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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2011
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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. |
format | Text |
id | pubmed-3063069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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