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Effects of molecular chirality on self-assembly and switching in liquid crystals at the cross-over between rod-like and bent shapes

dc.contributor.authorOcak, Hale
dc.contributor.authorPoppe, Marco
dc.contributor.authorBilgin-Eran, Belkiz
dc.contributor.authorKaranlik, Gurkan
dc.contributor.authorPrehm, Marko
dc.contributor.authorTschierske, Carsten
dc.date.accessioned2026-06-27T13:54:42Z
dc.date.issued2016
dc.description.abstractA bent-core compound derived from a 4-cyanoresorcinol core unit with two terephthalate based rodlike wings and carrying chiral 3,7-dimethyloctyloxy side chains has been synthesized in racemic and enantiomerically pure form and characterized by polarizing microscopy, differential scanning calorimetry, X-ray diffraction and electro-optical investigations to study the influence of molecular chirality on the superstructural chirality and polar order in lamellar liquid crystalline phases. Herein we demonstrate that the coupling of molecular chirality with superstructural layer chirality in SmCsPF domain phases (forming energetically distinct diastereomeric pairs) can fix the tilt direction and thus stabilize synpolar order, leading to bistable ferroelectric switching in the SmC star phases of the (S)-enantiomer, whereas tristable modes determine the switching of the racemate. Moreover, the mechanism of electric field induced molecular reorganization changes from a rotation around the molecular long axis in the racemate to a rotation on the tilt-cone for the (S)-enantiomer. At high temperature the enantiomer behaves like a rod-like molecule with a chirality induced ferroelectric SmC star phase and an electroclinic effect in the SmA'(star) phase. At reduced temperature sterically induced polarization, due to the bent molecular shape, becomes dominating, leading to much higher polarization values, thus providing access to high polarization ferroelectric materials with weakly bent compounds having only weakly chiral'' stereogenic units. Moreover, the field induced alignment of the SmCsPF(star) domains gives rise to a special kind of electroclinic effect appearing even in the absence of molecular chirality. Comparison with related compounds indicates that the strongest effects of chirality appear for weakly bent molecules with a relatively short coherence length of polar order, whereas for smectic phases with long range polar order the effects of the interlayer interfaces can override the chirality effects.en
dc.description.sponsorshipDFG [Ts 39/24-1]
dc.description.sponsorshipYildiz Technical University Scientific Research Projects Coordination Department [2014-01-02-KAP01]
dc.description.sponsorshipAlexander von Humboldt Foundation for a research fellowship at Martin Luther University, Halle, Germany
dc.description.urihttps://doi.org/10.1039/c6sm00960c
dc.identifier.doi10.1039/c6sm00960c
dc.identifier.eissn1744-6848
dc.identifier.endpage7422
dc.identifier.issn1744-683X
dc.identifier.issue35
dc.identifier.pubmed27510177
dc.identifier.startpage7405
dc.identifier.urihttps://hdl.handle.net/20.500.14981/55600
dc.identifier.volume12
dc.identifier.wos000382764700016
dc.language.isoeng
dc.publisherROYAL SOC CHEMISTRY
dc.relation.ispartofSOFT MATTER
dc.rightsopenAccess
dc.subjectPOLAR ORDER
dc.subjectCORE MESOGENS
dc.subjectACHIRAL MOLECULES
dc.subjectSYMMETRY-BREAKING
dc.subjectAZOBENZENE WINGS
dc.subjectEND-GROUPS
dc.subjectPHASES
dc.subjectFIELD
dc.subject4-CYANORESORCINOL
dc.subjectTILT
dc.subjectChemistry
dc.subjectMaterials Science
dc.subjectPhysics
dc.subjectPolymer Science
dc.titleEffects of molecular chirality on self-assembly and switching in liquid crystals at the cross-over between rod-like and bent shapes
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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