期刊
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 14, 期 11, 页码 2862-2868出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.3c00445
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This work presents a series of endohedral metallofullerene superatoms [Mg@ C20]n, with n = 4, 2, 0, -2, and -4. The study reveals that Mg donates most of its 3s electrons to the C20 shell, resulting in the ionic states of Mg2+@[C20]n-2. Calculations show that the superatomic electronic configuration of these clusters is 1S21P61D101F4-n. The interaction between Mg2+ ion and [C20]n-2 is predominantly ionic in nature. Ultraviolet-visible spectra offer a theoretical basis for identifying these clusters. This research aims to promote the synthesis of these smallest superatomic systems.
This work reports a series of endohedral metallofullerene superatoms [Mg@ C20]n, where n = 4, 2, 0, -2, and -4. It was found that Mg transfers virtually all of its 3s electrons to the C20 shell, resulting in the ionic states of Mg2+@[C20]n-2. Detailed calculations revealed that the superatomic electronic configuration of these clusters is 1S21P61D101F4-n. The first nine superatomic molecular orbitals (SAMOs), 1S21P61D10, housed with 18 electrons, are largely based on [C20]n-2 with small contributions from magnesium, while the outmost SAMOs, 1F4-n, with 4 - n extra electrons, reside solely on [C20]n-2. The interaction between the Mg2+ ion and [C20]n-2 was found to be predominately ionic in character. Furthermore, ultraviolet-visible spectra provide a theoretical basis for fingerprinting these clusters. It is hoped that this work will encourage the synthetic pursuit of these smallest superatomic systems.
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