RESUMEN
The biocatalytic system laccase/TEMPO/O2 has attracted the attention of researchers over the past two decades. A variety of applications for the system include organic synthesis, modification of cellulose, and oxidative degradation of environmental contaminants. A rigorous and predictable quantitative assessment of the change in enzymatic activity under the influence of a mediator is important for such a system. In this study, the operative conditions for carrying out a model reaction for the degradation of the synthetic dye Indigo Carmine in the presence of Trametes versicolor laccase/TEMPO were determined and the enzyme inactivation under the action of a mediator and substrate was studied. The long-term stability of Trametes versicolor laccase was assessed and the regression model of the response surface of laccase activity under the influence of TEMPO was created. It has been shown that laccase is inactivated in the presence of TEMPO, but the addition of the dye, CuSO4 or CuCl2 reduces this effect. The system under study can be used repeatedly for the Indigo Carmine decolorization, however, a gradual falling rate during the process is observed from cycle to cycle. This is due to two reasons - firstly, a decrease in the enzyme activity with each batch and secondly, the consumption of the mediator (22% within 5 days). Relatively high enzyme activity (>40%) is maintained after 73 cycles (1 portion of IC contained 25 µM) using 500 µM TEMPO and 0.12 U mL-1 laccase. The laccase/TEMPO system has shown its effectiveness in the treatment of artificial wastewater containing high concentrations of Indigo carmine (0.5 g L-1). In this case, the dye solution becomes 100% colorless within 5 hours in the presence of dye bath components and within 7.5 hours in a buffer solution.
RESUMEN
A model for predicting the rate constants of hydrogen atom transfer (HAT) from the α-C-H bond of p-substituted benzyl alcohols to N-oxyl radicals was proposed. To quantify the factors governing the reactivity of both N-oxyl radicals and benzyl alcohols, multivariate regression analysis was performed using various combinations of reactivity parameters. The analysis was based on a 2D array of 35 HAT reactions, the rate constants of which span 4 orders of magnitude. The proposed polyparameter equation approximates the experimental rate constants of reactions with high accuracy using three independent parameters: Brown and Okamoto's substituent constants σ+ in alcohol molecules and the spin population on O and N atoms in the N-O⢠fragment of N-oxyl radicals [calculated by DFT/B3LYP/6-31G(d,p)]. The rate constants of HAT reactions from p-substituted benzyl alcohols to a series of aryl-substituted phthalimide-N-oxyl radicals containing either electron-withdrawing or electron-donating substituents (4-Cl, 4-HOOC, 4-CH3O), quinolinimide-N-oxyl, benzotriazole-N-oxyl, and violuric acid radicals were experimentally determined at 30 °C in acetonitrile.
RESUMEN
Nitroxyl radicals are widely used in chemistry, materials sciences, and biology. Imide-N-oxyl radicals are subclass of unique nitroxyl radicals that proved to be useful catalysts and mediators of selective oxidation and CH-functionalization. An efficient metal-free method was developed for the generation of imide-N-oxyl radicals from N-hydroxyimides at room temperature by the reaction with (diacetoxyiodo)benzene. The method allows for the production of high concentrations of free radicals and provides high resolution of their EPR spectra exhibiting the superhyperfine structure from benzene ring protons distant from the radical center. An analysis of the spectra shows that, regardless of the electronic effects of the substituents in the benzene ring, the superhyperfine coupling constant of an unpaired electron with the distant protons at positions 4 and 5 of the aromatic system is substantially greater than that with the protons at positions 3 and 6 that are closer to the N-oxyl radical center. This is indicative of an unusual character of the spin density distribution of the unpaired electron in substituted phthalimide-N-oxyl radicals. Understanding of the nature of the electron density distribution in imide-N-oxyl radicals may be useful for the development of commercial mediators of oxidation based on N-hydroxyimides.
