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Molecular Catalysts for N2 Reduction: State of the Art, Mechanism, and Challenges

期刊

CHEMPHYSCHEM
卷 18, 期 19, 页码 2606-2617

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.201700665

关键词

bond dissociation energies; homogeneous catalysis; nitrogen fixation; reaction mechanism; transition metals

资金

  1. Agence Nationale pour la Recherche (grant CalixMo) [ANR-14-CE06_0002_01]
  2. Labex ARCANE [ANR-11-LABX-0003-01]

向作者/读者索取更多资源

Fixation of atmospheric nitrogen is central for the production of ammonia, which is the source of nitrogen fertilizers and is also emerging as a promising renewable fuel. While the development of efficient molecular-based artificial nitrogen fixation systems working under mild conditions is probably a Holy Grail, the catalytic reduction of N-2 by transition-metal complexes isabove allthe main instrument to progress in the mechanistic understanding of N-2 splitting. In this Minireview we first give an overview of molecular-based catalytic systems, including recent breakthroughs, and then we illustrate the alternative pathways for N-2 reduction. We mainly focus on multistep hydrogenation of N-2 by separated proton and electron sources, with a particular attention for the possibility of proton-coupled electron transfer events. Finally, we try to identify the key factors to achieve catalytic reduction of dinitrogen by metal complexes and to enhance their efficiency.

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