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首页> 外文期刊>Nature Communications >Remarkable catalytic activity of dinitrogen-bridged dimolybdenum complexes bearing NHC-based PCP-pincer ligands toward nitrogen fixation
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Remarkable catalytic activity of dinitrogen-bridged dimolybdenum complexes bearing NHC-based PCP-pincer ligands toward nitrogen fixation

机译:带有基于NHC的PCP-钳位配体的氮桥联二钼配合物对固氮的显着催化活性

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Intensive efforts for the transformation of dinitrogen using transition metal–dinitrogen complexes as catalysts under mild reaction conditions have been made. However, limited systems have succeeded in the catalytic formation of ammonia. Here we show that newly designed and prepared dinitrogen-bridged dimolybdenum complexes bearing N -heterocyclic carbene- and phosphine-based PCP-pincer ligands [{Mo(N2)2(PCP)}2(μ-N2)] ( 1 ) work as so far the most effective catalysts towards the formation of ammonia from dinitrogen under ambient reaction conditions, where up to 230?equiv. of ammonia are produced based on the catalyst. DFT calculations on 1 reveal that the PCP-pincer ligand serves as not only a strong σ -donor but also a π -acceptor. These electronic properties are responsible for a solid connection between the molybdenum centre and the pincer ligand, leading to the enhanced catalytic activity for nitrogen fixation.
机译:在温和的反应条件下,使用过渡金属-二氮配合物作为催化剂,已进行了大量努力来转化二氮。但是,有限的系统已成功催化形成氨。在这里,我们显示了新设计和制备的带有氮杂环卡宾和膦基PCP钳位配体[{Mo(N 2 2 ( PCP)} 2 (μ-N 2 )](1)是迄今为止在环境反应条件下,从二氮形成氨的最有效催化剂。至230?equiv。氨基于催化剂产生。 DFT对1的计算表明,PCP-pincer配体不仅充当强σ-供体,而且充当π-受体。这些电子性质负责钼中心与钳位配体之间的牢固连接,从而提高了固氮的催化活性。

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