期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 21, 期 4, 页码 1652-1659出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201405305
关键词
host-guest systems; macrocycles; scanning probe microscopy; self-assembly; surface analysis
资金
- China Scholarship Council
- Marie Curie European
- Fund of Scientific Research-Flanders (FWO) for postdoctoral fellowship
- Belgian Federal Science Policy Office via the IAP-PAI network Functional Supramolecular Systems [IAP 7/05]
- KU Leuven [GOA 11/003]
- FWO
- advanced ERC grant Oxide Surfaces
- Ministry of Education, Culture, Sports, Science, and Technology, Japan
- European Research Council under the European Union [340324]
Multicomponent network formation by using a shape-persistent macrocycle (MC6) at the interface between an organic liquid and Au(111) surface is demonstrated. MC6 serves as a versatile building block that can be co-adsorbed with a variety of organic molecules based on different types of noncovalent interactions at the liquid-solid interface. Scanning tunneling microscopy (STM) reveals the formation of crystalline bicomponent networks upon code-position of MC6 with aromatic molecules, such as fullerene (C-60) and coronene. Tetracyanoquinodimethane, on the other hand, was found to induce disorder into the MC6 networks by adsorbing on the rim of the macrocycle. Immobilization of MC6 itself was studied in two different noncovalently assembled host networks. MC6 assumed a rather passive role as a guest and simply occupied the host cavities in one network, whereas it induced a structural transition in the other. Finally, the central cavity of MC6 was used to capture C-60 in a complex three-component system. Precise immobilization of organic molecules at discrete locations within multicomponent networks, as demonstrated here, constitutes an important step towards bottom-up fabrication of functional surface-based nanostructures.
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