Radicals Derived from 1,4-Disubstituted Anthraquinones: Further Evidence for Association of Quinones in Solution

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dc.contributor.authorMcAlpine, Eoghan
dc.contributor.authorSinclair, Roy S.
dc.contributor.authorTruscott, T. George
dc.date.accessioned2025-04-21T10:10:21Z
dc.date.available2025-04-21T10:10:21Z
dc.date.issued1978
dc.description.abstractThe radicals derived from three 1,4-disubstituted anthraquinones containing NH;, NHMc and OH substituent groups have been studied in methanol solution using the technique of pulse radiolysis. Absorption spectra and rates of formation of semiquinone radical species (DH« and Dr),formed respectively under acidic and alkaline conditions, have been recorded. Aggregation of the ground state dye must be assumed to obtain positive extinction coefficients for the radical formed under alkaline conditionsen_US
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18707
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (3)en_US
dc.subjectChemistryen_US
dc.subjectRadicalsen_US
dc.subjectAnthraquinonesen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleRadicals Derived from 1,4-Disubstituted Anthraquinones: Further Evidence for Association of Quinones in Solutionen_US
dc.typeArticleen_US

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