Unique behaviour of dinitrogen-bridged dimolybdenum complexes bearing pincer ligand towards catalytic formation of ammonia

被引:136
作者
Tanaka, Hiromasa [1 ,2 ,3 ]
Arashiba, Kazuya [4 ]
Kuriyama, Shogo [4 ]
Sasada, Akira [1 ,2 ,3 ]
Nakajima, Kazunari [4 ]
Yoshizawa, Kazunari [1 ,2 ,3 ]
Nishibayashi, Yoshiaki [4 ]
机构
[1] Kyushu Univ, Inst Mat Chem & Engn, Nishi Ku, Fukuoka 8190395, Japan
[2] Kyushu Univ, Int Res Ctr Mol Syst, Nishi Ku, Fukuoka 8190395, Japan
[3] Kyoto Univ, Elements Strategy Initiat Catalysts & Batteries, Nishikyo Ku, Kyoto 6158520, Japan
[4] Univ Tokyo, Sch Engn, Inst Engn Innovat, Bunkyo Ku, Tokyo 1138656, Japan
基金
日本学术振兴会;
关键词
SINGLE MOLYBDENUM CENTER; SYNTHETIC NITROGEN-FIXATION; MILD REACTION CONDITIONS; TUNGSTEN-DINITROGEN; MOLECULAR NITROGEN; COORDINATED DINITROGEN; REDUCTION; DENSITY; REACTIVITY; PROTONATION;
D O I
10.1038/ncomms4737
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is vital to design effective nitrogen fixation systems that operate under mild conditions, and to this end we recently reported an example of the catalytic formation of ammonia using a dinitrogen-bridged dimolybdenum complex bearing a pincer ligand, where up to twenty three equivalents of ammonia were produced based on the catalyst. Here we study the origin of the catalytic behaviour of the dinitrogen-bridged dimolybdenum complex bearing the pincer ligand with density functional theory calculations, based on stoichiometric and catalytic formation of ammonia from molecular dinitrogen under ambient conditions. Comparison of di- and mono-molybdenum systems shows that the dinitrogen-bridged dimolybdenum core structure plays a critical role in the protonation of the coordinated molecular dinitrogen in the catalytic cycle.
引用
收藏
页数:11
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