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Multicomponent Self‐Assembly with a Shape‐Persistent N‐Heterotriangulene Macrocycle on Au(111)
Authors:Kang Cui  Dr Florian Schlütter  Dr Oleksandr Ivasenko  Dr Milan Kivala  Dr Matthias G Schwab  Dr Shern‐Long Lee  Dr Stijn F L Mertens  Dr Kazukuni Tahara  Prof Yoshito Tobe  Prof Klaus Müllen  Dr Kunal S Mali  Prof Steven De?Feyter
Affiliation:1. Division of Molecular Imaging and Photonics, Department of Chemistry, KU Leuven‐University of Leuven, Celestijnenlaan 200F, 3001 Leuven (Belgium);2. Max Planck Institute for Polymer Research, 55128 Mainz (Germany);3. Present address: BASF SE, Carl‐Bosch‐Strasse 38, 67056 Ludwigshafen (Germany);4. Present address: Vienna University of Technology, Institute of Applied Physics, 1040 Vienna (Austria);5. Division of Frontier Materials Science, Graduate School of Engineering Science, Osaka University Toyonaka, Osaka 560‐8531 (Japan)
Abstract: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 coadsorbed 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 codeposition of MC6 with aromatic molecules, such as fullerene (C60) 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 C60 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.
Keywords:host–  guest systems  macrocycles  scanning probe microscopy  self‐assembly  surface analysis
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