Biomimetic Mn(III) porphyrin-catalyzed aromaticity-breaking epoxidation of electron-deficient naphthalene

Selective catalytic aromaticity-breaking epoxidation of arenes remains an ongoing research challenge, attributed to the stability of aromatic systems, the occurrence of over-oxidation, and the instability of epoxides. Epoxides, recognized as short-lived and highly reactive intermediates, are prone to undergo the "NIH-shift" rearrangement to yield the hydroxylated products. Herein, we report the synthesis and characterization of several electron-deficient naphthalene epoxides that disrupt the aromaticity of naphthalene. Their formation is highly dependent on the substrate, especially on the specific substitution pattern. This achievement is enabled by using mild biomimetic manganese porphyrins as catalysts and iodosylbenzene as an oxidant. The strategic employment of electron-withdrawing substitution on naphthalenes enables a chemoselective switch from hydroxylation to epoxidation. Experimental studies and theoretical calculations elucidate the possible underlying mechanisms of epoxidation and hydroxylation: epoxidation is likely mediated by a radical mechanism, whereas hydroxylation predominantly follows a zwitterionic pathway.

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Journal
Nature Communications
Published
2025-12-22
DOI
https://doi.org/10.1038/s41467-025-67300-8
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Biomimetic Mn(III) porphyrin-catalyzed aromaticity-breaking epoxidation of electron-deficient naphthalene

Wu H-P, Guijie Li, Yuanbin She, Junjie Tai et al.
Nature Communications
Porphyrin and Phthalocyanine Chemistry
article

Biomimetic Mn(III) porphyrin-catalyzed aromaticity-breaking epoxidation of electron-deficient naphthalene

Wu H-P, Guijie Li, Yuanbin She, Junjie Tai, Juan Gao, Jiayi Xu, Yun-Fang Yang, Yunfei Ge
article en

Abstract

Selective catalytic aromaticity-breaking epoxidation of arenes remains an ongoing research challenge, attributed to the stability of aromatic systems, the occurrence of over-oxidation, and the instability of epoxides. Epoxides, recognized as short-lived and highly reactive intermediates, are prone to undergo the "NIH-shift" rearrangement to yield the hydroxylated products. Herein, we report the synthesis and characterization of several electron-deficient naphthalene epoxides that disrupt the aromaticity of naphthalene. Their formation is highly dependent on the substrate, especially on the specific substitution pattern. This achievement is enabled by using mild biomimetic manganese porphyrins as catalysts and iodosylbenzene as an oxidant. The strategic employment of electron-withdrawing substitution on naphthalenes enables a chemoselective switch from hydroxylation to epoxidation. Experimental studies and theoretical calculations elucidate the possible underlying mechanisms of epoxidation and hydroxylation: epoxidation is likely mediated by a radical mechanism, whereas hydroxylation predominantly follows a zwitterionic pathway.

Nature CommunicationsVol. 16(1)
State Key Laboratory of Chemical Engineering (CN), Zhejiang University of Technology (CN), Zhejiang University (CN)
National Natural Science Foundation of China, Zhejiang University, Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 49%
Porphyrin and Phthalocyanine Chemistry
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