Abstract
Isolable singlet carbenes are among the most important tools in chemistry, but generally require the interaction of two substituents with the electron deficient carbon atom. We herein report a synthetic approach to monosubstituted phosphinocarbenes via deprotonation of hitherto unknown diprotic terminal methylene phosphonium ions. Two methylene phosphonium salts bearing bulky N-heterocyclic imine substituents at the phosphorus atom were isolated and fully characterized. Deprotonation studies indicate the formation of transient monosubstituted carbenes that undergo intermolecular cycloadditions or intramolecular Buchner ring expansion to afford a cycloheptatriene derivative. The reaction mechanism of the latter transformation was elucidated using DFT calculations, which reveal the ambiphilic nature of the phosphinocarbene enabling the insertion into the aromatic C-C bond. Additional computational studies on the role of substituent effects are presented.