Semiheterogeneous Intrinsic FeTiO<sub>3</sub>-Photoredox/Ph<sub>3</sub>N Dual-Catalyzed Fluoroalkylation of N-Heteroarenes with Alkenes and R<sub>f</sub>SO<sub>2</sub>Cl

Herein, we report the sustainable semiheterogeneous synthesis of various fluoroalkylated <i>N</i>-heteroarenes using natural intrinsic iron(II) titanium oxide (FeTiO<sub>3</sub>) as a semiconductor photocatalyst and Ph<sub>3</sub>N as a redox mediator. This synergistic system combines photogenerated electron-mediated fluoroalkyl sulfonyl chloride (R<sub>f</sub>SO<sub>2</sub>Cl) reduction with photogenerated hole-induced oxidative dehydrogenation aromatization, enabling high-yielding transformations with excellent functional-group tolerance while avoiding stoichiometric redox reagents or sacrificial electron donors/acceptors.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-10-02
DOI
https://doi.org/10.1021/acs.joc.5c02000
Citations
7
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
5.54
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article

Semiheterogeneous Intrinsic FeTiO3-Photoredox/Ph3N Dual-Catalyzed Fluoroalkylation of N-Heteroarenes with Alkenes and RfSO2Cl

Chunlin Zhuang, Wei‐Min He, Shenghua Wang, Qiong-Hui Peng et al.
7 citations
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
5.54
article

Semiheterogeneous Intrinsic FeTiO3-Photoredox/Ph3N Dual-Catalyzed Fluoroalkylation of N-Heteroarenes with Alkenes and RfSO2Cl

Chunlin Zhuang, Wei‐Min He, Shenghua Wang, Qiong-Hui Peng, Jun Rong Jiang, Yue Cai, Zi Yang, Zu‐Li Wang, Hui Dai
article en
7 citations

Abstract

Herein, we report the sustainable semiheterogeneous synthesis of various fluoroalkylated <i>N</i>-heteroarenes using natural intrinsic iron(II) titanium oxide (FeTiO<sub>3</sub>) as a semiconductor photocatalyst and Ph<sub>3</sub>N as a redox mediator. This synergistic system combines photogenerated electron-mediated fluoroalkyl sulfonyl chloride (R<sub>f</sub>SO<sub>2</sub>Cl) reduction with photogenerated hole-induced oxidative dehydrogenation aromatization, enabling high-yielding transformations with excellent functional-group tolerance while avoiding stoichiometric redox reagents or sacrificial electron donors/acceptors.

The Journal of Organic ChemistryVol. 90(41)
Changsha Medical University (CN), Nanjing Forestry University (CN), University of South China (CN), Hunan Institute of Technology (CN)
Openalex Percentile: Top 4%
Fluorine in Organic Chemistry
5.54
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Semiheterogeneous Intrinsic FeTiO<sub>3</sub>-Photoredox/Ph<sub>3</sub>N Dual-Catalyzed Fluoroalkylation of N-Heteroarenes with Alkenes and R<sub>f</sub>SO<sub>2</sub>Cl — Chunlin Zhuang, Wei‐Min He, et al. · The Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS