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Issue 37, 2017
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Molecular dynamics simulations of oligoester brushes: the origin of unusual conformations

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Abstract

We present results from all-atom molecular dynamics simulations for the structural properties of oligomeric lactic acid chains (OLA) grafted to the surface of cellulose nanocrystals (CNCs) and immersed in the melt of polylactic acid (PLA). Earlier, we have found that the distribution of free ends of OLA molecules is bimodal [Glova et al., Polym. Int., 2016, 65(8), 892]. The results cannot be explained within the standard picture of uncharged polymer brushes exposed to the melt of a chemically identical polymer. Although the oligomeric brushes of the OLA chains are uncharged, they have partial polarization charges producing a non-zero dipole moment of the monomeric chain unit. We study the influence of partial charges on the structure of the layer of OLA chains grafted to the CNC surface. A detailed analysis of the conformations of the grafted chains shows that interaction of partial charges in the models causes bending of the OLA molecules toward the cellulose surface, forming a hairpin structure. The observed separation of the grafted chains into two populations increases with grafting density. We demonstrate that hydrogen bonds can be formed between the free ends of the grafted chains and the CNC surface, but they do not affect the brush structure significantly. Thus, dipole–dipole interactions turn out to be the key factor governing the unusual conformations of grafts.

Graphical abstract: Molecular dynamics simulations of oligoester brushes: the origin of unusual conformations

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Publication details

The article was received on 17 Jul 2017, accepted on 11 Sep 2017 and first published on 11 Sep 2017


Article type: Paper
DOI: 10.1039/C7SM01419H
Citation: Soft Matter, 2017,13, 6627-6638
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    Molecular dynamics simulations of oligoester brushes: the origin of unusual conformations

    A. D. Glova, S. V. Larin, S. G. Falkovich, V. M. Nazarychev, D. A. Tolmachev, N. V. Lukasheva and S. V. Lyulin, Soft Matter, 2017, 13, 6627
    DOI: 10.1039/C7SM01419H

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