Calculations on phenol and a large number of phenols substituted with methyl, methoxyl, and amino groups have yielded reliable gas-phase O-H bond dissociation energies, BDE(ArO-H)(gas). Geometries for the phenol, ArOH, and aryloxyl radical, ArO, were optimized at the (semiempirical) AM1 level followed by single point density functional theory (DFT) calculations using a 6-31G basis set supplemented with p-functions on the hydrogen atom and the B3LYP density functional. This gave BDE(PhO-H)(gas) = 86.46 kcal/mol, which is in good agreement with the experimental value of 87.3 ± 1.5 kcal/mol. All but one of the compounds and conformations examined had weaker O-H BDE's than phenol, the exception being o-methoxyphenol with the O-H group pointing toward this substituent (BDE = 87.8 kcal/mol). Where comparison was possible, calculated differences in O-H BDE's were in excellent agreement with experiment (better than 1 kcal/mol). A simple group additivity scheme also gave excellent agreement with calculated BDE (ArO-H)(gas) values. Some potential new leads to phenolic antioxidants more active than vitamin E have been uncovered.

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Persistent URL dx.doi.org/10.1021/ja963378z
Journal American Chemical Society Journal
Citation
Wright, J.S, Carpenter, D.J. (David J.), McKay, D.J. (Daniel J.), & Ingold, K.U. (1997). Theoretical calculation of substituent effects on the O-H bond strength of phenolic antioxidants related to vitamin E. American Chemical Society Journal, 119(18), 4245–4252. doi:10.1021/ja963378z