Issue 2, 1996

On the existence of quinone radical cations. A study in 1,1,1,3,3,3-hexafluoropropan-2-ol

Abstract

The strongly stabilizing influence of 1,1,1,3,3,3-hexafluoropropan-2-ol (HFP) upon radical cations has been utilized to study the photolysis of a few quinones (Q), viz. benzoquinone, duroquinone, anthraquinone and tetrafluorobenzoquinone, in HFP containing 6% trifluoroacetic acid. The EPR spectra of the photolysed solutions are assigned to the radical cations of the corresponding hydroquinones (QH2˙+, the three first-mentioned quinones) or the protonated semiquinone (QH˙, the tetrafluoro derivative), formed in a one-electron redox process involving excited Q as the reductant, in agreement with earlier studies in strongly acidic media.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1996, 151-154

On the existence of quinone radical cations. A study in 1,1,1,3,3,3-hexafluoropropan-2-ol

L. Eberson and M. P. Hartshorn, J. Chem. Soc., Perkin Trans. 2, 1996, 151 DOI: 10.1039/P29960000151

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