Activation of Dinitrogen by Polynuclear Metal Complexes.

Activation of Dinitrogen by Polynuclear Metal Complexes.
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DOI:
10.1021/acs.chemrev.0c00042
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发表时间:
2020-06-24
期刊:
影响因子:
62.1
通讯作者:
Murray LJ
Murray LJ
中科院分区:
化学1区
文献类型:
--
作者:
Singh D;Buratto WR;Torres JF;Murray LJ

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Activation of dinitrogen plays an important role in daily anthropogenic life and the processes by which this fixation occurs has been a longstanding and significant research focus within the community. One of the major fields of dinitrogen activation research is the use of multimetallic compounds to reduce and/or activate N2 into a more useful nitrogen-atom source, such as ammonia. Here we report a comprehensive review of multimetallic-dinitrogen complexes and their utility towards N2 activation, beginning with the d-block metals from Group 4 to Group 11, then extending to Group 13 (which is exclusively populated by B complexes), and finally the rare-earth and actinide species. The review considers all polynuclear metal aggregates containing two or more metal centers in which dinitrogen is coordinated or activated (i.e., partial or complete cleavage of the N2 triple bond in the observed product). Our survey includes complexes in which mononuclear N2 complexes are used as building blocks to generate homo- or hetero-multimetallic dinitrogen species, which allow one to evaluate the potential of heterometallic species for dinitrogen activation. We hightlight some of the common trends throughout the periodic table, such as the differences between coordination modes as it relates to N2 activation and potential functionalization, the effect of polarizing the bridging N2 ligand by employing different metal ions of differing Lewis acidities. By providing this comprehensive treatment of polynuclear metal dinitrogen species, this Review aims to outline the past and provide potential future directions for continued research in this area.
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