Cargando…
Mesogenic Polyelectrolyte Gels Absorb Organic Solvents and Liquid Crystalline Molecules
In this paper, mesogenic polyelectrolyte gels (MPEgels) tethering mesogenic groups on the side chains were synthesized from a mesogenic monomer and ionic monomer via a conventional radical polymerization process. The obtained MPEgels absorbed various organic solvents in a wide range of dielectric co...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432411/ https://www.ncbi.nlm.nih.gov/pubmed/30979242 http://dx.doi.org/10.3390/polym8040148 |
_version_ | 1783406129230905344 |
---|---|
author | Nishikori, Yusuke Iseda, Kazuya Kokado, Kenta Sada, Kazuki |
author_facet | Nishikori, Yusuke Iseda, Kazuya Kokado, Kenta Sada, Kazuki |
author_sort | Nishikori, Yusuke |
collection | PubMed |
description | In this paper, mesogenic polyelectrolyte gels (MPEgels) tethering mesogenic groups on the side chains were synthesized from a mesogenic monomer and ionic monomer via a conventional radical polymerization process. The obtained MPEgels absorbed various organic solvents in a wide range of dielectric constants from chloroform (ε = 7.6) to DMSO (ε = 46.5). The electrostatic repulsion among the polymer chains and the osmotic pressure between the interior and exterior of the MPEgel is responsible for the high swelling ability, revealed by the common ion effect using tetra(n-hexyl)ammonium tetra(3,5-bis(trifluoromethyl)phenylborate (THATFPB). The obtained MPEgels could also absorb liquid crystalline molecules such as 4-cyano-4’-pentylbiphenyl (5CB), analogously caused by the above-mentioned polyelectrolyte characteristic. The MPEgels exhibited liquid crystal transition temperature (T(NI)) on differential scanning calorimetry (DSC) measurement, and the increase of the ionic group content lowered T(NI). The MPEgels absorbing liquid crystalline molecules exhibited differing T(NI), dependent on the compatibility of the mesogenic group on the side chain to the liquid crystalline molecule. |
format | Online Article Text |
id | pubmed-6432411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64324112019-04-02 Mesogenic Polyelectrolyte Gels Absorb Organic Solvents and Liquid Crystalline Molecules Nishikori, Yusuke Iseda, Kazuya Kokado, Kenta Sada, Kazuki Polymers (Basel) Article In this paper, mesogenic polyelectrolyte gels (MPEgels) tethering mesogenic groups on the side chains were synthesized from a mesogenic monomer and ionic monomer via a conventional radical polymerization process. The obtained MPEgels absorbed various organic solvents in a wide range of dielectric constants from chloroform (ε = 7.6) to DMSO (ε = 46.5). The electrostatic repulsion among the polymer chains and the osmotic pressure between the interior and exterior of the MPEgel is responsible for the high swelling ability, revealed by the common ion effect using tetra(n-hexyl)ammonium tetra(3,5-bis(trifluoromethyl)phenylborate (THATFPB). The obtained MPEgels could also absorb liquid crystalline molecules such as 4-cyano-4’-pentylbiphenyl (5CB), analogously caused by the above-mentioned polyelectrolyte characteristic. The MPEgels exhibited liquid crystal transition temperature (T(NI)) on differential scanning calorimetry (DSC) measurement, and the increase of the ionic group content lowered T(NI). The MPEgels absorbing liquid crystalline molecules exhibited differing T(NI), dependent on the compatibility of the mesogenic group on the side chain to the liquid crystalline molecule. MDPI 2016-04-19 /pmc/articles/PMC6432411/ /pubmed/30979242 http://dx.doi.org/10.3390/polym8040148 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nishikori, Yusuke Iseda, Kazuya Kokado, Kenta Sada, Kazuki Mesogenic Polyelectrolyte Gels Absorb Organic Solvents and Liquid Crystalline Molecules |
title | Mesogenic Polyelectrolyte Gels Absorb Organic Solvents and Liquid Crystalline Molecules |
title_full | Mesogenic Polyelectrolyte Gels Absorb Organic Solvents and Liquid Crystalline Molecules |
title_fullStr | Mesogenic Polyelectrolyte Gels Absorb Organic Solvents and Liquid Crystalline Molecules |
title_full_unstemmed | Mesogenic Polyelectrolyte Gels Absorb Organic Solvents and Liquid Crystalline Molecules |
title_short | Mesogenic Polyelectrolyte Gels Absorb Organic Solvents and Liquid Crystalline Molecules |
title_sort | mesogenic polyelectrolyte gels absorb organic solvents and liquid crystalline molecules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432411/ https://www.ncbi.nlm.nih.gov/pubmed/30979242 http://dx.doi.org/10.3390/polym8040148 |
work_keys_str_mv | AT nishikoriyusuke mesogenicpolyelectrolytegelsabsorborganicsolventsandliquidcrystallinemolecules AT isedakazuya mesogenicpolyelectrolytegelsabsorborganicsolventsandliquidcrystallinemolecules AT kokadokenta mesogenicpolyelectrolytegelsabsorborganicsolventsandliquidcrystallinemolecules AT sadakazuki mesogenicpolyelectrolytegelsabsorborganicsolventsandliquidcrystallinemolecules |