
doi: 10.1039/c6pp00037a
pmid: 27265022
Betanin is the best known natural dye belonging to the betacyanin family. In this work, efficient singlet oxygen quenching by betanin in deuterated water with the rate constant 1.20 ± 0.15 × 10(8) M(-1) s(-1) is reported, deduced from the (1)O2 phosphorescence decays measured as a function of betanin concentration. The quenching occurs by a chemical mechanism, as confirmed by the analysis of the transient absorption kinetics at the probe λ ∼ 535 nm, by comparison of the initial triplet signal amplitude of perinaphthenone acting as the (1)O2 photosensitizer with the final bleaching signal of betanin. The main betanin oxidation product is 2-decarboxy-2,3-dehydrobetanin, with its formation observed as the transient absorption signal at λ ∼ 445 nm. LC-MS/MS analysis of the photolyzed solutions supports the product identification as 2-decarboxy-2,3-dehydrobetanin, based on the molecular ion [M](+) observed at m/z 505. Isobetanin also undergoes a similar photooxidation reaction.
Photolysis, Singlet Oxygen, Tandem Mass Spectrometry, Ultraviolet Rays, Betacyanins, Oxidation-Reduction, Chromatography, High Pressure Liquid
Photolysis, Singlet Oxygen, Tandem Mass Spectrometry, Ultraviolet Rays, Betacyanins, Oxidation-Reduction, Chromatography, High Pressure Liquid
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