Solvent controlled self-assembly at the liquid-solid interface revealed by STM

被引:201
|
作者
Mamdouh, W
Uji-i, H
Ladislaw, JS
Dulcey, AE
Percec, V
De Schryver, FC
De Feyter, S
机构
[1] Katholieke Univ Leuven, Dept Chem, Div Mol & Nanomat, Lab Photochem & Spect, B-3001 Louvain, Belgium
[2] Univ Penn, Dept Chem, Roy & Diana Vageols Labs, Philadelphia, PA 19104 USA
关键词
D O I
10.1021/ja056175w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The effect of solvent on the two-dimensional (2D) supramolecular ordering of monodendron 1 at the liquid-solid interface has been systematically investigated by means of scanning tunneling microscopy (STM). Solvents range from those with hydrophilic solvating properties, such as alkylated alcohols and acids, to hydrophobic solvents such as alkylated aromatics and alkanes. Dramatic differences in the 2D ordering are observed depending on the nature of the solvent. Of particular interest is the fact that in hydrophobic solvating solvents, such as aliphatic and aromatic hydrocarbons, solvent molecules are coadsorbed in the 2D molecular network while this is not the case for alkylated alcohols or acids. Furthermore, in the case of the coadsorbing solvents, a striking influence of the alkyl chain length has been observed on the 2D pattern formed. The solvent and alkyl chain length dependences are discussed in terms of molecule-molecule interactions (homo and hetero) and molecule-substrate interactions.
引用
收藏
页码:317 / 325
页数:9
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