首页> 外文期刊>Zeitschrift fur Kristallographie. New crystal structures >Crystal structure of tetraaqua-bis(4-(1,2,4-triazol-4-yl)benzoato-κN) - zinc(II) decahydrate, C_(18)H_(40)N_6O_(18)Zn
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Crystal structure of tetraaqua-bis(4-(1,2,4-triazol-4-yl)benzoato-κN) - zinc(II) decahydrate, C_(18)H_(40)N_6O_(18)Zn

机译:四水双(4-(1,2,4-三唑-4-基)苯并-κN)-十水合锌(II),C_(18)H_(40)N_6O_(18)Zn的晶体结构

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(Equation presentation) (Table presentation) Source of material The title complex was prepared by reaction of an aqueous solution of Zn(NO_3)2.6H2O (0.297 g, 1 mmol) with 4-(p-benzoxy)- 1,2,4-triazole (HL) (0.378 g, 2 mmol) in 18 mL water. This suspending solution was rigidly stirred at room temperature for 5 h and then was filtrated. The clear solution was sealed in a 25 mL acid digestion bomb at 140 °C for 4 days. Colourless block crystals were obtained by filtration and dried in air. Discussion Metal-organic supermolecular compounds with various network structures have received wide attention because of their attractive structures and potential application in many research areas [1]. Herein, we employed 4-(p-benzoxy)-1,2,4-triazole (L) ligand to construct a new zinc complex [2]. The title structure consists of mononuclear [Zn(L)2(H2O)4] units and lattice water molecules in the ratio 1:10 as shown in the figure. The [Zn(L)2(H2O)4] unit has a crystallographically imposed C2 symmetry. The ligand adopts the unique Zn-N coordination fashion, in which the uncoordinated carboxylate groups exhibits strong intermolecular hdyrogen bonding interaction with water molecules. It is noteworth that the title compound self-assembles into a three-dimensional (3D) supramolecular architecture through intermolecular O-H...O hydrogen-bonding interactions. (Table presentation).
机译:(方程式表示)(表式表示)原料来源通过将Zn(NO_3)2.6H2O(0.297 g,1 mmol)的水溶液与4-(对-苯并xy)-1,2,4反应制得标题配合物-18水中的三唑(HL)(0.378 g,2 mmol)。将该悬浮液在室温下严格搅拌5小时,然后过滤。将澄清的溶液在140°C的25 mL酸消解罐中密封4天。通过过滤获得无色块状晶体,并在空气中干燥。讨论具有各种网络结构的金属有机超分子化合物因其吸引人的结构和在许多研究领域中的潜在应用而受到广泛关注[1]。在本文中,我们采用了4-(对苯甲酰)-1,2,4-三唑(L)配体来构建新的锌络合物[2]。标题结构由单核[Zn(L)2(H2O)4]单元和点阵水分子组成,比例为1:10,如图所示。 [Zn(L)2(H 2 O)4]单元具有晶体学上强加的C 2对称性。配体采用独特的Zn-N配位方式,其中未配位的羧酸酯基团表现出与水分子的强分子间高氢键相互作用。值得注意的是,标题化合物通过分子间的O-H ... O氢键相互作用自组装成三维(3D)超分子结构。 (表演示)。

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