Chaur Manuel N, Melin Frederic, Elliott Bevan, Kumbhar Amar, Athans Andreas J, Echegoyen Luis
Chemistry Department, Clemson University, 219 Hunter Laboratories, Clemson, SC 29630-0973, USA.
Chemistry. 2008;14(15):4594-9. doi: 10.1002/chem.200800044.
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.
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。