Empirical Conversion of pKa Values between Different Solvents and Interpretation of the Parameters: Application to Water, Acetonitrile, Dimethyl Sulfoxide, and Methanol
| Autor: | Ernst-Walter Knapp, Emanuele Rossini, Art D. Bochevarov |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
010304 chemical physics
Dimethyl sulfoxide General Chemical Engineering Value (computer science) General Chemistry 010402 general chemistry 01 natural sciences Article 0104 chemical sciences Interpretation (model theory) lcsh:Chemistry Solvent chemistry.chemical_compound lcsh:QD1-999 chemistry Computational chemistry 0103 physical sciences Functional group Methanol Acetonitrile Equilibrium constant |
| Zdroj: | ACS Omega, Vol 3, Iss 2, Pp 1653-1662 (2018) ACS Omega |
| ISSN: | 2470-1343 |
| Popis: | An empirical conversion method (ECM) that transforms pKa values of arbitrary organic compounds from one solvent to the other is introduced. We demonstrate the method’s usefulness and performance on pKa conversions involving water and organic solvents acetonitrile (MeCN), dimethyl sulfoxide (Me2SO), and methanol (MeOH). We focus on the pKa conversion from the known reference value in water to the other three organic solvents, although such a conversion can also be performed between any pair of the considered solvents. The ECM works with an additive parameter that is specific to a solvent and a molecular family (essentially characterized by a functional group that is titrated). We formally show that the method can be formulated with a single additive parameter, and that the extra multiplicative parameter used in other works is not required. The values of the additive parameter are determined from known pKa data, and their interpretation is provided on the basis of physicochemical concepts. The data set of known pKa values is augmented with pKa values computed with the recently introduced electrostatic transform method, whose validity is demonstrated. For a validation of our method, we consider pKa conversions for two data sets of titratable compounds. The first data set involves 81 relatively small molecules belonging to 19 different molecular families, with the pKa data available in all four considered solvents. The second data set involves 76 titratable molecules from 5 additional molecular families. These molecules are typically larger, and their experimental pKa values are available only in Me2SO and water. The validation tests show that the agreement between the experimental pKa data and the ECM predictions is generally good, with absolute errors often on the order of 0.5 pH units. The presence of a few outliers is rationalized, and observed trends with respect to molecular families are discussed. |
| Databáze: | OpenAIRE |
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