Photochemical hydrogen production and cobaloximes: the influence of the cobalt axial N-ligand on the system stability

Abstract

We report on the first systematic study of cobaloxime-based hydrogen photoproduction in mixed pH 7 aqueous/acetonitrile solutions and demonstrate that H₂ evolution can be tuned through electronic modifications of the axial cobalt ligand or through introduction of TiO₂ nanoparticles. The photocatalytic systems consist of various cobaloxime catalysts [Co(dmgH)₂(L)Cl] (L = nitrogen-based axial ligands) and a water soluble porphyrin photosensitizer. They were assayed in the presence of triethanolamine as a sacrificial electron donor. Optimal turnover numbers related to the photosensitizer are obtained with electron-rich axial ligands such as imidazole derivatives (1131 TONs with N-methyl imidazole). Lower stabilities are observed with various pyridine axial ligands (443 TONs for para-methylpyridine), especially for those containing electron-acceptor substituents. Interestingly, when L is para-carboxylatopyridine the activity of the system is increased from 40 to 223 TONs in the presence of TiO₂ nanoparticles.