Radical trapping properties of imidazolyl nitrones - Archive ouverte HAL Access content directly
Journal Articles Free Radical Research Year : 2006

Radical trapping properties of imidazolyl nitrones


The ability of ten imidazolyl nitrones to directly scavenge free radicals (R√) generated in polar (√OH, cysteinyl, √CH3) or in apolar (CH3–√CH–CH3) media has been studied. When oxygen or sulfur-centered radicals are generated in polar media, EPR spectra are not or weakly observed with simple spectral features. Strong line intensities and more complicated spectra are observed with the isopropyl radical generated in an apolar medium. Intermediate results are obtained with √CH3 generated in a polar medium. EPR demonstrates the ability of these nitrones to trap radicals to the nitrone C(α) atom (alpha radical adduct) and to the imidazol C(5) atom (5-radical adduct). Beside the nucleophilic addition of the radical to the C(α) atom, the EPR studies suggest a two-step mechanism for the overall reaction of R√ attacking the imidazol core. The two steps seem to occur very fast with the √OH radical obtained in a polar medium and slower with the isopropyl radical prepared in benzene. In conclusion, imidazolyl nitrones present a high capacity to trap and stabilize carbon-centered radicals.
Fichier principal
Vignette du fichier
Reybier_23177.pdf (435.18 Ko) Télécharger le fichier
Origin Files produced by the author(s)

Dates and versions

hal-02143180 , version 1 (29-05-2019)



Karine Reybier, Jeremie Boyer, Vincent Farines, Fabrice Camus, Jean-Pierre Souchard, et al.. Radical trapping properties of imidazolyl nitrones. Free Radical Research, 2006, 40 (1), pp.11-20. ⟨10.1080/10715760500329598⟩. ⟨hal-02143180⟩
41 View
71 Download



Gmail Mastodon Facebook X LinkedIn More