Structure and function revealed with submolecular resolution at the liquid-solid interface

被引:57
|
作者
Elemans, Johannes A. A. W.
De Feyter, Steven [1 ]
机构
[1] Katholieke Univ Leuven, Dept Chem, Div Mol & Nanomat, B-3001 Louvain, Belgium
关键词
SCANNING-TUNNELING-MICROSCOPY; ASSEMBLED SUPRAMOLECULAR RECTANGLE; 2-DIMENSIONAL MOLECULAR NETWORK; SOLVENT-INDUCED POLYMORPHISM; SELECTIVE GUEST INCLUSION; AU(111) SURFACES; SELF-ORGANIZATION; TRIMESIC ACID; GRAPHITE SURFACE; NEAT LIQUID;
D O I
10.1039/b811090e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The liquid-solid interface is a unique medium to support the self-assembly of molecules into surface-confined networks. Non-covalent interactions are key in forming these two-dimensional (2D) architectures, and a deep understanding is crucial for successful 2D crystal engineering. Scanning tunnelling microscopy is the tool of choice to reveal the structure and function of these patterns with subnanometre resolution. A recent success is the formation of 2D nanoporous molecular patterns and their host guest chemistry. However, this is not the only functionality addressed by this review. Surface-confined molecular architectures at the liquid solid interface are also relevant in the field of molecular electronics. Furthermore, inducing and probing chemical reactivity at the single-molecule level at the liquid solid interface might turn out to be one of the most exciting developments.
引用
收藏
页码:721 / 735
页数:15
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