STM studies on double- and triple-decker porphyrin and phthalocyanine complexes

被引:11
作者
Otsuki, Joe [1 ]
机构
[1] Nihon Univ, Coll Sci & Technol, Chiyoda Ku, Tokyo 1018308, Japan
关键词
double-decker complexes; molecular devices; phthalocyanines; porphyrins; scanning tunnelling microscopy; SCANNING-TUNNELING-MICROSCOPY; LIQUID-SOLID INTERFACE; SUPRAMOLECULAR ASSEMBLIES; ROTATIONAL OSCILLATION; MOLECULAR ASSEMBLIES; SANDWICH COMPLEXES; CU(111) SURFACES; METAL-COMPLEXES; OXIDIZED FORMS; RECOGNITION;
D O I
10.1080/10610278.2010.515028
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Properly designed double- and triple-decker porphyrin and/or phthalocyanine complexes assemble themselves into ordered higher-order structures on substrate surfaces. One of the macrocyclic ligands adsorbs on the surface almost always in a face-on fashion on highly oriented pyrolytic graphite and Au(111) surfaces as revealed by means of scanning tunnelling microscopy. For example, well-ordered oriented monolayer assemblies of single-molecule magnets were fabricated. In some cases, the vertical orientation, that is, which ligand adsorbs on the surface, can be controlled by applied potentials. The rotational libration of the top ligand with respect to the adsorbed bottom ligand and hence to the surface has been visualised for a double-decker porphyrin with a molecular beacon. The electronic, magnetic and dynamic properties of double- and triple-decker complexes bode well for the development of molecular devices.
引用
收藏
页码:169 / 182
页数:14
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