化学
范德瓦尔斯力
二乙炔
扫描隧道显微镜
分子
分子间力
氢键
烷基
自组装
芳基
化学物理
结晶学
纳米技术
有机化学
聚合物
聚合
材料科学
作者
Zhongcheng Mu,Lijin Shu,Harald Fuchs,Marcel Mayor,Lifeng Chi
摘要
Self-assembly of the partially fluorinated rigid molecules physisorbed at solution/graphite interface has been investigated by scanning tunneling microscopy. Upon adsorption, both the branched star-shaped compound 1 and the angulate rod 2 compromising diacetylene and acetylene interlinked benzene and pentafluorobezene formed two-dimensional chiral porous networks. The spontaneous formation of these architectures is likely attributed to the two effects: the compensation of the dipole moments of the branches and the formation of Ar−H···F hydrogen bonds. These results demonstrate that the immobilization of molecules at the liquid/solid interface can be driven by these weak intermolecular interactions instead of van der Waals interactions between alkyl chains and substrate.
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