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Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities
A new family of valine-containing 3,5-diaminobenzoate derivatives 2 with N-alkylurea moieties attached to the valine moieties was prepared. By appending these two new N-alkylurea chains to the molecular structure, their organogelating properties were extended from only aromatic solvents, to a wide r...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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Beilstein-Institut
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2981810/ https://www.ncbi.nlm.nih.gov/pubmed/21085497 http://dx.doi.org/10.3762/bjoc.6.114 |
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author | Chow, Hak-Fun Cheng, Chin-Ho |
author_facet | Chow, Hak-Fun Cheng, Chin-Ho |
author_sort | Chow, Hak-Fun |
collection | PubMed |
description | A new family of valine-containing 3,5-diaminobenzoate derivatives 2 with N-alkylurea moieties attached to the valine moieties was prepared. By appending these two new N-alkylurea chains to the molecular structure, their organogelating properties were extended from only aromatic solvents, to a wide range of other types of solvents such as alicyclic hydrocarbons, alcohols and polar solvents such as DMSO and DMF. It was also found that a longer N-alkylurea chain conferred improved gelation power and higher thermal stability as compared to those of the shorter ones. |
format | Text |
id | pubmed-2981810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-29818102010-11-17 Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities Chow, Hak-Fun Cheng, Chin-Ho Beilstein J Org Chem Full Research Paper A new family of valine-containing 3,5-diaminobenzoate derivatives 2 with N-alkylurea moieties attached to the valine moieties was prepared. By appending these two new N-alkylurea chains to the molecular structure, their organogelating properties were extended from only aromatic solvents, to a wide range of other types of solvents such as alicyclic hydrocarbons, alcohols and polar solvents such as DMSO and DMF. It was also found that a longer N-alkylurea chain conferred improved gelation power and higher thermal stability as compared to those of the shorter ones. Beilstein-Institut 2010-10-26 /pmc/articles/PMC2981810/ /pubmed/21085497 http://dx.doi.org/10.3762/bjoc.6.114 Text en Copyright © 2010, Chow and Cheng 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 Chow, Hak-Fun Cheng, Chin-Ho Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities |
title | Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities |
title_full | Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities |
title_fullStr | Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities |
title_full_unstemmed | Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities |
title_short | Expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities |
title_sort | expanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with n-alkylurea functionalities |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2981810/ https://www.ncbi.nlm.nih.gov/pubmed/21085497 http://dx.doi.org/10.3762/bjoc.6.114 |
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