Dergi makalesi Açık Erişim
Caglar, Fatma Pinar; Akdas-Kilic, Huriye; Ocak, Hale; Eran, Belkiz Bilgin
<?xml version='1.0' encoding='utf-8'?> <oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"> <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> </oai_dc:dc>
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