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A self-assembled photoresponsive gel consisting of chiral nanofibers

A novel compound based on a glutamic acid skeleton, containing azobenzene as a photoresponsive group and ureidopyrimidinone (UPy) as a connection site, was designed and synthesized. The monomer is capable of forming an organogel in nonpolar organic solvents and different types of nanostructures in o...

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Detalles Bibliográficos
Autores principales: Zou, Lei, Han, Dan, Yuan, Zhiyi, Chang, Dongdong, Ma, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122117/
https://www.ncbi.nlm.nih.gov/pubmed/30202453
http://dx.doi.org/10.3762/bjoc.14.174
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author Zou, Lei
Han, Dan
Yuan, Zhiyi
Chang, Dongdong
Ma, Xiang
author_facet Zou, Lei
Han, Dan
Yuan, Zhiyi
Chang, Dongdong
Ma, Xiang
author_sort Zou, Lei
collection PubMed
description A novel compound based on a glutamic acid skeleton, containing azobenzene as a photoresponsive group and ureidopyrimidinone (UPy) as a connection site, was designed and synthesized. The monomer is capable of forming an organogel in nonpolar organic solvents and different types of nanostructures in other solvents. The state of the gel and the chirality of the nanostructures could both be adjusted by subsequent light irradiation at different wavelengths. The helical nanofiber-like morphology was verified in the internal structure of the gel. The performance of this gel was investigated by a series of methods, such as UV–vis absorption spectroscopy, circular dichroism, scanning electron microscopy and rheological techniques. This work provides a new method for facile synthesis of chiro-optical gels.
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spelling pubmed-61221172018-09-10 A self-assembled photoresponsive gel consisting of chiral nanofibers Zou, Lei Han, Dan Yuan, Zhiyi Chang, Dongdong Ma, Xiang Beilstein J Org Chem Letter A novel compound based on a glutamic acid skeleton, containing azobenzene as a photoresponsive group and ureidopyrimidinone (UPy) as a connection site, was designed and synthesized. The monomer is capable of forming an organogel in nonpolar organic solvents and different types of nanostructures in other solvents. The state of the gel and the chirality of the nanostructures could both be adjusted by subsequent light irradiation at different wavelengths. The helical nanofiber-like morphology was verified in the internal structure of the gel. The performance of this gel was investigated by a series of methods, such as UV–vis absorption spectroscopy, circular dichroism, scanning electron microscopy and rheological techniques. This work provides a new method for facile synthesis of chiro-optical gels. Beilstein-Institut 2018-08-01 /pmc/articles/PMC6122117/ /pubmed/30202453 http://dx.doi.org/10.3762/bjoc.14.174 Text en Copyright © 2018, Zou et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Zou, Lei
Han, Dan
Yuan, Zhiyi
Chang, Dongdong
Ma, Xiang
A self-assembled photoresponsive gel consisting of chiral nanofibers
title A self-assembled photoresponsive gel consisting of chiral nanofibers
title_full A self-assembled photoresponsive gel consisting of chiral nanofibers
title_fullStr A self-assembled photoresponsive gel consisting of chiral nanofibers
title_full_unstemmed A self-assembled photoresponsive gel consisting of chiral nanofibers
title_short A self-assembled photoresponsive gel consisting of chiral nanofibers
title_sort self-assembled photoresponsive gel consisting of chiral nanofibers
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122117/
https://www.ncbi.nlm.nih.gov/pubmed/30202453
http://dx.doi.org/10.3762/bjoc.14.174
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