Artículos de revistas
Energetics of neutral and deprotonated (Z)-cinnamic acid
Fecha
2016-01Registro en:
Dávalos, Juan Z.; Lima, Carlos F. R. A. C.; Silva, Artur M. S.; Santos, Luís M. N. B. F. ; Erra Balsells, Rosa; et al.; Energetics of neutral and deprotonated (Z)-cinnamic acid; Academic Press Ltd - Elsevier Science Ltd; Journal of Chemical Thermodynamics; 95; 1; 1-2016; 195-201
0021-9614
CONICET Digital
CONICET
Autor
Dávalos, Juan Z.
Lima, Carlos F. R. A. C.
Silva, Artur M. S.
Santos, Luís M. N. B. F.
Erra Balsells, Rosa
Salum, Maria Laura
Resumen
We have performed a study of structural, thermochemical and thermophysical properties of the (Z)-cinnamic acid neutral molecule and its corresponding oxyanion (formed by deprotonation of the carboxylic group). The thermophysical study (heat capacities, temperature and enthalpy of fusion) was made by DSC. The following intrinsic (gas-phase) thermochemical magnitudes have been experimentally determined: i/ standard enthalpy of formation, at 298.15 K, of the neutral molecule, (g) = -215.5 3.2 kJ?mol-1, by combustion calorimetry and by the Knudsen effusion technique, ii/ deprotonation enthalpy, ΔacidH0(g) = 1416.4 ± 8.8 kJ?mol-1 and acidity, GA = 1386.7 ± 8.8 kJ?mol-1, by the EKM method using ESI-TQ Mass Spectrometry. From these results we have also derived the enthalpy of formation of the oxyanion, (oxyanion,g) = -303.5 9.4 kJ?mol-1. A computational study, through density functional calculations at the B3LYP/6-311++G(d,p) level of theory, was used to check the good consistency of the experimental results. The global results show that (Z)-cinnamic acid is significantly less stable than the corresponding (E)-isomer, which can be related to the greater acidity of the (Z)-form found in both the gas and aqueous solution phases.