Theoretical pKa Calculations With Continuum Model Solvents, Alternative Protocols to Thermodynamic Cycles

Show simple item record

dc.contributor.author Casasnovas Parera, Rodrigo
dc.contributor.author Ortega Castro, Joaquín
dc.contributor.author Frau Munar, Juan
dc.contributor.author Donoso Pardo, Josefa Laurentina
dc.contributor.author Muñoz Izquierdo, Francisco
dc.date.accessioned 2018-11-21T10:51:03Z
dc.identifier.uri http://hdl.handle.net/11201/148563
dc.description.abstract [eng] This article reviews different formulations of the thermodynamic cycles used for the prediction of pKa values, their advantages, and disadvantages with special emphasis on the limitations resulting from the necessity of gas-phase calculations, which allow introducing some difficult cases that motivated alternative strategies. Before introducing the protocols that do not consider gas-phase calculations, the two current opinions available in the literature on the debate about the correct formalism for the calculation of free energies in solution are briefly introduced. Then, the isodesmic proton exchange reaction in solution is reviewed by analyzing its performance on difficult cases for thermodynamic cycles such as carbon acids and amino acids. The pKa values predicted by the isodesmic reaction for common acid species are also reviewed to compare their accuracy results in relation with those of thermodynamic cycles. Linear regressions between experimental pKa values and the calculated free energies obtained with the isodesmic reaction provide expressions for the dependence of the error in the calculated pKas on the pKa difference between the studied acid and the reference species. Finally, it is shown that linear regressions correct the calculated free energies of the isodesmic reaction, when high constant precision is required in a large pKa range. The deviations from the expected behavior are equivalent to those reported previously for different pKa calculation protocols and are determined by the inaccuracies of continuum solvent models on the interactions with ionic species
dc.format application/pdf
dc.relation.isformatof Versió preprint del document publicat a: https://doi.org/10.1002/qua.24699
dc.relation.ispartof International Journal of Quantum Chemistry, 2014, vol. 114, p. 1350-1363
dc.subject.classification 54 - Química
dc.subject.other 54 - Chemistry. Crystallography. Mineralogy
dc.title Theoretical pKa Calculations With Continuum Model Solvents, Alternative Protocols to Thermodynamic Cycles
dc.type info:eu-repo/semantics/article
dc.type info:eu-repo/semantics/submittedVersion
dc.date.updated 2018-11-21T10:51:03Z
dc.date.embargoEndDate info:eu-repo/date/embargoEnd/2075-01-01
dc.embargo 2075-01-01
dc.subject.keywords DFT
dc.subject.keywords pKa calculations
dc.subject.keywords AGE inhibitors
dc.subject.keywords Pyridoxamine (PM)
dc.subject.keywords metal complexes
dc.rights.accessRights info:eu-repo/semantics/embargoedAccess
dc.identifier.doi https://doi.org/10.1002/qua.24699


Files in this item

This item appears in the following Collection(s)

Show simple item record