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Computer simulation of the liquid crystal formation in a semi‐flexible polymer system
Author(s) -
Darinskii Anatoly A.,
Neelov Igor M.,
Zarembo Anna,
Balabaev Nikolai K.,
Sundholm Franciska,
Binder Kurt
Publication year - 2003
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.200390008
Subject(s) - liquid crystal , materials science , rigidity (electromagnetism) , anisotropy , spheres , hard spheres , polymer , phase (matter) , tangent , brush , molecular dynamics , chain (unit) , polymer brush , molecule , flexibility (engineering) , chemical physics , thermodynamics , physics , chemistry , composite material , computational chemistry , optics , geometry , mathematics , optoelectronics , quantum mechanics , astronomy , polymerization , statistics
Molecular dynamic simulations are reported for system of semi‐flexible linear rod‐like molecules. The molecules are composed of N c tangent soft spheres, connected by elastic springs. Rigidity is introduced by additional springs between all pairs of spheres along the molecule. The formation of only a nematic LC phase is shown for all systems with N c = 8 and different flexibility. The effect of flexibility on the order parameter and the volume fraction at the LC phase transition is compared with theoretical predictions by Khokhlov‐Semenov and with available simulation data. The dependence of the anisotropy of diffusion on chain flexibility in LC phase was studied. The polymer brushes consisting of flexible and semi‐flexible (composed of linear rod‐like segments) chains were simulated at different grafting densities. Height of brush, order parameter, distribution of density and chain ends in brush were obtained in both cases and compared with theoretical predictions.