National Repository of Grey Literature 7 records found  Search took 0.01 seconds. 
Differences in Oxidation Mechanism of Selected Bioflavonoids, UV-Vis and IR Spectroelectrochemical Study
Sokolová, Romana ; Fiedler, Jan ; Ramešová, Šárka ; Kocábová, Jana ; Degano, I. ; Quinto, A. ; Křen, Vladimír
The oxidation of selected bioflavonoids (quercetin, rhamnazin, fisetin, rhamnetin, taxifolin, luteolin, silybin and 2,3-dehydrosilybin) was studied by electrochemical and spectroscopic methods. The oxidation mechanism and formation of oxidation products depends on the chemical structure. Only small differences in the chemical structure of compounds with flavone, flavanone and flavonol motif result in extremely variable oxidation pathways and products. Products of oxidation and further decomposition were determined by HPLC-ESIMS/MS and HPLC-DAD.
Oxidation of Bioflavonoids in Respect to their Chemical Structure
Sokolová, Romana ; Ramešová, Šárka ; Kocábová, Jana ; Degano, I.
The electrochemical oxidation of flavone luteolin, flavanone taxifolin and flavonols derived from quercetin was studied by cyclic voltammetry. Only small differences in the chemical structure of bioflavonoids resulted in extremely variable oxidation pathways and products. Products of oxidation and further decomposition were determined by HPLC-ESI-MS/MS and HPLC-DAD.
Oxidation Mechanism of Rhamnetin, a Bioflavonoid Compound
Ramešová, Šárka ; Sokolová, Romana ; Degano, I.
The natural flavonoid rhamnetin (2-(3,4-dihydroxyfenyl)-3,5-dihydroxy-7-methoxychromen-4-one) is important bioactive compound. Rhamnetin was studied in aqueous solution by electrochemical methods. The oxidation mechanism proceeds in sequential steps, which correspond to the hydroxyl oxidation of groups in the three aromatic rings. The study is based on in situ spectroelectrochemistry and identification of products by HPLC-DAD and HPLC–ESI MS/MS.
Reduction and Oxidation of Hydroxyquinolines in Acetonitrile and Dimethylsulfoxide
Sokolová, Romana ; Ramešová, Šárka ; Fiedler, Jan ; Kolivoška, Viliam ; Degano, I. ; Gál, M. ; Szala, M. ; Nycz, J. E.
This study is focused on investigation of oxidation and reduction pathways of selected hydroxyquinoline compounds in nonaqueous solutions. The experimentally obtained reduction potentials are reported to well correlate with calculated values of LUMO energies as well as the obtained oxidation potentials are in a good agreement with theoretical HOMO energies. The cyclic voltammetry, in situ UV/Vis spectroelectrochemistry and in situ IR spectroelectrochemistry confirmed that the oxidation mechanism is complicated. Oxidation unexpectedly proceeds together with protonation of the starting compound. This behaviour was found for all studied compounds, hydroxyquinoline carboxylic acids and also for compounds, where a methyl group is present instead of carboxylic group.
Electrochemical Study of Rhamnazin
Ramešová, Šárka ; Sokolová, Romana ; Degano, I.
The natural flavonoid compound rhamanzin (3,5,4’-trihydroxy-7,3’-dimethoxyflavone) is important bioactive compound with antioxidative, anti-allergic, and anti-inflammatory properties. The cyclic voltammetry is used for the electrochemistry behavior of rhamnazin. The determination of oxidation pathways is supported by the identification of degradation products using separation technique.
The Electrochemistry of Natural Pigments
Sokolová, Romana ; Degano, I. ; Hromadová, Magdaléna ; Pospíšil, Lubomír
The electrochemical properties of flavonoid compounds (hemotoxylin, quercetin) were studied in buffered aqueous and non-aqueous solutions. The role of the preceding protonation/deprotonation on the electron transfer was estimated. The absorption spectra of these compounds, which contain a chromophore, were recorded during their oxidation. The electrochemical techniques were combined with GC-MS analysis in order to identify the degradation products. The mechanism of the formation of degradation products will be discussed.
Electrochemical study of degradation of natural dyes used in artworks
Sokolová, Romana ; Degano, I. ; Hromadová, Magdaléna
This work is focused on the electrochemical study of natural flavonoid dyes used in artworks. Electrochemical behaviour of hematoxylin was studied in 0.1 M KCl, phosphate buffers of pH 5 – 12 and in acetonitrile. The mechanism of oxidation and the stability of intermediates as a function of pH are discussed. The electrochemical techniques are combined with spectrophotometry, LC/DAD and GC-MS analysis in order to identify the degradation products.

Interested in being notified about new results for this query?
Subscribe to the RSS feed.