Utilizing a zwitterionic approach for the synthesis of late transition metal – triphosphenium ion coordination compounds

Abstract

Zwitterionic dicoordinate phosphorus(I) compounds (1 and 2), formally a charge neutral triphosphenium ion or phosphanide, are shown to coordinate to a variety of late transition metals. The reaction of the phosphanide proligands with {Rh(COD)Cl}2 results in an equilibrium process that varies as a function of temperature or reaction stoichiometry. Palladium(II) compounds have a tendency to chlorinate the borate backbone while giving dimeric coordination compounds (1Pd) and also a decomposition product (3) where the P(I) atom was replaced. Both “lone pairs” of electrons on phosphorus are utilized simultaneously in the dominant product from the reaction of 1 and [PtMe2(μ-SMe2)]2, while each platinum center ortho-metallated a phenyl substituent on the flanking phosphorus atoms (1Pt). Stable, isolable, and fully characterized dimeric mercury complexes (1Hg and 2Hg) are produced nearly quantitatively from the reaction of the phosphanide proligand with HgCl2. All compounds described were structurally characterized using single crystal X-ray diffraction and represent a growing series of zwitterionic P(I) coordination compounds that cannot be isolated when a cationic triphosphenium ion is used.