4.8 Article

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

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NATURE COMMUNICATIONS
卷 3, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms2264

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资金

  1. Japan Society for the Promotion of Science (JSPS) [22245028, 24109014]
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
  3. Nanotechnology Support Project of MEXT
  4. MEXT Project of Integrated Research on Chemical Synthesis
  5. Kyushu University Global COE Project
  6. Funding Program for Next Generation World-Leading Researchers [GR025]
  7. Toyota Motor Corporation
  8. Grants-in-Aid for Scientific Research [22245028, 24109014] Funding Source: KAKEN

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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.

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