Synthesis of Endohedral 133Xe-Fullerenol by Using Higher Fullerene

Sou Watanabe, T. Katabuchi, N. Ishioka, S. Matsuhashi
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Abstract

2.1. Production of endohedral higher 133Xe-fullerenes. The endohedral higher 133Xe-fullerenes (133Xe@C76 and 133Xe@C8 4) were synthesized in a manner as described in detail in our previous paper. Fullerene targets for ion implantation were prepared by vacuum evaporation of fullerenes (C76 or C84) on Ni foil. Xenon-133 ions were implanted into the targets with an isotope separator (Takasaki Institute, JAEA) at an acceleration energy of 30 keV. After the ion implantation, the fullerenes on the target foil were dissolved in o-dichlorobenzene. The solution was filtered through a membrane filter of 0.2 ƒÊm in pore size (Millipore, JGWP) to remove insoluble materials. The filtrate was purified by HPLC with a Cosmosil Buckyprep Figure 1. A Schematic diagram of a synthetic procedure for 133 Xe@C76(OH)x. The same proedure was also used for 133Xe@C60 (OH)x, 133Xe@C70(OH)x, and133Xe@C84,(OH)x.
用高级富勒烯合成内嵌133xe -富勒烯醇
2.1. 内生高133xe -富勒烯的产生。内嵌高133xe -富勒烯(133Xe@C76和133Xe@C8 4)的合成方法在我们之前的文章中有详细的描述。采用真空蒸发法制备了富勒烯(C76或C84)在镍箔上的离子注入靶。利用同位素分离器(日本高崎研究所)将氙-133离子以30 keV的加速能量注入靶中。离子注入后,靶箔上的富勒烯溶解在邻二氯苯中。溶液通过0.2 ƒÊm孔径的膜过滤器(Millipore, JGWP)过滤,去除不溶性物质。滤液采用Cosmosil Buckyprep高效液相色谱纯化(图1)。133 Xe@C76(OH)x的合成过程示意图。同样的方法也用于133Xe@C60 (OH)x, 133Xe@C70(OH)x, and133Xe@C84,(OH)x。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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