Reactivities of diphenylfuran (a singlet oxygen trap) with singlet oxygen and hydroxyl radical in aqueous systems. |
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Authors: | K Takayama T Noguchi M Nakano |
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Affiliation: | Department of Biochemistry, School of Medicine, Gunma University Maebashi, Gunma 371, Japan;Department of Chemistry, Gunma University, Kiryu, Gunma 376, Japan |
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Abstract: | ![]() It has been studied whether 2,5-diphenylfuran is a specific singlet oxygen trap in aqueous systems. With certain 1O2 generating systems (Rose Bengal photooxygenation and NaOClH2O2 systems) and·OH generating systems (Fenton's reagent and acetaldehyde-xanthine oxidase system), diphenylfuran was chiefly converted in all cases to cis-dibenzoyl-ethylene, but not to trans-dibenzoylethylene. Low but detectable conversion of diphenylfuran to a hydroperoxide, probably a distinct 1O2-derived reaction in aqueous media, was found only in the Rose Bengal photooxygenation system. |
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Keywords: | singlet molecular oxygen DPF 2,5-diphenylfuran cis-DBE cis-1,2-dibenzoylethylene trans-DBE trans-1,2-dibenzoylethylene NMR nuclear magnetic resonance IR infrared |
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