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过渡金属的驮运:外核金属富勒烯在碳纳米管中的封装。

A piggyback ride for transition metals: encapsulation of exohedral metallofullerenes in carbon nanotubes.

机构信息

School of Chemistry, University of Nottingham, Nottingham, NG7 2RD, UK.

出版信息

Chemistry. 2011 Jan 10;17(2):668-74. doi: 10.1002/chem.201001288. Epub 2010 Nov 9.

Abstract

We have developed a method that enables the efficient insertion of transition-metal atoms and their small clusters into carbon nanotubes. As a model system, Os complexes attached to the exterior of fullerene C60 (exohedral metallofullerenes) were shown to be dragged into the nanotube spontaneously and irreversibly due to strong van der Waals interactions, specific to fullerenes and carbon nanotubes. The size of the metal-containing groups attached to C60 was shown to be critical for successful insertion, as functional groups too bulky to enter the nanotube were stripped off the fullerene during the encapsulation process. Once inside the nanotube, Os atoms catalyse polymerisation and decomposition of fullerene cages, which is related to a much higher catalytic activity of metal atoms situated on the surface of the fullerene cage, as compared to metal atoms in endohedral fullerenes, such as M@C82. Thus, exohedral metallofullerenes show promise for applications in catalysis in carbon “nano” test tubes.

摘要

我们开发了一种方法,能够有效地将过渡金属原子及其小团簇插入碳纳米管中。作为模型体系,附着在富勒烯 C60 外部的 Os 配合物(外配位金属富勒烯)由于与富勒烯和碳纳米管具有特异性的强范德华相互作用,而被自发且不可逆地拖入纳米管中。附着在 C60 上的含金属基团的大小对于成功插入至关重要,因为太大而无法进入纳米管的官能团在封装过程中会从富勒烯上剥离。一旦进入纳米管,Os 原子就会催化富勒烯笼的聚合和分解,这与位于富勒烯笼表面的金属原子的催化活性相比,要高得多,而位于金属原子位于内配位金属富勒烯(如 M@C82)中的金属原子则要低得多。因此,外配位金属富勒烯有望在碳“纳米”试管中的催化应用中得到应用。

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