Towards Supramolecular Engineering of Functional Nanomaterials: Pre-Programming Multi-Component 2D Self-Assembly at Solid-Liquid Interfaces

被引:265
作者
Ciesielski, Artur [1 ,2 ]
Palma, Carlos-Andres [1 ,2 ]
Bonini, Massimo [3 ]
Samori, Paolo [1 ,2 ]
机构
[1] Univ Strasbourg, Nanochem Lab, ISIS, F-67000 Strasbourg, France
[2] CNRS, UMR 7006, F-67000 Strasbourg, France
[3] BASF SE, D-67056 Ludwigshafen, Germany
关键词
SCANNING-TUNNELING-MICROSCOPY; HEXA-PERI-HEXABENZOCORONENE; ORIENTED PYROLYTIC-GRAPHITE; HYDROGEN-BONDED COMPLEXES; 1D COORDINATION NETWORKS; AB-INITIO HF; MOLECULAR RECOGNITION; SUBMOLECULAR RESOLUTION; ORDERED ARCHITECTURES; THIOPHENE DERIVATIVES;
D O I
10.1002/adma.201001582
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Materials with a preprogrammed order at the supramolecular level can be engineered with a sub-nanometer precision making use of reversible non-covalent interactions. The intrinsic ability of supramolecular materials to recognize and exchange their constituents makes them constitutionally dynamic materials. The tailoring of the materials properties relies on the full control over the self-assembly behavior of molecular modules exposing recognition sites and incorporating functional units. In this review we focus on three classes of weak-interactions to form complex 2D architectures starting from properly designed molecular modules: van der Waals, metallo-ligand and hydrogen bonding. Scanning tunneling microscopy studies will provide evidence with a sub-nanometer resolution, on the formation of responsive multicomponent architectures with controlled geometries and properties. Such endeavor enriches the scientist capability of generating more and more complex smart materials featuring controlled functions and unprecedented properties.
引用
收藏
页码:3506 / 3520
页数:15
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