A "Push-Pull" Stabilized Phosphinidene Supported by a Phosphine-Functionalized β-Diketiminato Ligand.

The use of a bis(diphenyl)phosphine functionalized β-diketiminato ligand, [HC{(CH3 )C}2 {(ortho-[P(C6 H5 )2 ]2 C6 H4 )N}2 ]- (PNac), as a support for germanium(II) and tin(II) chloride and phosphaketene compounds, is described. The conformational flexibility and hemilability of this unique ligand provide a versatile coordination environment that can accommodate the electronic needs of the ligated elements. For example, chloride abstraction from [(PNac)ECl] (E=Ge, Sn) affords the cationic germyliumylidene and stannyliumylidene species [(PNac)E]+ in which the pendant phosphine arms associate more strongly with the Lewis acidic main group element centers, providing further electronic stabilization. In a similar fashion, chemical decarbonylation of the germanium phosphaketene [(PNac)Ge(PCO)] with tris(pentafluorophenyl)borane affords a "push-pull" stabilized phosphinidene in which one of the phosphine groups of the ligand backbone associates with the low valent phosphinidene center.