Maitra, Uday and Kumar, Vijay P and Chandra, Nividh and DSouza, Lawrence J and Prasanna, MD and Raju, AR (1999) First donor-acceptor interaction promoted gelation of organic fluids. In: Chemical Communications (7). pp. 595-596.
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Abstract
In recent years there has been considerable interest in developing new types of gelators of organic solvents.1 Despite the recent advances, a priori design of a gelator for gelling a given solvent has remained a challenging task. Various noncovalent interactions like hydrogen-bonding,2 metal coordination3 etc. have been used as the driving force for the gelation process. A special class of cholesterol-based gelators were reported by Weiss,4 and by Shinkai.5 Gels derived from these molecules have been used for chiral recognition/sensing,6 for studying photo- and metal-responsive functions,7 and as templates to make hollow fiber silica.8 Other types of organogels have been used for designing polymerized 9 and reverse aerogels,10 and in molecular imprinting.11 Hanabusa’s group has recently reported organogels with a bile acid derivative.12 This has prompted us to disclose our results on a novel electron donor–acceptor (EDA) interaction mediated two-component13 gelator system based on the bile acid14 backbone.
Item Type: | Journal Article |
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Publication: | Chemical Communications |
Publisher: | The Royal Society of Chemistry |
Additional Information: | Copyright of this article belongs to The Royal Society of Chemistry. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 21 Jul 2009 11:16 |
Last Modified: | 19 Sep 2010 05:28 |
URI: | http://eprints.iisc.ac.in/id/eprint/19513 |
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