A molybdenum complex bearing PNP-type pincer ligands leads to the catalytic reduction of dinitrogen into ammonia

被引:609
作者
Arashiba, Kazuya [1 ]
Miyake, Yoshihiro [1 ]
Nishibayashi, Yoshiaki [1 ]
机构
[1] Univ Tokyo, Sch Engn, Inst Engn Innovat, Bunkyo Ku, Tokyo 1138656, Japan
关键词
DENSITY-FUNCTIONAL THEORY; NITROGEN-FIXATION; TUNGSTEN-DINITROGEN; MOLECULAR NITROGEN; COORDINATED DINITROGEN; FEMO-COFACTOR; PROTONATION; ACTIVATION; CHEMISTRY; N-2;
D O I
10.1038/NCHEM.906
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis of transition metal-dinitrogen complexes and the stoichiometric transformation of their coordinated dinitrogen into ammonia and hydrazine have been the subject of considerable research, with a view to achieving nitrogen fixation under ambient conditions. Since a single example in 2003, no examples have been reported of the catalytic conversion of dinitrogen into ammonia under ambient conditions. The dimolybdenum-dinitrogen complex bearing PNP pincer ligands was found to work as an effective catalyst for the formation of ammonia from dinitrogen, with 23 equiv. of ammonia being produced with the catalyst (12 equiv. of ammonia are produced based on the molybdenum atom of the catalyst). This is another successful example of the catalytic and direct conversion of dinitrogen into ammonia under ambient reaction conditions. We believe that the results described in this Article provide valuable information with which to develop a more effective nitrogen-fixation system under mild reaction conditions.
引用
收藏
页码:120 / 125
页数:6
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