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.
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http://dx.doi.org/10.1021/acs.jpca.0c01228 | DOI Listing |
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