TY - JOUR
T1 - Structural Diversity of Diosgenin Hydrates
T2 - Effect of Initial Concentration, Water Volume Fraction, and Solvent on Crystallization
AU - Wang, Yajing
AU - Chi, Yingnan
AU - Zhang, Wenwen
AU - Yang, Qiuhong
AU - Yang, Song
AU - Su, Chong
AU - Lin, Zhengguo
AU - Gu, Jingkai
AU - Hu, Changwen
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/3/2
Y1 - 2016/3/2
N2 - Four hemihydrates (HH-I, HH-II, HH-III, and HH-IV) and two monohydrates (MH-I, MH-II) of diosgenin, a steroid sapogenin, have been prepared. Hydrates HH-I, HH-III, HH-IV, MH-I, and MH-II have been thoroughly characterized by single-crystal X-ray diffraction, powder X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetry, and differential scanning calorimetry. Although in these cases diosgenin has a similar conformation, hydrogen bonding interactions connect diosgenin and the lattice water molecule into different supermolecular structures. More importantly, three controlling factors, including initial concentration, water volume fraction, and solvent, have been investigated in the crystallization of diosgenin hydrates. The control experiments in ethanol display that as the initial concentration increases, HH-III, HH-I, and HH-II appear in order, and with the increase of water content, HH-I, HH-III, MH-I, and MH-II are obtained correspondingly. When acetone is used as solvent, HH-IV was synthesized. Moreover, we observed that stick-like crystals of HH-III gradually transform to plate-like ones of MH-I in solution at ambient conditions. This transformation is prevented by lowering temperature and is accelerated by adding water.
AB - Four hemihydrates (HH-I, HH-II, HH-III, and HH-IV) and two monohydrates (MH-I, MH-II) of diosgenin, a steroid sapogenin, have been prepared. Hydrates HH-I, HH-III, HH-IV, MH-I, and MH-II have been thoroughly characterized by single-crystal X-ray diffraction, powder X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetry, and differential scanning calorimetry. Although in these cases diosgenin has a similar conformation, hydrogen bonding interactions connect diosgenin and the lattice water molecule into different supermolecular structures. More importantly, three controlling factors, including initial concentration, water volume fraction, and solvent, have been investigated in the crystallization of diosgenin hydrates. The control experiments in ethanol display that as the initial concentration increases, HH-III, HH-I, and HH-II appear in order, and with the increase of water content, HH-I, HH-III, MH-I, and MH-II are obtained correspondingly. When acetone is used as solvent, HH-IV was synthesized. Moreover, we observed that stick-like crystals of HH-III gradually transform to plate-like ones of MH-I in solution at ambient conditions. This transformation is prevented by lowering temperature and is accelerated by adding water.
UR - http://www.scopus.com/inward/record.url?scp=84960192451&partnerID=8YFLogxK
U2 - 10.1021/acs.cgd.5b01609
DO - 10.1021/acs.cgd.5b01609
M3 - Article
AN - SCOPUS:84960192451
SN - 1528-7483
VL - 16
SP - 1492
EP - 1501
JO - Crystal Growth and Design
JF - Crystal Growth and Design
IS - 3
ER -