Preassembly‐Controlled Radical Recombination at Bismuth: Decarboxylative C─N Coupling with Sulfonamides

Persistent transition metal radicals form the foundation for many metallaphotoredox protocols. Their ability to efficiently trap organic radicals and convert them into various coupling products has inspired the exploration of selective radical reactions even beyond the d-block. Radical processes involving bismuth hold great potential, but innovative strategies are required to control the reactivity of bismuth intermediates. Herein, we report preassembly as a powerful strategy to enforce a selective recombination of a bismuth(II) radical and an organic radical. As a result, an inner-sphere pathway is accessed, enabling the formation of C─N coupling products.

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Publication Details

Journal
Chemistry - A European Journal
Published
2025-04-07
DOI
https://doi.org/10.1002/chem.202500396
Citations
3
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
2.81

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article

Preassembly‐Controlled Radical Recombination at Bismuth: Decarboxylative C─N Coupling with Sulfonamides

Esko Taskinen, Dominik Birnthaler, Burkhard Koenig, Vid Kermelj
3 citations
Chemistry - A European Journal
Radical Photochemical Reactions
2.81
article

Preassembly‐Controlled Radical Recombination at Bismuth: Decarboxylative C─N Coupling with Sulfonamides

Esko Taskinen, Dominik Birnthaler, Burkhard Koenig, Vid Kermelj
article en
3 citations

Abstract

Persistent transition metal radicals form the foundation for many metallaphotoredox protocols. Their ability to efficiently trap organic radicals and convert them into various coupling products has inspired the exploration of selective radical reactions even beyond the d-block. Radical processes involving bismuth hold great potential, but innovative strategies are required to control the reactivity of bismuth intermediates. Herein, we report preassembly as a powerful strategy to enforce a selective recombination of a bismuth(II) radical and an organic radical. As a result, an inner-sphere pathway is accessed, enabling the formation of C─N coupling products.

Chemistry - A European JournalVol. 31(28)
University of Ljubljana (SI), University of Regensburg (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 11%
Radical Photochemical Reactions
2.81
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