| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 215066 | The Journal of Chemical Thermodynamics | 2016 | 8 Pages |
•Determination of the enthalpy of sublimation of phthalide and phthalic anhydride.•Measurement of the massic energy of combustion, in oxygen, of the crystalline phthalide and phthalic anhydride.•Gas-phase enthalpies of formation derived experimentally for phthalide and phthalic anhydride.•Correlations for the enthalpic effects of one and two ketone groups in the main structure of phthalan.•Gas-phase enthalpies of formation estimated from G3(MP2)//B3LYP approach.
In the present work the energetic properties of phthalide and phthalic anhydride are assessed experimental and computationally allowing to calculate the standard molar enthalpy of formation, in the gaseous phase, of each compound. These results enabled to analyze and interpret the enthalpic and structural molecular effects of one and two ketone groups in the main structure of phthalan.The high-temperature Calvet microcalorimetry and the static bomb combustion calorimetry were used to measure, respectively, the enthalpy of sublimation and the massic energy of combustion of the two compounds. These data were combined to derive the standard molar enthalpy of formation, in the gaseous phase, of phthalide and phthalic anhydride.The gas-phase enthalpies of formation of phthalide and phthalic anhydride compounds were estimated using the composite G3(MP2)//B3LYP approach together with adequate gas-phase working reactions. The computational study was also extended to phthalan and the reliability of the value obtained for the correspondent gas-phase enthalpy of formation, when compared with the experimental value reported in the literature, contributes to validate the computational methodology used. The good agreement verified between computational and experimental results for the other two phthalan derivatives studied gave us confidence to estimate the gas-phase enthalpy of formation of the 2,5-dihydrofuran that was not studied experimentally.Complementary, natural bond orbital (NBO) calculations were also performed, allowing an advance on the analysis of the structural and reactivity characteristics of this type of compounds.
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