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Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid
In order to have access to chiral gels, a series of salts derived from (1R,3S)-(+)-camphoric acid and various secondary amines were prepared based on supramolecular synthon rationale. Out of seven salts prepared, two showed moderate gelation abilities. The gels were characterized by differential sca...
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/PMC2956458/ https://www.ncbi.nlm.nih.gov/pubmed/20978610 http://dx.doi.org/10.3762/bjoc.6.100 |
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author | Adalder, Tapas Kumar Adarsh, N N Sankolli, Ravish Dastidar, Parthasarathi |
author_facet | Adalder, Tapas Kumar Adarsh, N N Sankolli, Ravish Dastidar, Parthasarathi |
author_sort | Adalder, Tapas Kumar |
collection | PubMed |
description | In order to have access to chiral gels, a series of salts derived from (1R,3S)-(+)-camphoric acid and various secondary amines were prepared based on supramolecular synthon rationale. Out of seven salts prepared, two showed moderate gelation abilities. The gels were characterized by differential scanning calorimetry, table top rheology, scanning electron microscopy, single crystal and powder X-ray diffraction. Structure property correlation based on X-ray diffraction techniques remain inconclusive indicating that some of the integrated part associated with the gelation phenomena requires a better understanding. |
format | Text |
id | pubmed-2956458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-29564582010-10-26 Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid Adalder, Tapas Kumar Adarsh, N N Sankolli, Ravish Dastidar, Parthasarathi Beilstein J Org Chem Full Research Paper In order to have access to chiral gels, a series of salts derived from (1R,3S)-(+)-camphoric acid and various secondary amines were prepared based on supramolecular synthon rationale. Out of seven salts prepared, two showed moderate gelation abilities. The gels were characterized by differential scanning calorimetry, table top rheology, scanning electron microscopy, single crystal and powder X-ray diffraction. Structure property correlation based on X-ray diffraction techniques remain inconclusive indicating that some of the integrated part associated with the gelation phenomena requires a better understanding. Beilstein-Institut 2010-09-21 /pmc/articles/PMC2956458/ /pubmed/20978610 http://dx.doi.org/10.3762/bjoc.6.100 Text en Copyright © 2010, Adalder 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 Adalder, Tapas Kumar Adarsh, N N Sankolli, Ravish Dastidar, Parthasarathi Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid |
title | Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid |
title_full | Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid |
title_fullStr | Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid |
title_full_unstemmed | Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid |
title_short | Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid |
title_sort | chiral gels derived from secondary ammonium salts of (1r,3s)-(+)-camphoric acid |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956458/ https://www.ncbi.nlm.nih.gov/pubmed/20978610 http://dx.doi.org/10.3762/bjoc.6.100 |
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