Dow Corning Corporation

Other

Aroop K Roy

Gary T Burns

Toshio Suzuki

Rudolf Faust

Savvas E Hadjikyriacou

Howard M Bank

Arthur James Tselepis

Gary T Decker

Linda Denise Kennan

Michael Kang-Jen Lee

Richard Bruce Taylor

Alkene-platinum-silyl complexes described by formula (COD)Pt(SiR ) Y are claimed, where each R is independently selected from organic groups, halo atoms, and siloxy groups, each Y is an independently selected divalent bridging group between the silicon atoms bonded to platinum, n is 0, 1, 2, or 3, and COD is 1,5-cyclooctadiene.

Alkene-platinum-silyl complexes

Virtually telechelic silyl-functional polyisobutylene

Method for preparing functional halosilanes

Living cationic polymers prepared from silyl-functional aromatic initiators

A hydrosilation process where a silicon hydride is reacted with an unsaturated reactant in the presence of a platinum catalyst and an accelerator selected from the group consisting of 1,7-octadiyne, 1,5-hexadiyne, cyclooctadiene, 5-vinyl-2-norbornene, 4-vinyl-1-cyclohexene, 2,5-bis(t-butylperoxy)-2,5-dimethylhexane, furan, 4H-Pyran-4-one, cis-4,7-dihydro-1,3-dioxepin, maleic anhydride, and dimethyldiallylmalonate. The accelerators are especially useful for facilitating the hydrosilation of unsaturated reactants where the unsaturation is in the internal portion of the reactant's structure, for example, as in cyclopentene and cyclohexene.

Unsaturated accelerators for hydrosilation

A method of hydrophobing fillers such as inorganic pigments, metal oxides, metal hydroxides, and silicate minerals, involves contacting a filler with an oxa-silacycloalkane, until hydroxyl functionality on the filler is replaced with carbinol functionality (i.e. .tbd.C--OH). The preferred oxa-silacycloalkane is 2,2,4-trimethyl-1-oxa-2-silacyclopentane.

Treatment of fillers with oxa-silacycloalkanes

An improved process for hydrosilating alkynes with hydridosilane using a cycloalkadiene-platinum complex as catalyst. The use of the cycloalkadiene-platinum complex as catalyst in the process reduces formation of the bis-silated adduct of the alkynes, when compared to the use of standard platinum-based hydrosilation catalysts.

Alkyne hydrosilation using cycloalkadiene-platinum complex as catalyst

An improved process for hydrosilating alkynes with organodihalosilanes and trihalosilanes in the presence of a platinum catalyst selected from a group consisting of platinum halides and reaction product of platinum halides with organosilicon compounds having terminal aliphatic unsaturation. The process uses a cycloalkene comprising about six to 20 carbon atoms as a catalyst modifier to reduce formation of the bis-silated adduct of the alkynes.

Process for alkyne hydrosilation using cycloalkenes as catalyst modifiers

An improved process for hydrosilating alkynes with hydridosilane in the presence of a platinum catalyst selected from a group consisting of platinum halides and reaction product of platinum halides with organosilicon compounds having terminal aliphatic unsaturation. The process uses a cycloalkadiene comprising about six to 20 carbon atoms as a catalyst modifier to reduce formation of the bis-silated adduct of the alkynes.

Alkyne hydrosilation using cycloalkadiene as catalyst modifier

A method for preparing a telechelic polydiene having at least 70% 1,4-microstructure and at least 70% of its end groups capped by silanol-terminated siloxane functionality is disclosed, said method comprising: (I) reacting, in a non-polar solvent solution,

Synthesis of siloxane-functional telechelic hydrocarbon polymers

A method for preparing a telechelic polydiene having at least 70% 1,4-microstructure and at least 70% of its end groups capped by reactive silyl functionality is disclosed, said method comprising:

Synthesis of silyl-functional telechelic hydrocarbon polymers

The present invention is a method for the preparation of carbinol-functional organosiloxanes and carbinol-functional organosiloxane resins. The method comprises contacting a cyclic silyl ether with an organosiloxane or an organosiloxane resin at a temperature within a range of about 25.degree. C. to 150.degree. C. The method may be conducted in the presence of an inert organic solvent to facilitate dissolution and contact of the reactants.

Method for preparation of carbinol-functional siloxanes

This invention provides novel organosulfonimidates and a method for preparing both the present sulfonimidates and those disclosed in the prior art. Some of the sufonimidates can be condensed under relatively mild conditions to form polyorganooxothiazenes.

Sulfonimidates and method for preparing same

This invention provides novel organosulfonimidates and a method for preparing both the present sulfonimidates and those disclosed in the prior art. Some of the sulfonimidates can be condensed under relatively mild conditions to form polyorganooxothiazenes.

This invention provides polyorganooxothiazenes exhibiting levels of molecular weight and properties not heretofore achieved by similar polymers reported in the prior art. The sulfonimidates that are condensed to form the polymers are prepared using a novel reaction between an N-triorganosilylsulfonamide and a triorganodihalophosphorane to form the corresponding N-triorganosilylsulfonimidoyl halide that is subsequently reacted with a fluorinated alcohol or phenol to form the N-triorgano-silylsulfonimidate.

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Midland, MI, United States of America

Aroop K Roy