Photoredox Oxidation of Alkanes by Monometallic Copper–Oxygen Complexes Using Visible Light Including One Sun Illumination

• Published in: Journal of the American Chemical Society Vol. 146; no. 42; pp. 28612 - 28617
• Main Authors: Nascimento, Daniel L., Gygi, David, Drummer, Matthew C., Gonzalez, Miguel I., Zheng, Shao-Liang, Nocera, Daniel G.
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 23-10-2024
• ISSN: 0002-7863; 1520-5126; 1520-5126
• DOI: 10.1021/jacs.4c08377

Oxygenation of hydrocarbons offers versatile catalytic routes to more valuable compounds, such as alcohols, aldehydes, and ketones. Despite the importance of monometallic copper–oxygen species as hydroxylating agents in biology, few synthetic model compounds are known to react with hydrocarbons, owing to high C–H bond dissociation energies. To overcome this challenge, the photoredox chemistry of monometallic copper (pyrazolyl)­borate complexes coordinated by chlorate has been explored in the presence of C1–C6 alkanes with BDEs ≥ 93 kcal/mol. Ethane is photooxidized at room temperature under N2 with yields of 15–30%, which increases to 77% for the most oxidizing tris­(3,5-trifluoromethyl-pyrazolyl)­borate complex (Cu-3). This complex also promotes the photooxidation of methane to methanol in significant yield (38%) when the photoredox reaction is run under aerobic conditions. Ligand modification alters the reaction selectivity by tuning the redox potential. The ability to activate 1° C–H bonds of C1–C6 alkanes using visible light is consistent with the photogeneration of a powerfully oxidizing copper-oxyl, which is supported by photocrystallographic studies of the tris­(3,4,5-tribromopyrazolyl)­borate chlorate complex. Mechanistic studies are consistent with the hydrogen atom abstraction of the C–H bond by the copper-oxyl intermediate. We demonstrate for Cu-3 with hexane as an exemplar, that the photoredox chemistry may be achieved under solar conditions of one-sun illumination.