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新型M(3)N@C(2n)内嵌金属富勒烯家族(M = Nd、Pr、Ce;n = 40 - 53):扩展C(88)笼的优先模板化并接近C(96)笼。

New M(3)N@C(2n) endohedral metallofullerene families (M=Nd, Pr, Ce; n=40-53): expanding the preferential templating of the C(88) cage and approaching the C(96) cage.

作者信息

Chaur Manuel N, Melin Frederic, Elliott Bevan, Kumbhar Amar, Athans Andreas J, Echegoyen Luis

机构信息

Chemistry Department, Clemson University, 219 Hunter Laboratories, Clemson, SC 29630-0973, USA.

出版信息

Chemistry. 2008;14(15):4594-9. doi: 10.1002/chem.200800044.

Abstract

Three new families of trimetallic nitride template endohedral metallofullerenes (TNT EMFs), based on cerium, praseodymium, and neodymium clusters, were synthesized by vaporizing packed graphite rods in a conventional Krätschmer-Huffman arc reactor. Each of these families of metallofullerenes was identified and characterized by mass spectroscopy, HPLC, UV/Vis-NIR spectroscopy, and cyclic voltammetry. The mass spectra and HPLC chromatograms show that these larger metallic clusters are preferentially encapsulated by a C(88) cage. When the size of the cluster is increased, the C(96) cage is progressively favored over the predominant C(88) cage. It is also observed that the smaller cages (C(80)-C(86)) almost disappear on going from neodymium to cerium endohedral metallofullerenes. The UV/Vis-NIR spectra and cyclic voltammograms confirm the low HOMO-LUMO gap and reversible electrochemistry of these M(3)N@C(88) metallofullerenes.

摘要

通过在传统的克拉斯奇默尔-霍夫曼电弧反应器中蒸发填充的石墨棒,合成了基于铈、镨和钕簇的三个三金属氮化物模板内嵌金属富勒烯(TNT EMF)新家族。这些金属富勒烯家族中的每一个都通过质谱、高效液相色谱、紫外/可见-近红外光谱和循环伏安法进行了鉴定和表征。质谱图和高效液相色谱图表明,这些较大的金属簇优先被C(88)笼包裹。当簇的尺寸增加时,C(96)笼逐渐比主要的C(88)笼更受青睐。还观察到,从钕内嵌金属富勒烯到铈内嵌金属富勒烯时,较小的笼(C(80)-C(86))几乎消失。紫外/可见-近红外光谱和循环伏安图证实了这些M(3)N@C(88)金属富勒烯的低最高占据分子轨道-最低未占据分子轨道能隙和可逆电化学性质。

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