Structural and energetic characterization of anhydrous and hemihydrated 2-mercaptoimidazole: Calorimetric, X-ray diffraction, and computational studies. (April 2016)

• Record Type: Journal Article
• Authors: Silva, Ana L.R.; Morais, Victor M.F.; Ribeiro da Silva, Maria D.M.C.; Simões, Ricardo G.; Bernardes, Carlos E.S.; Piedade, M. Fátima M.; Minas da Piedade, Manuel E.
• Is Part Of: Journal of chemical thermodynamics. Volume 95(2016:Apr.)
• Page Start: 35
• Page End: 48
• Publication Date: 2016-04
• Subjects: Anhydrous/hydrated 2-mercaptoimidazole -- Tautomerism -- X-ray diffraction -- Enthalpy of formation -- Enthalpy of sublimation -- Heat capacity; Thermodynamics -- Periodicals; Thermochemistry -- Periodicals; Thermodynamique -- Périodiques; Thermochimie -- Périodiques; Thermochemistry; Thermodynamics; Periodicals; 541.369
• DOI: 10.1016/j.jct.2015.11.010
• Languages: English
• ISSNs: 0021-9614

Abstract

Highlights: Rotating-bomb combustion calorimetry was used to obtain the enthalpy of formation of crystalline 2-mercaptoimidazole. Enthalpy of sublimation of 2-mercaptoimidazole was measured by Calvet microcalorimetry. Enthalpy of interaction between substituents is calculated using isodesmic reactions. Crystal X-ray diffraction determinations for anhydrous and hemihydrate 2-mercaptoimidazole forms were carried. Gas-phase enthalpies of formation of 2-mercaptoimidazole and 1, 3-dihydro-2 H -imidazole-2-thione estimated by the G3 method. Abstract: This paper reports an experimental and theoretical study on the structural and energetic characterization of the 2-mercaptoimidazole (2-MI) in the solid and in the gaseous phases. The single crystal X-ray diffraction determinations on the anhydrous and hemihydrate 2-MI forms were carried out at T = (296 ± 2) K and T = (150 ± 2) K, respectively, and suggest that in both forms the 2-MI molecule is closer to the thione conformation, albeit some single bond character is possible. The energy of combustion of the title compound was measured by rotating-bomb combustion calorimetry, being used to derive the corresponding enthalpy of formation in the crystalline-phase. The enthalpy of sublimation of 2-MI, at T = 298.15 K, was obtained from high temperature Calvet microcalorimetry measurements. These two parameters yielded the gas-phase enthalpy of formation, allowing the inherent energetic analysis of the molecule. This result was discussed together with the corresponding predictions for 2-MI and its tautomer, 1, 3-dihydro-2 H -imidazole-2-thione, by the G3 method. The dehydration reaction of 2-MI · 0.5H2 O(cr) was also investigated and the corresponding enthalpy of dehydration was determined by Calvet microcalorimetry.