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富勒烯笼内超级原子的发现。

Discovery of a Superatom inside the Fullerene Cage.

作者信息

Hao Debo, Yang Le, Li Bo, Hou Qinghua, Li Lanlan, Jin Peng

机构信息

School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130, P. R. China.

出版信息

J Phys Chem A. 2020 Apr 2;124(13):2694-2699. doi: 10.1021/acs.jpca.0c01228. Epub 2020 Mar 24.

Abstract

The stability of endohedral clusterfullerenes is generally understood in terms of the metal cluster shape, cage structure, and metal-cage interactions, with the electronic state of the internal cluster mostly neglected. Herein, theoretical calculations reveal that the (TiC) unit of recently synthesized TiC@(7)-C exhibits a superatomic state with a perfect closed-shell 1S1P1D electronic configuration in accordance with the famous jellium model. This "trapped superatom" features considerable aromaticity and hyperconjugation interactions never reported for other clusterfullerenes. Besides the localized two-center two-electron (2c-2e) Ti-C/C-C bonds, it also has two 3c-2e Ti-C-Ti bonds. Furthermore, the ring strain of the cyclopropane-like C core is effectively released upon the metal coordination. All these factors greatly stabilize the (TiC) cluster, showing the critical role of metal-to-cage charge transfer and cage encapsulation in enhancing the stability of this exotic metal cluster.

摘要

内嵌富勒烯的稳定性通常根据金属簇形状、笼状结构和金属-笼相互作用来理解,而内部簇的电子态大多被忽略。在此,理论计算表明,最近合成的TiC@(7)-C的(TiC)单元呈现出一种超原子态,根据著名的电子气模型,其具有完美的闭壳层1S1P1D电子构型。这种“捕获的超原子”具有相当大的芳香性和超共轭相互作用,这是其他簇富勒烯从未报道过的。除了局域化的双中心双电子(2c-2e) Ti-C/C-C键外,它还具有两个3c-2e Ti-C-Ti键。此外,类环丙烷C核的环张力在金属配位时有效地释放。所有这些因素极大地稳定了(TiC)簇,表明金属到笼的电荷转移和笼包封在增强这种奇异金属簇稳定性方面的关键作用。

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