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Research Article | Open Access

Co7-cluster metal–organic frameworks for photocatalytic dehalogenation reduction

Sumeng LiuSaiyu LiuYiying WeiLanjv WangPengcheng Jiang ( )Haitao Yu ( )Jianwei Wei ( )
Hebei Technology Innovation Center for Energy Conversion Materials and Devices, College of Chemistry and Materials Science, Hebei Normal University, Shijiazhuang 050024, China
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Abstract

Photocatalytic dehalogenation reduction, which converts a C–X bond into a C–H bond, plays a significant role in synthetic catalysis and pollutant remediation. However, the reduction is significantly affected by photoinduced electron transfer (PET) from organic photoredox catalysts to metal ions or clusters. By introducing photosensitive ligands and cluster-based nodes into metal–organic frameworks (MOFs), we synthesized Co73-O)3-cluster MOFs using the easily redox cobalt ions and a tetraphenylbenzene-1,4-diamine-based ligand modified by the central skeleton, effectively regulating the redox potential. The synergistic interactions between the Co73-O)3 cluster and the photosensitive ligands enable efficient PET process. This synergy provides a concise strategy for photocatalytic dehalogenation reduction using cobalt-cluster MOFs under mild conditions, which can be extended to aryl halide and halogenated aromatic pollutants.

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Polyoxometalates
Article number: 9140120

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Cite this article:
Liu S, Liu S, Wei Y, et al. Co7-cluster metal–organic frameworks for photocatalytic dehalogenation reduction. Polyoxometalates, 2026, 5(2): 9140120. https://doi.org/10.26599/POM.2026.9140120

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Received: 13 October 2025
Revised: 31 December 2025
Accepted: 23 January 2026
Published: 06 March 2026
© The Author(s) 2026. Published by Tsinghua University Press.

Open Access This article is licensed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, sharing, distribution and reproduction in any medium, provided the original work is properly cited.