Please use this identifier to cite or link to this item: https://doi.org/10.1021/la103921e
Title: Effect of intermolecular dipole-dipole interactions on interfacial supramolecular structures of C3-symmetric hexa-peri-hexabenzocoronene derivatives
Authors: Mu, Z.
Shao, Q.
Ye, J.
Zeng, Z.
Zhao, Y.
Hng, H.H.
Boey, F.Y.C.
Wu, J. 
Chen, X.
Issue Date: 15-Feb-2011
Citation: Mu, Z., Shao, Q., Ye, J., Zeng, Z., Zhao, Y., Hng, H.H., Boey, F.Y.C., Wu, J., Chen, X. (2011-02-15). Effect of intermolecular dipole-dipole interactions on interfacial supramolecular structures of C3-symmetric hexa-peri-hexabenzocoronene derivatives. Langmuir 27 (4) : 1314-1318. ScholarBank@NUS Repository. https://doi.org/10.1021/la103921e
Abstract: Two-dimensional (2D) supramolecular assemblies of a series of novel C 3-symmetric hexa-peri-hexabenzocoronene (HBC) derivatives bearing different substituents adsorbed on highly oriented pyrolytic graphite were studied by using scanning tunneling microscopy at a solid-liquid interface. It was found that the intermolecular dipole-dipole interactions play a critical role in controlling the interfacial supramolecular assembly of these C 3-symmetric HBC derivatives at the solid-liquid interface. The HBC molecule bearing three-CF3 groups could form 2D honeycomb structures because of antiparallel dipole-dipole interactions, whereas HBC molecules bearing three-CN or-NO2 groups could form hexagonal superstructures because of a special trimeric arrangement induced by dipole-dipole interactions and weak hydrogen bonding interactions ([C-H· ·· NC-] or [C-H···O2N-]). Molecular mechanics and dynamics simulations were performed to reveal the physics behind the 2D structures as well as detailed functional group interactions. This work provides an example of how intermolecular dipole-dipole interactions could enable fine control over the self-assembly of disklike π-conjugated molecules. © 2010 American Chemical Society.
Source Title: Langmuir
URI: http://scholarbank.nus.edu.sg/handle/10635/93649
ISSN: 07437463
DOI: 10.1021/la103921e
Appears in Collections:Staff Publications

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