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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17287
Title: Photochemistry and Radiation Chemistry of Anthraquinone-2-sodium-sulphonate in Aqueous Solution: Part 1.—Photochemical Kinetics in Aerobic Solution
Authors: Clark, K. P.
Stonehill, H. I.
Keywords: Chemistry
Photochemistry
Radiation Chemistry
Anthraquinone-2-sodium-sulphonate
Journal of the Chemical Society : Faraday Transaction - I
Issue Date: 1972
Publisher: Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (4)
Abstract: When 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.
URI: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17287
Appears in Collections:Journal Articles (before-1995)

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