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室温下异核金属簇阴离子FeVC对氮气的活化与官能团化

Dinitrogen Activation and Functionalization by Heteronuclear Metal Cluster Anions FeVC at Room Temperature.

作者信息

Mou Li-Hui, Li Yao, Li Zi-Yu, Liu Qing-Yu, Ren Yi, Chen Hui, He Sheng-Gui

机构信息

State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.

University of Chinese Academy of Sciences, Beijing 100049, P. R. China.

出版信息

J Phys Chem Lett. 2020 Dec 3;11(23):9990-9994. doi: 10.1021/acs.jpclett.0c02921. Epub 2020 Nov 12.

Abstract

It is of great importance to study the mechanisms to activate dinitrogen (N), the very inert molecule, under mild conditions. Gas-phase metal clusters are being actively generated to react with N to identify new reaction types and mechanisms. Herein, an unprecedented, mechanistically unique metal atom (Fe or V) ejection in the thermal reaction of FeVC with N has been identified using mass spectrometry, photoelectron imaging spectroscopy, and quantum chemistry calculations. Strong evidence suggests that the complete cleavage of the N≡N triple bond and subsequent functionalization of two N atoms via C-N coupling were achieved in this reaction. The complementary cooperation between V atoms with strong electron-donating ability and an Fe atom with large electron-withdrawing ability as well as the geometric flexibility of the Fe-V-V ring drives the whole reaction. The important role of C ligands in N≡N cleavage was also revealed. This study emphasizes the importance of heteronuclear metal systems for N fixation.

摘要

研究在温和条件下激活非常惰性的分子二氮(N₂)的机制具有极其重要的意义。气相金属簇正被积极地生成以与N₂反应,从而识别新的反应类型和机制。在此,通过质谱、光电子成像光谱和量子化学计算,在FeVC与N₂的热反应中发现了前所未有的、机制独特的金属原子(Fe或V)喷射。有力的证据表明,在该反应中实现了N≡N三键的完全断裂以及两个N原子随后通过C-N偶联的官能化。具有强给电子能力的V原子与具有大吸电子能力的Fe原子之间的互补协同作用以及Fe-V-V环的几何灵活性驱动了整个反应。还揭示了C配体在N≡N断裂中的重要作用。这项研究强调了异核金属体系在固氮中的重要性。

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