Comparison of the rare earth complexes iodides and polyiodides with biuret

A. Kornilov, M. S. Grigoriev, E. Savinkina
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Abstract

Objectives. Currently, several hundred polyiodide compounds have been synthesized and structurally characterized, but so far, no formation patterns for certain polyiodide ions have been revealed. The purpose of this work is to continue the search for formation regularities of polyiodides, including polyiodides of lanthanide complexes.Methods. Iodide and polyiodide of samarium complexes with biuret (BU), [Sm(BU)4]I3·BU·2H2O and [Sm(BU)4][I5][I]2, were first synthesized and characterized by X-ray diffraction analysis and infrared spectroscopy, respectively.Results. The obtained compounds complement the row of isostructural lanthanide (La–Gd) complexes. Structures of corresponding iodides and polyiodides were compared in detail. Both types of the compounds contain complex cations of the same composition; however, their structures differ significantly. The central atom coordination polyhedron can be described as a distorted square antiprism and a distorted dodecahedron, respectively. Even greater differences are observed in the outer sphere of complex compounds. The iodide compound crystals contain uncoordinated iodide ions, a biuret molecule and two water molecules. In the polyiodide compound, cations together with isolated I– ions form a three-dimensional framework with the channels, in which linear I5– ions are united in infinite linear chains by weak interactions.Conclusions. The replacement of an iodide ion with a polyiodide ion in complex compounds of lanthanides with BU leads to changes in both the inner sphere and the outer sphere of the cation complex, including the supramolecular level. The presence of iodine atom infinite linear chains in polyiodides allows expecting the presence of anisotropic electrical conductivity along this direction.
稀土配合物碘化物与聚碘化物与双缩脲的比较
目标。目前,已经合成了数百种聚碘化合物并对其结构进行了表征,但迄今为止还没有发现某些聚碘离子的形成模式。本工作的目的是继续探索多碘化物的形成规律,包括镧系配合物的多碘化物。首次合成了钐与双缩脲(BU)配合物的碘化物和多碘化物[Sm(BU)4]I3·BU·2H2O和[Sm(BU)4][I5][I]2,并分别用x射线衍射分析和红外光谱对其进行了表征。得到的化合物补充了同结构镧系(La-Gd)配合物。详细比较了相应的碘化物和多碘化物的结构。两种类型的化合物含有相同组成的复合阳离子;然而,它们的结构有很大的不同。中心原子配位多面体可以分别描述为扭曲的方形反棱镜和扭曲的十二面体。在复杂化合物的外层可以观察到更大的差异。碘化物化合物晶体包含不配位的碘离子、一个双缩脲分子和两个水分子。在多碘化合物中,阳离子与孤立的I -离子在通道中形成三维框架,其中线性的I5 -离子通过弱相互作用结合成无限的线性链。在含BU的镧系元素络合物中,碘离子被多碘离子取代,导致阳离子络合物的内外球发生变化,包括超分子水平。多碘化物中碘原子无限线性链的存在使得沿此方向存在各向异性电导率。
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