N-Heterocyclic Carbene Stabilized Dicarbondiphosphides: Strong Neutral Four-Membered Heterocyclic 6π-Electron Donors
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Updated: Dec 31, 2025

Preparation and Use of Carbonyl-decorated Carbenes in the Activation of White Phosphorus
Published on: October 3, 2014
Zhongshu Li1,2, Xiaodan Chen3, Liu Leo Liu4
1Lehn Institute of Functional Materials (LIFM), School of Chemistry, Sun Yat-Sen University, 510275, Guangzhou, China.
Abstract:
In contrast to cyclic π-conjugated hydrocarbons, the coordination chemistry of inorganic heterocycles is less developed. Dicarbondiphosphides stabilized by N-heterocyclic carbenes (NHCs) NHC→C2 P2 ←NHC (1 a,b) (NHC=IPr or SIPr) contain a four-membered C2 P2 ring with an aromatic 6π-electron configuration. These heterocycles coordinate to a variety of complex fragments with metals from groups 6, 9, and 10, namely [M0 (CO)3 ] (M=Cr, Mo), [CoI (CO)2 ]+ , or [NiII Br2 ], through an η4 -coordination mode, leading to complexes 2 a,b, 3 a,b, 5 a,b, and 6 a,b, respectively. These complexes were characterized by X-ray diffraction methods using single crystals, IR spectroscopy, and DFT calculations. In combination these methods indicate that 1 a,b behave as exceptionally strong 6π-electron donors.
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