Abstract
Aryl chlorides and fluorides are inexpensive and readily available feedstocks; however, the high bond dissociation energies and low polarizability of CAr─X (Cl, F) bonds have long posed significant challenges to classical thermal activation, which is often harsh and poorly compatible with functional groups. Visible-light photocatalysis has emerged as a powerful strategy that overcomes these limitations by leveraging single-electron transfer to highly reactive radical intermediates under mild conditions. This review provides a mechanistically guided overview of recent advances in photocatalytic functionalization of aryl chlorides and fluorides, encompassing oxidative and reductive radical activation, radical–polar crossover, homolytic aromatic substitution, and synergistic photoredox/transition-metal catalysis.
| Original language | English |
|---|---|
| Journal | Chemistry - A European Journal |
| DOIs | |
| State | Accepted/In press - 2026 |
Keywords
- aryl cation radicals
- aryl radical anions
- cross-coupling
- inert C─X bonds
- photocatalysis
- radical–polar crossover
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