Iron-catalysed transformation of molecular dinitrogen into silylamine under ambient conditions

被引:112
|
作者
Yuki, Masahiro [1 ]
Tanaka, Hiromasa [2 ]
Sasaki, Kouitsu [1 ]
Miyake, Yoshihiro [1 ]
Yoshizawa, Kazunari [2 ]
Nishibayashi, Yoshiaki [1 ]
机构
[1] Univ Tokyo, Inst Engn Innovat, Sch Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Kyushu Univ, Inst Mat Chem & Engn, Int Res Ctr Mol Syst, Nishi Ku, Fukuoka 8190395, Japan
来源
NATURE COMMUNICATIONS | 2012年 / 3卷
基金
日本学术振兴会;
关键词
UNSATURATED TRIS(TRIMETHYLSILYL)SILYL COMPLEXES; DENSITY FUNCTIONALS; REDUCTION; NITROGEN; ENERGY; MOLYBDENUM; AMMONIA; SILYLATION; FIXATION; METAL;
D O I
10.1038/ncomms2264
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
Although stoichiometric transformations using transition metal-N-2 complexes have been well investigated towards the goal of nitrogen fixation under mild reaction conditions, only a few examples of the catalytic transformations of N-2 using transition metal-N-2 complexes as catalysts have been reported. In almost all the catalytic systems, the use of Mo is essential to realize the catalytic transformation of N-2, where Mo-N-2 complexes are considered to work as effective catalysts. Here we show the first successful example of the Fe-catalysed transformation of N-2 into N(SiMe3)(3) under ambient conditions, in which iron complexes such as iron pentacarbonyl [Fe(CO)(5)] and ferrocenes have been found to work as effective catalysts. A plausible reaction pathway is proposed, where Fe(II)-N-2 complex bearing two Me3Si groups as ancillary ligands has an important role as a key reactive intermediate, with the aid of density-functional-theory calculations.
引用
收藏
页数:6
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