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Effects of chain branching and chirality on liquid crystalline phases of bent-core molecules: blue phases, de Vries transitions and switching of diastereomeric states

dc.contributor.authorOcak, Hale
dc.contributor.authorBilgin-Eran, Belkiz
dc.contributor.authorPrehm, Marko
dc.contributor.authorSchymura, Stefan
dc.contributor.authorLagerwall, Jan P. F.
dc.contributor.authorTschierske, Carsten
dc.contributor.institutionauthorOCAK GÜMRÜKÇÜ, Hale
dc.date.accessioned2026-06-27T13:15:23Z
dc.date.issued2011
dc.description.abstractBent-core molecules based on a resorcinol bisbenzoate core with a series of distinct substituents in different positions at the central resorcinol core have been synthesized and characterized. The focus is on the effect of branched terminal groups in the racemic and chiral forms on the mesomorphic properties. These were investigated by differential scanning calorimetry, optical polarizing microscopy, X-ray diffraction, electro-optic and dielectric methods. Only bent-core mesogens derived from 4-cyanoresorcinol exhibit liquid crystalline phases and the mesophases of these compounds are strongly influenced by the branching and enantiomeric composition of the terminal chains. Depending on the structure of the rod-like wings and the enantiomeric composition, cybotactic nematic phases (N-cybC), BPIII-like isotropic mesophases (BPIIIcybC*) and various polar and apolar smectic phases (SmA, SmC, SmC*, SmCsPA, SmCsPA*) are formed. For one compound, a de Vries type smectic phase is observed and it appears that with decreasing temperature, order develops in two steps. First, at the SmA to SmC transition, the tilt direction becomes long range ordered and in a second step a long range ordering in bend direction takes place. Hence, for the optically active compound a transition from chirality induced polar switching to bend induced (shape induced) antiferroelectricity takes place. In this SmCsPA* phase a homogeneous layer chirality is induced under an applied electric field which interacts with the fixed molecular chirality leading to the energetically favoured diastereomeric state and giving rise to a field direction dependent uniform tilt director orientation. Field reversal induces a flipping of the layer chirality, which first leads to the less favorable diastereomeric state, and then this slowly relaxes to the more stable one by a spontaneous reversal of the tilt direction.en
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK)
dc.description.sponsorshipDeutsche Forschungsgemeinschaft [TS 39/23-1]
dc.description.sponsorshipAlexander von Humboldt Foundation
dc.description.urihttps://doi.org/10.1039/c1sm05826f
dc.identifier.doi10.1039/c1sm05826f
dc.identifier.eissn1744-6848
dc.identifier.endpage8280
dc.identifier.issn1744-683X
dc.identifier.issue18
dc.identifier.startpage8266
dc.identifier.urihttps://hdl.handle.net/20.500.14981/51105
dc.identifier.volume7
dc.identifier.wos000294447600051
dc.language.isoeng
dc.publisherROYAL SOC CHEMISTRY
dc.relation.ispartofSOFT MATTER
dc.subjectUNUSUAL MESOMORPHIC BEHAVIOR
dc.subjectBANANA-SHAPED MESOGENS
dc.subjectSMECTIC PHASE
dc.subjectNEMATIC PHASE
dc.subjectLATERAL SUBSTITUENTS
dc.subjectMESOPHASE BEHAVIOR
dc.subjectORGANIZATION
dc.subjectCOMPLEXES
dc.subjectDOMAINS
dc.subjectLATTICE
dc.subjectChemistry
dc.subjectMaterials Science
dc.subjectPhysics
dc.subjectPolymer Science
dc.titleEffects of chain branching and chirality on liquid crystalline phases of bent-core molecules: blue phases, de Vries transitions and switching of diastereomeric states
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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