Photocatalytic aerobic oxidative cleavage of olefins in pure water

Abstract

The photocatalytic oxidative cleavage of C[double bond, length as m-dash]C bonds to generate aldehydes, ketones and α-halo acetophenones using pure water as a solvent is proposed and designed. A green route is realized in the presence of an FeOx/C3N4 composite catalyst under aerobic conditions. The specially prepared FeOx on C3N4 improved the amphiphilicity of the catalyst, thus avoiding the agglomeration of the photocatalyst in water, and enhanced the utilization efficiency of photo-induced charges. Control experiments and ESR results confirmed both hydroxyl and hydrosuperoxide radicals as the key oxidative species in the reaction, which play a crucial role in the efficient activation of the C[double bond, length as m-dash]C bond. Furthermore, the catalyst is highly stable and can be reused at least 20 times without significant loss of activity.

Graphical abstract: Photocatalytic aerobic oxidative cleavage of olefins in pure water

Supplementary files

Article information

Article type
Paper
Submitted
16 Nov 2025
Accepted
24 Dec 2025
First published
26 Dec 2025

Catal. Sci. Technol., 2026, Advance Article

Photocatalytic aerobic oxidative cleavage of olefins in pure water

T. Niu, Y. Yang, F. Zhang, S. Chen, Y. Guo, Y. Li, B. Ni and Y. Dong, Catal. Sci. Technol., 2026, Advance Article , DOI: 10.1039/D5CY01371B

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