Cholesteric Liquid Crystalline Copolymers for Gas Chromatographic Separation of Polycyclic Aromatic Compounds

A novel series of side-chain liquid crystalline copolysiloxanes containing [S]-1-(2-naphthyl) ethyl 6-[4-(10-undecen-1-yloxy) biphenyl--carbonyloxy]-2-naphthoate mesogenic and 4-biphenyl -allyloxybenzoate mesogenic side groups in the backbone and side chains liquid crystalline copolymers were prepar...

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Main Author: Chih-Hung Lin
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Advances in Materials Science and Engineering
Online Access:http://dx.doi.org/10.1155/2012/904354
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author Chih-Hung Lin
author_facet Chih-Hung Lin
author_sort Chih-Hung Lin
collection DOAJ
description A novel series of side-chain liquid crystalline copolysiloxanes containing [S]-1-(2-naphthyl) ethyl 6-[4-(10-undecen-1-yloxy) biphenyl--carbonyloxy]-2-naphthoate mesogenic and 4-biphenyl -allyloxybenzoate mesogenic side groups in the backbone and side chains liquid crystalline copolymers were prepared and evaluated as possible stationary phases for gas chromatography capillary columns. All copolymers display enantiotropic cholesteric phases. These mesomorphic polysiloxanes specimens with the widest temperature range were used as the stationary phase in a gas chromatography capillary column, and it showed good thermal and physical stability, excellent chemical inertness, and unique separation properties for polycyclic aromatic compounds. These cholesteric LC copolysiloxane stationary phases show much better separation effect for the polycyclic aromatic compound than those of the nematic and smectic LC copolysiloxanes.
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spelling doaj-art-5e109cbdf3814ed5b01ccc2d01e21c2e2025-08-20T02:06:00ZengWileyAdvances in Materials Science and Engineering1687-84341687-84422012-01-01201210.1155/2012/904354904354Cholesteric Liquid Crystalline Copolymers for Gas Chromatographic Separation of Polycyclic Aromatic CompoundsChih-Hung Lin0Center for General Education, Chang Gung University of Science and Technology, 261 Wen-Hwa 1st Road, Kwei-Shan, Tao-Yuan, TaiwanA novel series of side-chain liquid crystalline copolysiloxanes containing [S]-1-(2-naphthyl) ethyl 6-[4-(10-undecen-1-yloxy) biphenyl--carbonyloxy]-2-naphthoate mesogenic and 4-biphenyl -allyloxybenzoate mesogenic side groups in the backbone and side chains liquid crystalline copolymers were prepared and evaluated as possible stationary phases for gas chromatography capillary columns. All copolymers display enantiotropic cholesteric phases. These mesomorphic polysiloxanes specimens with the widest temperature range were used as the stationary phase in a gas chromatography capillary column, and it showed good thermal and physical stability, excellent chemical inertness, and unique separation properties for polycyclic aromatic compounds. These cholesteric LC copolysiloxane stationary phases show much better separation effect for the polycyclic aromatic compound than those of the nematic and smectic LC copolysiloxanes.http://dx.doi.org/10.1155/2012/904354
spellingShingle Chih-Hung Lin
Cholesteric Liquid Crystalline Copolymers for Gas Chromatographic Separation of Polycyclic Aromatic Compounds
Advances in Materials Science and Engineering
title Cholesteric Liquid Crystalline Copolymers for Gas Chromatographic Separation of Polycyclic Aromatic Compounds
title_full Cholesteric Liquid Crystalline Copolymers for Gas Chromatographic Separation of Polycyclic Aromatic Compounds
title_fullStr Cholesteric Liquid Crystalline Copolymers for Gas Chromatographic Separation of Polycyclic Aromatic Compounds
title_full_unstemmed Cholesteric Liquid Crystalline Copolymers for Gas Chromatographic Separation of Polycyclic Aromatic Compounds
title_short Cholesteric Liquid Crystalline Copolymers for Gas Chromatographic Separation of Polycyclic Aromatic Compounds
title_sort cholesteric liquid crystalline copolymers for gas chromatographic separation of polycyclic aromatic compounds
url http://dx.doi.org/10.1155/2012/904354
work_keys_str_mv AT chihhunglin cholestericliquidcrystallinecopolymersforgaschromatographicseparationofpolycyclicaromaticcompounds