Issue 0, 1978

Radicals derived from 1,4-disubstituted anthraquinones. Further evidence for association of quinones in solution

Abstract

The radicals derived from three 1,4-disubstituted anthraquinones containing NH2, NHMe 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 D.), 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.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 1, 1978,74, 597-602

Radicals derived from 1,4-disubstituted anthraquinones. Further evidence for association of quinones in solution

E. McAlpine, R. S. Sinclair, T. G. Truscott and E. J. Land, J. Chem. Soc., Faraday Trans. 1, 1978, 74, 597 DOI: 10.1039/F19787400597

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements