Carbene-Stabilized Phosphorus(III)-Centered Cations [LPX<sub>2</sub>]<sup>+</sup> and [L<sub>2</sub>PX]<sup>2+</sup> (L = NHC; X = Cl, CN, N<sub>3</sub>)

Jan J. Weigand, K.‐O. Feldmann, F. D. Henne

Journal of the American Chemical Society · 2010 · 100 citations · 28 references

Concepts

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.

References

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