TY - JOUR
T1 - Efficient Polymorph Screening through Crystallization from Bulk and Confined Melts
AU - Fellah, Noalle
AU - Tahsin, Lamia
AU - Zhang, Carolyn Jin
AU - Kahr, Bart
AU - Ward, Michael D.
AU - Shtukenberg, Alexander G.
N1 - Funding Information:
This work was supported by the National Science Foundation by DMREF Program under Award Number DMR-2118890, National Science Foundation Awards DMR-1708716 and DMR-2003968, and the National Science Foundation MRSEC Program under Award Number DMR-1420073. The X-ray microdiffractometer with GADDS was acquired through the support of the National Science Foundation under Award Number CRIF/CHE-0840277 and NSF MRSEC Program under Award Number DMR-0820341. The authors thank Prof. John H. Perepezko and Dr. Chengrong Cao (University of Wisconsin-Madison) for the glass transition temperature measurements of coumarin and isonicotinamide using their Mettler Toledo Flash DSC 2+ system. The authors thank Dr. Martin Ward (University of Strathclyde, Glasgow) for the matching chlorpropamide powder diffraction pattern obtained for our samples crystallized in nanopores with the unpublished crystal structure of form ζ.
Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/12/7
Y1 - 2022/12/7
N2 - Crystallization from the melt can allow the achievement of high driving force for crystallization accompanied by relatively slow growth, nucleation, and transformation rates, features that favor its use as an efficient polymorph screening method. Surprisingly, even though melt crystallization has a long history, it has been employed less often in the search for new polymorphs than solution crystallization. Applications of melt crystallization to 21 highly polymorphic, well-characterized compounds with at least five ambient polymorphs revealed that melt crystallization afforded more than half of the known polymorphs and in many cases revealed new polymorphs not detected by other screening methods. A statistical analysis revealed that polymorphs grown from the melt have a greater propensity for high Z′ values, which are not easily accessible by other crystallization protocols and are often not detectable by crystal structure prediction methods. Melt crystallization within nanopores (8-100 nm) performed for 19 of the 21 compounds mostly resulted in polymorphs that dominated crystallization from the bulk melt at similar temperatures. The total number of polymorphs observed in nanopores was less than that observed during crystallization from the bulk melt, however, and melt crystallization under confinement revealed new polymorphs not detected by other crystallization methods.
AB - Crystallization from the melt can allow the achievement of high driving force for crystallization accompanied by relatively slow growth, nucleation, and transformation rates, features that favor its use as an efficient polymorph screening method. Surprisingly, even though melt crystallization has a long history, it has been employed less often in the search for new polymorphs than solution crystallization. Applications of melt crystallization to 21 highly polymorphic, well-characterized compounds with at least five ambient polymorphs revealed that melt crystallization afforded more than half of the known polymorphs and in many cases revealed new polymorphs not detected by other screening methods. A statistical analysis revealed that polymorphs grown from the melt have a greater propensity for high Z′ values, which are not easily accessible by other crystallization protocols and are often not detectable by crystal structure prediction methods. Melt crystallization within nanopores (8-100 nm) performed for 19 of the 21 compounds mostly resulted in polymorphs that dominated crystallization from the bulk melt at similar temperatures. The total number of polymorphs observed in nanopores was less than that observed during crystallization from the bulk melt, however, and melt crystallization under confinement revealed new polymorphs not detected by other crystallization methods.
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U2 - 10.1021/acs.cgd.2c01065
DO - 10.1021/acs.cgd.2c01065
M3 - Article
AN - SCOPUS:85142750709
SN - 1528-7483
VL - 22
SP - 7527
EP - 7543
JO - Crystal Growth and Design
JF - Crystal Growth and Design
IS - 12
ER -