TY - JOUR
T1 - The Very Different Effect of Water on Nucleation, Crystallization, and Hydrate Stability of Zingerone and Vanillate Esters
AU - Aljohani, Marwah
AU - McArdle, Patrick
AU - Erxleben, Andrea
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/2/5
Y1 - 2020/2/5
N2 - Vanillin and vanillate esters are widely used as flavorings in the food industry, and the vanillin derivative zingerone is one of the compounds found in the spice ginger. Neither the growth of single crystals of zingerone or methyl or ethyl vanillate nor their crystal structures or the crystal structures of their hydrates have been reported. In this paper a detailed study of the crystallization of methyl vanillate, ethyl vanillate, and zingerone is described and the relationship among crystal growth, habit, and intermolecular interactions in the crystal lattice is discussed. Adventitious or deliberately added water suppressed the crystal nucleation and growth of zingerone from cyclohexane solution. Good-quality single crystals of zingerone can be grown from a cyclohexane solution in closed vials if water is excluded. It was not possible to isolate a hydrate of zingerone. In contrast, the crystallization of methyl and ethyl vanillates from cyclohexane is not affected by adventitious water from the air and monohydrates are easily isolated. The crystal structures of zingerone, methyl and ethyl vanillates, and the monohydrates of the vanillates have been determined and analyzed using the PIXEL program. Observed crystal morphologies have been rationalized using intermolecular interaction energies and slice attachment energy calculations.
AB - Vanillin and vanillate esters are widely used as flavorings in the food industry, and the vanillin derivative zingerone is one of the compounds found in the spice ginger. Neither the growth of single crystals of zingerone or methyl or ethyl vanillate nor their crystal structures or the crystal structures of their hydrates have been reported. In this paper a detailed study of the crystallization of methyl vanillate, ethyl vanillate, and zingerone is described and the relationship among crystal growth, habit, and intermolecular interactions in the crystal lattice is discussed. Adventitious or deliberately added water suppressed the crystal nucleation and growth of zingerone from cyclohexane solution. Good-quality single crystals of zingerone can be grown from a cyclohexane solution in closed vials if water is excluded. It was not possible to isolate a hydrate of zingerone. In contrast, the crystallization of methyl and ethyl vanillates from cyclohexane is not affected by adventitious water from the air and monohydrates are easily isolated. The crystal structures of zingerone, methyl and ethyl vanillates, and the monohydrates of the vanillates have been determined and analyzed using the PIXEL program. Observed crystal morphologies have been rationalized using intermolecular interaction energies and slice attachment energy calculations.
UR - https://www.scopus.com/pages/publications/85081078420
U2 - 10.1021/acs.cgd.9b00960
DO - 10.1021/acs.cgd.9b00960
M3 - Article
SN - 1528-7483
VL - 20
SP - 627
EP - 635
JO - Crystal Growth and Design
JF - Crystal Growth and Design
IS - 2
ER -