Literature DB >> 26935882

Polymorphs and Versatile Solvates of 7-Hydroxyisoflavone.

Ningbo Gong1, Guoshun Zhang1, Guimin Jin1, Guanhua Du2, Yang Lu3.   

Abstract

7-hydroxyisoflavone has been crystallized, identified, and characterized as 2 solvent-free conformational polymorphs and 5 solvates, which differ from each other in the mode of packing and in molecular conformation. All the 7 crystal structures were previously unreported. The conformational polymorphs and solvates were compared by Hirshfeld surface and fingerprint plot analysis and were spectroscopically characterized by powder X-ray diffraction, differential scanning calorimetry, and thermal gravimetric analysis. Hydrogen bond played an important role in the formation of polymorphs. From this study, we can predict that more solvates could be cultivated in other polarity solvents such as isopropanol or 2-butanol at appropriate conditions.
Copyright © 2016 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

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Keywords:  crystal polymorphism; crystal structure; crystallization; physical characterization; physicochemical properties; stability

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Year:  2016        PMID: 26935882     DOI: 10.1016/j.xphs.2016.01.011

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  1 in total

1.  Structure of 7-hy-droxy-3-(2-meth-oxy-phen-yl)-2-tri-fluoro-meth-yl-4H-chromen-4-one.

Authors:  John Nicolson Low; Ligia R Gomes; Alexandra Gaspar; Fernanda Borges
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2017-07-07
  1 in total

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