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Structural diversity of neutral bis-(beta-iminoaldehyde) complexes of nickel(II)

机译:镍(II)的中性双-(β-亚氨基醛)配合物的结构多样性

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Series of Ni-II and Cu-II complexes with dianionic [N2O2] ligands were synthesized and characterised applying spectroscopic and X-ray diffraction techniques. The ligands were obtained by 1:2 condensation of ethylene- and propylenediamine with malonic aldehyde derivatives (R-2 = H, R-1 = H or OCH3). Although the molecular formulae of the complexes are quite similar, the X-ray investigations have proved a significant structural diversity in the solid state. Among others, we found some simple nearly planar molecules stacked in the crystal lattice with electron density of six-membered rings delocalised over the chelate rings as well as some very complex polymeric or nickel acetate bridged trinuclear complexes. The coordination of the nickel ion by surrounding oxygen and nitrogen atoms is square-planar in the simplest case and octahedral in the most complex one. Small topological differences in similar molecules generate completely different crystal structures.
机译:合成了一系列具有阴离子[N2O2]配体的Ni-II和Cu-II配合物,并使用光谱和X射线衍射技术对其进行了表征。通过将乙二胺和丙二胺与丙二醛醛衍生物(R-2 = H,R-1 = H或OCH3)1:2缩合获得配体。尽管配合物的分子式非常相似,但X射线研究证明了固态具有显着的结构多样性。除其他外,我们发现一些简单的近乎平面的分子堆积在晶格中,六元环的电子密度在螯合环上散布,以及一些非常复杂的聚合物或乙酸镍桥联的三核络合物。在最简单的情况下,镍离子与周围氧原子和氮原子的配位为方形,在最复杂的情​​况下为八面体。相似分子中的微小拓扑差异会产生完全不同的晶体结构。

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