Semiheterogeneous Intrinsic CoS <sub>2</sub> -Photoredox/Cp <sub>2</sub> Fe Dual-Catalyzed Synthesis of Selenylated Phenanthrene

Herein, we report a practical semiheterogeneous strategy for the photosynthesis of diverse selanyl phenanthrenes, employing CoS<sub>2</sub> as a heterogeneous photocatalyst in combination with ferrocene (Cp<sub>2</sub>Fe) as a homogeneous redox catalyst. This synergistic system combines photogenerated electron-mediated reduction of selenyl cations into diselenide with photogenerated hole oxidation of Cp<sub>2</sub>Fe to its oxidized form, which not only oxidizes diselenide into selenyl radicals but also mediates oxidative dehydroaromatization, leading to high-yielding transformations with broad functional group compatibility. Notably, this method eliminates the need for stoichiometric oxidants or reductants and avoids sacrificial electron donors or acceptors.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-12-11
DOI
https://doi.org/10.1021/acs.joc.5c02498
Primary Topic
Organoselenium and organotellurium chemistry
Type
article
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article

Semiheterogeneous Intrinsic CoS 2 -Photoredox/Cp 2 Fe Dual-Catalyzed Synthesis of Selenylated Phenanthrene

Wei‐Min He, Peng Mei, Jun Rong Jiang, Hai‐Tao Zhu et al.
The Journal of Organic Chemistry
Organoselenium and organotellurium chemistry
article

Semiheterogeneous Intrinsic CoS 2 -Photoredox/Cp 2 Fe Dual-Catalyzed Synthesis of Selenylated Phenanthrene

Wei‐Min He, Peng Mei, Jun Rong Jiang, Hai‐Tao Zhu, Zi Yang, Ting Li, Yaohui Wang
article en

Abstract

Herein, we report a practical semiheterogeneous strategy for the photosynthesis of diverse selanyl phenanthrenes, employing CoS<sub>2</sub> as a heterogeneous photocatalyst in combination with ferrocene (Cp<sub>2</sub>Fe) as a homogeneous redox catalyst. This synergistic system combines photogenerated electron-mediated reduction of selenyl cations into diselenide with photogenerated hole oxidation of Cp<sub>2</sub>Fe to its oxidized form, which not only oxidizes diselenide into selenyl radicals but also mediates oxidative dehydroaromatization, leading to high-yielding transformations with broad functional group compatibility. Notably, this method eliminates the need for stoichiometric oxidants or reductants and avoids sacrificial electron donors or acceptors.

The Journal of Organic ChemistryVol. 90(51)
Changsha Medical University (CN), Baoji University of Arts and Sciences (CN), University of South China (CN)
Openalex Percentile: Top 59%
Organoselenium and organotellurium chemistry
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