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

McAlpine, Eoghan; Sinclair, Roy S.; Truscott, T. George

dc.contributor.author	McAlpine, Eoghan
dc.contributor.author	Sinclair, Roy S.
dc.contributor.author	Truscott, T. George
dc.date.accessioned	2025-04-21T10:10:21Z
dc.date.available	2025-04-21T10:10:21Z
dc.date.issued	1977
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18707
dc.description.abstract	The 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 conditions	en_US
dc.language.iso	en	en_US
dc.publisher	Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 74 (3)	en_US
dc.subject	Chemistry	en_US
dc.subject	Radicals	en_US
dc.subject	Anthraquinones	en_US
dc.subject	Journal of the Chemical Society : Faraday Transaction - I	en_US
dc.title	Radicals Derived from 1,4-Disubstituted Anthraquinones: Further Evidence for Association of Quinones in Solution	en_US
dc.type	Article	en_US