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一系列带有全氟棱纹取代基的新型钴和铁包合螯合物。

A New Series of Cobalt and Iron Clathrochelates with Perfluorinated Ribbed Substituents.

作者信息

Zelinskii Genrikh E, Pavlov Alexander A, Belov Alexander S, Belaya Irina G, Vologzhanina Anna V, Nelyubina Yulia V, Efimov Nikolay N, Zubavichus Yan V, Bubnov Yurii N, Novikov Valentin V, Voloshin Yan Z

机构信息

Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences, 119991 Moscow, Russia.

Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences, 119991 Moscow, Russia.

出版信息

ACS Omega. 2017 Oct 18;2(10):6852-6862. doi: 10.1021/acsomega.7b01088. eCollection 2017 Oct 31.

Abstract

The study tackles one of the challenges in developing platinum-free molecular electrocatalysts for hydrogen evolution, which is to seek for new possibilities to ensure large turnover numbers by stabilizing electrocatalytic intermediates. These species are often much more reactive than the initial electrocatalysts, and if not properly stabilized by a suitable choice of functionalizing substituents, they have a limited long-time activity. Here, we describe new iron and cobalt(II) cage complexes (clathrochelates) that in contrast to many previously reported complexes of this type do not act as electrocatalysts for hydrogen evolution. We argue that the most probable reason for this behavior is an excessive stabilization of the metal(I) species by perfluoroaryl ribbed groups, resulting in an unprecedented long-term stability of the metal(I) complexes even in acidic solutions.

摘要

该研究解决了开发用于析氢的无铂分子电催化剂的挑战之一,即通过稳定电催化中间体来寻找确保高周转数的新可能性。这些物种通常比初始电催化剂的反应活性高得多,如果没有通过合适的官能化取代基的选择进行适当的稳定,它们的长期活性就会受到限制。在这里,我们描述了新的铁和钴(II)笼状配合物(包合螯合物),与许多先前报道的此类配合物不同,它们不作为析氢的电催化剂。我们认为这种行为最可能的原因是全氟芳基肋状基团对金属(I)物种的过度稳定,导致金属(I)配合物即使在酸性溶液中也具有前所未有的长期稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f629/6645064/54fbf7115488/ao-2017-01088c_0010.jpg

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