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Multicomponent Solvate Crystals of 3,5-Dinitrobenzoic Acid and Acetamide and CSD Analysis of Solvates

[Image: see text] Twelve multicomponent solvate crystals (cocrystal solvates) of 3,5-dinitrobenzoic acid and acetamide were synthesized via slow evaporation method. All crystalline materials were characterized by single-crystal X-ray diffraction. All cocrystal solvates are isostructural, and crystal...

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Detalles Bibliográficos
Autores principales: Shaikh, Tabrez Rafique, Shelke, Nikita, Tothadi, Srinu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10339403/
https://www.ncbi.nlm.nih.gov/pubmed/37457492
http://dx.doi.org/10.1021/acsomega.3c03091
Descripción
Sumario:[Image: see text] Twelve multicomponent solvate crystals (cocrystal solvates) of 3,5-dinitrobenzoic acid and acetamide were synthesized via slow evaporation method. All crystalline materials were characterized by single-crystal X-ray diffraction. All cocrystal solvates are isostructural, and crystal packing forms continuous channels where some solvent molecules are connected via weak intermolecular interactions with 3,5-dinitrobenzoic acid and acetamide. All multicomponent solvate crystals encompass amide–amide dimer homo synthons and form R(2)(2) (8) motifs. Moreover, the phase purity of solvate crystals was analyzed by powder X-ray diffraction. Further, most of the cocrystal solvates were analyzed by nuclear magnetic resonance and differential scanning calorimetry. Cambridge structural database analysis categorizes solvate propensity in single-crystal structures. The importance of hydrogen bond donor/acceptor nature, size, and shape of solvents is also discussed in the context of crystallization and crystal packing.