Molecular dynamics simulation of the mesophase behaviour of a model bolaamphiphilic liquid crystal with a lateral flexible chain

被引:64
作者
Crane, Andrew J. [1 ]
Martinez-Veracoechea, Francisco J. [1 ,2 ]
Escobedo, Fernando A. [2 ]
Mueller, Erich A. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, England
[2] Cornell Univ, Dept Chem & Biomol Engn, Ithaca, NY USA
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1039/b802452a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present simulations of a coarse-grained model of a bolaamphiphile liquid crystal molecule with a grafted flexible side chain. The coarse-graining approach employed is based on minimising the attractions present in the system, on the premise that the most important features of the liquid structure stem from the balance between the close range repulsions and the strong directional forces typical of hydrogen bonding and association. The model consists of six fused rigid spheres, where the two end spheres have a significant attraction amongst themselves while the rest are repulsive in nature. A weakly self-attracting lateral chain consisting of fully flexible tangently bonded spheres is attached to one of the central spheres. A parametric study is made of the configurations of collectives of these molecules at temperatures that span from the isotropic fluid range down to the onset of crystallisation. The underlying rigid core molecules ( with no side chain) are set up to exhibit a smectic liquid crystal behaviour. Upon increasing the number of spheres in the lateral chains from 1 to 12, the liquid regions exhibit a rich variety of self-assembled structures; for small number of lateral chain spheres columnar arrays of different cross sections ( triangular, square, rectangular, hexagonal) are obtained and for the longer chains lamellar structures of different interlayer spacing are observed. We showcase and give a rational physical explanation for the global phase behaviour of the model, based on pertinent order parameters and apparent diffusivities of the several regimes encountered. Although no attempt has been made to fit the parameters of the model to real molecules, the model is inspired by the reported synthesis of a family of T-shaped polyphilic molecules ( C. Tschierske, Chem. Soc. Rev., 2007, 36, 1930 1970) where some of the above mentioned phases have been inferred from experimental measurements.
引用
收藏
页码:1820 / 1829
页数:10
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