Institute for Chemical Research, Kyoto University , Uji 611-0011, Japan.
J Am Chem Soc. 2014 Feb 12;136(6):2284-7. doi: 10.1021/ja413214q. Epub 2014 Jan 30.
The synthesis of highly strained [5]cycloparaphenylene ([5]CPP), a structural unit of the periphery of C60 and the shortest possible structural constituent of the sidewall of a (5,5) carbon nanotube, was achieved in nine steps in 17% overall yield. The synthesis relied on metal-mediated ring closure of a triethylsilyl (TES)-protected masked precursor 1c followed by removal of the TES groups and subsequent reductive aromatization. UV-vis and electrochemical studies revealed that the HOMO-LUMO gap of [5]CPP is narrow and is comparable to that of C60, as predicted by theoretical calculations. The results suggest that [5]CPP should be an excellent lead compound for molecular electronics.
高度应变的[5]环对苯撑([5]CPP)的合成,C60 外围的结构单元和(5,5)碳纳米管侧壁的最短可能结构组成部分,以 17%的总收率通过九步反应实现。该合成依赖于三乙基硅基(TES)保护的掩蔽前体 1c 的金属介导环闭合,然后去除 TES 基团并随后进行还原芳构化。UV-vis 和电化学研究表明,[5]CPP 的 HOMO-LUMO 能隙较窄,与理论计算预测的 C60 相当。这些结果表明[5]CPP 应该是分子电子学的一个极好的先导化合物。