Nature of the radical formed during electrolytic reduction of 4-(2'-thienyl)quinazoline in dimethylformamide

Priyamvada Devi, T. ; Gopinathan, M. S. ; Venkatachalam, C. S. (1980) Nature of the radical formed during electrolytic reduction of 4-(2'-thienyl)quinazoline in dimethylformamide Electrochimica Acta, 25 (9). pp. 1173-1176. ISSN 0013-4686

Full text not available from this repository.

Official URL: http://linkinghub.elsevier.com/retrieve/pii/001346...

Related URL: http://dx.doi.org/10.1016/0013-4686(80)87115-5

Abstract

EPR studies and HMO calculations are carried out in order to understand the nature of the electrolytically generated radical of 4(2'-thienyl)quinazoline (4-TQ) in dimethylformamide (DMF). Single broad EPR signal obtained is explained on the basis of theoretical hyperfine splitting constants. By correlating the experimental half-wave potentials and the colour of the radical with HMO energies, it is concluded that 4-TQ protonated at N1-position is getting reduced to give the neutral radical.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:15176
Deposited On:13 Nov 2010 06:36
Last Modified:02 Jun 2011 07:04

Repository Staff Only: item control page