Cyaphide, , is the phosphorus analogue of cyanide. It is not known as a discrete salt; however, in silico measurements reveal that the âÂÂ1 charge in this ion is located mainly on carbon (0.65), as opposed to phosphorus.
The word "cyaphide" was first coined in 1992, by analogy with cyanide.
Organometallic complexes of cyaphide were first reported in 1992. More recent preparations use two other routes:
Treatment of the ÷<sup>1</sup>-coordinated phosphaalkyne complex trans– with an alkoxide resulted in desilylation, followed by subsequent rearrangement to the corresponding carbon-bound cyaphide complex. Cyaphide-alkynyl complexes are prepared similarly.
An actinide cyaphide complex can be prepared by CâÂÂO bond cleavage of the phosphaethynolate anion, the phosphorus analogue of cyanate. Reaction of the uranium complex [] with [ in the presence of 2.2.2-cryptand results in the formation of a dinuclear, oxo-bridged uranium complex featuring a Câ¡P ligand.