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A comparative study of ferrocenyl carboxylate cadmium(II) complexes prepared by two different synthetic methods

机译:两种不同合成方法制备二茂铁羧酸羧镉(II)配合物的比较研究

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摘要

Reaction of ferrocenyl carboxylate H_2bfcs with Cd(Ac)_2 _ 2H_2O (H_2bfcs = 1,1'-bis(3-carboxy-1-oxopropyl)ferrocene) gives the mononuclear tetrahydrate precursor Cd(Hbfcs)_2(H_2O)_4 (1). Investigation on the substitution reactions of 1 with imidazole or 2,2'-bpy afforded two one-dimensional (ID) complexes {[Cd_2(bfcs)_2(C_3H_4N_2)_6] . 4H_2O}_n (2) and {[Cd(bfcs)(2,2'-bpy)(H_2O)1 _ 2H_2O}_n (4) (2,2'-bpy = 2,2'-bipyridine), respectively. However, the one-step reactions of H_2bfcs, Cd(Ac)_2 _2H_2O with imidazole or 2,2'bpy result in the formation of two different 1D complexes {[Cd(bfcs)(C_3H_4N_2)_2] _ CH_3OH _ 2H_20}_n (3) and [Cd(bfcs)(CH_3OH)]_n (5). It can be seen from the results that applying different synthetic routes produce dissimilar complexes from however the same materials and under the same reaction conditions. In addition, investigations of differential pulse voltammetry of these four 1D complexes indicate that their half-wave potentials are slightly higher than that of H2bfcs.
机译:二茂铁基羧酸盐H_2bfcs与Cd(Ac)_2 _ 2H_2O(H_2bfcs = 1,1'-双(3-羧基-1-氧丙基)二茂铁)反应生成单核四水合物前体Cd(Hbfcs)_2(H_2O)_4(1) 。研究1与咪唑或2,2'-bpy的取代反应可得到两个一维(ID)配合物{[Cd_2(bfcs)_2(C_3H_4N_2)_6]。 4H_2O} _n(2)和{[Cd(bfcs)(2,2'-bpy)(H_2O)1 _ 2H_2O} _n(4)(2,2'-bpy = 2,2'-联吡啶)。但是,H_2bfcs,Cd(Ac)_2 _2H_2O与咪唑或2,2'bpy的一步反应导致形成两个不同的1D络合物{[Cd(bfcs)(C_3H_4N_2)_2] _ CH_3OH _2H_20} _n (3)和[Cd(bfcs)(CH_3OH)] _ n(5)。从结果可以看出,采用不同的合成路线,在相同的反应条件下,由相同的材料会产生不同的络合物。此外,对这四个一维复合物的差分脉冲伏安法的研究表明,它们的半波电势略高于H2bfcs。

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