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β-cyclodextrin as an end-to-end connector

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dc.contributor.author Retheesh, K
dc.contributor.author Gopidas, K R
dc.date.accessioned 2013-11-21T08:42:26Z
dc.date.available 2013-11-21T08:42:26Z
dc.date.issued 2011
dc.identifier.citation Journal of Physical Chemistry Letters 2(17):2094-2098;01 Sep 2011 en_US
dc.identifier.issn 1948-7185
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/793
dc.description.abstract Interaction 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.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Benzenes en_US
dc.subject Molecules en_US
dc.subject Polymers en_US
dc.subject Derivatives en_US
dc.subject Complexation en_US
dc.subject Supramolecular hydrogels en_US
dc.subject Induced circular-dichroism en_US
dc.title β-cyclodextrin as an end-to-end connector en_US
dc.type Article en_US


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