Ring-opening and dimerisation of a 1H-diphosphirene–tungsten pentacarbonyl complex
Abstract
The 1H-diphosphirene complex 6, generated by [2 + 1] cycloaddition of the short-lived phosphinidene species 5 to the phosphaalkyne 4, undergoes dimerisation with elimination of a W(CO)5 fragment to give the tricyclotetraphosphahexane 11; reaction of 6 with tetrachloro-o-quinone gives rise to the 1 : 2-adduct 13 in which the P–P bond of the former has been cleaved.