4.6 Article

Solvent-Controlled 2D Host-Guest (2,7,12-Trihexyloxytruxene/Coronene) Molecular Nanostructures at Organic Liquid/Solid Interface Investigated by Scanning Tunneling Microscopy

Journal

LANGMUIR
Volume 26, Issue 11, Pages 8195-8200

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la904568q

Keywords

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Funding

  1. National Natural Science Foundation of China [20821003, 20733004, 20821120291, 20905069]
  2. National Key Project on Basic Research [2006CB806100, 2006CBON0100]
  3. Chinese Academy of Sciences

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The two-dimensional (2D) self-assembled networks of 2,7,12-trihexyloxytruxene (Tr) are shown to accommodate coronene guest molecules on highly oriented pyrolytic graphite (HOPG) surfaces. The host-guest structures are revealed by scanning tunneling microscopy (STM) at liquid/solid interfaces. The effect of solvents on the host-guest structures is intensively investigated in different solvents such as 1,2,4-trichlorobenzene (TCB), 1-phenyloctane, 1-octanol, and tetradecane. In contrast to the similar 2D hexagonal self-assembly of Tr host template on HOPG in different solvents, the formation of host-guest nanostructures of coronene in Tr 2D network strongly depend on the polarity of the solvents. The thermodynamic equilibrium during the host-guest assembly process is discussed, and the solvent guest interaction is proposed as a main contributor for the observed solvent effect in the 2D host-guest self-assembly process. The results are significant to surface host-guest chemistry and nanopatterning.

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