扫描隧道显微镜
卤键
卤素
超分子化学
自组装
密度泛函理论
纳米技术
纳米结构
氢键
晶体工程
非共价相互作用
结晶学
分子
化学
取代基
分子间力
材料科学
化学物理
计算化学
晶体结构
有机化学
烷基
作者
Yi Wang,Xinrui Miao,Wenli Deng
出处
期刊:Crystals
[Multidisciplinary Digital Publishing Institute]
日期:2020-11-20
卷期号:10 (11): 1057-1057
被引量:18
标识
DOI:10.3390/cryst10111057
摘要
Halogen bonds are currently new noncovalent interactions due to their moderate strength and high directionality, which are widely investigated in crystal engineering. The study about supramolecular two-dimensional architectures on solid surfaces fabricated by halogen bonding has been performed recently. Scanning tunneling microscopy (STM) has the advantages of realizing in situ, real-time, and atomic-level characterization. Our group has carried out molecular self-assembly induced by halogen bonds at the liquid–solid interface for about ten years. In this review, we mainly describe the concept and history of halogen bonding and the progress in the self-assembly of halogen-based organic molecules at the liquid/graphite interface in our laboratory. Our focus is mainly on (1) the effect of position, number, and type of halogen substituent on the formation of nanostructures; (2) the competition and cooperation of the halogen bond and the hydrogen bond; (3) solution concentration and solvent effects on the molecular assembly; and (4) a deep understanding of the self-assembled mechanism by density functional theory (DFT) calculations.
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