Grochala Wojciech
Interdisciplinary Center for Mathematical and Computational Modeling, University of Warsaw, Pawińskiego 5a, 02106 Warsaw, Poland.
Phys Chem Chem Phys. 2006 Mar 21;8(11):1340-5. doi: 10.1039/b516113d. Epub 2006 Feb 9.
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.
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。