Electrochemical behavior of 4-(5',6',7', 8'-Tetrahydro-naphthalene)-1-tetralone in aprotic media

Shekhawat, K, Sharma, H, Bhargava, S and Sharma, D 2013, 'Electrochemical behavior of 4-(5',6',7', 8'-Tetrahydro-naphthalene)-1-tetralone in aprotic media', Chemical Science Transactions, vol. 2, no. 4, pp. 1334-1339.


Document type: Journal Article
Collection: Journal Articles

Attached Files
Name Description MIMEType Size
n2006048784.pdf Published Version application/pdf 174.00KB
Title Electrochemical behavior of 4-(5',6',7', 8'-Tetrahydro-naphthalene)-1-tetralone in aprotic media
Author(s) Shekhawat, K
Sharma, H
Bhargava, S
Sharma, D
Year 2013
Journal name Chemical Science Transactions
Volume number 2
Issue number 4
Start page 1334
End page 1339
Total pages 6
Publisher WWW Publications Private
Abstract The electrochemical reduction of 4-(5',6',7',8'-tetrahydro-naphthalene)-1-tetralone was investigated in aprotic solvent dimethylsulphoxide at glassy carbon electrode (GCE) using the technique of cyclic voltammetry at room temperature. The reduction of tetralone carried out in acidic medium which is irreversible and involves transfer of two electrons. The intensity of cathodic peak current increases with increasing scan rate consistent with Randles-Sevcik equation. A linear behavior of peak current versus square root of scan rate indicates that the electrochemical reduction processes are diffusion controlled.
Subject Electrochemistry
Keyword(s) Tetralone
Cyclic voltammetry (Glassy carbon electrode)
Reduction
Irreversible
DOI - identifier 10.7598/cst2013.574
Copyright notice All rights reserved. Copyright © 2012 WWW Publications(P)- India. This is an open access article, distribution, and reproduction in any medium, provided the original work is properly cited.
ISSN 2278-3318
Versions
Version Filter Type
Altmetric details:
Access Statistics: 138 Abstract Views, 7 File Downloads  -  Detailed Statistics
Created: Thu, 15 Jan 2015, 13:42:00 EST by Catalyst Administrator
© 2014 RMIT Research Repository • Powered by Fez SoftwareContact us