Novel Isoniazid cocrystals with aromatic carboxylic acids: Crystal engineering, spectroscopy and thermochemical investigations

dc.contributor.authorDiniz, Luan F.
dc.contributor.authorSouza, Matheus S.
dc.contributor.authorCarvalho Jr., Paulo S.
dc.contributor.authorP. da Silva, Cecilia C.
dc.contributor.authorD'Vries, Richard F.
dc.contributor.authorEllena, Javier
dc.date.accessioned2019-08-05T23:02:52Z
dc.date.available2019-08-05T23:02:52Z
dc.date.issued2017
dc.description.abstractFour novel cocrystals of the anti-tuberculosis drug Isoniazid (INH), including two polymorphs, with the aromatic carboxylic acids p-nitrobenzoic (PNBA), p-cyanobenzoic (PCNBA) and p-aminobenzoic (PABA) were rationally designed and synthesized by solvent evaporation. Aiming to explore the possible supramolecular synthons of this API, these cocrystals were fully characterized by X-ray diffraction (SCXRD, PXRD), spectroscopic (FT-IR) and thermal (TGA, DSC, HSM) techniques. The cocrystal formation was found to be mainly driven by the synthons formed by the pyridine and hydrazide moieties. In both INH−PABA polymorphs, the COOH acid groups are H-bonded to pyridine and hydrazide groups giving rise to the acid⋯pyridine and acid⋯hydrazide heterosynthons. In INH−PNBA and INH−PCNBA cocrystals these acid groups are only related to the pyridine moiety. In addition to the structural study, supramolecular and Hirshfeld surface analysis were also performed based on the structural data. The cocrystals were identified from the FT-IR spectra and their thermal behaviors were studied by a combination of DSC, TGA and HSM techniques.en_US
dc.identifier.issn0022-2860
dc.identifier.urihttps://repositorio.usc.edu.co/handle/20.500.12421/484
dc.language.isoenen_US
dc.publisherJournal of Molecular Structureen_US
dc.subjectTuberculosisen_US
dc.subjectIsoniaziden_US
dc.subjectCocrystalsen_US
dc.subjectCrystal engineeringen_US
dc.subjectX-ray diffractionen_US
dc.titleNovel Isoniazid cocrystals with aromatic carboxylic acids: Crystal engineering, spectroscopy and thermochemical investigationsen_US
dc.typeArticleen_US

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