| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 219175 | Journal of Electroanalytical Chemistry | 2013 | 9 Pages |
A selected series of new different substituted 3-arylcoumarins have been designed, synthesized, and evaluated their electrochemical redox mechanisms. The relevant structural information about coumarins was considered in order to better understand the structure/electrochemical relationship. The influence of bromine, methyl or other hydroxyl groups in different positions of the coumarin scaffold, by cyclic, differential pulse and square wave voltammetry at a glassy carbon electrode at different pHs was investigated. A comparative study of differently substituted 8-hydroxy-3-arylcoumarins was performed.
► New different substituted 3-arylcoumarins have been designed and synthesized, and evaluated their electrochemical redox mechanisms. ► pH-dependent oxidation and reduction processes investigated using a glassy carbon electrode. ► Influence of bromine, methyl or other hydroxyl groups in different positions of the coumarin scaffold.
