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Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
Published on: November 22, 2016
Stable phosphonium sila-ylide with reactivity as a sila-Wittig reagent
David Gau1, Tsuyoshi Kato, Nathalie Saffon-Merceron
1Universite de Toulouse, UPS, LHFA, and CNRS, LHFA UMR 5069, F-31062 Toulouse, France.
Abstract:
The silicon congeners of well-known phosphonium ylides have been considered only as short-lived reactive intermediates. We successfully synthesized a remarkably stable phosphonium sila-ylide. Its X-ray structure reveals a long Si-P bond and a strongly pyramidalized silicon center, indicating a very weak P-Si pi interaction. In addition, it exhibits an alpha,beta-ambiphilic character with a nucleophilic silicon center, similar to its carbon-congener phosphonium ylides. This property of the phosphonium sila-ylide allows its use as a sila-Wittig reagent with carbonyl derivatives.
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