Experimental and theoretical treatment of hydrogen splitting and storage in boron-nitrogen systems

被引:83
|
作者
Sumerin, Victor [1 ]
Schulz, Felix [2 ]
Nieger, Martin [1 ]
Atsumi, Michiko [1 ]
Wang, Cong [1 ]
Leskela, Markku [1 ]
Pyykko, Pekka [1 ]
Repo, Timo [1 ]
Rieger, Bernhard [2 ]
机构
[1] Univ Helsinki, Dept Chem, FIN-00014 Helsinki, Finland
[2] Tech Univ Munich, WACKER Lehrstuhl Makromol Chem, D-85747 Garching, Germany
基金
芬兰科学院;
关键词
Hydrogen; Boron; Nitrogen; Activation; Liberation; FRUSTRATED LEWIS PAIRS; FREE CATALYTIC-HYDROGENATION; HETEROLYTIC DIHYDROGEN ACTIVATION; METAL-FREE; H-2; ACTIVATION; BORANE; REACTIVITY; IMINES; BOND; CLEAVAGE;
D O I
10.1016/j.jorganchem.2009.03.023
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Hydrogen gas serves as a reducing agent and hydrogen atom source in numerous industrially important chemical processes and also has a great potential as a clean power source for fuel cells. In this respect, the reversible storage of hydrogen and the development of new metal-free hydrogenation catalysts are important tasks. Here, we review the recent literature, primarily on cases where the split H(2) forms an N-H center dot center dot center dot H-B dihydrogen bond. In these systems dihydrogen interaction was found to be the key actor in the hydrogen liberating process. Accordingly, the intramolecular ansa-aminoboranes (where B and N atoms are situated within each other's range) can reversibly activate hydrogen. Moreover, the theoretical studies of the hydrogen splitting by bulky Lewis acid-Lewis base systems are discussed. (C) 2009 Elsevier B. V. All rights reserved.
引用
收藏
页码:2654 / 2660
页数:7
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