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dc.contributor.authorRetheesh, K-
dc.contributor.authorGopidas, K R-
dc.date.accessioned2013-11-21T08:42:26Z-
dc.date.available2013-11-21T08:42:26Z-
dc.date.issued2011-
dc.identifier.citationJournal of Physical Chemistry Letters 2(17):2094-2098;01 Sep 2011en_US
dc.identifier.issn1948-7185-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/793-
dc.description.abstractInteraction of beta-cyclodextrin (beta-CD) with a ditopic molecule having adamantane (AD) at one end and a pyromellitic diimide (PMDI) moiety at the other is studied. The AD moiety undergoes inclusion binding with the beta-CD cavity, and the PMDI undergoes binding with the primary rim of beta-CD. In an equimolar solution of beta-CD and the ditopic molecule in water, beta-CD accommodates both modes of complexation simultaneously, leading to the formation of long fibers. The fibers get entangled to give a supramolecular hydrogel with very high water content.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectBenzenesen_US
dc.subjectMoleculesen_US
dc.subjectPolymersen_US
dc.subjectDerivativesen_US
dc.subjectComplexationen_US
dc.subjectSupramolecular hydrogelsen_US
dc.subjectInduced circular-dichroismen_US
dc.titleβ-cyclodextrin as an end-to-end connectoren_US
dc.typeArticleen_US
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