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Zinc(II) and Nickel(II) Benzoate Complexes from the Use of 1-methyl-4,5-diphenylimidazole

机译:使用1-甲基-4,5-二苯基咪唑的苯甲酸锌(II)和镍(II)配合物

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摘要

Two new complexes, [Zn(O2CPh)2(L)2]·2MeOH (1·2MeOH) and [Ni2(O2CPh))4(L)2]·2MeCN (2·2MeCN), have been synthesized and characterized by X-ray analysis in the course of an ongoing investigation of the MII/X−/L [MII = Co, Ni, Cu, Zn; X− = Cl−, Br−, I−, NCS−, NO3−, N3−, PhCO2−; L = 1-methyl-4,5-diphenylimidazole] reaction system, aiming at understanding and assessing the relative strength and the way in which the intermolecular interactions control the supramolecular organization of these compounds. In the mononuclear complex 1·2MeOH, the benzoate ion acts as a monodentate ligand resulting in a distorted tetrahedral N2O2 coordination environment. Complex 2·2MeCN exhibits a dinuclear paddle-wheel structure; each NiII has a square pyramidal NiNO4 chromophore with four benzoate oxygens in the basal plane and the pyridine-type nitrogen atom of one ligand L at the apex. The structure of 1·2MeOH is stabilized by intramolecular π-π interactions between aromatic rings of adjacent 4,5-diphenylimidazole moieties; it is a feature also evidenced in similar compounds of the type [MX2L2].
机译:合成了两个新的配合物[Zn(O2CPh)2(L)2]·2MeOH(1·2MeOH)和[Ni2(O2CPh))4(L)2]·2MeCN(2·2MeCN)并用X表征正在进行的MII / X- / L研究中的射线分析[MII = Co,Ni,Cu,Zn; X-= Cl-,Br-,I-,NCS-,NO 3-,N 3-,PhCO 2-; L = 1-甲基-4,5-二苯基咪唑]反应体系,旨在理解和评估相对强度以及分子间相互作用控制这些化合物的超分子结构的方式。在单核络合物1·2MeOH中,苯甲酸酯离子充当单齿配体,导致扭曲的四面体N2O2配位环境。络合物2·2MeCN呈双核桨轮结构。每个NiII都有一个方形金字塔形的NiNO4发色团,在基面上有四个苯甲酸酯氧,在顶点有一个配体L的吡啶型氮原子。相邻4,5-二苯基咪唑部分的芳环之间的分子内π-π相互作用可稳定1·2MeOH的结构;在[MX2L2]类型的类似化合物中也证实了这一特征。

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