(L)2C2P2: Dicarbondiphosphide Stabilized by N-Heterocyclic Carbenes or Cyclic Diamido Carbenes

Zhongshu Li, Xiaodan Chen, Diego M. Andrada, Gernot Frenking, Zoltán Benkö, Yaqi Li, Jeffrey R. Harmer, Cheng Yong Su, Hansjörg Grützmacher

Research output: Contribution to journalArticlepeer-review

88 Scopus citations

Abstract

Carbon phosphides, CnPm, may have highly promising electronic, optical, and mechanical properties, but they are experimentally almost unexplored materials. Phosphaheteroallenes stabilized by N-heterocyclic carbenes undergo a one-electron reduction to yield compounds of the type (L)2C2P2 with diverse structures. The use of imidazolylidenes as ligands L give complexes with a central four-membered ring C2P2, while more electrophilic cyclic diamidocarbenes (DAC) give a compound with an acyclic π-conjugated CP−PC unit. Cyclic C2P2 compounds are best described as non-Kekulé molecules that are stabilized by coordination to the NHC ligands NHC→(C2P2)←NHC. These species can be easily oxidized to give stable radical cations [(NHC)2C2P2]+.. The remarkably stable molecules with an acylic C2P2 core are best described with electron-sharing bonds (DAC)=C=P−P=C=(DAC).

Original languageEnglish
Pages (from-to)5744-5749
Number of pages6
JournalAngewandte Chemie - International Edition
Volume56
Issue number21
DOIs
StatePublished - 15 May 2017

Keywords

  • bonding analysis
  • carbenes
  • carbon phosphide
  • heterocycles
  • phosphorus

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