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Structural Landscape of an Antimicrobial Sulfa Drug Sulfachloropyridazine: Polymorphs, Solvates, and Cocrystals

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dc.contributor.author S, SeethaLekshmi
dc.contributor.author S, Amrutha
dc.contributor.author M S R N, Kiran
dc.contributor.author S, Varughese
dc.date.accessioned 2020-02-26T09:27:57Z
dc.date.available 2020-02-26T09:27:57Z
dc.date.issued 2019-04-17
dc.identifier.citation Crystal Growth & Design; 19(6):3222-3232 en_US
dc.identifier.uri https://pubs.acs.org/doi/pdf/10.1021/acs.cgd.9b00083
dc.identifier.uri http://10.10.100.66:8080/xmlui/handle/123456789/3607
dc.description.abstract Experimentally identified unique crystal forms (polymorphs, solvates, and molecular complexes) of a particular compound logically reside in a certain low-energy point in the crystal landscape. The observed crystal forms offer an effective route to access different landmarks in the crystal landscape of a compound, which in turn is a profile of the structural and energetic changes occurring at the late stage of crystallization. We experimentally determined nine novel crystal forms—a polymorph, two solvates, and six cocrystals—of the sulfa drug sulfachloropyridazine. The spectral, thermal, and diffraction studies unequivocally establish the structural characteristics and the stability relationship of the polymorphs. The added coformers, with no specific chemical similarity but related by geometric and interaction types, lead to the convergence of torsional preferences and supramolecular synthons and hence a modular design of crystal structures. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Crystal forms en_US
dc.subject Crystal landscape en_US
dc.subject Crystallization en_US
dc.subject Supramolecular synthons en_US
dc.title Structural Landscape of an Antimicrobial Sulfa Drug Sulfachloropyridazine: Polymorphs, Solvates, and Cocrystals en_US
dc.type Article en_US


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  • 2019
    Research articles authored by NIIST researchers published in 2019

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