Please use this identifier to cite or link to this item:
Full metadata record
DC FieldValueLanguage
dc.contributor.authorBhat, P.B.
dc.contributor.authorBhat, B.R.
dc.identifier.citationNew Journal of Chemistry, 2015, Vol.39, 6, pp.4933-4938en_US
dc.description.abstractA Schiff base immobilised nanocatalyst was synthesized via copper catalysed alkyne azide cycloaddition (CuAAC) on a magnetic support. The nanocatalyst exhibited high accessible active sites with a surface area of 76 m2 g-1 for a cobalt complex and 57 m2 g-1 for a nickel complex. A strong interaction between the magnetic support and the Schiff base was achieved by avoiding leaching during the course of reaction. The nanocatalyst efficiently oxidised both primary and secondary alcohols to carbonyl with improved yield in a solventless system rendering a greener approach. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2015.en_US
dc.titleAn immobilised Co(ii) and Ni(ii) Schiff base magnetic nanocatalyst via a click reaction: A greener approach for alcohol oxidationen_US
Appears in Collections:1. Journal Articles

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.