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Structure and structural transition of chiral domains in oligo(p-phenylenevinylene) assembly investigated by scanning tunneling microscopy
Author(s) -
Qing Chen,
Ting Chen,
Dong Wang,
Hui-Biao Liu,
Yuliang Li,
LiJun Wan
Publication year - 2010
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1000120107
Subject(s) - scanning tunneling microscope , crystallography , molecule , highly oriented pyrolytic graphite , chirality (physics) , materials science , intermolecular force , self assembly , chemistry , nanotechnology , organic chemistry , chiral symmetry breaking , physics , quantum mechanics , quark , nambu–jona lasinio model
OPV3-CHO molecules are employed to prepare assembly on highly oriented pyrolytic graphite, and the so-prepared assembly is investigated by scanning tunneling microscopy. In the assembly chiral domains are observed with various structures such as linear and windmill. The chiral structural formation, stability, transition, and possible unification are intensively studied. After thermal annealing, linear structure was the only structure. To achieve a unified assembly with a single structure, an efficient method is proposed by coadsorption of OPV3-CHO with selected molecules. For example, an assembly with side-by-side helix structure is formed by a simple coadsorption of OPV3-CHO with alkyl bromide (C(n)H(2n+1)Br, n = 15-18). The experiments by cocrystallization of OPV3-CHO/C(n)H(2n+1)X (X = Cl, Br, and I) show the important role of halogen bonding in formation of the uniform structure. The results are significant in understanding the intermolecular noncovalent interactions that dominate the surface structure and chirality.

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