Activation and C−C Coupling of Aryl Iodides via Bismuth Photocatalysis
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(sp 2 )−C(sp 2 ) 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.
Authors
- Paolo Cleto Bruzzese (ORCID: https://orcid.org/0000-0002-2070-836X)
- Mauro Mato (ORCID: https://orcid.org/0000-0002-2931-5060)
- Alexios Stamoulis (ORCID: https://orcid.org/0000-0003-4886-0512)
- Josep Cornellà (ORCID: https://orcid.org/0000-0003-4152-7098)
Institutions
- Max-Planck-Institut für Kohlenforschung (DE)
- Max Planck Institute for Chemical Energy Conversion (DE)
Publication Details
- Journal
- Angewandte Chemie
- Published
- 2024-10-22
- DOI
- https://doi.org/10.1002/ange.202418367
- Primary Topic
- Chemical Synthesis and Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Deutsche Forschungsgemeinschaft
- Max-Planck-Gesellschaft
- H2020 European Research Council
- H2020 Marie Skłodowska-Curie Actions