Acid- and Base-Catalyzed Hydrolytic Hydrogen Evolution from Diboronic Acid

被引:20
|
作者
Wang, Yi [1 ]
Shen, Jialu [1 ]
Huang, Yu [1 ]
Liu, Xiang [1 ]
Zhao, Qiuxia [2 ]
Astruc, Didier [2 ]
机构
[1] China Three Gorges Univ, Coll Mat & Chem Engn, Key Lab Inorgan Nonmetall Crystalline & Energy Co, Mat Anal & Testing Ctr, Yichang 443002, Hubei, Peoples R China
[2] Univ Bordeaux, ISM, UMR CNRS 5255, 351 Cours Liberat, F-33405 Talence, France
基金
中国国家自然科学基金;
关键词
Acid catalysis; Base catalysis; Boron; Hydrogen evolution; Reaction mechanisms; AMMONIA-BORANE; WATER; REDUCTION; EFFICIENT; TETRAHYDROXYDIBORON; DEHYDROGENATION; NANOPARTICLES; GENERATION; MECHANISM; MILD;
D O I
10.1002/ejic.202100093
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The efficient production of H-2 from hydrogen-rich sources, particularly from water, is a crucial task and a great challenge, both as a sustainable energy source and on the laboratory scale for hydrogenation reactions. Herein, a facile and effective synthesis of H-2 and D-2 from only acid- or base-catalyzed metal-free hydrolysis of B-2(OH)(4), a current borylation reagent, has been developed without any transition metal or ligand. Acid-catalyzed H-2 evolution was completed in 4 min, whereas the base-catalyzed process needed 6 min. The large kinetic isotopic effects for this reaction with D2O, deuteration experiments and mechanistic studies have confirmed that both H atoms of H-2 originate from water using either of these reactions. This new, metal-free catalytic system holds several advantages, such as high efficiency, simplicity of operation, sustainability, economy, and potential further use.
引用
收藏
页码:3013 / 3018
页数:6
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