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
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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 |
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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 |
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