New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization

The first example of non-symmetric isoflavone-based fast photo-switchable liquid crystals with different functional groups at theterminalposition were synthesized and characterized. Polarizing optical microscopy study revealed that the compounds showed least ordered nematic phase. Optical photo swi...

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Main Authors: Hegde, Gurumurthy, A. R., Yuvaraj, Wan, Sinn Yam, Tze, Nee Chan, Yit, Peng Goh
Format: Article
Language:en
en
Published: Elsevier 2015
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Online Access:http://umpir.ump.edu.my/id/eprint/8071/1/New%20para-substituted%20non-symmetric%20isoflavones%20for%20their%20fast%20photo-switching%20ability-%20Synthesis%20and%20their%20liquid%20crystal%20characterization.pdf
http://umpir.ump.edu.my/id/eprint/8071/7/New%20Para-substituted%20Non-symmetric%20Isoflavones%20for%20their%20Fast%20Photo-switching%20Ability-%20Synthesis%20and%20their%20Liquid%20Crystal%20Characterization.pdf
http://umpir.ump.edu.my/id/eprint/8071/
http://dx.doi.org/10.1016/j.saa.2014.08.009
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author Hegde, Gurumurthy
A. R., Yuvaraj
Wan, Sinn Yam
Tze, Nee Chan
Yit, Peng Goh
author_facet Hegde, Gurumurthy
A. R., Yuvaraj
Wan, Sinn Yam
Tze, Nee Chan
Yit, Peng Goh
author_sort Hegde, Gurumurthy
building UMPSA Library
collection Institutional Repository
content_provider Universiti Malaysia Pahang Al-Sultan Abdullah
content_source UMPSA Institutional Repository
continent Asia
country Malaysia
description The first example of non-symmetric isoflavone-based fast photo-switchable liquid crystals with different functional groups at theterminalposition were synthesized and characterized. Polarizing optical microscopy study revealed that the compounds showed least ordered nematic phase. Optical photo switching study exhibited very fast photoisomerization effect in solution. TheE–ZandZ–Econversion occurred around 3–5 s and 40–700 s respectively. This is also the first example ofpara-substituted non-symmetric isoflavone liquid crystals exhibiting very fast photo switching property in solution. Argument based on non-symmetrical behaviour might be the reason for the observed behaviour.
format Article
id my.ump.umpir.8071
institution Universiti Malaysia Pahang
language en
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publishDate 2015
publisher Elsevier
record_format eprints
spelling my.ump.umpir.80712018-05-17T05:24:53Z http://umpir.ump.edu.my/id/eprint/8071/ New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization Hegde, Gurumurthy A. R., Yuvaraj Wan, Sinn Yam Tze, Nee Chan Yit, Peng Goh QD Chemistry QC Physics The first example of non-symmetric isoflavone-based fast photo-switchable liquid crystals with different functional groups at theterminalposition were synthesized and characterized. Polarizing optical microscopy study revealed that the compounds showed least ordered nematic phase. Optical photo switching study exhibited very fast photoisomerization effect in solution. TheE–ZandZ–Econversion occurred around 3–5 s and 40–700 s respectively. This is also the first example ofpara-substituted non-symmetric isoflavone liquid crystals exhibiting very fast photo switching property in solution. Argument based on non-symmetrical behaviour might be the reason for the observed behaviour. Elsevier 2015-01-25 Article PeerReviewed application/pdf en http://umpir.ump.edu.my/id/eprint/8071/1/New%20para-substituted%20non-symmetric%20isoflavones%20for%20their%20fast%20photo-switching%20ability-%20Synthesis%20and%20their%20liquid%20crystal%20characterization.pdf application/pdf en http://umpir.ump.edu.my/id/eprint/8071/7/New%20Para-substituted%20Non-symmetric%20Isoflavones%20for%20their%20Fast%20Photo-switching%20Ability-%20Synthesis%20and%20their%20Liquid%20Crystal%20Characterization.pdf Hegde, Gurumurthy and A. R., Yuvaraj and Wan, Sinn Yam and Tze, Nee Chan and Yit, Peng Goh (2015) New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 135. pp. 1115-1122. ISSN 1386-1425 (print); 1873-3557 (online). (Published) http://dx.doi.org/10.1016/j.saa.2014.08.009 DOI: org/10.1016/j.saa.2014.08.009
spellingShingle QD Chemistry
QC Physics
Hegde, Gurumurthy
A. R., Yuvaraj
Wan, Sinn Yam
Tze, Nee Chan
Yit, Peng Goh
New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization
title New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization
title_full New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization
title_fullStr New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization
title_full_unstemmed New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization
title_short New Para-substituted Non-symmetric Isoflavones for Their Fast Photo-switching Ability: Synthesis and Their Liquid Crystal Characterization
title_sort new para-substituted non-symmetric isoflavones for their fast photo-switching ability: synthesis and their liquid crystal characterization
topic QD Chemistry
QC Physics
url http://umpir.ump.edu.my/id/eprint/8071/1/New%20para-substituted%20non-symmetric%20isoflavones%20for%20their%20fast%20photo-switching%20ability-%20Synthesis%20and%20their%20liquid%20crystal%20characterization.pdf
http://umpir.ump.edu.my/id/eprint/8071/7/New%20Para-substituted%20Non-symmetric%20Isoflavones%20for%20their%20Fast%20Photo-switching%20Ability-%20Synthesis%20and%20their%20Liquid%20Crystal%20Characterization.pdf
http://umpir.ump.edu.my/id/eprint/8071/
http://dx.doi.org/10.1016/j.saa.2014.08.009
url_provider http://umpir.ump.edu.my/