Photochemical thiylation of Si-methoxy-substituted 1, 2-disilylethylenes

M. G. Voronkov, L. V. Tsvetaeva, M. V. Sigalov, Z. I. Mikhailov, N. F. Chernov, O. G. Yarosh, V. A. Pestunovich

Research output: Contribution to journalArticlepeer-review

Abstract

1. A number of new sulfur-containing organosilicon monomers was synthesized by the reaction of 1,2-bis(alkylmethoxysilyl)- and 1-(trimethylsilyl)-2-(methylmethoxysilyi)ethylenes with mercaptans and thioacetic acid. 2. Based on the NMR spectral data, the 1-(trimethylsilyl)-2-(methylmethoxysilyl)ethylenes form two isomeric adducts in a 1:1 ratio.

Original languageEnglish
Pages (from-to)160-163
Number of pages4
JournalBulletin of the Academy of Sciences of the USSR Division of Chemical Science
Volume25
Issue number1
DOIs
StatePublished - 1 Jan 1976
Externally publishedYes

ASJC Scopus subject areas

  • General Chemistry

Fingerprint

Dive into the research topics of 'Photochemical thiylation of Si-methoxy-substituted 1, 2-disilylethylenes'. Together they form a unique fingerprint.

Cite this