Abstract

4-Hydroxyproline, 8-hydroxyquinoline, 4-hydroxyquinoline-2-carboxylic acid and 4-hydroxyphenylacetic acid (HPA) react with H 2O 2 when irradiated with UV light to yield fluorescent products. Sub-micromolar detection limits of H 2O 2 are possible with HPA. The fluorescent product is the same as that formed in the peroxidase enzyme-mediated H 2O 2 oxidation of HPA. Several compounds that participate in the photomediated reaction do not react in the enzyme-mediated system. A mechanism for the photomediated reaction involving an aryloxy radical derived from the substrate is suggested. Although the limits of detection for H 2O 2 do not equal the best achievable with the enzyme-mediated systems, the simplicity of a single-step reaction and an ability to “photodevelop” the product offer a range of novel analytical possibilities.

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