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dc.contributor.authorClark, K. P.-
dc.contributor.authorStonehill, H. I.-
dc.date.accessioned2025-02-07T02:15:05Z-
dc.date.available2025-02-07T02:15:05Z-
dc.date.issued1972-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17287-
dc.description.abstractWhen aqueous solutions of anthraquinone-2-sodium-sulphonate (D) are photolyzed the quinone becomes hydroxylated and (in the absence of oxygen) reduced. On the basis of the kinetics of the photohydroxylation in air or oxygen saturated solutions (pH 2–14), two alternative mechanisms are proposed, the 3D*/S (S = H2O or OH–) and the 3D*/D. In the former, D attacks S to produce an adduct DOH– which is converted by ground-state D to the radical DOH·. In the latter, 3D* attacks D to form a solvent caged radical pair {D·+ D·–}, the D·+ constituent then reacting with S to give OH· radicals which with D yield DOH·. This intermediate is converted by oxygen to hydroxy product. Neither continuous irradiation kinetics nor conventional µs flash photolysis permits discrimination between these schemes. The thermodynamic feasibility of OH· production by the 3D*/D reaction is demonstrated.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (4)en_US
dc.subjectChemistryen_US
dc.subjectPhotochemistryen_US
dc.subjectRadiation Chemistryen_US
dc.subjectAnthraquinone-2-sodium-sulphonateen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titlePhotochemistry and Radiation Chemistry of Anthraquinone-2-sodium-sulphonate in Aqueous Solution: Part 1.—Photochemical Kinetics in Aerobic Solutionen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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