Large-Scale and Facile Preparation of Pure Ammonia Borane through Displacement Reactions

被引:42
|
作者
Chen, Xuenian [1 ,2 ]
Bao, Xiaoguang [1 ]
Billet, Beau [2 ]
Shore, Sheldon G. [1 ]
Zhao, Ji-Cheng [2 ]
机构
[1] Ohio State Univ, Dept Chem, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Mat Sci & Engn, Columbus, OH 43210 USA
关键词
boranes; displacement reactions; hydrogen storage; Lewis acid-base; synthetic methods; MOLECULAR ADDITION-COMPOUNDS; AMORPHOUS BORON-NITRIDE; UNSYMMETRICAL CLEAVAGE; ASYMMETRIC CLEAVAGE; AMINE COMPLEXES; HYDROGEN; DIBORANE; ENERGY; STORAGE; HYDROBORATION;
D O I
10.1002/chem.201201342
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ammonia borane (AB) is the most widely studied hydride for hydrogen storage in addition to being a useful reducing agent. Attempts to synthesize pure AB through simple displacement reactions date back to the 1960s; but have been thwarted by the formation of the diammoniate of diborane (DADB), an ionic byproduct. Based on our recent characterization of the formation mechanism of DADB, we have developed a large-scale synthesis of pure AB by both increasing the basicity of the Lewis base of the borane carrier and using a nonpolar solvent to limit the formation of an intermediate, the ammonia diborane (AaDB). Conditions were optimized for the preparation of pure AB by two displacement reactions, either ammonia with dimethylsulfide borane or ammonia with dimethylaniline borane in toluene at room temperature. These procedures are also suitable for preparation of other amine boranes which had the same problem of forming ionic byproducts during displacement reactions.
引用
收藏
页码:11994 / 11999
页数:6
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