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首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >FIRST OXALATE-BRIDGED HETEROBINUCLEAR CO(II)-MN(III) COMPLEXES - SYNTHESIS AND MAGNETISM
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FIRST OXALATE-BRIDGED HETEROBINUCLEAR CO(II)-MN(III) COMPLEXES - SYNTHESIS AND MAGNETISM

机译:首次草酸盐桥接的异核CO(II)-MN(III)配合物-合成和磁性

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摘要

Three novel Co(II)-Mn(III) oxalato heterobinuclear complexes have been synthesized and characterized, namely K[Co(L)(2)Mn(ox)(3)] (L denotes 1,10-phenanthroline (phen), 2,2'-bipyridyl (bpy), 4,4'-dimethyl-2,2'-bipyridyl (Me(2)bpy), respectively), where ox stands for the oxalate dianion. Based on IR, elemental analyses, electronic spectra and ESR, these complexes are proposed to have extended oxalato-bridged structures consisting of manganese(III) ions and cobalt(II) ions, in which each manganese(III) and each cobalt(II) ion has a distorted octahedral environment. The temperature dependance of the magnetic susceptibility for K[Co(bpy)(2)Mn(ox)(3)] and K[Co(Me(2)bpy)(2)Mn(ox)(3)]. 2H(2)O was measured over the range 77 - 300 K and the observed data were simulated by an equation based on the spin Hamiltonian operator (H = -2JS(1) . S-2), giving the exchange integral J = -0.311 cm(-1) or -0.335 cm(-1), respectively. This indicates a very weak antiferromagnetic interaction between Co(II) ion and Mn(III) ion. [References: 16]
机译:合成并表征了三种新型Co(II)-Mn(III)草酸杂双核配合物,即K [Co(L)(2)Mn(ox)(3)](L表示1,10-菲咯啉(phen), 2,2'-联吡啶基(bpy),4,4'-二甲基-2,2'-联吡啶基(分别为Me(2)bpy),其中ox代表草酸二阴离子。基于红外光谱,元素分析,电子光谱和ESR,提出了这些配合物具有由草锰(III)离子和钴(II)离子组成的扩展草酸酯桥接的结构,其中每种锰(III)和每种钴(II)离子具有扭曲的八面体环境。 K [Co(bpy)(2)Mn(ox)(3)]和K [Co(Me(2)bpy)(2)Mn(ox)(3)]的磁化率的温度依赖性。在77-300 K范围内测量了2H(2)O,并通过基于自旋哈密顿算子(H = -2JS(1)。S-2)的方程对模拟的观测数据进行了模拟,得出交换积分J =-分别为0.311厘米(-1)或-0.335厘米(-1)。这表明Co(II)离子和Mn(III)离子之间的反铁磁相互作用非常弱。 [参考:16]

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