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Chiral polymorphism in new imine based rod-like liquid crystals

Caglar, Fatma Pinar; Akdas-Kilic, Huriye; Ocak, Hale; Eran, Belkiz Bilgin


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  <dc:creator>Caglar, Fatma Pinar</dc:creator>
  <dc:creator>Akdas-Kilic, Huriye</dc:creator>
  <dc:creator>Ocak, Hale</dc:creator>
  <dc:creator>Eran, Belkiz Bilgin</dc:creator>
  <dc:date>2020-01-01</dc:date>
  <dc:description>New imine based rod-like compounds, composed of three-benzene-ring molecular core linked with azomethine as well as ester groups and terminated with (S)-3,7-dimethyloctyloxy chiral unit at one side have been synthesized. The other terminal position has been varied by using n-octyloxy/decyloxy/dodecyloxy groups to reveal chain length effect on mesophase behavior. The liquid crystalline properties of the new compounds have been investigated by polarizing optical microscopy, differential scanning calorimetry and electro-optic studies. The novel chiral calamitics derived from Schiff base or salicylaldimine-core show a chiral polymorphism comprising of blue phase and chiral nematic as well as smectics such as chiral tilted smectic and unidentified smectic mesophase. (C) 2020 Elsevier B.V. All rights reserved.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/7713</dc:identifier>
  <dc:identifier>oai:zenodo.org:7713</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>JOURNAL OF MOLECULAR STRUCTURE 1220</dc:source>
  <dc:title>Chiral polymorphism in new imine based rod-like liquid crystals</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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