Moroni Aldana B, Bottoso Tiago, Lionello Diego F, Vega Daniel R, Kaufman Teodoro S, Calvo Natalia L
Instituto de Química Rosario (IQUIR CONICET-UNR) and Facultad de Ciencias Bioquímicas y Farmacéuticas Universidad Nacional de Rosario. Suipacha 531 2000 Rosario Argentina.
Departamento Física de la Materia Condensada, Gerencia de Investigación y, Aplicaciones, Centro Atómico Constituyentes, Comisión Nacional de Energía, Atómica, Av. Gral. Paz 1499, B1650KNA, San Martín, Buenos Aires, Argentina.
Acta Crystallogr E Crystallogr Commun. 2024 Sep 24;80(Pt 10):1064-1068. doi: 10.1107/S2056989024009204. eCollection 2024 Sep 1.
The mol-ecular salt sulfamethoxazolium {or 4-[(5-methyl-1,2-oxazol-3-yl)sulf-amo-yl]anilinium methyl sulfate monohydrate}, CHNOS·CHOS·HO, was prepared by the reaction of sulfamethoxazole and HSO in methanol and crystallized from methanol-ether-water. Protonation takes place at the nitro-gen atom of the primary amino group. In the crystal, N-H⋯O hydrogen bonds (water and methyl-sulfate anion) and inter-molecular N-H⋯N inter-actions involving the sulfonamide and isoxazole nitro-gen atoms, link the components into a tri-dimensional network, additional cohesion being provided by face-to-face π-π inter-actions between the phenyl rings of adjacent mol-ecules. A Hirshfeld surface analysis was used to verify the contributions of the different inter-molecular inter-actions, showing that the three most important contributions for the crystal packing are from H⋯O (54.1%), H⋯H (29.2%) and H⋯N (5.0%) inter-actions.
分子盐磺胺甲恶唑鎓(或4 - [(5 - 甲基 - 1,2 - 恶唑 - 3 - 基)磺酰胺基]苯胺甲基硫酸盐一水合物),CHNOS·CHOS·HO,通过磺胺甲恶唑与HSO在甲醇中反应制备,并从甲醇 - 乙醚 - 水体系中结晶得到。质子化发生在伯氨基的氮原子上。在晶体中,N - H⋯O氢键(水和甲基硫酸根阴离子)以及涉及磺酰胺和异恶唑氮原子的分子间N - H⋯N相互作用,将各组分连接成三维网络,相邻分子苯环之间的面对面π - π相互作用提供了额外的内聚力。使用 Hirshfeld 表面分析来验证不同分子间相互作用的贡献,结果表明晶体堆积的三个最重要贡献来自H⋯O(54.1%)、H⋯H(29.2%)和H⋯N(5.0%)相互作用。