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 language | English |
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Pages (from-to) | 5744-5749 |
Number of pages | 6 |
Journal | Angewandte Chemie - International Edition |
Volume | 56 |
Issue number | 21 |
DOIs | |
State | Published - 15 May 2017 |
Keywords
- bonding analysis
- carbenes
- carbon phosphide
- heterocycles
- phosphorus