Two I(h)-symmetry-breaking C60 isomers stabilized by chlorination.
Two I(h)-symmetry-breaking C60 isomers stabilized by chlorination.
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DOI:
10.1038/nmat2275
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发表时间:
2008
期刊:
影响因子:
41.2
通讯作者:
Yuanzhi Tan;Zhao-Jiang Liao;Zhuo-Zhen Qian;Rui-ting Chen;Xin Wu;Hua Liang;Xiao Han;Feng Zhu
中科院分区:
文献类型:
--
作者:
Yuanzhi Tan;Zhao-Jiang Liao;Zhuo-Zhen Qian;Rui-ting Chen;Xin Wu;Hua Liang;Xiao Han;Feng Zhu
One abiding surprise in fullerene science is thatIh-symmetric buckminsterfullerene C60(ref. ) (Ih–C60or#1,812C60, the nomenclature specified by symmetry or by Fowler’s spiral algorithm) remains the sole C60species experimentally available. Setting it apart from the other 1,811 topological isomers (isobuckminsterfullerenes) is its exclusive conformity with the isolated-pentagon rule, which states that stable fullerenes have isolated pentagons. Although gas-phase existence of isobuckminsterfullerenes has long been suspected,,,, synthetic efforts have yet to yield successful results. Here, we report the realization of two isobuckminsterfullerenes by means of chlorination of the respectiveC2v- andCs-symmetric C60cages. These chlorinated species,#1,809C60Cl8(1) and#1,804C60Cl12(2), were isolated in experimentally useful yields. Structural characterization by crystallography unambiguously established the unique pentagon–pentagon ring fusions. These distinct structural features are directly responsible for the regioselectivity observed in subsequent substitution of chlorines, and also render these unprecedented derivatives of C60isomers important for resolving the long-standing puzzle of fullerene formation by the Stone–Wales transformation scheme,,,.