Interaction of pyromellitic diimide derivatives with beta-cyclodextrin and anthracene-appended beta-cyclodextrin: Rim binding vs inclusion complexation

dc.contributor.author	Bijitha, B
dc.contributor.author	Deepthi, L S
dc.contributor.author	Gopidas, K R
dc.date.accessioned	2014-04-17T08:54:56Z
dc.date.available	2014-04-17T08:54:56Z
dc.date.issued	2007
dc.identifier.citation	Organic Letters 9(14):2709-2712;5 Jul 2007	en_US
dc.identifier.issn	1523-7060
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/1327
dc.description.abstract	Complex formation of pyromellitic diimide derivatives with beta-cyclodextrin and anthracene-appended beta-cyclodextrin was studied with use of induced circular dichroism and H-1 NMR spectroscopies. It is revealed that pyromellitic diimides form rim-binding type complexes with beta-CD and in these complexes the pyromellitic diimides lie just outside of the narrow rim of the CD. With anthracene-appended beta-CD the pyromellitic diimides form true inclusion complexes. Implications of the formation of rim-binding type complexes are also discussed.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Induced circular dichroism	en_US
dc.subject	Benzenes	en_US
dc.title	Interaction of pyromellitic diimide derivatives with beta-cyclodextrin and anthracene-appended beta-cyclodextrin: Rim binding vs inclusion complexation	en_US
dc.type	Article	en_US