Synthesis of cupric acetate selective receptor derived from alanyl glycoconjugate and their application in selective oxidation of benzylic alcohols

Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2785

Full metadata record

DC Field	Value	Language
dc.contributor.author	Sah, Ajay Kumar	-
dc.date.accessioned	2021-10-14T13:07:57Z	-
dc.date.available	2021-10-14T13:07:57Z	-
dc.date.issued	2012-11	-
dc.identifier.uri	https://www.sciencedirect.com/science/article/abs/pii/S1566736712003287?via%3Dihub	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2785	-
dc.description.abstract	Cupric acetate sensing ability of alanyl-(4,6-O-ethylidene-β-D-glucopyranosylamine) derived receptor (L-N2O2) has been explored using fluorescence and UV–visible absorption spectroscopy. Cupric acetate quenches the fluorescence intensity of L-N2O2 with a correlation coefficient, R = 0.978 and Stern Volmer constant, KSV = 38,067 M− 1 revealing the possibilities of interaction via dynamic mode. Further, copper complex of L-N2O2 has been utilized in selective oxidation of primary and secondary alcohols into the corresponding carbonyl compounds.	en_US
dc.language.iso	en	en_US
dc.publisher	ACS	en_US
dc.subject	Chemistry	en_US
dc.subject	Glucopyranosylamine	en_US
dc.subject	Copper	en_US
dc.subject	Fluorescence	en_US
dc.title	Synthesis of cupric acetate selective receptor derived from alanyl glycoconjugate and their application in selective oxidation of benzylic alcohols	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

Files in This Item:

There are no files associated with this item.