Li P, Bourgois C, Glaser F, De Kreijger S, Cadranel A, Troian-Gautier L, Hu K (2025)
Publication Type: Journal article
Publication year: 2025
DOI: 10.1021/jacs.5c00129
Trifluoromethylation is a key transformation in drug and agrochemical synthesis, yet current reagents often suffer from high cost, low atom economy, and low scalability. Trifluoroacetate derivatives represent ideal reagents as they are highly abundant and cheap, but their very positive one electron oxidation potential (∼2.3 V vs NHE) often hampers their widespread use in photoredox catalysis. Indeed, at these potentials, selectively oxidizing trifluoroacetate over reaction solvent or partner substrates becomes challenging. Herein, we present a novel approach that circumvents these limitations through the use of a pentacationic Ir(III) photosensitizer that forms a strong 1:1 ion-pair with trifluoroacetate in acetonitrile (K
APA:
Li, P., Bourgois, C., Glaser, F., De Kreijger, S., Cadranel, A., Troian-Gautier, L., & Hu, K. (2025). Outcompeting Thermodynamics: Ion-Pairing and Coulombic Interactions to Trigger Perfluoroacetate Intra-Ionic Photooxidation for Perfluoroalkylation Reactions. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.5c00129
MLA:
Li, Pengju, et al. "Outcompeting Thermodynamics: Ion-Pairing and Coulombic Interactions to Trigger Perfluoroacetate Intra-Ionic Photooxidation for Perfluoroalkylation Reactions." Journal of the American Chemical Society (2025).
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