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EPR and UV−Vis−NIR spectroscopic features of radical ions of amino substituted thienyl ketones

Year: 2025
Type: article
Abstract: A series of amino-substituted mono- and bis-thienyl ketones were characterized by means of cyclic voltammetry, ultraviolet−visible−near infrared (UV−Vis−NIR) absorption spectroscopy, and in situ electron paramagnetic resonance (EPR)/UV−Vis−NIR spectroelectrochemistry. The molecular structures of bis-thienyl ketones contain morpholine ( 3a–c ) or N,N ´-disubstituted amino ( 3d–f ) groups. The electrochemical reduction of the ketones leads to the formation of stable radical anions, and their EPR and UV−Vis−NIR spectral features were analyzed in detail. In contrast, the radical cations are not stable and undergo follow-up chemical reactions with formation of redox-active dimers. The EPR data and DFT calculations provide information about the charge/spin localization in the electrochemically generated radical ions.
Language: English
Subfield: Biophysics
Open Access status: hybrid
Estimated APC paid: $3,790
OpenAlex ID: W4416898759
FWCI: 0.745
Cites: 20
Cited by: 2
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