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Updated: Jun 7, 2026

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
Published on: November 22, 2016
Carbene-stabilized phosphorus(III)-centered cations [LPX(2)](+) and [L(2)PX](2+) (L = NHC; X = Cl, CN, N(3))
Jan J Weigand1, Kai-Oliver Feldmann, Florian D Henne
1Anorganische und Analytische Chemie and Graduate School of Chemistry, Westfälische Wilhelms-Universität Münster, Corrensstrasse 30, 48149 Münster, Germany. jweigand@uni-muenster.de
Abstract:
A versatile, high-yielding synthesis of NHC-stabilized [PCl(2)](+) and [PCl](2+) phosphorus synthons has been achieved by using an "onio-substituent transfer" reagent. Subsequent functionalization yields access to cationic cyano- and azido-substituted derivatives which represent first examples of a displacement reaction on NHC-stabilized phosphorus(III)-centered cations. The new salts have been fully characterized by NMR spectroscopy and X-ray crystallography.
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