Combining the Advantages of Powder X-ray Diffraction and NMR Crystallography in Structure Determination of the Pharmaceutical Material Cimetidine Hydrochloride
Author(s) -
Abigail E. Watts,
Keisuke Maruyoshi,
Colan E. Hughes,
Steven P. Brown,
Kenneth D. M. Harris
Publication year - 2016
Publication title -
crystal growth and design
Language(s) - English
Resource type - Journals
eISSN - 1528-7505
pISSN - 1528-7483
DOI - 10.1021/acs.cgd.6b00016
Subject(s) - powder diffraction , microcrystalline , crystal structure , crystallography , solid state nuclear magnetic resonance , chemistry , x ray crystallography , rietveld refinement , diffraction , materials science , nuclear magnetic resonance , physics , optics
We report the crystal structure of the anhydrous phase of cimetidine hydrochloride, determined directly from powder X-ray diffraction data. The material was prepared by dehydration of the readily obtained monohydrate form of cimetidine hydrochloride, the only form for which a crystal structure has previously been reported. As such, solid-state dehydration processes typically yield the product phase as a microcrystalline powder, and structure determination was carried out directly from powder X-ray diffraction data, using the direct-space genetic algorithm technique for structure solution followed by Rietveld refinement. The structure determined from powder X-ray diffraction was further validated by calculating solid-state 13C NMR data for the crystal structure (using first-principles periodic DFT techniques within the GIPAW approach) and assessing the quality of agreement with the corresponding experimental solid-state 13C CPMAS NMR data. This strategy provides a robust vindication of the correctness of t...
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom