Electrophotochemical Decarboxylative C−H Fluoroalkylation via a Fe <sub>2</sub> O <sub>3</sub> −FTO Active Photoanode

C−H fluoroalkylation of heteroarenes and biomolecules employing inexpensive carboxylic acids based on electrophotochemical oxidation on a Fe2O3 photoanode was developed. Notably, the devised approach proved amenable to a wide range of versatile late-stage C−H fluoroalkylations of biorelevant heterocycles. Mechanistic studies supported a direct electron transfer to form a fluoroalkyl radical with a cost-efficient heterogeneous iron catalyst.

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Publication Details

Journal
ACS Catalysis
Published
2026-03-12
DOI
https://doi.org/10.1021/acscatal.5c07973
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Electrophotochemical Decarboxylative C−H Fluoroalkylation via a Fe 2 O 3 −FTO Active Photoanode

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ACS Catalysis
Fluorine in Organic Chemistry
article

Electrophotochemical Decarboxylative C−H Fluoroalkylation via a Fe 2 O 3 −FTO Active Photoanode

Vladimir Motornov, Kentaro Imaoka, Sven Trienes, H. Kang, Prof. Dr. Lutz Ackermann, Zhi Liu, R. Thomas Weitz
article en

Abstract

C−H fluoroalkylation of heteroarenes and biomolecules employing inexpensive carboxylic acids based on electrophotochemical oxidation on a Fe2O3 photoanode was developed. Notably, the devised approach proved amenable to a wide range of versatile late-stage C−H fluoroalkylations of biorelevant heterocycles. Mechanistic studies supported a direct electron transfer to form a fluoroalkyl radical with a cost-efficient heterogeneous iron catalyst.

ACS Catalysis
German Centre for Cardiovascular Research (DE), University of Göttingen (DE)
Clean water and sanitation
Openalex Percentile: Top 23%
Fluorine in Organic Chemistry
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