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Freestanding organogels by molecular velcro of unsaturated amphiphiles
A simple amphiphile, N -cardanyltaurine amide (NCT) with different degrees of cis -unsaturation in its tail resulted in the formation of strong organogels. Interestingly, this is in contrast to the commonly accepted notion that introducing unsaturation in alkyl chains enhances fluidity in lipid asse...
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Published in: | Soft matter 2019-08, Vol.15 (31), p.6263-6268 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A simple amphiphile,
N
-cardanyltaurine amide (NCT) with different degrees of
cis
-unsaturation in its tail resulted in the formation of strong organogels. Interestingly, this is in contrast to the commonly accepted notion that introducing unsaturation in alkyl chains enhances fluidity in lipid assemblies. The physico-chemical and first-principles DFT calculations confirmed the pegging of 'kinked' unsaturated side chains, where the hydrophobic interlocking as in Velcro fasteners leads to a network of cylindrical micelles, resulting in self-standing organogels. Textural profile analysis and spectroscopic details substantiated the dynamic assembly to resemble a 3D network of gelators rather than being a cross-linked or polymerized matrix of monomers.
Gelation of amphiphiles due to the formation of networks of cylindrical chains of reverse micelles is observed. |
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ISSN: | 1744-683X 1744-6848 |
DOI: | 10.1039/c9sm00378a |