Uranyl Polyoxotungstate Cluster for Visible-Light-Driven Heterogeneous C-H Selective Fluorination

被引:2
|
作者
Chen, Chao-Long [1 ,2 ]
Wang, Hai-Ying [1 ,2 ]
Weng, Zhen-Zhang [1 ,2 ]
Long, La-Sheng [1 ,2 ]
Zheng, Lan-Sun [1 ,2 ]
Kong, Xiang-Jian [1 ,2 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Collaborat Innovat Ctr Chem Energy Mat, State Key Lab Phys Chem Solid Surface, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTOCATALYSIS; FLUORIDE; CATION; MONO;
D O I
10.1021/acs.inorgchem.3c02531
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The selective fluorination of C-H bonds at room temperature using heterogeneous visible-light catalysts is both interesting and challenging. Herein, we present the heterogeneous sandwich-type structure uranyl-polyoxotungstate cluster Na-17{Na@[(SbW9O33)(2)(UO2)(6)(PO3OH)(6)]}<middle dot>46H(2)O (denoted as U6P6) to regulate the selective fluorination of the C-H bond under visible light and room temperature. This is the first report in which uranyl participates in the fluorination reaction in the form of an insoluble substance. U6P6 is capable of the effective selective fluorination of cycloalkanes and the recyclability of the photocatalyst due to the synergistic effect of multiple uranyl (UO2)(2+) and the insolubility of organic reagents of polyoxotungstate. In situ electron paramagnetic resonance spectroscopy captured the generation of cycloalkane radicals during the photoreaction, confirming the mechanism of direct hydrogen atom transfer.
引用
收藏
页码:17041 / 17045
页数:5
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