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

Tabrez Rafique Shaikh, Nikita Shelke, Srinu Tothadi

2023ACS Omega11 citationsDOIOpen Access PDF

Abstract

High Resolution Image Download MS PowerPoint Slide 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.

Topics & Concepts

CocrystalCrystallographyAcetamideDifferential scanning calorimetryCrystallizationChemistryDimerCrystal engineeringAmideHydrogen bondIsostructuralCrystal (programming language)MoleculeCrystal structureSupramolecular chemistryOrganic chemistryPhysicsComputer scienceThermodynamicsProgramming languageCrystallography and molecular interactionsCrystallization and Solubility StudiesNonlinear Optical Materials Research