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• W2028102706 abstract "A new version of the single-reference-extended kinetic method is presented in which direct entropy correction is incorporated. Results of calibration experiments with the monodentate base pyridine and the bidentate base ethylenediamine are presented for which the method provides proton affinities in excellent agreement with published values and reasonable predictions for the protonation entropies. The method is then used to determine the proton affinity and protonation entropy of the non-protein amino acid beta-oxalylaminoalanine (BOAA). The PA of BOAA is found to be 933.1 +/- 7.8 kJ/mol and a prediction for the protonation entropy of -39 J mol(-1) K(-1) is also obtained, indicating a significant degree of intramolecular hydrogen bonding in the protonated form. These results are supported by hybrid density functional theory calculations at the B3LYP/6-311++G**//B3LYP/6-31+G* level. They indicate that the preferred site of protonation is the alpha-nitrogen atom (PA = 935.0 kJ/mol) and that protonated BOAA has a strong hydrogen bond between the hydrogen on the alpha-amino group and one of the carbonyl oxygen atoms on the side chain." @default.
• W2028102706 created "2016-06-24" @default.
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• W2028102706 date "2005-07-01" @default.
• W2028102706 modified "2023-10-16" @default.
• W2028102706 title "Proton affinity of β-oxalylaminoalanine (BOAA): Incorporation of direct entropy correction into the single-reference kinetic method" @default.
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• W2028102706 doi "https://doi.org/10.1016/j.jasms.2005.03.011" @default.
• W2028102706 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15921924" @default.
• W2028102706 hasPublicationYear "2005" @default.
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