Dinitrogen photoactivation: status quo and future perspectives

被引:29
作者
Krewald, Vera [1 ]
机构
[1] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
基金
欧盟地平线“2020”;
关键词
TRANSITION-METAL-COMPLEXES; DRIVEN NITROGEN-FIXATION; CATALYTIC-REDUCTION; PHOTOCHEMICAL ACTIVATION; COMPETITIVE CATALYSTS; MOLECULAR DINITROGEN; NITRIDE COMPLEXES; AMMONIA-SYNTHESIS; VISIBLE-LIGHT; N-2; CLEAVAGE;
D O I
10.1039/c8dt00418h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
While the thermal activation of the dinitrogen molecule has been demonstrated in numerous examples with a variety of transition metals and ligand frameworks, the use of light to induce a weakening or splitting of the strong N-N bond is less well explored. Six complexes that bind N-2 in a linear -(1):(1)-end-on fashion between two transition metals are known to cleave dinitrogen after absorbing a photon and relaxing from an electronically excited state. This Perspective article reviews the molecular complexes known to be capable of dinitrogen photocleavage, and discusses mechanistic insights into the photoactivation process gained from experimental and computational studies. In an extension of previous hypotheses for pathways to dinitrogen photoactivation that would facilitate easy protonation of the -N atoms, a scheme is presented that may help to identify other complexes that could be capable of dinitrogen photoactivation.
引用
收藏
页码:10320 / 10329
页数:10
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