Influence of Multidirectional Interactions on Domain Size and Shape of 2-D Molecular Assemblies

被引:7
|
作者
Nishitani, Nobuhiko [1 ]
Hirose, Takashi [1 ]
Matsuda, Kenji [1 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Synthet Chem & Biol Chem, Nishikyo Ku, Kyoto 6158510, Japan
关键词
SOLID-LIQUID INTERFACE; SCANNING-TUNNELING-MICROSCOPY; HYDROGEN-BONDS; SUPRAMOLECULAR POLYMERIZATION; DIPOLE-DIPOLE; THIN-FILM; SURFACES; NANOSTRUCTURES; CHEMISTRY; SYSTEMS;
D O I
10.1021/acs.langmuir.7b02094
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The effect of molecule-molecule interactions on the size and shape of two-dimensional (2-D) ordering domains was investigated using scanning tunneling microscopy (STM) at the liquid/solid interface. Synthesized alkoxybenzene derivatives bearing amide group tend to form very large domains of 2-D orderings (>0.25 mu m(2)), whereas the domain size of corresponding urea derivatives was significantly small in the same condition. The quantitative analysis of the concentration dependence of surface coverage using a nucleation-elongation model suggests that the replacement of amide functionality by urea increased the equilibrium constant of the nucleation process of 2-D self-assembly, which is a key factor for the domain size at the liquid/solid interface. Interestingly, the STM observation revealed that a slight difference of molecular structure influences the shape of 2-D ordering domains, and needle-shaped domains with large aspect ratio around 10 were observed by tuning molecule-molecule intramolecular interactions in 2-D self-assembly formed at a liquid/graphite interface.
引用
收藏
页码:9151 / 9159
页数:9
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