Issue 84, 2015

1,2-Halosilane vs. 1,2-alkylborane elimination from (boryl)(silyl) complexes of iron: switching between borylenes and silylenes just by changing the alkyl group

Abstract

Reaction of different combinations of aryl(dihalo)boranes and trialkylsilyl iron metallates, a route previously used to prepare a terminal iron arylborylene complex, is found to lead to three distinct new reaction outcomes, including unselective decomposition, an inert iron(II) (boryl)(silyl) complex, and a dinuclear bis(μ-silylene) complex. The latter result is to our knowledge the first example of a 1,2-alkylborane elimination, in contrast to the facile and ubiquitous 1,1-alkylborane elimination observed from (alkyl)(boryl) transition metal complexes, and is also a novel route to bridging silylene complexes.

Graphical abstract: 1,2-Halosilane vs. 1,2-alkylborane elimination from (boryl)(silyl) complexes of iron: switching between borylenes and silylenes just by changing the alkyl group

Supplementary files

Article information

Article type
Communication
Submitted
31 Jul 2015
Accepted
28 Aug 2015
First published
08 Sep 2015

Chem. Commun., 2015,51, 15465-15468

1,2-Halosilane vs. 1,2-alkylborane elimination from (boryl)(silyl) complexes of iron: switching between borylenes and silylenes just by changing the alkyl group

H. Braunschweig, R. D. Dewhurst, K. Radacki, B. Wennemann and Q. Ye, Chem. Commun., 2015, 51, 15465 DOI: 10.1039/C5CC06425B

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