Vaporization, Sublimation Enthalpy, and Crystal Structures of Imidazo[1,2‑a]pyrazine and Phthalazine

• Published in: Journal of chemical and engineering data 2016-01, Vol.61 (1), p.370-379
• Main Authors: Mori, Massiel, Rath, Nigam, Gobble, Chase, Chickos, James, Samarov, Artemiy A, Verevkin, Sergey P
• Format: Article
• Language: English
• ISSN: 0021-9568; 1520-5134
• DOI: 10.1021/acs.jced.5b00606

The vaporization enthalpy of imidazo­[1,2-a]­pyrazine is evaluated by correlation gas chromatography using two sets of standards and by transpiration. Vaporization enthalpies were evaluated using heterocyclic standards with dipole moments that vary from 0 to 3.0 D and using standards with dipole moments > 3.0 D. A value of (70.7 ± 1.0) kJ·mol–1 measured by transpiration compares to (67.9 ± 1.4) kJ·mol–1 measured by correlation gas chromatography using standards characterized by dipole moments > 3.0 D. The results suggest that imidazo­[1,2-a]­pyrazine is a member of this series of compounds whose vaporization enthalpies exceed those less polar heterocycles by a fairly constant amount, (6.9 ± 0.3) kJ·mol–1, in this case by (5.9 ± 3.0) kJ·mol–1 using the less polar heterocycles. The crystal structures of phthalazine, another member of the polar series, and of imidazo­[1,2-a]­pyrazine were determined to examine whether π–π stacking, present in the solid state of two other members of the polar series, was a characteristic of this series. If present in the liquid, π–π stacking could offer a possible explanation for the vaporization enthalpy differences observed. The sublimation enthalpy of imidazo­[1,2-a]­pyrazine was also evaluated.