Hydrogen Evolution Mediated by Cobalt Diimine-Dioxime Complexes: Insights into the Role of the Ligand Acid/Base Functionalities.
Résumé
The benchmarking of the performance for H-2 evolution of cobalt diimine-dioxime catalysts is provided based on a comprehensive study of their catalytic mechanism. The latter follows an ECE'CC pathway with intermediate formation of a Co(II)-hydride intermediate and second protonation possibly at a basic site of the ligand, acting as a proton relay. This suggests an intramolecular coupling between the hydride and protonated ligand as the proton concentration-independent rate-determining step controlling the turnover frequency for H-2 evolution.
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