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Synthetic Mn3Ce2O5-Cluster Mimicking the Oxygen-Evolving Center in Photosynthesis.
Chen, Yang; Su, Yao; Han, Juanjuan; Chen, Changhui; Fan, Hongjun; Zhang, Chunxi.
Affiliation
  • Chen Y; Beijing National Laboratory for Molecular Sciences and Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
  • Su Y; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Han J; Beijing National Laboratory for Molecular Sciences and Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
  • Chen C; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Fan H; Center for Physicochemical Analysis and Measurement, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
  • Zhang C; Beijing National Laboratory for Molecular Sciences and Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
ChemSusChem ; : e202401031, 2024 Jun 03.
Article in En | MEDLINE | ID: mdl-38829180
ABSTRACT
The photosynthetic oxygen-evolving center (OEC) is a unique Mn4CaO5-cluster that catalyses water splitting into electrons, protons, and dioxygen. Precisely structural and functional mimicking of the OEC is a long-standing challenge and pressingly needed for understanding the structure-function relationship and catalytic mechanism of O-O bond formation. Herein we report two simple and robust artificial Mn3Ce2O5-complexes that display a remarkable structural similarity to the OEC in regarding of the ten-atom core (five metal ions and five oxygen bridges) and the alkyl carboxylate peripheral ligands. This Mn3Ce2O5-cluster can catalyse the water-splitting reaction on the surface of ITO electrode. These results clearly show that cerium can structurally and functionally replace both calcium and manganese in the cluster. Mass spectroscopic measurements demonstrate that the oxide bridges in the cluster are exchangeable and can be rapidly replaced by the isotopic oxygen of H2 18O in acetonitrile solution, which supports that the oxide bridge(s) may serve as the active site for the formation of O-O bond during the water-splitting reaction. These results would contribute to our understanding of the structure-reactivity relationship of both natural and artificial clusters and shed new light on the development of efficient water-splitting catalysts in artificial photosynthesis.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: ChemSusChem Journal subject: QUIMICA / TOXICOLOGIA Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: ChemSusChem Journal subject: QUIMICA / TOXICOLOGIA Year: 2024 Document type: Article Affiliation country: China