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US4143089A Expired / Lapsed US ⏱️ 0.0 years remaining

Silylated polymers

Assignee: Wacker Chemical Corp
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Filing: 1976-11-22
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Granted: 1979-03-06
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Expires: 1996-11-22
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Abstract

Abstract Alkali metal terminated organic polymers are reacted with silicon containing compounds having aliphatic unsaturation to produce a new class of reactive silylated organic polymers. These silyated organic polymers can be in turn reacted with cyclic siloxanes to produce silylated organic-organopolysiloxane block copolymers which are useful as protective coatings, surfactants and as elastomers.

Inventors

  • 👤 Eugene R. Martin

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 19:48
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/42; C08G77/442; C08C; C08C19/00; C08C19/30; C08C19/42; C08C19/44; C08F; C08F12/00; C08F12/02; C08F12/04; C08F12/06; C08F12/08; C08F212/00; C08F212/02; C08F212/04; C08F212/06; C08F212/12; C08F297/00; C08F297/02; C08G77/48; C08G77/50; C08G81/00; C08G81/02; C08G85/00; C08G85/004; C08K; C08K5/00; C08K5/0008; C08K5/0025; C08L; C08L43/00; C08L43/04

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 118 words
A carbanion containing silylated organic polymer obtained from the reaction of a silane of the formula ##STR16## where R is a monovalent hydrocarbon radical, X is selected from the class consisting of halogen, acyloxy radicals, hydrocarbonoxy radicals, sulfato radicals, phosphato radicals and perchlorato radicals, a is a number of from 1 to 3, b is a number of from 0 to 2 and the sum of (a + b) is a number of from 1 to 3, with a carbanion containing organic polymer at a temperature up to about 150° C., said carbanion containing organic polymer is obtained from the polymerization of an unsaturated organic monomer having carbon-to-carbon double bonds in the presence of a carbanion forming catalyst.
Claim 2
Dependent Claim 118 words
A carbanion containing silylated organic polymer obtained from the reaction of a silane of the formula ##STR16## where R is a monovalent hydrocarbon radical, X is selected from the class consisting of halogen, acyloxy radicals, hydrocarbonoxy radicals, sulfato radicals, phosphato radicals and perchlorato radicals, a is a number of from 1 to 3, b is a number of from 0 to 2 and the sum of (a + b) is a number of from 1 to 3, with a carbanion containing organic polymer at a temperature up to about 150° C., said carbanion containing organic polymer is obtained from the polymerization of an unsaturated organic monomer having carbon-to-carbon double bonds in the presence of a carbanion forming catalyst.
Claim 3
Dependent Claim 17 words
The silylated organic polymer of claim 1 where the organic monomer is a hydrocarbon having carbon-to-carbon unsaturation.
Claim 4
Dependent Claim 12 words
The silylated organic polymer of claim 1 where the monomer is styrene.
Claim 5
Dependent Claim 12 words
The silylated organic polymer of claim 1 where the silane is vinyltrichlorosilane.
Claim 6
Dependent Claim 12 words
The silylated organic polymer of claim 1 where the silane is methylvinyldichlorosilane.
Claim 7
Dependent Claim 12 words
The silylated organic polymer of claim 1 where the monomer is isoprene.
Claim 8
Dependent Claim 14 words
The silylated organic polymer of claim 1 where the monomer is an alkyl acrylate.
Claim 9
Dependent Claim 12 words
The silylated organic polymer of claim 1 where the monomer is acrylonitrile.
Claim 10
Dependent Claim 12 words
The silylated organic polymer of claim 1 wherein the monomer is butadiene.
Claim 11
Dependent Claim 12 words
The silylated organic polymer of claim 1 where the silane is vinyltriacetoxysilane.
Claim 12
Dependent Claim 18 words
The silylated organic polymer of claim 1 where the monomer consists of a mixture of styrene and isoprene.
Claim 13
Independent Claim 132 words
A method for preparing a carbanion containing silylated organic polymer which comprises reacting in the presence of an aprotic solvent a silane of the formula ##STR17## where R is selected from the class consisting of a monovalent hydrocarbon radical, X is selected from the class consisting of halogen, acyloxy radicals, hydrocarbonoxy radicals, sulfato radicals, phosphato radicals and perchlorato radicals, a is a number of from 1 to 3, b is a number of from 0 to 2 and the sum of (a + b) is a number of from 1 to 3 with a carbanion containing organic polymer at a temperature up to about 150° C., said carbanion containing organic polymer is obtained from the polymerization of an unsaturated organic monomer having carbon-to-carbon unsaturation in the presence of a carbanion forming catalyst.
Claim 14
Independent Claim 132 words
A method for preparing a carbanion containing silylated organic polymer which comprises reacting in the presence of an aprotic solvent a silane of the formula ##STR17## where R is selected from the class consisting of a monovalent hydrocarbon radical, X is selected from the class consisting of halogen, acyloxy radicals, hydrocarbonoxy radicals, sulfato radicals, phosphato radicals and perchlorato radicals, a is a number of from 1 to 3, b is a number of from 0 to 2 and the sum of (a + b) is a number of from 1 to 3 with a carbanion containing organic polymer at a temperature up to about 150° C., said carbanion containing organic polymer is obtained from the polymerization of an unsaturated organic monomer having carbon-to-carbon unsaturation in the presence of a carbanion forming catalyst.
Claim 15
Dependent Claim 11 words
The method of claim 12 where the aprotic solvent is tetrahydrofuran.
Claim 16
Dependent Claim 12 words
The method of claim 13 where the carbanion producing catalyst is 9-fluorenylsodium.
Claim 17
Dependent Claim 12 words
The method of claim 12 where the carbanion producing catalyst is butyllithium.
Claim 18
Dependent Claim 12 words
The method of claim 12 where the unsaturated organic monomer is styrene.

References Cited (Backward Citations)

US3051684A Cited
US3483270A Cited
US3637899A Cited
US3870766A Cited
US3956419A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-03-05 1982-09-04 1983-03-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-03-05 1986-09-04 1987-03-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-03-05 1990-09-04 1991-03-06 $7700.00 Window Closed / Lapsed

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