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ortho-Substituted (aryl)(3-nitrobenzo[b]thiophen-2-yl)amines: study of the electrochemical behavior.

Authors :
Cosimelli B
Lanza CZ
Scavetta E
Severi E
Spinelli D
Stenta M
Tonelli D
Source :
The journal of physical chemistry. A [J Phys Chem A] 2009 Sep 24; Vol. 113 (38), pp. 10260-3.
Publication Year :
2009

Abstract

The reduction potentials of the title compounds 4 have been measured by cyclic voltammetry. The effect of the substituents has been evaluated by using a linear free energy relationship treatment, thus evidencing that the present ortho-substituents affect the Epc values basically by electronic effects. A comparison with data previously collected on ortho-substituted (aryl)(2-nitrobenzo[b]thiophen-3-yl)amines 3 has provided some interesting information. Different electrochemical behaviors are observed during the reduction (a reversible process and an irreversible process are operating in 3 and 4, respectively): to elucidate the reasons for this different behavior, the "reversible" reduction potentials of 5 and of 6 have been measured. Moreover, higher susceptibility constants have been calculated for compounds of series 4 with respect to those of series 3 (rho4 = 329 and rho3 = 182, respectively). A rationale for all of these findings has been offered.

Details

Language :
English
ISSN :
1520-5215
Volume :
113
Issue :
38
Database :
MEDLINE
Journal :
The journal of physical chemistry. A
Publication Type :
Academic Journal
Accession number :
19708677
Full Text :
https://doi.org/10.1021/jp9056972