Self-templating 2D supramolecular networks: a new avenue to reach control over a bilayer formation

被引:46
作者
Ciesielski, Artur [1 ]
Cadeddu, Andrea [1 ]
Palma, Carlos-Andres [1 ]
Gorczynski, Adam [1 ,2 ]
Patroniak, Violetta [2 ]
Cecchini, Marco [1 ]
Samori, Paolo [1 ]
机构
[1] Univ Strasbourg, Nanochem Lab, ISIS UMR CNRS 7006, F-67000 Strasbourg, France
[2] Adam Mickiewicz Univ, Fac Chem, PL-60780 Poznan, Poland
关键词
LIQUID-SOLID INTERFACE; SCANNING-TUNNELING-MICROSCOPY; MOLECULAR CRYSTALLIZATION; BONDED ASSEMBLIES; TRIMESIC ACID; SURFACE; SYSTEMS; ORGANIZATION; POLYMORPHISM; AGGREGATION;
D O I
10.1039/c1nr10485c
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
One of the greatest challenges in 2D self-assembly at interfaces is the ability to grow spatially controlled supramolecular motifs in the third dimension, exploiting the surface as a template. In this manuscript a concentration-dependent study by scanning tunneling microscopy at the solid-liquid interface, corroborated by Molecular Dynamics (MD) simulations, reveals the controlled generation of mono- or bilayer self-assembled Kagome networks based on a fully planar tetracarboxylic acid derivative. By programming the backbone of the molecular building blocks, we present a strategy to gain spatial control over the adlayer structure by conferring self-templating capacity to the 2D self-assembled network.
引用
收藏
页码:4125 / 4129
页数:5
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