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Preparation of siloxylated metal-containing catalysts

Assignee: Witco Corp
•
Filing: 1981-12-30
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Granted: 1983-08-23
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Expires: 2001-12-30
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Abstract

Abstract Reaction of silylamine with a metallic carboxylate produces siloxylated organometallic compounds with M-O-Si bonds. These siloxylated organometallic compounds are useful catalysts in the preparation of urethane foams and elastomers, especially when prepared in situ with the urethane foam or elastomer reactants.

Inventors

  • 👤 Baskent Feyyaz O
  • 👤 James D. Reedy

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 10:06
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/16; C08G18/22; C08G18/24; C07; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/0834; C07F7/0836; C07F7/22; C07F7/2224; C07F7/24; C07F7/28

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 141 words
A process for preparing a siloxylated organometallic catalyst which comprises reacting below 100° C. a silylamine of the formula: R.sub.4-n Si(NR'R").sub.n wherein R is a alkyl, alkaryl, alkenyl, alkynyl, aryl cycloaliphatic, or heteroatom substituted aliphatic siloxy or substituted siloxy group; R' and R" are individually hydrogen, alkyl, alkenyl, alkynyl, aryl, cycloaliphatic, or heteroatom substituted aliphatic, groups provided R' and R" cannot both be hydrogen; and n is one to four inclusive, with a metallic carboxylate of the formula: M(OCOR'").sub.x R"".sub.y wherein M is a metal with an oxidation state, R'" and R"" are individually an alkyl, alkaryl, alkenyl, alkynyl, aryl, cycloaliphatic, or heteroatom substituted aliphatic, group; x is at least one but no more than the oxidation state of M and y is equal to the oxidation state of M minus x, and M is greater than or equal to two.
Claim 2
Dependent Claim 141 words
A process for preparing a siloxylated organometallic catalyst which comprises reacting below 100° C. a silylamine of the formula: R.sub.4-n Si(NR'R").sub.n wherein R is a alkyl, alkaryl, alkenyl, alkynyl, aryl cycloaliphatic, or heteroatom substituted aliphatic siloxy or substituted siloxy group; R' and R" are individually hydrogen, alkyl, alkenyl, alkynyl, aryl, cycloaliphatic, or heteroatom substituted aliphatic, groups provided R' and R" cannot both be hydrogen; and n is one to four inclusive, with a metallic carboxylate of the formula: M(OCOR'").sub.x R"".sub.y wherein M is a metal with an oxidation state, R'" and R"" are individually an alkyl, alkaryl, alkenyl, alkynyl, aryl, cycloaliphatic, or heteroatom substituted aliphatic, group; x is at least one but no more than the oxidation state of M and y is equal to the oxidation state of M minus x, and M is greater than or equal to two.
Claim 3
Dependent Claim 27 words
The process of claim 1 wherein the R, R' and R" groups of the silylamine employed are alkyl groups containing no more than twenty-four carbon atoms each.
Claim 4
Dependent Claim 23 words
The process of claim 2 wherein the R, R' and R" groups of the silylamine employed contain no more than twelve carbons each.
Claim 5
Dependent Claim 20 words
The process of claim 3 where in the R, R' and R" groups of the silylamine employed are methyl groups.
Claim 6
Dependent Claim 14 words
The process of claim 1 wherein the value of n is equal to one.
Claim 7
Dependent Claim 26 words
The process of claim 1 wherein the R'" and R"" groups of the metallic carboxylate are alkyl groups containing no more than twenty-four carbon atoms each.
Claim 8
Dependent Claim 22 words
The process of claim 6 wherein the R'" and R"" groups of the metallic carboxylate contain no more than twelve carbon atoms.
Claim 9
Dependent Claim 35 words
The process of claim 1 wherein M is a metal selected from the group consisting of the metals of group IB, IIB, IIIB, IVB, VB, VIB, VIIB, VIII, gallium, indium, thallium, germanium, tin and lead.
Claim 10
Dependent Claim 21 words
The process of claim 8 wherein M is selected from the group consisting of iron, tin, lead, titanium, cerium and mercury.

References Cited (Backward Citations)

US2872168A Cited
US3927052A Cited
US3681266A Cited
US3993606A Cited
US3919276A Cited
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US4152343A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1986-08-22 1987-02-21 1987-08-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1990-08-22 1991-02-21 1991-08-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1994-08-22 1995-02-21 1995-08-23 $7700.00 Window Closed / Lapsed

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