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Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity

While only a few studies have investigated the synthesis of main chain-type polyazobenzenes, they continue to draw an increasing amount of attention owing to their industrial applications in holography, dyes, and functional adhesives. In this study, dibromoazobenzene was prepared as a monomer for co...

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Detalles Bibliográficos
Autores principales: Otaki, Masashi, Kumai, Reiji, Sagayama, Hajime, Goto, Hiromasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419163/
https://www.ncbi.nlm.nih.gov/pubmed/30960332
http://dx.doi.org/10.3390/polym11020348
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author Otaki, Masashi
Kumai, Reiji
Sagayama, Hajime
Goto, Hiromasa
author_facet Otaki, Masashi
Kumai, Reiji
Sagayama, Hajime
Goto, Hiromasa
author_sort Otaki, Masashi
collection PubMed
description While only a few studies have investigated the synthesis of main chain-type polyazobenzenes, they continue to draw an increasing amount of attention owing to their industrial applications in holography, dyes, and functional adhesives. In this study, dibromoazobenzene was prepared as a monomer for constructing azo-based π-conjugated polymers. Miyaura–Suzuki cross-coupling polymerization was conducted to develop copolymers containing an azobenzene unit as a photoisomerization block and a pyrimidine-based liquid crystal generator block. The prepared polymers exhibited thermotropic liquid crystallinity and underwent cis and trans photoisomerization upon irradiation with ultraviolet and visible light. Furthermore, the photoisomerization behavior was examined using optical absorption spectroscopy and synchrotron X-ray diffraction spectrometry.
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spelling pubmed-64191632019-04-02 Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity Otaki, Masashi Kumai, Reiji Sagayama, Hajime Goto, Hiromasa Polymers (Basel) Communication While only a few studies have investigated the synthesis of main chain-type polyazobenzenes, they continue to draw an increasing amount of attention owing to their industrial applications in holography, dyes, and functional adhesives. In this study, dibromoazobenzene was prepared as a monomer for constructing azo-based π-conjugated polymers. Miyaura–Suzuki cross-coupling polymerization was conducted to develop copolymers containing an azobenzene unit as a photoisomerization block and a pyrimidine-based liquid crystal generator block. The prepared polymers exhibited thermotropic liquid crystallinity and underwent cis and trans photoisomerization upon irradiation with ultraviolet and visible light. Furthermore, the photoisomerization behavior was examined using optical absorption spectroscopy and synchrotron X-ray diffraction spectrometry. MDPI 2019-02-17 /pmc/articles/PMC6419163/ /pubmed/30960332 http://dx.doi.org/10.3390/polym11020348 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Otaki, Masashi
Kumai, Reiji
Sagayama, Hajime
Goto, Hiromasa
Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity
title Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity
title_full Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity
title_fullStr Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity
title_full_unstemmed Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity
title_short Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity
title_sort synthesis of polyazobenzenes exhibiting photoisomerization and liquid crystallinity
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419163/
https://www.ncbi.nlm.nih.gov/pubmed/30960332
http://dx.doi.org/10.3390/polym11020348
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