkyltin hydride in which each alkyl is straight-chain alkyl of from 3 to 6 carbon atoms inclusive.
Claim 15
Dependent Claim 28 words
The process of claim 13 wherein the boron halide promoter is present in an amount from about 0.05 mole to about 2 moles per mole of tungsten compound.
Claim 16
Dependent Claim 27 words
The process of claim 14 wherein the boron halide is boron trifluoride, the diethyl ether complex of boron trifluoride or the dibutyl ether complex of boron trifluoride.
Claim 17
Dependent Claim 12 words
The process of claim 13 wherein the tungsten halide is bis(2,6-diisopropylphenoxy)tungsten oxydichloride.
Claim 18
Dependent Claim 12 words
The process of claim 16 wherein the tin hydride is tributylin hydride.
Claim 19
Dependent Claim 12 words
The hard, infusible polymeric product produced by the process of claim 1.
Claim 20
Dependent Claim 12 words
The hard, infusible polymeric product produced by the process of claim 6.
Claim 21
Dependent Claim 64 words
A polymerizable mixture of (1) adducts of a divinyl cyclohydrocarbon compound of up to 20 carbon atoms, inclusive, containing two vinyl groups as substituents on carbon atoms at least one carbon atom apart on an aliphatic ring system of from 5 to 10 carbon atoms and 1 ring or 2 fused rings and cyclopentadiene, and (2) cyclopentadiene oligomers, optionally in the presence of dicyclopentadiene.
Claim 22
Dependent Claim 64 words
A polymerizable mixture of (1) adducts of a divinyl cyclohydrocarbon compound of up to 20 carbon atoms, inclusive, containing two vinyl groups as substituents on carbon atoms at least one carbon atom apart on an aliphatic ring system of from 5 to 10 carbon atoms and 1 ring or 2 fused rings and cyclopentadiene, and (2) cyclopentadiene oligomers, optionally in the presence of dicyclopentadiene.
Claim 23
Dependent Claim 79 words
The mixture of claim 20 wherein the divinyl cyclohydrocarbon compound is of the formula ##STR7## wherein z is 0 or 1 and A individually is hydrogen, alkyl of from 1 to 4 carbon atoms inclusive, or the two A groups taken together form a second valence bond between the two carbon atoms to which they are attached or a divalent linking group of from 3 to 4 carbon atoms in the bridge and up to 1 carbon-carbon double bond.
Claim 24
Dependent Claim 12 words
The mixture of claim 21 wherein the divinyl cyclohydrocarbon compound is 3,5-divinylcyclopentene.
Claim 25
Dependent Claim 12 words
The mixture of claim 21 wherein the divinyl cyclohydrocarbon compound is 1,3-divinylcyclopentane.
Claim 26
Dependent Claim 11 words
The mixture of claim 21 wherein the divinyl cyclohydrocarbon is 2,4-divinylbicyclo[3.3.0]oct-6-ene.
Claim 27
Dependent Claim 42 words
A process for providing the adduct mixture of claim 20 comprising contacting the divinylcyclohydrocarbon and dicyclopentadiene at a temperature of at least about 160° C. and such that the molar ratio of divinylcyclohydrocarbon to dicyclopentadiene is from about 0.5 to about 2.
Claim 28
Dependent Claim 10 words
The process of claim 25 wherein the divinylcyclohydrocarbon is 3,5-divinylcyclopentene.
Claim 29
Dependent Claim 10 words
The process of claim 25 wherein the divinylcyclohydrocarbon is 1,3-divinylcyclopentane.
Claim 30
Dependent Claim 10 words
The process of claim 25 wherein the divinylcyclohydrocarbon is 2,4-divinylbicyclo[3.3.0]oct-6-ene.

References Cited (Backward Citations)

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1995-09-01 1996-03-02 1996-09-01 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1999-09-01 2000-03-02 2000-09-01 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2003-09-01 2004-03-02 2004-09-01 $7700.00 Window Closed / Lapsed

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