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ortho-Substituted (aryl)(3-nitrobenzo[b]thiophen-2-yl)amines: study of the electrochemical behavior
- Source :
- The journal of physical chemistry. A. 113(38)
- 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.
- Subjects :
- Molecular Structure
Chemistry
Aryl
Stereoisomerism
Reversible process
Free-energy relationship
Electrochemistry
Medicinal chemistry
Irreversible process
studio elettrochimico
chemistry.chemical_compound
Electronic effect
Organic chemistry
Physical and Theoretical Chemistry
Cyclic voltammetry
Amines
Subjects
Details
- ISSN :
- 15205215
- Volume :
- 113
- Issue :
- 38
- Database :
- OpenAIRE
- Journal :
- The journal of physical chemistry. A
- Accession number :
- edsair.doi.dedup.....16f26ca85d64dcb27f82f76293e9ad76