Identity-reaction proton transfers from oxygen acids yielding localized vs. delocalized conjugate bases. An ab initio study

Abstract

Identity-reaction proton transfers from a series of oxygen acids to the corresponding conjugate bases have been studied by ab initio methods at the MP2/6-31+G*//MP2/6-31+G* level. The acids are H 3 O + , CH 3 OH 2 + , CH 2 = OH + , HC(O)OH 2 + , CH 2 = CHOH 2 + , H 2 O, CH 3 OH, HOOH, HOCH 2 OH, FOH, FCH 2 OH, HC(O)OH, and CH 2 = CHOH. Gas-phase acidities were calculated at the G2(MP2) level in order to have benchmark values for all acidities regardless of whether experimental values were available. Barriers to proton transfer relative to the separated reactants, ΔH TS , show a straight-line relation to acidity for all but two of the neutral acids and for all but one of the cationic acids. Two neutral acids, HOOH and FOH, show negative deviations that can be attributed to polarizability of the atoms attached to the proton donor oxygens. The cationic acid HC(O)OH 2 + shows a large positive deviation, which probably arises from substantial heavy-atom reorganization from reactant to TS. Charges provide evidence of a lag in delocalization in the reaction of CH 2 = CHOH 2 + , though it does not show an elevated ΔH TS .Key words: ab initio, oxygen acids, proton transfer, acidity.