Double Insertion of Coordinated Phosphanylalkyne Ligands into a Pt−C6F5 Bond

J.P.H. Charmant, J. Forniés, Julio Goméz, Elena Lalinde, M. Teresa Moreno, A.G. Orpen, Santiago Solano

Angewandte Chemie International Edition · 1999 · 36 citations · 0 references

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Abstract

Enhanced reactivity is shown by uncoordinated C identical withC bonds in the proximity of a metal in phosphanylacetylene complexes. cis-[Pt(C(6)F(5))(2)(thf)(2)] reacts with [M(C(6)F(5))(2)(PPh(2)C identical withCPh)(2)] (M=Pt, Pd) to form binuclear complexes containing the novel 2,3-bis(diphenylphosphanyl)-1,3-butadien-1-yl bridging ligand. Substitution of the solvent ligands with, for example, PPh(2)H (see picture) provides species that could be characterized by X-ray crystallography.