New cholesteryl containing bent core liquid crystals

The paper presents the synthesis and mesomorphic behavior of two new series of bent core liquid crystalline compounds based on a 1,3-dihydroxybezene core and containing a cholesteryl 6-oxyhexanoate wing. The two series were obtained by the esterification of the cholesteryl 6-(3-hydroxyphenoxy)he...

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Main Authors: Huzum Cosmin-Constantin, Carlescu Irina, Lisa Gabriela, Scutaru Dan
Format: Article
Language:English
Published: Serbian Chemical Society 2013-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200114H.pdf
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spelling doaj-f28a97be7cf6443cb097bf0746a064262020-11-25T00:26:13ZengSerbian Chemical Society Journal of the Serbian Chemical Society0352-51392013-01-0178566968010.2298/JSC120810114HNew cholesteryl containing bent core liquid crystalsHuzum Cosmin-ConstantinCarlescu IrinaLisa GabrielaScutaru DanThe paper presents the synthesis and mesomorphic behavior of two new series of bent core liquid crystalline compounds based on a 1,3-dihydroxybezene core and containing a cholesteryl 6-oxyhexanoate wing. The two series were obtained by the esterification of the cholesteryl 6-(3-hydroxyphenoxy)hexanoate core with some 4-((4-(n-alkyloxy)phenyl)azo)benzoic acids (n-alkyl = n-hexyl ÷ n-dodecyl) or 4-(4-(n-alkyloxy)benzoyloxy)benzoic acids (n-alkyl = n-hexyl ÷ n-decyl). The esterification reactions were performed via the corresponding acyl chlorides or with the DCC / DMAP system. All the synthesized compounds evidenced enantiotropic liquid crystalline properties, with smectic type textures, when investigated by means of differential scanning calorimetry and polarized optical microscopy. Isotropisation and isotropic to liquid crystal transitions were relatively low (between 89 ÷ 1460C). The compounds containing the azo-aromatic linking group presented the largest range of stability of the mesophases (between 42 and 870C). All the investigated compounds were thermally stable in the existence range of the mesophases.http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200114H.pdfliquid crystalsbanana shapedcholesterolresorcinol
collection DOAJ
language English
format Article
sources DOAJ
author Huzum Cosmin-Constantin
Carlescu Irina
Lisa Gabriela
Scutaru Dan
spellingShingle Huzum Cosmin-Constantin
Carlescu Irina
Lisa Gabriela
Scutaru Dan
New cholesteryl containing bent core liquid crystals
Journal of the Serbian Chemical Society
liquid crystals
banana shaped
cholesterol
resorcinol
author_facet Huzum Cosmin-Constantin
Carlescu Irina
Lisa Gabriela
Scutaru Dan
author_sort Huzum Cosmin-Constantin
title New cholesteryl containing bent core liquid crystals
title_short New cholesteryl containing bent core liquid crystals
title_full New cholesteryl containing bent core liquid crystals
title_fullStr New cholesteryl containing bent core liquid crystals
title_full_unstemmed New cholesteryl containing bent core liquid crystals
title_sort new cholesteryl containing bent core liquid crystals
publisher Serbian Chemical Society
series Journal of the Serbian Chemical Society
issn 0352-5139
publishDate 2013-01-01
description The paper presents the synthesis and mesomorphic behavior of two new series of bent core liquid crystalline compounds based on a 1,3-dihydroxybezene core and containing a cholesteryl 6-oxyhexanoate wing. The two series were obtained by the esterification of the cholesteryl 6-(3-hydroxyphenoxy)hexanoate core with some 4-((4-(n-alkyloxy)phenyl)azo)benzoic acids (n-alkyl = n-hexyl ÷ n-dodecyl) or 4-(4-(n-alkyloxy)benzoyloxy)benzoic acids (n-alkyl = n-hexyl ÷ n-decyl). The esterification reactions were performed via the corresponding acyl chlorides or with the DCC / DMAP system. All the synthesized compounds evidenced enantiotropic liquid crystalline properties, with smectic type textures, when investigated by means of differential scanning calorimetry and polarized optical microscopy. Isotropisation and isotropic to liquid crystal transitions were relatively low (between 89 ÷ 1460C). The compounds containing the azo-aromatic linking group presented the largest range of stability of the mesophases (between 42 and 870C). All the investigated compounds were thermally stable in the existence range of the mesophases.
topic liquid crystals
banana shaped
cholesterol
resorcinol
url http://www.doiserbia.nb.rs/img/doi/0352-5139/2013/0352-51391200114H.pdf
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