Show simple item record

dc.contributor.authorBilici, A. and Geçibesler, I.H. and Kaya, I.
dc.date.accessioned2021-04-08T12:08:28Z
dc.date.available2021-04-08T12:08:28Z
dc.date.issued2016
dc.identifier10.1139/cjc-2016-0210
dc.identifier.issn00084042
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85008367769&doi=10.1139%2fcjc-2016-0210&partnerID=40&md5=13b8ae8534d95c6f2d6a23ff40481d2e
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4611
dc.description.abstractThe compound 5-aminoquinoline (AQ) was treated with horseradish peroxidase (HRP) and H2O2 in a reaction medium containing a dioxane:phosphate buffer mixture (70:30). Products (OAQ) with a degree of polymerization ranging from 4 to 12 were obtained. 1H NMR, FTIR, UV-vis, SEM, TG-DTA, DSC, XRD analysis, and conductivity measurements were conducted for characterization of OAQ. Compared with a monomer, OAQ showed higher thermal stability. After heating to 1000 °C, 46% of the initial weight of the OAQ remained. The antioxidant efficiencies of the monomer and oligomer were evaluated by the typical spectrophotometric method such as the bleaching of 2,2-diphenyl-1-picrylhydrazyl (DPPH) radicals. OAQ showed improved DPPH activity compared with the AQ monomer. © 2017 Published by NRC Research Press.
dc.language.isoEnglish
dc.sourceCanadian Journal of Chemistry
dc.titleEnzymatic synthesis of 5-amino quinoline oligomers and evaluation of their free radical scavenging activity


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record