Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1449
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dc.contributor.authorAneesh, P S-
dc.contributor.authorSaleesh Kumar, N S-
dc.contributor.authorPrabhu, D D-
dc.contributor.authorShinto Varghese-
dc.contributor.authorKrishna Prasad, S-
dc.contributor.authorShankar Rao, D S-
dc.contributor.authorSuresh Das-
dc.date.accessioned2014-05-26T05:30:05Z-
dc.date.available2014-05-26T05:30:05Z-
dc.date.issued2014-
dc.identifier.citationJournal of the American Chemical Society 136(14):5416−5423;Apr 2014en_US
dc.identifier.issn0002-7863-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1449-
dc.description.abstractA series of highly luminescent oxadiazole-based stilbene molecules (OXD4, OXD8, OXD10, and OXD12) exhibiting interesting enantiotropic liquid crystalline and gelation properties have been synthesized and characterized. The molecules possessing longer alkyl substituents, OXD10 and OXD12, possess a pseudodisc shape and are capable of behaving as supergelators in nonpolar solvents, forming self-standing gels with very high thermal and mechanical stability. Notably the self-assembly of these molecules, which do not possess any hydrogen-bonding motifs normally observed in most reported supergelators, is driven purely by pi-stacking interactions of the constituent molecules. The d-spacing ratios estimated from XRD analysis of OXD derivatives possessing longer alkyl chains show that the molecules are arranged in a columnar fashion in the mesogens and the self-assembled nanofibers formed in the gelation process.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectSupergelatorsen_US
dc.subjectOxadiazole-based stilbene moleculesen_US
dc.subjectSupramolecular gelsen_US
dc.subjectOrganogelatorsen_US
dc.titleSupergelation via purely aromatic pi-pi driven self-assembly of pseudodiscotic oxadiazole mesogensen_US
dc.typeArticleen_US
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