Within the emerging field of bismuth redox catalysis, the catalytic formation of C−C bonds using aryl halides would be highly desirable; yet such a process remains a synthetic challenge. Herein, we present a chemoselective bismuth-photocatalyzed activation and subsequent coupling of (hetero)aryl iodides with pyrrole derivatives to access C(sp2)−C(sp2) linkages through C−H functionalization. This unique reactivity is the result of the bismuth complex featuring two redox state-dependent interactions with light, which 1) activates the Bi(I) complex for oxidative addition via MLCT, and 2) promotes the homolytic cleavage of aryl Bi(III) intermediates through a LLCT process.

Activation and C−C Coupling of Aryl Iodides via Bismuth Photocatalysis

Cleto Bruzzese, Paolo;
2025-01-01

Abstract

Within the emerging field of bismuth redox catalysis, the catalytic formation of C−C bonds using aryl halides would be highly desirable; yet such a process remains a synthetic challenge. Herein, we present a chemoselective bismuth-photocatalyzed activation and subsequent coupling of (hetero)aryl iodides with pyrrole derivatives to access C(sp2)−C(sp2) linkages through C−H functionalization. This unique reactivity is the result of the bismuth complex featuring two redox state-dependent interactions with light, which 1) activates the Bi(I) complex for oxidative addition via MLCT, and 2) promotes the homolytic cleavage of aryl Bi(III) intermediates through a LLCT process.
2025
64
5
1
6
aryl halide activation; bismuth catalysis; cross-coupling reactions; photocatalysis; radical catalysis
Mato, Mauro; Stamoulis, Alexios; Cleto Bruzzese, Paolo; Cornella, Josep
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/2107040
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