O–H bond strengths and one-electron reduction potentials of multisubstituted phenols and phenoxyl radicals. Predictions using free energy relationships-Reference-Cited by-同舟云学术

O–H bond strengths and one-electron reduction potentials of multisubstituted phenols and phenoxyl radicals. Predictions using free energy relationships

Published:1993 Issue:9 Volume: Page:1567-1568
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Jonsson Mats,Lind Johan,Eriksen Trygve E.,Merényi Gabor

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1993/P2/P29930001567

Reference21 articles.

1. Oxygen-hydrogen bond dissociation energies in para-substituted phenols

2. The one-electron reduction potential of 4-substituted phenoxyl radicals in water

3. Substituent effects on the stabilities of phenoxyl radicals and the acidities of phenoxyl radical cations

4. The two hydrogen-oxygen bond-dissociation energies of hydroquinone

5. Radical cation acidities in dimethyl sulfoxide solution

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