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dc.contributor.authorIreland, J. F.-
dc.contributor.authorWyatt, P. A. H.-
dc.date.accessioned2025-02-08T02:47:11Z-
dc.date.available2025-02-08T02:47:11Z-
dc.date.issued1972-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17392-
dc.description.abstractXanthone, which Ikis a ground state pK of -4.1, is shown to have a pK^j) value of +0.96 by fluorescence intensity measurements and a pK(7\) of +3.0 by triplet-triplet absorption measurements. The unusual order pK(7\) >pK(5i) >pK(5’0) is also reproduced in the Forster cycle values calculated from the absorption, fluorescence, and phosphorescence maxima, though the numbers thus obtained for pK(Ti) and pKGS^) arc 2 to 3 units more positive. Forster’s Cycle applied to the triplettriplet absorption spectra of the protonated and unprotonated species indicates that pK(T2) is —0.7, so that in basic strength the second triplet state lies between So and S1.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (6)en_US
dc.subjectChemistryen_US
dc.subjectXanthoneen_US
dc.subjectAqueous Solutionen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleExcited Singlet and Triplet pK Values of Xanthone in Aqueous Solutionen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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