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 SiH 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