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Abstract
Removing carbon dioxide from the atmosphere is an attractive way to mitigate the greenhouse gas effect that contributes to climate change. A series of donor-pi (D-π), acceptor-pi (A-π), and π Re(i) pyridyl imidazole complexes have been synthesized and examined under photocatalytic conditions for the photocatalytic reduction of CO2. The catalytic activity of the complexes was further supported by cyclic voltammetry through the presence of a catalytic current under CO2 atmosphere. The D-π, π, and A-π complexes were studied to elucidate the effects of incorporating conjugated electron donating vs. withdrawing groups on the catalytic rates and product selectivity. The synthesized complexes were compared with Re(bpy)(CO)3Br (where bpy is 2,2′-bipyridine), the benchmark catalyst for this transformation. Remarkably, the complex with A-π pendant (RC4) outperformed the π (RC2-3) and D-π (RC5) complexes for the production of formic acid (HCO2H) in the presence of photosensitizer [Ru(bpy)3]2+ and sacrificial electron donor BIH (1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]-imidazoline). Among the investigated catalysts, RC4 with the A-π pendant showed the highest turnover number (TON) value of 844 for HCO2H production with 86% carbon selectivity. In stark contrast to the imidazole-pyridine based catalysts reported here that favor formic acid as a product, Re(bpy)(CO)3Br generated no formic acid under the same conditions. The imidazole-pyridine complexes also function as catalysts for CO2 reduction without an added photosensitizer, however, the TON values under self-sensitized conditions are poor.
Document Type
Article
Publication Date
4-22-2025
Digital Object Identifier (DOI)
10.1039/d5ra01561h
Archival?
Archival
Repository Citation
Chafin, Ryan; Sujan, Majharul Islam; Parkin, Sean; Jurss, Jonah W.; and Huckaba, Aron J., "Light-driven CO2 reduction with substituted imidazole-pyridine Re catalysts favoring formic acid production" (2025). Chemistry Faculty Publications. 247.
https://uknowledge.uky.edu/chemistry_facpub/247

Notes/Citation Information
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