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Ligand-dependent structural diversity and optimizable CO chemical fixation activities of Cu-doped polyoxo-titanium clusters.

作者信息

Lin Xin, Yu Ying-Hua, Chen Guang-Hui, Li Qiao-Hong, Zhang Lei, Zhang Jian

机构信息

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, P. R. China.

University of Chinese Academy of Sciences, Beijing 100049, P. R. China.

出版信息

Dalton Trans. 2023 Aug 22;52(33):11451-11457. doi: 10.1039/d3dt01718d.

DOI:10.1039/d3dt01718d
PMID:37547997
Abstract

Heterometallic oxo clusters have been attracting intensive interest due to their unique properties originating from the synergistic interactions between different components. Herein, we report the construction and catalytic applications of a family of copper-doped polyoxo-titanium clusters (Cu-PTCs) coordinated with different acetate derivative ligands. The solvothermal reactions of metal salts and trimethylacetic acid or 1,2-phenylenediacetic acid in ethanol produced TiCu(μ-O)(μ-O)(OEt)(L1) (L1 = trimethyl acetate, PTC-367) and HTiCuBr(μ-O)(μ-O)(OEt)(L2) (L2 = 1,2-phenylenediacetate, PTC-368), respectively. When smaller acetic acid was introduced as a stabilizing ligand, higher nuclei HTiCu(μ-O)(μ-O)(μ-O)(OPr)(Ac) (Ac = acetate, PTC-369) and HTiCu(μ-O)(μ-O)(μ-O)(OPr)(Ac) (PTC-370) were prepared. The number of metal ions exposed on the surface of the four clusters changes due to variations in the steric hindrance of functionalizing ligands, and theoretically, so does their catalytic activity as Lewis acids. In light of this, we conducted a carbon dioxide cycloaddition reaction in an atmospheric environment and the four obtained compounds displayed increasing catalytic activities from PTC-367 to PTC-370. These results provide a feasible synthetic method for modulating the structures of Cu-doped titanium oxide materials and improving their catalytic activities.

摘要

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