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Hydrosilane cleavage reactions accelerated by...
Journal article

Hydrosilane cleavage reactions accelerated by tartaric acid and dimethyl sulphoxide

Abstract

Tartaric acid reacts spontaneously with triethoxysilane (HTES) liberating hydrogen gas, but alkyl- or arylhydrosilanes are essentially inert under these conditions. Other α-hydroxyacids reacted similarly with HTES. The reaction of tartaric acid in tetrahydrofuran is a second order process, consistent with a reaction pathway involving first transesterification of HTES by tartaric acid and subsequent SiH cleavage. In dimethyl sulphoxide (DMSO) …

Authors

Roth MJ; Brook MA; Penny HB

Journal

Journal of Organometallic Chemistry, Vol. 521, No. 1-2, pp. 65–74

Publisher

Elsevier

Publication Date

August 1996

DOI

10.1016/0022-328x(96)06299-7

ISSN

0022-328X