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Supergelation via purely aromatic pi-pi driven self-assembly of pseudodiscotic oxadiazole mesogens

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dc.contributor.author Aneesh, P S
dc.contributor.author Saleesh Kumar, N S
dc.contributor.author Prabhu, D D
dc.contributor.author Shinto Varghese
dc.contributor.author Krishna Prasad, S
dc.contributor.author Shankar Rao, D S
dc.contributor.author Suresh Das
dc.date.accessioned 2014-05-26T05:30:05Z
dc.date.available 2014-05-26T05:30:05Z
dc.date.issued 2014
dc.identifier.citation Journal of the American Chemical Society 136(14):5416−5423;Apr 2014 en_US
dc.identifier.issn 0002-7863
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/1449
dc.description.abstract A 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.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Supergelators en_US
dc.subject Oxadiazole-based stilbene molecules en_US
dc.subject Supramolecular gels en_US
dc.subject Organogelators en_US
dc.title Supergelation via purely aromatic pi-pi driven self-assembly of pseudodiscotic oxadiazole mesogens en_US
dc.type Article en_US


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