M
Mino R. Caira
Researcher at University of Cape Town
Publications - 335
Citations - 6687
Mino R. Caira is an academic researcher from University of Cape Town. The author has contributed to research in topics: Crystal structure & Hydrogen bond. The author has an hindex of 33, co-authored 324 publications receiving 6296 citations. Previous affiliations of Mino R. Caira include Rhodes University & University of Port Elizabeth.
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Book ChapterDOI
Crystalline Polymorphism of Organic Compounds
TL;DR: A wide variety of techniques appropriate to the study of organic crystalline polymorphism and pseu-dopolymorphism is then surveyed, ranging from simple crystal density measurement to observation of polymorphic transformations using variable-temperature synchrotron X-ray diffraction methods.
Journal ArticleDOI
Physicochemical properties and x-ray structural studies of the trigonal polymorph of carbamazepine
TL;DR: The trigonal polymorph of carbamazepine (alpha-carbamazepines) was obtained by crystallization from a number of solvents by means of differential scanning calorimetry, thermogravimetric analysis, infrared spectroscopy, X-ray power diffraction, thermal microscopy, and powder and intrinsic dissolution rates.
Journal ArticleDOI
Preparation and Crystal Characterization of a Polymorph, a Monohydrate, and an Ethyl Acetate Solvate of the Antifungal Fluconazole
TL;DR: Referencing PXRD patterns computed from the refined single-crystal X-ray data for the title compounds are presented, which clarified previous findings relating to the polymorphism of this compound.
BookDOI
Design of organic solids
Edwin Weber,Y. Aoyama,Mino R. Caira,Gautam R. Desiraju,J. P. Glusker,Andrew D. Hamilton,Rosa E. Meléndez,Ashwini Nangia +7 more
TL;DR: Directional Aspects of Intermolecular Interactions and Supramolecular Synthons and Pattern Recognition are discussed in this article, where hydrogen-bonded ribbons, Tapes and Sheets as Motifs for Crystal Engineering.
Journal ArticleDOI
Sulfa drugs as model cocrystal formers.
TL;DR: A review of several aspects of cocrystalization involving sulfonamide drugs is presented, with a focus on other drug molecules as cocrystallization partners, with reference to the drug sulfadimidine, which featured prominently as a model cocystal former.