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OXIDATION PATHWAYS OF NATURAL DYE HEMATOXYLIN IN AQUEOUS SOLUTION

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    SYSNO ASEP0354402
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleOXIDATION PATHWAYS OF NATURAL DYE HEMATOXYLIN IN AQUEOUS SOLUTION
    Author(s) Sokolová, Romana (UFCH-W) RID, ORCID, SAI
    Degano, I. (IT)
    Hromadová, Magdaléna (UFCH-W) RID, ORCID, SAI
    Kocábová, Jana (UFCH-W) RID
    Gál, Miroslav (UFCH-W)
    Valášek, Michal (UOCHB-X)
    Source TitleCollection of Czechoslovak Chemical Communications. - : Ústav organické chemie a biochemie AV ČR, v. v. i. - ISSN 0010-0765
    Roč. 75, č. 11 (2010), s. 1097-1114
    Number of pages18 s.
    Languageeng - English
    CountryCZ - Czech Republic
    Keywordshemotoxylin ; oxidation ; dye degradation ; cyclic voltammetry
    Subject RIVCG - Electrochemistry
    R&D ProjectsGA203/09/1607 GA ČR - Czech Science Foundation (CSF)
    GA203/08/1157 GA ČR - Czech Science Foundation (CSF)
    OC 140 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    AV0Z40550506 - UOCHB-X (2005-2011)
    UT WOS000284230500003
    DOI10.1135/cccc2010096
    AnnotationThe oxidation mechanism of hematoxylin was studied in phosphate buffers and 0.1 M KCl by cyclic voltammetry and UV-Vis spectroscopy under deaerated conditions. The redox potential of hematoxylin in buffered solution strongly depends on pH. A two electron oxidation is preceded by deprotonation. The homogeneous rate of deprotonation process of hematoxylin in 0.1 M phosphate buffer is k(d) = (2.5 +/- 0.1) x 10(4) s(-1). The cyclic voltammetry under unbuffered conditions shows the distribution of various dissociation forms of hematoxylin. The dissociation constants pK(1) = 4.7 +/- 0.2 and pK(2) = 9.6 +/- 0.1 were determined using UV-Vis spectroscopy. The final oxidation product was identified by gas chromatography with mass spectrometry detection as hemathein. The distribution of oxidation products differs under buffered and unbuffered conditions. The dye degradation in natural unbuffered environment yields hemathein and hydroxyhematoxylin, which is absent in buffered solution.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2011
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