Instituto de Farmacobiología, Universidad de la Cañada, Carretera Teotitlán-San Antonio Nanahuatipán km 1.7 s/n, Teotitlán de Flores Magón, Oaxaca 68540, México.
Facultad de Química, Universidad Nacional Autónoma de México, Ciudad de México 04510, México.
Acta Crystallogr C Struct Chem. 2022 May 1;78(Pt 5):280-286. doi: 10.1107/S2053229622003734. Epub 2022 Apr 11.
Cocrystals of 2,7-dihydroxynaphthalene (DHN, or naphthalene-2,7-diol) with isoniazid (pyridine-4-carbohydrazide) (INH), denoted DHN-INH [CHO·CHNO, (I)], and piracetam [2-(2-oxopyrrolidin-1-yl)acetamide] (PIR), denoted DHN-PIR [CHO·CHNO, (II)], were obtained by the solvent-assisted grinding method and characterized by IR spectroscopy, powder X-ray diffraction and single-crystal X-ray diffraction. Cocrystal (I) crystallized in the triclinic space group P-1 and showed a 2:2 stoichiometry. DHN and INH molecules are connected by O-H...N(pyridine) and O-H...N(hydrazide) hydrogen bonds. Cocrystal (II) crystallized in the space group Pca2 with a 1:1 stoichiometry. DHN and PIR molecules are connected by O-H...O=C hydrogen bonds. The supramolecular architecture of cocrystal (I) showed interlinked supramolecular tapes; meanwhile, in cocrystal (II), interlinked supramolecular sheets were observed.
2,7-二羟基萘(DHN,或萘-2,7-二醇)与异烟肼(吡啶-4-甲酰肼)(INH)的共晶,标记为 DHN-INH [CHO·CHNO,(I)],以及吡拉西坦[2-(2-氧代吡咯烷-1-基)乙酰胺](PIR),标记为 DHN-PIR [CHO·CHNO,(II)],通过溶剂辅助研磨法获得,并通过红外光谱、粉末 X 射线衍射和单晶 X 射线衍射进行了表征。共晶(I)结晶于三斜空间群 P-1,表现出 2:2 的化学计量比。DHN 和 INH 分子通过 O-H…N(吡啶)和 O-H…N(酰肼)氢键连接。共晶(II)结晶于 Pca2 空间群,具有 1:1 的化学计量比。DHN 和 PIR 分子通过 O-H…O=C 氢键连接。共晶(I)的超分子结构表现为互穿的超分子带;而在共晶(II)中,则观察到互穿的超分子片。