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The EPR spectrum of the reaction mixture showed strong signals due to the phenoxyl radical from 2b.
-
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26
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13044281148
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note
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One of the reviewers has suggested that alkylated benzene derivatives resulting from the addition of alkyl radicals to the solvent are the source of hydrogen atoms.
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31
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13044279837
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note
-
The previously unreported BDE value for the O-H bond in p-fluorophenol in benzene was measured as 881 kcal/mol by using the same procedure of ref 29.
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38
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0001736705
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The failure of 2.6-di-tert-butylphenols to form hydrogen bonds was originally recognized in the early sixties. See for instance: Ingold. K. U. Can. J. Chem. 1960, 38, 1092. Ingold, K. U.; Taylor, D. R. Can. J. Chem. 1961, 39, 471. Ingold, K. U. Can. J. Chem. 1962, 40, 111.
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41
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0000644116
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The failure of 2.6-di-tert-butylphenols to form hydrogen bonds was originally recognized in the early sixties. See for instance: Ingold. K. U. Can. J. Chem. 1960, 38, 1092. Ingold, K. U.; Taylor, D. R. Can. J. Chem. 1961, 39, 471. Ingold, K. U. Can. J. Chem. 1962, 40, 111.
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42
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0001680006
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The failure of 2.6-di-tert-butylphenols to form hydrogen bonds was originally recognized in the early sixties. See for instance: Ingold. K. U. Can. J. Chem. 1960, 38, 1092. Ingold, K. U.; Taylor, D. R. Can. J. Chem. 1961, 39, 471. Ingold, K. U. Can. J. Chem. 1962, 40, 111.
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Ingold, K.U.1
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