Metal-Ligand Cooperative Synthesis of Benzonitrile by Electrochemical Reduction and Photolytic Splitting of Dinitrogen

被引:77
|
作者
Schendzielorz, Florian [1 ]
Finger, Markus [1 ]
Abbenseth, Josh [1 ]
Wuertele, Christian [1 ]
Krewald, Vera [2 ]
Schneider, Sven [1 ]
机构
[1] Georg August Univ, Inst Anorgan Chem, Tammannstr 4, D-37077 Gottingen, Germany
[2] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
基金
欧洲研究理事会;
关键词
electrochemistry; nitrogen fixation; photochemistry; pincer ligands; rhenium; NITROGEN-FIXATION; CATALYTIC-REDUCTION; CLEAVAGE; N-2; AMMONIA; MOLYBDENUM; CONVERSION; COMPLEXES; RUTHENIUM; FUNCTIONALIZATION;
D O I
10.1002/anie.201812125
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thermal nitrogen fixation relies on strong reductants to overcome the extraordinarily large N-N bond energy. Photochemical strategies that drive N-2 fixation are scarcely developed. Here, the synthesis of a dinuclear N-2-bridged complex is presented upon reduction of a rhenium(III) pincer platform. Photochemical splitting into terminal nitride complexes is triggered by visible light. Clean nitrogen transfer with benzoyl chloride to free benzamide and benzonitrile is enabled by cooperative 2 H+/2 e(-) transfer of the pincer ligand. A three-step cycle is demonstrated for N-2 to nitrile fixation that relies on electrochemical reduction, photochemical N-2-splitting and thermal nitrogen transfer.
引用
收藏
页码:830 / 834
页数:5
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