Iron porphyrin-catalyzed bromination of unactivated C–H bonds: inhibition of oxygen rebound by redox-inactive metal ions

Biomimetic bromination of unactivated C–H bonds catalyzed by an iron porphyrin complex with LiBr was achieved. Introduction of Li + completely inhibited the oxygen-rebound pathway. A carbocation was proposed as the key intermediate for the reaction.

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Publication Details

Journal
Inorganic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qi00508f
Citations
4
Primary Topic
Vanadium and Halogenation Chemistry
Type
article
Field-Weighted Citation Impact
2.15

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article

Iron porphyrin-catalyzed bromination of unactivated C–H bonds: inhibition of oxygen rebound by redox-inactive metal ions

Peng Wu, Binju Wang, Yiran Xu, Yue Cui et al.
4 citations
Inorganic Chemistry Frontiers
Vanadium and Halogenation Chemistry
2.15
article

Iron porphyrin-catalyzed bromination of unactivated C–H bonds: inhibition of oxygen rebound by redox-inactive metal ions

Peng Wu, Binju Wang, Yiran Xu, Yue Cui, Mian Guo, Yuheng Zhang, Duanfeng Xie
article en
4 citations

Abstract

Biomimetic bromination of unactivated C–H bonds catalyzed by an iron porphyrin complex with LiBr was achieved. Introduction of Li + completely inhibited the oxygen-rebound pathway. A carbocation was proposed as the key intermediate for the reaction.

Inorganic Chemistry FrontiersVol. 12(13)
Xiamen University (CN), Ningxia University (CN), Wuhan University (CN)
National Natural Science Foundation of China, Wuhan University, Northwest Fisheries Science Center
Openalex Percentile: Top 13%
Vanadium and Halogenation Chemistry
2.15
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