Ebrahimi Arash, Gyepes Róbert, Bujdoš Marek, Krivosudský Lukáš
Comenius University in Bratislava, Faculty of Natural Sciences, Department of Inorganic Chemistry, Mlynská dolina, Ilkovičova 6, 842 15 Bratislava, Slovakia.
Charles University, Department of Inorganic Chemistry, Hlavova 2030, Prague, 128 00, Czech Republic.
Acta Crystallogr E Crystallogr Commun. 2022 Apr 5;78(Pt 5):481-484. doi: 10.1107/S2056989022003449. eCollection 2022 May 1.
The crystalline product (NH)[Zn(CHNO)(HO)][VO]·4HO was success-fully isolated from an HO/DMF solvent combination by evaporation at ambient temperature. The salt crystallizes in the 2/ space group. Imidazole, initially used in the synthesis but not present in the product, and DMF solvent appear to affect the synthesis and crystallization as structural-directing agents. In the title compound, the complex cation [Zn(HO)(DMF)] acts as a counter-ion without being directly coordinated to the deca-vanadate anion. An extensive framework of hydrogen bonds integrates the whole architecture as evidenced by X-ray crystallography. The polyoxometalate [VO] lies on a center of symmetry while the complex cation [Zn(HO)(DMF)] links three adjacent anions through a set of 2 + 2 + 3 hydrogen bonds.
通过在室温下蒸发,从水/二甲基甲酰胺(HO/DMF)溶剂组合中成功分离出结晶产物(NH)[Zn(CHNO)(HO)][VO]·4HO。该盐在2/空间群中结晶。咪唑最初用于合成但产物中不存在,二甲基甲酰胺溶剂似乎作为结构导向剂影响合成和结晶。在标题化合物中,络合阳离子[Zn(HO)(DMF)]作为抗衡离子,而不直接与十钒酸盐阴离子配位。如X射线晶体学所示,广泛的氢键框架整合了整个结构。多金属氧酸盐[VO]位于对称中心,而络合阳离子[Zn(HO)(DMF)]通过一组2 + 2 + 3氢键连接三个相邻阴离子。