二维三金属[CoCl(NH3)5][KCr(C2O4)3]·0.5H2O配合物中不寻常的草酸钾配位

G. Wrzeszcz, A. Wojtczak, M. Zawadzka
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引用次数: 1

摘要

合成了一种新的杂金属化合物[CoCl(NH3)5][KCr(C2O4)3]·0.5H2O(1),并用元素分析、红外光谱和电子能谱、热分析、变温磁化率测量和单晶x射线衍射对其进行了表征。化合物1由二维[{KCr(C2O4)3}n]2n−层、[CoCl(NH3)5]2+离子和水分子组成。在二维层中,存在三种不同类型的草酸盐配位模式。每个K阳离子由来自草酸基团的8个氧原子配位,并与第9个氧原子弱相互作用。[KCr(C2O4)3]2−层与[CoCl(NH3)5]2+离子之间形成了广泛的氢键网络。这些相互作用涉及氨配体中的所有氢原子和水分子。
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Unusual potassium-oxalate coordination in the two-dimensional trimetallic [CoCl(NH3)5][KCr(C2O4)3]·0.5H2O complex
A new heterometallic compound, [CoCl(NH3)5][KCr(C2O4)3]·0.5H2O (1), has been synthesized and characterized by elemental analysis, IR and electronic spectra, thermal analysis, variable temperature magnetic susceptibility measurements, and single crystal X-ray diffraction. Compound 1 consists of two-dimensional [{KCr(C2O4)3}n]2n− layers, [CoCl(NH3)5]2+ ions and water molecules. Within the 2-D layer, three different types of oxalate coordination modes are present. Each K cation is coordinated by eight oxygen atoms from oxalate groups and also weakly interacts with the ninth oxygen atom. The extensive network of hydrogen bond is formed between the [KCr(C2O4)3]2− layer and the [CoCl(NH3)5]2+ ions. These interactions involve all hydrogen atoms of ammonia ligads and water molecule.
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