Journal
CHINESE CHEMICAL LETTERS
Volume 30, Issue 2, Pages 398-402Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2018.06.021
Keywords
RuCl3; MIL-101(Cr)-DPPB; Post-synthetic modification; Anchoring Ru(III); Electron-donor substituent
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Funding
- National Natural Science Foundation of China (NSFC) [21776211, 21325626]
- Program for New Century Excellent Talents in University [NCET-13-0411]
- Program of Introducing Talents of Discipline to Universities [B06006]
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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.
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