Insights into Formate Oxidation by a Series of Cobalt Piano-Stool Complexes Supported by Bis(phosphino)amine Ligands.

Abstract

A series of (cyclopentadienyl)cobalt(III) half-sandwich complexes (1-4) supported by bidentate bis(phosphino)amine ligands was synthesized and characterized by NMR spectroscopy, X-ray crystallography, and cyclic voltammetry. The CoIII-hydride complex 4-H bearing the bis(cyclohexylphosphine) ligand derivative was successfully isolated via protonation of the neutral reduced CoI complex 5 with a weak acid. Experimental and computational methods were used to determine the thermodynamic hydride accepting ability of these CoIII centers and to evaluate their reactivity toward the oxidation of formate. We find that the hydride accepting ability of 1-4 ranges from 71 to 74 kcal/mol in acetonitrile, which should favor a highly exergonic reaction with formate through direct hydride transfer. Formate oxidation was demonstrated at elevated temperatures in the presence of stoichiometric quantities of 4, generating carbon dioxide and the CoIII-hydride complex 4-H in 72% yield.