Search:
Computing and Library Services - delivering an inspiring information environment

Thermodynamics of the self-assembly of non-ionic chromonic molecules using atomistic simulations. The case of TP6EO2M in aqueous solution

Akinshina, Anna, Walker, Martin, Wilson, Mark R, Tiddy, Gordon TJ, Masters, Andrew J and Carbone, Paola (2015) Thermodynamics of the self-assembly of non-ionic chromonic molecules using atomistic simulations. The case of TP6EO2M in aqueous solution. Soft Matter, 4. pp. 680-691. ISSN 1744-683X

[img]
Preview
PDF - Accepted Version
Download (1MB) | Preview

Abstract

Atomistic molecular dynamic simulations have been performed for the non-ionic chromonic liquid crystal
2,3,6,7,10,11-hexa-(1,4,7-trioxa-octyl)-triphenylene (TP6EO2M) in aqueous solution. TP6EO2M molecules
consist of a central poly-aromatic core (a triphenylene ring) functionalized by six hydrophilic ethyleneoxy
(EO) chains, and have a strong tendency to aggregate face-to-face into stacks even in very dilute
solution. We have studied self-assembly of the molecules in the low concentration range corresponding
to an isotropic solution of aggregates, using two force fields GAFF and OPLS. Our results reveal that the
GAFF force field, even though it was successfully used previously for modelling of ionic chromonics,
overestimates the attraction of TP6EO2M molecules in water. This results in an aggregation free energy
which is too high, a reduced hydration of EO chains and, therefore, molecular self-assembly into
compact disordered clusters instead of stacks. In contrast, use of the OPLS force field, leads to selfassembly
into ordered stacks in agreement with earlier experimental studies of triphenylene-based
chromonics. The free energy of association follows a “quasi-isodesmic” pattern, where the binding free
energy of two molecules to form a dimer is of the order of 2.5 RT larger than the corresponding energy
of addition of a molecule into a stack. The obtained value for the binding free energy, dG
agg = -12 RT, is
found to be in line with the published values for typical ionic chromonics (-7 to -12 RT), and agrees
reasonably well with the experimental results for this system. The calculated interlayer distance between
the molecules in a stack is 0.37 nm, which is at the top of the range found for typical chromonics (0.33–
0.37 nm). We suggest that the relatively large layer spacing can be attributed to the repulsion between
EO side chains.

Item Type: Article
Subjects: Q Science > QC Physics
Q Science > QD Chemistry
Schools: School of Human and Health Sciences
Depositing User: Anna Akinshina
Date Deposited: 03 Mar 2016 10:10
Last Modified: 30 Nov 2016 20:57
URI: http://eprints.hud.ac.uk/id/eprint/27838

Downloads

Downloads per month over past year

Repository Staff Only: item control page

View Item View Item

University of Huddersfield, Queensgate, Huddersfield, HD1 3DH Copyright and Disclaimer All rights reserved ©