Effect of Intermolecular Dipole-Dipole Interactions on Interfacial Supramolecular Structures of C3-Symmetric Hexa-peri-hexabenzocoronene Derivatives

被引:28
作者
Mu, Zhongcheng [2 ]
Shao, Qi [3 ]
Ye, Jun [3 ]
Zeng, Zebing [1 ]
Zhao, Yang [3 ]
Hng, Huey Hoon [3 ]
Boey, Freddy Yin Chiang [3 ]
Wu, Jishan [1 ]
Chen, Xiaodong [3 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] NE Normal Univ, Fac Chem, Changchun 130024, Jilin, Peoples R China
[3] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
关键词
SCANNING-TUNNELING-MICROSCOPY; SOLVENT-INDUCED POLYMORPHISM; NETWORKS; ELECTRONICS; SURFACES; NANOGRAPHENES; SUBSTITUENTS; ORGANIZATION; MOLECULES; ACID;
D O I
10.1021/la103921e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 center dot center dot center dot NC-] or [C-H center dot center dot center dot 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 disldike pi-conjugated molecules.
引用
收藏
页码:1314 / 1318
页数:5
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