Pentagon, Hexagon, or Bridge? Identifying the Location of a Single Vanadium Cation on Buckminsterfullerene Surface

Jianzhi Xu, Joost M. Bakker, Olga V. Lushchikova, Peter Lievens, Ewald Janssens, Gao-Lei Hou
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Abstract

Buckminsterfullerene C60 has received extensive research interest ever since its discovery. In addition to its interesting intrinsic properties of exceptional stability and electron-accepting ability, the broad chemical tunability by decoration or substitution on the C60-fullerene surface makes it a fascinating molecule. However, to date there is uncertainty about the binding location of such decorations on the C60 surface, even for a single adsorbed metal atom. In this work, we report the gas-phase synthesis of the C60V+ complex and its in-situ characterization by mass spectrometry and in-frared spectroscopy with the help of quantum chemical calculations and molecular dynamics simulations. We identify the most probable binding position of a vanadium cation on C60 above a pentagon center in eta5-fashion, demonstrate a high thermal stability for this complex, and explore the bonding nature between C60 and the vanadium cation, reveal-ing that large orbital and electrostatic interactions lie at the origin of the stability of the eta5-C60V+ complex.
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五边形,六边形,还是桥?确定单个钒离子在巴克敏斯特富勒烯表面的位置
巴克敏斯特富勒烯C60自从被发现以来就受到了广泛的研究兴趣。除了其独特的稳定性和电子接受能力等有趣的内在特性外,c60 -富勒烯表面通过修饰或取代的广泛化学可调性使其成为一种迷人的分子。然而,到目前为止,这种修饰在C60表面的结合位置还不确定,即使是单个吸附的金属原子。在这项工作中,我们报道了C60V+配合物的气相合成及其在量子化学计算和分子动力学模拟的帮助下,通过质谱和红外光谱的原位表征。我们确定了C60上最可能的钒离子以eta5方式在五边形中心上方的结合位置,证明了该配合物具有较高的热稳定性,并探索了enc60与钒离子之间的键合性质,揭示了eta5-C60V+配合物稳定性的根源在于大的轨道和静电相互作用。
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