Ioffe Ilya N, Yang Shangfeng, Wang Song, Kemnitz Erhard, Sidorov Lev N, Troyanov Sergey I
Department of Chemistry, Moscow State University, Leninskie gory, 119991 Moscow (Russia).
Chemistry. 2015 Mar 23;21(13):4904-7. doi: 10.1002/chem.201406487. Epub 2015 Feb 12.
Chlorination of the C100 (18) fullerene with a mixture of VCl4 and SbCl5 gives rise to branched skeletal transformations affording non-classical (NC) C94 (NC1)Cl22 with one heptagon in the carbon cage together with the previously reported C96 (NC3)Cl20 with three heptagons. The three-step pathway to C94 (NC1)Cl22 starts with two successive C2 losses of 5:6 CC bonds to give two cage heptagons, whereas the third C2 loss of the 5:5 CC bond from a pentalene fragment eliminates one of the heptagons. Quantum-chemical calculations demonstrate that the two unusual skeletal transformations-creation of a heptagon in C96 (NC3)Cl20 through a Stone-Wales rearrangement and the presently reported elimination of a heptagon through C2 loss-are both characterized by relatively low activation energy.
用VCl₄和SbCl₅的混合物对C100(18)富勒烯进行氯化,会引发支链骨架转变,生成碳笼中有一个七边形的非经典(NC)C94(NC1)Cl22,以及先前报道的有三个七边形的C96(NC3)Cl20。生成C94(NC1)Cl22的三步途径始于5:6 CC键连续两次失去C₂,形成两个笼状七边形,而来自并五苯片段的5:5 CC键的第三次C₂损失消除了其中一个七边形。量子化学计算表明,两个不寻常的骨架转变——通过斯通-威尔士重排在C96(NC3)Cl20中形成一个七边形,以及目前报道的通过失去C₂消除一个七边形——都具有相对较低的活化能。