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 |