A cobalt complex with a bioinspired molybdopterin-like ligand: a catalyst for hydrogen evolution

Abstract

Cobalt dithiolene complexes are a new class of H₂-evolving catalysts. Here we describe the preparation, the structure and the catalytic activity of an original cobalt complex using a bioinspired ligand, a quinoxaline–pyran-fused dithiolene derivative (qpdt²⁻) that mimics the molybdopterin cofactor present in the active sites of formate dehydrogenases. This complex displays very good activity for electrochemical proton reduction under weak acid conditions in terms of turnover frequency, faradic yields and stability. Density functional theory calculations show that protonation of a nitrogen atom of the ligand decreases overpotentials by 520 mV and H₂ formation proceeds via protonation of an intermediate Co–H hydride, with an adjacent S atom of the dithiolene ligand serving as a proton relay.