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handle: 1822/64867
This work reports on cyclic voltammetry and spectroscopic UV-Vis investigations of some pyridazine derivatives 1-8 in dimethylformamide. In the electrochemical study, monochlorinated pyridazines 2-8 exhibit two reductions but in the case of dichlorinated derivative 1 an additional wave is seen for the reduction of the second carbon-chloride bond. The electronic absorption spectra display an intramolecular charge transfer band π-π* in the UV region of which depend substantially on the nature of both donor and acceptor moieties. These results indicate the π-electron delocalization in the conjugated system.
Pyridazines, Synthesis, push-pull pi-congugated molecules, electrochemistry, Electrochemistry, donor- -bridge-acceptor systems, pyridazines, UV-Vis spectroscopy, electronic spectra
Pyridazines, Synthesis, push-pull pi-congugated molecules, electrochemistry, Electrochemistry, donor- -bridge-acceptor systems, pyridazines, UV-Vis spectroscopy, electronic spectra
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