Crystal Structures of Prulifloxacin and its Solvates
Inspite of the well-known antibacterial activity of Prulifloxacin, structural studies of this molecule are not reported. We discuss three new X-ray crystal structures of Prulifloxacin guest free form and its solvates with methyl ethyl ketone and nitromethane. The role of the solvent molecules in altering the crystal packing and hydrogen bonding is discussed. All the novel solid-state forms were characterized by PXRD, DSC and IR techniques.
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Document Type: Research Article
Publication date: June 1, 2013
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- Advanced Chemistry Letters is an international multidisciplinary peer-reviewed journal covering all fundamental and applied research areas of chemical sciences including organic chemistry, inorganic chemistry, synthetic chemistry, medicinal chemistry, analytical chemistry, organometallic chemistry, nuclear chemistry, electrochemistry, atmospheric chemistry, environmental chemistry, materials chemistry, materials science, supramolecular chemistry, physical chemistry, polymer chemistry, bioinorganic chemistry, physical organic chemistry, surface chemistry, biochemistry, molecular biology, chemical biology, food chemistry, natural product chemistry, neurochemistry, pharmacology, photochemistry, photobiology, toxicology, nanoscience, nanotechnology, agrochemistry, green chemistry, marine chemistry, geochemistry, petrochemistry, radiochemistry, astrochemistry, molecular physics, chemical engineering, quantum chemistry, and theoretical and computational chemistry.
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