Catalytic transformation of dinitrogen into ammonia and hydrazine by iron-dinitrogen complexes bearing pincer ligand

被引:232
作者
Kuriyama, Shogo [1 ]
Arashiba, Kazuya [1 ]
Nakajima, Kazunari [1 ]
Matsuo, Yuki [2 ,3 ]
Tanaka, Hiromasa [2 ,3 ]
Ishii, Kazuyuki [4 ]
Yoshizawa, Kazunari [2 ,3 ,5 ]
Nishibayashi, Yoshiaki [1 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Syst Innovat, Bunkyo Ku, Tokyo 1138656, Japan
[2] Kyushu Univ, Inst Mat Chem & Engn, Nishi Ku, Fukuoka 8190395, Japan
[3] Kyushu Univ, Int Res Ctr Mol Syst, Nishi Ku, Fukuoka 8190395, Japan
[4] Univ Tokyo, Inst Ind Sci, Meguro Ku, 4-6-1 Komaba, Tokyo 1538505, Japan
[5] Kyoto Univ, ESICB, Nishikyo Ku, Kyoto 6158520, Japan
关键词
N BOND-CLEAVAGE; MOLECULAR DINITROGEN; NITROGEN-FIXATION; UNIQUE BEHAVIOR; FE-N-2; COMPLEX; SQUARE-PLANAR; REDUCTION; N-2; MOLYBDENUM; (FEFEI)-FE-II;
D O I
10.1038/ncomms12181
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
Synthesis and reactivity of iron-dinitrogen complexes have been extensively studied, because the iron atom plays an important role in the industrial and biological nitrogen fixation. As a result, iron-catalyzed reduction of molecular dinitrogen into ammonia has recently been achieved. Here we show that an iron-dinitrogen complex bearing an anionic PNP-pincer ligand works as an effective catalyst towards the catalytic nitrogen fixation, where a mixture of ammonia and hydrazine is produced. In the present reaction system, molecular dinitrogen is catalytically and directly converted into hydrazine by using transition metal-dinitrogen complexes as catalysts. Because hydrazine is considered as a key intermediate in the nitrogen fixation in nitrogenase, the findings described in this paper provide an opportunity to elucidate the reaction mechanism in nitrogenase.
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页数:9
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