ORGANOSILYLAMINES

1,179,509. Silylamines; siloxanes. GENERAL ELECTRIC CO. 5 Dec., 1967 [20 Dec., 1966], No.55232/67. Headings C3S and C3T. The invention comprises organosilylamines and their higher molecular weight reaction products with silanol-containing materials, the silylamines having the general formula where Y...

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description 1,179,509. Silylamines; siloxanes. GENERAL ELECTRIC CO. 5 Dec., 1967 [20 Dec., 1966], No.55232/67. Headings C3S and C3T. The invention comprises organosilylamines and their higher molecular weight reaction products with silanol-containing materials, the silylamines having the general formula where Y is -NZZ1 or a heterocyclic amino radical, Z being alkyl and Z1 hydrogen or alkyl, R is a monovalent hydrocarbon or halohydrocarbon radical and R1 is a divalent hydrocarbon radical which may be interrupted by hetero elements. In particular, R1 is alkylene, arylene, alkylenearylene alkylene, alkyleneoxy-arylene or -alkylene, aryleneoxyarylene or R11TR11 where R11 is alkylene or arylene and T is -C(R111 )2 -, -S(O)-, -SO 2 or -Si(R111) 2 -, where R111 is hydrogen or one of R. They are prepared by reacting the appropriate primary or secondary amine with the corresponding bis- (halosilyl) compound. Suitable amines are dimethyl, diethyl, isopropyl, n-butyl and methylethyl amines, piperidine, pyrrolidine and morpholine. The groups R and R1 may be aliphatic, saturated or unsaturated, or aromatic. The higher molecular weight products are obtained by reacting (1) the above silylamines, or mixtures thereof with a monofunctional silylamine R 3 SiY, with (2) a silanol or siloxanol of the formula or mixture thereof with a monofunctional silylamine or silanol-terminated polysiloxane, where Q is R or a cyanoalkyl radical. The products consist of combined Q 2 SiO units and (R 2 )SiR1- Si(R 2 )O units. They may be vulcanized at room temperature by adding silica filler together with ethylpolysilicate and a metal soap catalyst. Or the gums may be mixed with fumed silica or titania and a peroxy catalyst in the usual way for elastomers. Specification 1,089,227 is referred to.
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The invention comprises organosilylamines and their higher molecular weight reaction products with silanol-containing materials, the silylamines having the general formula where Y is -NZZ1 or a heterocyclic amino radical, Z being alkyl and Z1 hydrogen or alkyl, R is a monovalent hydrocarbon or halohydrocarbon radical and R1 is a divalent hydrocarbon radical which may be interrupted by hetero elements. In particular, R1 is alkylene, arylene, alkylenearylene alkylene, alkyleneoxy-arylene or -alkylene, aryleneoxyarylene or R11TR11 where R11 is alkylene or arylene and T is -C(R111 )2 -, -S(O)-, -SO 2 or -Si(R111) 2 -, where R111 is hydrogen or one of R. They are prepared by reacting the appropriate primary or secondary amine with the corresponding bis- (halosilyl) compound. Suitable amines are dimethyl, diethyl, isopropyl, n-butyl and methylethyl amines, piperidine, pyrrolidine and morpholine. The groups R and R1 may be aliphatic, saturated or unsaturated, or aromatic. The higher molecular weight products are obtained by reacting (1) the above silylamines, or mixtures thereof with a monofunctional silylamine R 3 SiY, with (2) a silanol or siloxanol of the formula or mixture thereof with a monofunctional silylamine or silanol-terminated polysiloxane, where Q is R or a cyanoalkyl radical. The products consist of combined Q 2 SiO units and (R 2 )SiR1- Si(R 2 )O units. They may be vulcanized at room temperature by adding silica filler together with ethylpolysilicate and a metal soap catalyst. Or the gums may be mixed with fumed silica or titania and a peroxy catalyst in the usual way for elastomers. 