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Synthesis and Thermotropic Studies of a New Series of Teraryl Liquid Crystals 2-(4′-Alkoxybiphen-4-yl)-5-Cyanopyridines
A new series of teraryl 2-(4′-alkoxybiphen-4-yl)-5-cyanopyridines (nO-PPPyCN, n = 2–8) compounds, bearing a cyanopyridine terminus, were synthesized using a short 2-step reaction with overall yields between 33% and 69%. Spectral analyses were in accord with the expected structures. Thermotropic beha...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794808/ https://www.ncbi.nlm.nih.gov/pubmed/24036442 http://dx.doi.org/10.3390/ijms140918809 |
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author | Chia, Win-Long Lin, Xue-Ming |
author_facet | Chia, Win-Long Lin, Xue-Ming |
author_sort | Chia, Win-Long |
collection | PubMed |
description | A new series of teraryl 2-(4′-alkoxybiphen-4-yl)-5-cyanopyridines (nO-PPPyCN, n = 2–8) compounds, bearing a cyanopyridine terminus, were synthesized using a short 2-step reaction with overall yields between 33% and 69%. Spectral analyses were in accord with the expected structures. Thermotropic behavior of the teraryl compounds was investigated using polarised optical microscopy and differential scanning calorimetry. All compounds exhibited both enantiotropic nematic and smectic A phases, with an additional enantiotropic smectic C phase when n = 7 and 8. Polymesomorphism appears to be a common behavior in this series of linear liquid crystal compounds. |
format | Online Article Text |
id | pubmed-3794808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-37948082013-10-21 Synthesis and Thermotropic Studies of a New Series of Teraryl Liquid Crystals 2-(4′-Alkoxybiphen-4-yl)-5-Cyanopyridines Chia, Win-Long Lin, Xue-Ming Int J Mol Sci Article A new series of teraryl 2-(4′-alkoxybiphen-4-yl)-5-cyanopyridines (nO-PPPyCN, n = 2–8) compounds, bearing a cyanopyridine terminus, were synthesized using a short 2-step reaction with overall yields between 33% and 69%. Spectral analyses were in accord with the expected structures. Thermotropic behavior of the teraryl compounds was investigated using polarised optical microscopy and differential scanning calorimetry. All compounds exhibited both enantiotropic nematic and smectic A phases, with an additional enantiotropic smectic C phase when n = 7 and 8. Polymesomorphism appears to be a common behavior in this series of linear liquid crystal compounds. MDPI 2013-09-12 /pmc/articles/PMC3794808/ /pubmed/24036442 http://dx.doi.org/10.3390/ijms140918809 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Chia, Win-Long Lin, Xue-Ming Synthesis and Thermotropic Studies of a New Series of Teraryl Liquid Crystals 2-(4′-Alkoxybiphen-4-yl)-5-Cyanopyridines |
title | Synthesis and Thermotropic Studies of a New Series of Teraryl Liquid Crystals 2-(4′-Alkoxybiphen-4-yl)-5-Cyanopyridines |
title_full | Synthesis and Thermotropic Studies of a New Series of Teraryl Liquid Crystals 2-(4′-Alkoxybiphen-4-yl)-5-Cyanopyridines |
title_fullStr | Synthesis and Thermotropic Studies of a New Series of Teraryl Liquid Crystals 2-(4′-Alkoxybiphen-4-yl)-5-Cyanopyridines |
title_full_unstemmed | Synthesis and Thermotropic Studies of a New Series of Teraryl Liquid Crystals 2-(4′-Alkoxybiphen-4-yl)-5-Cyanopyridines |
title_short | Synthesis and Thermotropic Studies of a New Series of Teraryl Liquid Crystals 2-(4′-Alkoxybiphen-4-yl)-5-Cyanopyridines |
title_sort | synthesis and thermotropic studies of a new series of teraryl liquid crystals 2-(4′-alkoxybiphen-4-yl)-5-cyanopyridines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794808/ https://www.ncbi.nlm.nih.gov/pubmed/24036442 http://dx.doi.org/10.3390/ijms140918809 |
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