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Encapsulation of Organic Dyes within an Electron‐Deficient Redox Metal‐Organic Tetrahedron for Photocatalytic Proton Reduction
Author(s) -
Wang Hailing,
Li Lili,
Li Xuezhao,
He Cheng
Publication year - 2019
Publication title -
israel journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.908
H-Index - 54
eISSN - 1869-5868
pISSN - 0021-2148
DOI - 10.1002/ijch.201800145
Subject(s) - chemistry , redox , photocatalysis , supramolecular chemistry , artificial photosynthesis , photochemistry , tetrahedron , metal , catalysis , ligand (biochemistry) , inorganic chemistry , crystallography , organic chemistry , crystal structure , biochemistry , receptor
The design of artificial systems that mimic highly evolved and finely tuned natural photosynthetic systems is a subject of intensive research. By incorporating electron‐deficient anthraquinone within the ligand backbone, a redox‐active Ni‐based tetrahedron was developed as a redox vehicle for the construction of an artificial photosynthesis system. The tetrahedron can encapsulate fluorescein within its cavity for light‐driven H 2 evolution, with the turnover number reaching 1200 moles H 2 per mole redox catalyst. This well‐designed supramolecular system displayed a significantly superior activities compared with the reference mononuclear compound or introducing an inactive inhibitor (ATP), which confirmed this enzymatic photocatalytic behaviour.

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