DMAP-stabilized bis(silyl)silylenes as versatile synthons for organosilicon compounds

Richard Holzner; Dominik Reiter; Philipp Frisch; Shigeyoshi Inoue

doi:10.1039/c9ra10628f

DMAP-stabilized bis(silyl)silylenes as versatile synthons for organosilicon compounds

Richard Holzner, Dominik Reiter, Philipp Frisch, Shigeyoshi Inoue

Chair of Silicon Chemistry

Technical University of Munich

Research output: Contribution to journal › Article › peer-review

23 Scopus citations

Abstract

DMAP-stabilized silylenes 1a-c are obtained from the reductive debromination of the corresponding dibromosilanes in the presence of DMAP. Their distinctly different thermal isomerization reactions via C-H bond activation, dearomative ring expansion and silyl migration are discussed. Furthermore, complexes 1 dissociate at elevated temperatures, providing the corresponding free silylenes in situ, which are even capable of single-site activation of H₂.

Original language	English
Pages (from-to)	3402-3406
Number of pages	5
Journal	RSC Advances
Volume	10
Issue number	6
DOIs	https://doi.org/10.1039/c9ra10628f
State	Published - 2020

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abstract = "DMAP-stabilized silylenes 1a-c are obtained from the reductive debromination of the corresponding dibromosilanes in the presence of DMAP. Their distinctly different thermal isomerization reactions via C-H bond activation, dearomative ring expansion and silyl migration are discussed. Furthermore, complexes 1 dissociate at elevated temperatures, providing the corresponding free silylenes in situ, which are even capable of single-site activation of H2.",

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AU - Inoue, Shigeyoshi

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AB - DMAP-stabilized silylenes 1a-c are obtained from the reductive debromination of the corresponding dibromosilanes in the presence of DMAP. Their distinctly different thermal isomerization reactions via C-H bond activation, dearomative ring expansion and silyl migration are discussed. Furthermore, complexes 1 dissociate at elevated temperatures, providing the corresponding free silylenes in situ, which are even capable of single-site activation of H2.

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DMAP-stabilized bis(silyl)silylenes as versatile synthons for organosilicon compounds

Abstract

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