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US3966531A Expired / Lapsed US ⏱️ 0.0 years remaining

Compositions containing silanes possessing imide groups

Assignee: Rhone Poulenc Industries SA
•
Filing: 1975-02-03
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Granted: 1976-06-29
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Expires: 1995-02-03
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Abstract

Abstract Compositions are prepared by reacting one mol of a bis-imide of the formula: ##EQU1## with at least one mol of an amino-silane of the formula: ##EQU2## IN WHICH R represents a divalent hydrocarbon radical with 2 to 20 carbon atoms which is free from unsaturated bonds other than aromatic bonds, a divalent mono- or bis-heterocyclic radical with 2 to 10 carbon atoms, or a divalent organic radical with 4 to 20 carbon atoms which consists of more than one said divalent hydrocarbon radical bonded to one another via --O--, --S--, --CO-- or --SO 2 --, R' represents a divalent hydrocarbon radical with 1 to 20 carbon atoms or a divalent radical with 4 to 20 carbon atoms which consists of more than one hydrocarbon radical bonded to one another via --NH-- or --O--, Z represents a hydrolysable group, R" represents a monovalent radical with 1 to 6 carbon atoms and x is 0 or 1. These compositions are particularly useful, especially as solutions, as undercoats for adhering organopolysiloxane compositions to a variety of substrates.

Inventors

  • 👤 Michel Bargain

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 00:49
CPC Classifications
C; C09; C09D; C09D183/00; C09D183/14; C07; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/18; C07F7/1804; C09D4/00; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31652; Y10T428/31663

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 166 words
Process for the preparation of a composition based on imide-group containing organosilicon compound which comprises reacting one mol of a bis-imide of the formula: ##EQU15## with at least one mole of an amino-silane of the formula: ##EQU16## in which R represents a divalent hydrocarbon radical with 2 to 20 carbon atoms which is free from unsaturated bonds other than aromatic bonds, a divalent mono- or bis-heterocyclic radical with 2 to 10 carbon atoms, or a divalent organic radical with 4 to 20 carbon atoms which consists of more than one said divalent hydrocarbon radical bonded to one another via --O--, --S--, --CO-- or --SO 2 --, R' represents a divalent hydrocarbon radical with 1 to 20 carbon atoms or a divalent radical with 4 to 20 carbon atoms which consists of more than one hydrocarbon radical bonded to one another via --NH-- or --O--, Z represents a hydrolysable group, R" represents a monovalent radical with 1 to 6 carbon atoms and x is 0 or 1.
Claim 2
Dependent Claim 166 words
Process for the preparation of a composition based on imide-group containing organosilicon compound which comprises reacting one mol of a bis-imide of the formula: ##EQU15## with at least one mole of an amino-silane of the formula: ##EQU16## in which R represents a divalent hydrocarbon radical with 2 to 20 carbon atoms which is free from unsaturated bonds other than aromatic bonds, a divalent mono- or bis-heterocyclic radical with 2 to 10 carbon atoms, or a divalent organic radical with 4 to 20 carbon atoms which consists of more than one said divalent hydrocarbon radical bonded to one another via --O--, --S--, --CO-- or --SO 2 --, R' represents a divalent hydrocarbon radical with 1 to 20 carbon atoms or a divalent radical with 4 to 20 carbon atoms which consists of more than one hydrocarbon radical bonded to one another via --NH-- or --O--, Z represents a hydrolysable group, R" represents a monovalent radical with 1 to 6 carbon atoms and x is 0 or 1.
Claim 3
Dependent Claim 16 words
Process according to claim 1, in which the molar ratio ##EQU17## is from 1 to 2.
Claim 4
Dependent Claim 34 words
Process according to claim 1, in which the bis-imide contains up to 20 mol % of a monoimide which is a maleimide, N-alkyl- or aryl-maleimide, or a maleimide possessing an acetoxy or acetamido group.
Claim 5
Dependent Claim 28 words
Process according to claim 1, in which the reaction is carried out at a temperature of 0° to 100°C in at least a partial solvent for the bis-imide.
Claim 6
Dependent Claim 40 words
A composition based on imide group-containing organosilicon compound which comprises a compound of the formula: ##EQU18## in which R, R', R"Z and x are as defined in claim 1 and Σ represents a radical of the formula: ##EQU19## or ##EQU20##
Claim 7
Dependent Claim 13 words
A composition according to claim 5, which contains a solvent for the compound.
Claim 8
Dependent Claim 11 words
A composition according to claim 5, which contains a curing accelerator.
Claim 9
Dependent Claim 66 words
A composition according to claim 5, in which Z represents a group of the formula: --OG, ##EQU21## --NHG, --N(G) 2 , ##EQU22## --ON=CHG, --ON=C(G) 2 , --ON(G) 2 in which each of the G radicals, which may be the same or different, represents a monovalent hydrocarbon radical containing at most 15 carbon atoms or two G radicals together form a divalent radical optionally containing a heteroatom.
Claim 10
Dependent Claim 54 words
A composition according to claim 8, in which G represents a methyl, ethyl, propyl, hexyl, cyclohexenyl, cyclohexyl, phenyl, benzyl or tolyl radical, or two G radicals form a radical of formula: --(CH 2 ) n or --(CH 2 ) n --O(CH 2 ) n in which n is an integer from 1 to 5.
Claim 11
Dependent Claim 53 words
In a process for adhering an organopolysiloxane composition which can be vulcanised at ambient temperature in the presence of water in the liquid or vapour state to a substrate which comprises placing an adhesive between the composition and the substrate, the improvement wherein the adhesive is a composition as defined in claim 5.
Claim 12
Dependent Claim 22 words
A process according to claim 10, in which the substrate is wood, concrete, a metal, polyethylene, glass or a glass fibre material.

References Cited (Backward Citations)

US2721873A Cited
US2818405A Cited
US3185704A Cited
US3379607A Cited
US3562223A Cited
US3499870A Cited
US3717615A Cited
US3759779A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-06-29 1979-12-29 1980-06-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-06-29 1983-12-29 1984-06-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-06-29 1987-12-29 1988-06-29 $7700.00 Window Closed / Lapsed

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