The relationship between the proton-donating and proton-accepting powers and the structures of various proton donors and acceptors was studied in the liquid phase by means of an infrared spectrophotometer. The proton-donating powers of the donors were evaluated by means of the ratios of the O–H shifts of the donors (RO–H) to those of methanol in various proton acceptor solutions. The proton-accepting powers of the acceptors were evaluated by means of the division of the O–H shifts by the proton-donating powers of the donors used. The proton-donating powers increased with the decrease in the pKa or the ionic RO–H bond dissociation energies and with the increase in the electron affinities of RO radicals, i. e., t-butanol
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Kagiya et al. (1970) studied this question.
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