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关于一价镍对二氧化碳、氢离子和氢气的催化还原的评述

Remarks on catalytic reduction of CO2, H+ and H2 by monovalent Ni.

作者信息

Grochala Wojciech

机构信息

Interdisciplinary Center for Mathematical and Computational Modeling, University of Warsaw, Pawińskiego 5a, 02106 Warsaw, Poland.

出版信息

Phys Chem Chem Phys. 2006 Mar 21;8(11):1340-5. doi: 10.1039/b516113d. Epub 2006 Feb 9.

Abstract

Prompted by catalysis of CO2 electroreduction by a tetraazamacrocyclic Ni(i)(cyclam) complex (cyclam = 1,4,8,11-tetraazacyclotetradecane), we examine theoretically the possibility of H2 reduction by this molecule. We show that the process 2 Ni(i) + H2 --> 2 [Ni(ii)(H-)] is thermodynamically facile, and that H2 could be reduced by a binuclear Ni(i) complex in two concerted 1e- processes. Our calculations also indicate that hydride complexes of Ni(iii)(cyclam) are significantly unstable thermodynamically and therefore they are unlikely to serve as intermediates in process of H2 evolution from water.

摘要

受四氮大环镍(Ⅰ)(环胺)配合物(环胺 = 1,4,8,11 - 四氮杂环十四烷)催化二氧化碳电还原的启发,我们从理论上研究了该分子还原氢气的可能性。我们表明,2Ni(Ⅰ) + H₂ → 2[Ni(Ⅱ)(H⁻)] 这一过程在热力学上是容易发生的,并且氢气可以通过双核镍(Ⅰ)配合物以两个协同的单电子过程被还原。我们的计算还表明,镍(Ⅲ)(环胺)的氢化物配合物在热力学上非常不稳定,因此它们不太可能作为从水中析出氢气过程的中间体。

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