Fereidouni Nazanin, Aljohani Marwah, Erxleben Andrea
School of Biological and Chemical Sciences, University of Galway, Galway H91TK33, Ireland.
Department of Chemistry, College of Science, Imam Abdulrahman Bin Faisal University, P.O. Box 76971, Dammam 31441, Saudi Arabia.
Cryst Growth Des. 2025 Jul 29;25(15):5954-5959. doi: 10.1021/acs.cgd.5c00373. eCollection 2025 Aug 6.
Aspartame crystallizes as very long, thin needles. The crystallization behavior of extreme needle formers not only causes problems in industrial processing and handling but is also of interest in fundamental research. Cocrystallization is a popular approach to expand the solid-state landscape of a compound and often leads to improved physicochemical properties such as stability, dissolution behavior, particle size, and morphology. No crystal structure of an aspartame cocrystal has been reported in the literature up to now. In this work, a comprehensive screening study for aspartame cocrystals was performed. Cocrystals with fumaric acid and 4-hydroxybenzoic acid were detected by powder X-ray diffraction analysis. Growing X-ray suitable cocrystals, however, proved extremely difficult, as both cocrystals, like aspartame, crystallized as very fine needles. Nevertheless, in the case of 4-hydroxybenzoic acid, crystals of sufficient quality for single-crystal X-ray analysis could be grown, and the first crystal structure of an aspartame cocrystal is reported. In the cocrystal aspartame·4-hydroxybenzoic acid dihydrate (), the coformer forms the OH···OOC synthon with aspartame. The aspartame zwitterions in are connected through charge-assisted NH ···OOC hydrogen bonds into a spiral along a 2 screw axis, the same structural feature that drives the needle growth of aspartame and that seems to be the reason why the isolation of X-ray-quality cocrystals of aspartame is so challenging.
阿斯巴甜结晶为非常长的细针状。极端针状结晶物的结晶行为不仅在工业加工和处理中会引发问题,在基础研究中也备受关注。共结晶是拓展化合物固态形态的常用方法,通常会带来诸如稳定性、溶解行为、粒径和形态等物理化学性质的改善。截至目前,文献中尚未报道过阿斯巴甜共晶体的晶体结构。在这项工作中,对阿斯巴甜共晶体进行了全面的筛选研究。通过粉末X射线衍射分析检测到了与富马酸和4-羟基苯甲酸形成的共晶体。然而,生长适合X射线分析的共晶体被证明极其困难,因为这两种共晶体与阿斯巴甜一样,都结晶为非常细的针状。尽管如此,在4-羟基苯甲酸的情况下,能够生长出质量足以进行单晶X射线分析的晶体,并报道了阿斯巴甜共晶体的首个晶体结构。在共晶体阿斯巴甜·4-羟基苯甲酸二水合物( )中,共形成物与阿斯巴甜形成了OH···OOC合成子。 中的阿斯巴甜两性离子通过电荷辅助的NH···OOC氢键沿着2螺旋轴连接成螺旋结构,这与驱动阿斯巴甜针状生长的结构特征相同,似乎也是分离出X射线质量的阿斯巴甜共晶体极具挑战性的原因。