CORRELATION OF THE HOMO–LUMO GAP IN FURYL AND THIENYL NITRONES AND NITROETHENES WITH THEIR ELECTROCHEMICAL REDOX POTENTIALS
DOI:
https://doi.org/10.1007/966Ключевые слова:
organylsilylfuryl(thienyl)nitrones, organylsilylfuryl(thienyl)nitroethenes, IR spectroscopy, 1H, 13C, 29Si NMR spectroscopy, electrochemical redox potentials, synthesisАннотация
Two series of potentially biologically active heteroaryl derivatives of nitrones and nitroethenes have been prepared and studied by cyclic voltammetry and DFT modeling. Satisfactory correlations of experimental first peak potentials Ep, both in oxidation and in
reduction, with the energies of the corresponding frontier orbitals were found.
How to Cite
Boulkroune, M.; Ignatovich, L.; Muravenko, V.; Spura, J.; Chibani, A.; Jouikov, V. Chem. Heterocycl. Compd. 2014, 49, 1579. [Khim. Geterotsikl. Soedin. 2013, 1706.]
For this article in the English edition see DOI 10.1007/s10593-014-1409-3
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Опубликован
2013-10-22
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Оригинальные статьи