Direct Synthesis of Organonitrogen Compounds from Dinitrogen Using Transition Metal Complexes: Leap from Stoichiometric Reactions to Catalytic Reactions

被引:3
|
作者
Suginome, Shun [1 ]
Nishibayashi, Yoshiaki [1 ]
机构
[1] Univ Tokyo, Dept Appl Chem, Sch Engn, Bunkyo ku, Tokyo 1138656, Japan
关键词
Nitrogen Fixation; Organonitrogen Compound; Nitride Complex; Dinitrogen; Reduction reaction; CARBON BOND FORMATION; COORDINATED DINITROGEN; MOLECULAR NITROGEN; LIGATING DINITROGEN; PYRROLYLIMIDO COMPLEXES; MOLYBDENUM COMPLEXES; TUNGSTEN; CONVERSION; FIXATION; CLEAVAGE;
D O I
10.1002/cctc.202300850
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Organonitrogen compounds are of vital importance to our lives. For almost all organonitrogen compounds, ammonia is only the feedstock as a nitrogen source. Ammonia is produced from dinitrogen (N2) and dihydrogen (H2) by the Haber-Bosch process, which consumes an enormous amount of energy. As an alternative method to convert N2 into organonitrogen compounds under milder conditions, various stoichiometric reactions with transition metal complexes have been explored for the last 50 years. However, the field of catalytic formation of organonitrogen compounds directly from N2 with transition metal complexes is still in its infancy. This short review summarizes strategies to achieve the direct synthesis of organonitrogen compounds from N2 under mild reaction conditions using transition metal complexes ranging from stoichiometric reactions to catalytic reactions. This short review summarizes strategies to achieve the direct synthesis of organonitrogen compounds from N2 under mild reaction conditions using transition metal complexes ranging from stoichiometric reactions to catalytic reactions.image
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页数:12
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