Recent advances in catalytic nitrogen fixation using transition metal-dinitrogen complexes under mild reaction conditions

被引:31
|
作者
Tanabe, Yoshiaki [1 ]
Nishibayashi, Yoshiaki [1 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Appl Chem, Bunkyo Ku, Hongo, Tokyo 1138656, Japan
关键词
Ammonia; Catalysis; Catalyst; Dinitrogen; Dinitrogen complex; Electrochemistry; Nitrogen fixation; Proton-coupled electron transfer; Proton source; Reductant; COUPLED ELECTRON-TRANSFER; AMBIENT REACTION CONDITIONS; PINCER LIGANDS; MOLYBDENUM-DINITROGEN; MOLECULAR DINITROGEN; N-2; REDUCTION; N-2-TO-NH3; CONVERSION; NITRIDE COMPLEXES; SAMARIUM DIIODIDE; AMMONIA FORMATION;
D O I
10.1016/j.ccr.2022.214783
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Recent advances in catalytic nitrogen fixation using well-defined molecular transition metal-dinitrogen complexes and their precursors as catalysts under ambient or mild reaction conditions are summarized in terms of varieties of transition metals, ligands, reductants and proton sources, and catalytic reaction pathways. Several transition metal complexes have been applied as catalysts for nitrogen fixation, while Mo catalytic systems successfully fix nitrogen under ambient conditions. H2O becomes available as a pro-ton source for the formation of NH3 via proton-coupled electron transfer processes, and turnover fre-quencies for the formation of NH3 are now relevant to the biological nitrogen fixation, making gram -scale preparation of NH3 possible. Pioneering electrochemical nitrogen fixation systems mediated by molecular catalysts have been also under development. Targets and strategies for future research plans for improving catalytic systems are further discussed.(c) 2022 Elsevier B.V. All rights reserved.
引用
收藏
页数:19
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