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  • The 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.
  • The 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. (en)
Title
  • OXIDATION PATHWAYS OF NATURAL DYE HEMATOXYLIN IN AQUEOUS SOLUTION
  • OXIDATION PATHWAYS OF NATURAL DYE HEMATOXYLIN IN AQUEOUS SOLUTION (en)
skos:prefLabel
  • OXIDATION PATHWAYS OF NATURAL DYE HEMATOXYLIN IN AQUEOUS SOLUTION
  • OXIDATION PATHWAYS OF NATURAL DYE HEMATOXYLIN IN AQUEOUS SOLUTION (en)
skos:notation
  • RIV/61388955:_____/10:00354402!RIV11-GA0-61388955
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA203/08/1157), P(GA203/09/1607), P(OC 140), Z(AV0Z40400503), Z(AV0Z40550506)
http://linked.open...iv/cisloPeriodika
  • 11
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 277867
http://linked.open...ai/riv/idVysledku
  • RIV/61388955:_____/10:00354402
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • hemotoxylin; oxidation; dye degradation; cyclic voltammetry (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • CZ - Česká republika
http://linked.open...ontrolniKodProRIV
  • [2DC2451470BD]
http://linked.open...i/riv/nazevZdroje
  • Collection of Czechoslovak Chemical Communications
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 75
http://linked.open...iv/tvurceVysledku
  • Gál, Miroslav
  • Hromadová, Magdaléna
  • Sokolová, Romana
  • Valášek, Michal
  • Degano, I.
  • Bulíčková, Jana
http://linked.open...ain/vavai/riv/wos
  • 000284230500003
http://linked.open...n/vavai/riv/zamer
issn
  • 0010-0765
number of pages
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