Diop Mouhamadou Birame, Diop Libasse, Maris Thierry
Laboratoire de Chimie Minérale et Analytique, Département de Chimie, Faculté des Sciences et Techniques, Université Cheikh Anta Diop, Dakar, Senegal.
Département de Chimie, Université de Montréal, 2900 Boulevard Édouard-Montpetit, Montréal, Québec, H3C 3J7, Canada.
Acta Crystallogr E Crystallogr Commun. 2016 Mar 11;72(Pt 4):482-5. doi: 10.1107/S2056989016003789. eCollection 2016 Apr 1.
The title salts, C4H7N2 (+)·NO3 (-)·C4H6N2, (I), and C4H7N2 (+)·NO3 (-), (II), were obtained from solutions containing 2-methyl-imidazole and nitric acid in different concentrations. In the crystal structure of salt (I), one of the -NH H atoms of the imidazole ring shows half-occupancy, hence only every second mol-ecule is in its cationic form. The nitrate anion in this structure lies on a twofold rotation axis. The neutral 2-methyl-imidazole mol-ecule and the 2-methyl-1H-imidazol-3-ium cation inter-act through N-H⋯N hydrogen bonds to form [(C4H6N2)⋯(C4H7N2)(+)] pairs. These pairs are linked with two nitrate anions on both sides through bifurcated N-H⋯(O,O) hydrogen bonds into chains running parallel to [001]. In the crystal structure of salt (II), the C4H7N2 (+) cation and the NO3 (-) anion are both located on a mirror plane, leading to a statistical disorder of the methyl H atoms. The cations and anions again inter-act through bifurcated N-H⋯(O,O) hydrogen bonds, giving rise to the formation of chains consisting of alternating anions and cations parallel to [100].
标题盐C₄H₇N₂⁺·NO₃⁻·C₄H₆N₂(I)和C₄H₇N₂⁺·NO₃⁻(II)是从含有不同浓度的2-甲基咪唑和硝酸的溶液中获得的。在盐(I)的晶体结构中,咪唑环的一个-NH氢原子显示出半占据状态,因此只有每隔一个分子处于其阳离子形式。该结构中的硝酸根阴离子位于一个二次旋转轴上。中性的2-甲基咪唑分子和2-甲基-1H-咪唑-3-鎓阳离子通过N-H⋯N氢键相互作用形成[(C₄H₆N₂)⋯(C₄H₇N₂)⁺]对。这些对通过分叉的N-H⋯(O,O)氢键在两侧与两个硝酸根阴离子相连,形成平行于[001]的链。在盐(II)的晶体结构中,C₄H₇N₂⁺阳离子和NO₃⁻阴离子都位于一个镜面平面上,导致甲基氢原子的统计无序。阳离子和阴离子再次通过分叉的N-H⋯(O,O)氢键相互作用,形成由交替的阴离子和阳离子组成的平行于[100]的链。