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- W2160992053 abstract "A Quantitative Structure-Property Relationship (QSPR) is developed for the O-H bond dissociation energy (BDE) of a set of 78 phenols. The data set was composed of monosubstituted, disubstituted, and polysubstituted phenolic derivatives containing substituents with different steric and electronic effects in the ortho-, meta-, and para-positions of the aromatic ring. The proposed model, derived from multiple linear regression, contains seven descriptors calculated solely from the molecular structure of compounds. The average absolute relative errors are 1.37% (R(2) = 0.8978; SD: 6.67) and 1.13% (R(2) = 0.9076; SD: 4.26) for the working set (62 compounds) and the prediction set (16 compounds), respectively. These results are better than those obtained from DFT calculations, QSAR approach, and correlations with Hammet parameters." @default.
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- W2160992053 date "2003-01-25" @default.
- W2160992053 modified "2023-10-06" @default.
- W2160992053 title "A QSPR Study of O−H Bond Dissociation Energy in Phenols" @default.
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- W2160992053 doi "https://doi.org/10.1021/ci025632e" @default.
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