Institute for Chemical Research , Kyoto University , Kyoto , 611-0011 , Japan.
Org Lett. 2018 Sep 21;20(18):5973-5976. doi: 10.1021/acs.orglett.8b02715. Epub 2018 Sep 13.
Fluorinated [6]- and [9]cycloparaphenylene (CPP) derivatives, 8F-[6]CPP and 12F-[9]CPP, were synthesized based on the previous synthesis of the parent CPPs. While the reductive aromatization conditions used in the final step of the synthesis of the parent CPPs did not work for the fluorinated compounds, the use of PBr and SnCl in acetonitrile successfully accomplished the desired transformation. The structures of F-CPPs were determined by single-crystal X-ray analysis. Photo- and electrochemical analyses and host-guest chemistry revealed the effects of the introduction of fluorine atoms.
基于之前对母体 CPP 的合成,我们合成了氟化[6]-和[9]环并对苯撑(CPP)衍生物 8F-[6]CPP 和 12F-[9]CPP。虽然母体 CPP 合成的最后一步中使用的还原芳构化条件不适用于氟化化合物,但在乙腈中使用 PBr 和 SnCl 成功地完成了所需的转化。F-CPP 的结构通过单晶 X 射线分析确定。光化学和电化学分析以及主客体化学揭示了引入氟原子的影响。