RuCl3 anchored onto post-synthetic modification MIL-101(Cr)-NH2 as heterogeneous catalyst for hydrogenation of CO2 to formic acid

被引:71
作者
Wang, Shengping [1 ,2 ]
Hou, Shihui [1 ,2 ]
Wu, Chao [1 ,2 ]
Zhao, Yujun [1 ,2 ]
Ma, Xinbin [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Tianjin 300350, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
RuCl3; MIL-101(Cr)-DPPB; Post-synthetic modification; Anchoring Ru(III); Electron-donor substituent; METAL-ORGANIC FRAMEWORKS; CARBON-DIOXIDE; NANOPARTICLES; PALLADIUM; KINETICS; COMPLEX; LIGAND;
D O I
10.1016/j.cclet.2018.06.021
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of efficient ruthenium chloride (RuCl3)-anchored MOF catalysts, such as RuCl3 @MIL-101(Cr)-Sal, and RuCl3@MIL-101(Cr)-DPPB, have been successfully synthesized by post-synthetic modification (PSM) of the terminal amino of MIL-101(Cr)-NH2 with salicylaldehyde, 2-diphenylphosphinobenzaldehyde (DPPBde) and anchoring of Ru(III) ions. The stronger coordination electron donor interaction between Ru(III) ions and chelating groups in the RuCl3@MIL-101(Cr)-DPPB enhances its catalytic performance for CO2 hydrogenation to formic acid. The turnover number (TON) of formic acid was up to 831 in reaction time of 2 h with dimethyl sulfoxide (DMSO) and water (H2O) as mixed solvent, trimethylamine (Et3N) as organic base, and PPh3 as electronic additive. (C) 2018 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:398 / 402
页数:5
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