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GOOSSENS</creatorcontrib><title>ORGANOSILYLAMINES</title><description>1,179,509. Silylamines; siloxanes. GENERAL ELECTRIC CO. 5 Dec., 1967 [20 Dec., 1966], No.55232/67. Headings C3S and C3T. The invention comprises organosilylamines and their higher molecular weight reaction products with silanol-containing materials, the silylamines having the general formula where Y is -NZZ1 or a heterocyclic amino radical, Z being alkyl and Z1 hydrogen or alkyl, R is a monovalent hydrocarbon or halohydrocarbon radical and R1 is a divalent hydrocarbon radical which may be interrupted by hetero elements. In particular, R1 is alkylene, arylene, alkylenearylene alkylene, alkyleneoxy-arylene or -alkylene, aryleneoxyarylene or R11TR11 where R11 is alkylene or arylene and T is -C(R111 )2 -, -S(O)-, -SO 2 or -Si(R111) 2 -, where R111 is hydrogen or one of R. They are prepared by reacting the appropriate primary or secondary amine with the corresponding bis- (halosilyl) compound. Suitable amines are dimethyl, diethyl, isopropyl, n-butyl and methylethyl amines, piperidine, pyrrolidine and morpholine. The groups R and R1 may be aliphatic, saturated or unsaturated, or aromatic. The higher molecular weight products are obtained by reacting (1) the above silylamines, or mixtures thereof with a monofunctional silylamine R 3 SiY, with (2) a silanol or siloxanol of the formula or mixture thereof with a monofunctional silylamine or silanol-terminated polysiloxane, where Q is R or a cyanoalkyl radical. The products consist of combined Q 2 SiO units and (R 2 )SiR1- Si(R 2 )O units. They may be vulcanized at room temperature by adding silica filler together with ethylpolysilicate and a metal soap catalyst. Or the gums may be mixed with fumed silica or titania and a peroxy catalyst in the usual way for elastomers. 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GOOSSENS</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>JOHN C. GOOSSENS</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>ORGANOSILYLAMINES</title><date>1970-02-24</date><risdate>1970</risdate><abstract>1,179,509. Silylamines; siloxanes. GENERAL ELECTRIC CO. 5 Dec., 1967 [20 Dec., 1966], No.55232/67. Headings C3S and C3T. The invention comprises organosilylamines and their higher molecular weight reaction products with silanol-containing materials, the silylamines having the general formula where Y is -NZZ1 or a heterocyclic amino radical, Z being alkyl and Z1 hydrogen or alkyl, R is a monovalent hydrocarbon or halohydrocarbon radical and R1 is a divalent hydrocarbon radical which may be interrupted by hetero elements. In particular, R1 is alkylene, arylene, alkylenearylene alkylene, alkyleneoxy-arylene or -alkylene, aryleneoxyarylene or R11TR11 where R11 is alkylene or arylene and T is -C(R111 )2 -, -S(O)-, -SO 2 or -Si(R111) 2 -, where R111 is hydrogen or one of R. They are prepared by reacting the appropriate primary or secondary amine with the corresponding bis- (halosilyl) compound. Suitable amines are dimethyl, diethyl, isopropyl, n-butyl and methylethyl amines, piperidine, pyrrolidine and morpholine. The groups R and R1 may be aliphatic, saturated or unsaturated, or aromatic. The higher molecular weight products are obtained by reacting (1) the above silylamines, or mixtures thereof with a monofunctional silylamine R 3 SiY, with (2) a silanol or siloxanol of the formula or mixture thereof with a monofunctional silylamine or silanol-terminated polysiloxane, where Q is R or a cyanoalkyl radical. The products consist of combined Q 2 SiO units and (R 2 )SiR1- Si(R 2 )O units. They may be vulcanized at room temperature by adding silica filler together with ethylpolysilicate and a metal soap catalyst. Or the gums may be mixed with fumed silica or titania and a peroxy catalyst in the usual way for elastomers. Specification 1,089,227 is referred to.</abstract><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMISTRY
COMPOSITIONS BASED THEREON
MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
METALLURGY
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
THEIR PREPARATION OR CHEMICAL WORKING-UP
title ORGANOSILYLAMINES
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