Surface-assisted coordination chemistry and self-assembly

被引:58
作者
Lin, Nian
Stepanow, Sebastian
Vidal, Franck
Kern, Klaus
Alam, Mohammad S.
Stroemsdoerfer, Stefan
Dremov, Viacheslav
Mueller, Paul
Landa, Aitor
Ruben, Mario
机构
[1] Max Planck Inst Festkorperforsch, D-70569 Stuttgart, Germany
[2] Ecole Polytech Fed Lausanne, Inst Phys Nanostruct, CH-1015 Lausanne, Switzerland
[3] Univ Erlangen Nurnberg, Inst Phys 3, D-91058 Erlangen, Germany
[4] Forschungszentrum Karlsruhe, Inst Nanotechnol, D-76021 Karlsruhe, Germany
关键词
D O I
10.1039/b515728e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This article discusses different approaches to build up supramolecular nanoarchitectures on surfaces, which were simultaneously investigated by scanning tunneling microscopy (STM) on the single-molecule level. Following this general road map, first, the hydrogen-bonding guided self-assembly of two different, structural-equivalent molecular building blocks, azobenzene dicarboxylic acid and stilbene dicarboxylic acid, was studied. Secondly, the coordination chemistry of the same building blocks, now acting as ligands in metal coordination reactions, towards co-sublimed Fe atoms was studied under near surface-conditions. Extended two-dimensional tetragonal network formation with unusual Fe2L4/2-dimers at the crossing points was observed on copper surfaces. Complementary to the first two experiments, a two-step approach based on the solution-based self-assembly of square-like tetranuclear complexes of the M4L4-type with subsequent deposition on graphite surfaces was investigated. One-and two-dimensional arrangements as well as single molecules of the M4L4-complexes could be observed. Moreover, the local electronic properties of a single M4L4-complexes could be probed with submolecular resolution by means of scanning tunnelling spectroscopy (STS).
引用
收藏
页码:2794 / 2800
页数:7
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