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首页> 外文期刊>Inorganic Chemistry Communications >Iron(III), cobalt(II) and zinc(II) coordination compounds with a carboximidamide ligand: Synthesis, structures and properties
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Iron(III), cobalt(II) and zinc(II) coordination compounds with a carboximidamide ligand: Synthesis, structures and properties

机译:铁(III),钴(II)和锌(II)配合化合物,具有羧酰胺酰胺配体:合成,结构和性能

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Coordination complexes of iron(III), cobalt(II) and zinc(II) with the ligand N '-{[1-(pyridin-2-yl)ethylidene] amino}pyridine-2-carboximidamide (pmhpa) have been synthesised and were structurally characterized by elemental analysis, mass spectrometry, X-ray diffraction and infrared spectroscopy. The mononuclear iron(III) complex, [Fe(pmhap)2][FeCl4], (1), adopts the orthorhombic non-centric space group P2(1)2(1)2(1). The iron is present in an octahedral environment in the ion [Fe(pmhap)(2)](+). The crystallographically-determined formula of the cobalt(II) complex (2) is [Co-2(pmhap)(2)Cl-3](2)[CoCl4].4MeOH. The compound crystallizes in the non-centric space group P42(1)c with a single cobalt ion in the asymmetric unit. The complex is dinuclear, with two cobalt ions bridged by chloride and the two nitrogen atoms of N=N of the pmhap ligand. The zinc(II) complex; [Zn-2(pmhpa)(3)](NO3)(4).2.75MeOH (3) crystallizes in the cubic space group Paa with disordered methanol molecules present. This is dinuclear with the two zinc atoms being bridged by three N=N links from the ligand to form a threefold symmetric rotor. Infrared spectroscopy confirms that coordination occurs through the azide bridge. Measurements of magnetic susceptibility for the iron(III) and cobalt(II) complexes show that they are paramagnetic between 5 and 300 K. Mossbauer spectroscopic data supports the structure of the iron(III) complex being composed of an octahedral and a tetrahedral iron atom.
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