Energy & Environmental Science · 2008 · 187 citations · 66 references
Natural SciencesChemical EngineeringChemistryCatalysisElectrochemistryInorganic ChemistryCatalyst DesignCatalyst SynthesisCoordination ChemistryMetal CatalysisTransition Metal ChemistryTransition Metal ComplexesCatalyst Structure - Activity RelationshipsCatalytic Reaction MechanismsCobalt CatalysisCoordinationHydrogen ProductionMolecular CatalystsProton Relay NetworksTurnover Frequency
The cobalt analogue of a highly active nickel electrocatalyst for hydrogen production has been synthesized and characterized as [Co(PPh2NPh2)2(CH3CN)](BF4)2. In the presence of triflic acid in acetonitrile solution, the complex loses one cyclic diphosphine ligand to form [Co(PPh2NPh2)(CH3CN)3](BF4)2, which has been synthesized independently and stucturally characterized. The latter complex serves as an electrocatalyst for hydrogen formation with a turnover frequency of 90 s−1 and an overpotential of 285 mV using bromoanilinium tetrafluoroborate as the acid. A similar cobalt complex with a related diphosphine ligand that does not contain a pendant base is not catalytically active, confirming an important role for the pendant amine in the catalytic reaction.
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Ivari Kaljurand, Agnes Kütt, Lilli Sooväli et al. · The Journal of Organic Chemistry · 2005 · 942 citations
Yvain Nicolet, António L. De Lacey, X. Vernède et al. · Journal of the American Chemical Society · 2001 · 780 citations