Chemical water oxidation by nonheme iron catalysts supported by di- and trinucleating N4 donor ligands: unveiling the role of coordinating buffer in directing cooperative catalysis

In a borate buffer, a trinuclear non-heme iron complex exhibits higher catalytic water-oxidation activity than its mononuclear or dinuclear counterparts. Borate-assisted metal–metal cooperativity enhances catalytic efficiency.

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Publication Details

Journal
Inorganic Chemistry Frontiers
Published
2025-12-31
DOI
https://doi.org/10.1039/d5qi01852h
Primary Topic
Metal-Catalyzed Oxygenation Mechanisms
Type
article
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article

Chemical water oxidation by nonheme iron catalysts supported by di- and trinucleating N4 donor ligands: unveiling the role of coordinating buffer in directing cooperative catalysis

Sachidulal Biswas, Sabyasachi Mahapatra, Tapan Kanti Paine, Achintesh Narayan Biswas et al.
Inorganic Chemistry Frontiers
Metal-Catalyzed Oxygenation Mechanisms
article

Chemical water oxidation by nonheme iron catalysts supported by di- and trinucleating N4 donor ligands: unveiling the role of coordinating buffer in directing cooperative catalysis

Sachidulal Biswas, Sabyasachi Mahapatra, Tapan Kanti Paine, Achintesh Narayan Biswas, Subhankar Sutradhar
article en

Abstract

In a borate buffer, a trinuclear non-heme iron complex exhibits higher catalytic water-oxidation activity than its mononuclear or dinuclear counterparts. Borate-assisted metal–metal cooperativity enhances catalytic efficiency.

Inorganic Chemistry FrontiersVol. 13(6)
National Institute of Technology Sikkim (IN), Indian Association for the Cultivation of Science (IN)
Clean water and sanitation
Openalex Percentile: Top 43%
Metal-Catalyzed Oxygenation Mechanisms
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