Cyclic voltametric study of some alkyl substituted N-hydroxy-2,6-diarylpiperidin-4-one semicarbazone and the antibacterial studies of the products Online publication date: Sun, 09-Jul-2017
by J.B. Veeramalini; G. Baskar; N. Sheeja
International Journal of Materials and Product Technology (IJMPT), Vol. 55, No. 1/2/3, 2017
Abstract: A series of 3-ethyl-2,6-diarylpiperidin-4-one semicarbazone and 3,5-dimethyl-2,6-diarylpiperidin-4-one semicarbazone were synthesised. The semicarbazones were subjected to cyclic voltammetric analysis using glassy carbon electrode with variable scan rate. The method involves electron transfer without the use of oxidising or reducing agents. The study of cyclic voltammogram showed that all the compounds have undergone irreversible reduction. The peak potential values, the number of peaks formed during the anodic and cathodic scan and the different scan rate used have established irreversible reduction reaction. The reduction products were isolated and purified by column chromatography. The structure is proved by 1H and 13C NMR spectroscopy. Further five products were analysed for anti bacterial activity and the nitro substituted compound showed a high inhibition towards Salmonella typii among the eight bacterial cultures.
Existing subscribers:
Go to Inderscience Online Journals to access the Full Text of this article.
If you are not a subscriber and you just want to read the full contents of this article, buy online access here.Complimentary Subscribers, Editors or Members of the Editorial Board of the International Journal of Materials and Product Technology (IJMPT):
Login with your Inderscience username and password:
Want to subscribe?
A subscription gives you complete access to all articles in the current issue, as well as to all articles in the previous three years (where applicable). See our Orders page to subscribe.
If you still need assistance, please email subs@inderscience.com
Our Blog 
Follow us on Twitter 
Visit us on Facebook