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Université de Fribourg

Tautomerism in azo dyes: Border cases of azo and hydrazo tautomers as possible NMR reference compounds

Deneva, Vera ; Lyčka, Antonin ; Hristova, S. ; Crochet, Aurélien ; Fromm, Katharina M. ; Antonov, Liudmil

In: Dyes and Pigments, 2019, vol. 165, p. 157–163

In order to meet the need for NMR reference compounds in the study of tautomeric azo dyes, two series of azo dyes, derived from 3-methyl-1-phenyl-4- (phenyldiazenyl)-1H-pyrazol-5-amine and 5-methyl-2-phenyl-4-(2- phenylhydrazono)-2,4-dihydro-3H-pyrazol-3-one, have been studied by using molecular spectroscopy (UV–Vis and NMR) and quantum-chemical calculations (M06- 2X/TZVP) in solution. The...

Université de Fribourg

Hydrogen atom transfer (HAT) processes promoted by the quinolinimide-N-oxyl radical: a kinetic and theoretical study

DiLabio, Gino A. ; Franchi, Paola ; Lanzalunga, Osvaldo ; Lapi, Andrea ; Lucarini, Fiorella ; Lucarini, Marco ; Mazzonna, Marco ; Prasad, Viki Kumar ; Ticconi, Barbara

In: The Journal of Organic Chemistry, 2017, vol. 82, no. 12, p. 6133–6141

A kinetic study of the hydrogen atom transfer (HAT) reactions from a series of organic compounds to the quinolinimide-N-oxyl radical (QINO) was performed in CH3CN. The HAT rate constants are significantly higher than those observed with the phthalimide- N-oxyl radical (PINO) as a result of enthalpic and polar effects due to the presence of the N-heteroaromatic ring in QINO. The relevance of...