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dc.contributor.authorHaege, Christian-
dc.contributor.authorJagiella, Stefan-
dc.contributor.authorGiesselmann, Frank-
dc.date.accessioned2023-08-31T13:13:05Z-
dc.date.available2023-08-31T13:13:05Z-
dc.date.issued2022de
dc.identifier.issn1439-7641-
dc.identifier.issn1439-4235-
dc.identifier.other1860332080-
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-134800de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/13480-
dc.identifier.urihttp://dx.doi.org/10.18419/opus-13461-
dc.description.abstractIonic liquid crystals (ILCs) are soft matter materials with broad liquid crystalline phases and intrinsic electric conductivity. They typically consist of a rod‐shaped mesogenic ion and a smaller spherical counter‐ion. Their mesomorphic properties can be easily tuned by exchanging the counter ion. ILCs show a strong tendency to form smectic A phases due to the segregation of ionic and the non‐ionic molecular segments. Nematic phases are therefore extremely rare in ILCs and the question of why nematic phases are so exceptional in existing ILCs, and how nematic ILCs might be obtained in the future is of vital interest for both the fundamental understanding and the potential applications of ILCs. Here, we present the result of a simulation study, which highlights the crucial role of the location of the ionic charge on the rod‐like mesogenic ions in the phase behaviour of ILCs. We find that shifting the charge from the ends towards the centre of the mesogenic ion destabilizes the liquid crystalline state and induces a change from smectic A to nematic phases.en
dc.description.sponsorshipDeutsche Forschungsgemeinschaftde
dc.description.sponsorshipProjekt DEALde
dc.language.isoende
dc.relation.uridoi:10.1002/cphc.202200424de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/de
dc.subject.ddc540de
dc.titleTowards nematic phases in ionic liquid crystals : a simulation studyen
dc.typearticlede
dc.date.updated2023-04-19T20:03:21Z-
ubs.fakultaetChemiede
ubs.institutInstitut für Physikalische Chemiede
ubs.publikation.seiten7de
ubs.publikation.sourceChemPhysChem 24 (2023), No. e202200424de
ubs.publikation.typZeitschriftenartikelde
Enthalten in den Sammlungen:03 Fakultät Chemie

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