Replacing Pyridine with Pyrazine in Molecular Cobalt Catalysts: Effects on Electrochemical Properties and Aqueous H2 Generation

Four new molecular Co(II)tetrapyridyl complexes were synthesized and evaluated for their activity as catalysts for proton reduction in aqueous environments. The pyridine groups around the macrocycle were substituted for either one or two pyrazine groups. Single crystal X-ray analysis shows that the pyrazine groups have minimal impact on the Co(II)-N bond lengths and molecular geometry in general. X-band EPR spectroscopy confirms the Co(II) oxidation state and the electronic environment of the Co(II) center are only very slightly perturbed by the substitution of pyrazine groups around the macrocycle. The substitution of pyrazine groups has a substantial impact on the observed metal- and ligand-centered reduction potentials as well as the overall H-2 catalytic activity in a multimolecular system using the [Ru(2,2 '-bipyridine)(3)]Cl-2 photosensitizer and ascorbic acid as a sacrificial electron donor. The results reveal interesting trends between the H-2 catalytic activity for each catalyst and the driving force for electron transfer between either the reduced photosensitizer to catalyst step or the catalyst to proton reduction step. The work presented here showcases how even the difference of a single atom in a molecular catalyst can have an important impact on activity and suggests a pathway to optimize the photocatalytic activity and stability of molecular systems.

Automated summary

Four new molecular Co(II) tetrapyridyl complexes were synthesized and evaluated for their activity as catalysts for proton reduction in aqueous environments. The substitution of pyrazine groups around the macrocycle had a substantial impact on the observed metal- and ligand-centered reduction potentials as well as the overall H-2 catalytic activity. The study highlights how even small differences in molecular catalysts can have significant effects on activity and provides insights into optimizing the photocatalytic activity and stability of molecular systems.