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Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions

We report herein the use of an aromatic–aromatic interaction to produce small molecule hydrogelators that self-assemble in water and form molecular nanofibers in the resulting hydrogels. Among these hydrogelators, a hydrogelator (6) made from a phenylalanine and a cinnamoyl group represents the lowe...

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Detalles Bibliográficos
Autores principales: Shi, Junfeng, Gao, Yuan, Yang, Zhimou, Xu, Bing
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063069/
https://www.ncbi.nlm.nih.gov/pubmed/21448260
http://dx.doi.org/10.3762/bjoc.7.23
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author Shi, Junfeng
Gao, Yuan
Yang, Zhimou
Xu, Bing
author_facet Shi, Junfeng
Gao, Yuan
Yang, Zhimou
Xu, Bing
author_sort Shi, Junfeng
collection PubMed
description We report herein the use of an aromatic–aromatic interaction to produce small molecule hydrogelators that self-assemble in water and form molecular nanofibers in the resulting hydrogels. Among these hydrogelators, a hydrogelator (6) made from a phenylalanine and a cinnamoyl group represents the lowest molecular weight (MW = 295.33 g/mol) peptide-based hydrogelator prepared to date. The supramolecular hydrogels were characterized by transmission electron micrograph (TEM) and fluorescence spectroscopy, and the results obtained by both techniques correlate well with their rheological properties. Notably, compound 6 can undergo cis/trans-isomerization upon UV irradiation.
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spelling pubmed-30630692011-03-28 Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions Shi, Junfeng Gao, Yuan Yang, Zhimou Xu, Bing Beilstein J Org Chem Full Research Paper We report herein the use of an aromatic–aromatic interaction to produce small molecule hydrogelators that self-assemble in water and form molecular nanofibers in the resulting hydrogels. Among these hydrogelators, a hydrogelator (6) made from a phenylalanine and a cinnamoyl group represents the lowest molecular weight (MW = 295.33 g/mol) peptide-based hydrogelator prepared to date. The supramolecular hydrogels were characterized by transmission electron micrograph (TEM) and fluorescence spectroscopy, and the results obtained by both techniques correlate well with their rheological properties. Notably, compound 6 can undergo cis/trans-isomerization upon UV irradiation. Beilstein-Institut 2011-02-07 /pmc/articles/PMC3063069/ /pubmed/21448260 http://dx.doi.org/10.3762/bjoc.7.23 Text en Copyright © 2011, Shi et al. https://creativecommons.org/licenses/by/2.0https://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/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Shi, Junfeng
Gao, Yuan
Yang, Zhimou
Xu, Bing
Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions
title Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions
title_full Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions
title_fullStr Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions
title_full_unstemmed Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions
title_short Exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions
title_sort exceptionally small supramolecular hydrogelators based on aromatic–aromatic interactions
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063069/
https://www.ncbi.nlm.nih.gov/pubmed/21448260
http://dx.doi.org/10.3762/bjoc.7.23
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