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首页> 外文期刊>New Journal of Chemistry >Electrochemical properties of [Fe-III(L)(2)Cl-2] [PF6] and [(Fe2O)-O-III,III(L)(4)Cl-2] [PF6](2) [L=2,2 '-bipyridine (bpy) and 4,4 '-dimethyl-2,2 '-bipyridine (dmbpy)]. Crystal structures of the dmbpy derivatives
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Electrochemical properties of [Fe-III(L)(2)Cl-2] [PF6] and [(Fe2O)-O-III,III(L)(4)Cl-2] [PF6](2) [L=2,2 '-bipyridine (bpy) and 4,4 '-dimethyl-2,2 '-bipyridine (dmbpy)]. Crystal structures of the dmbpy derivatives

机译:[Fe-III(L)(2)Cl-2] [PF6]和[(Fe2O)-O-III,III(L)(4)Cl-2] [PF6](2)的电化学性质[L = 2,2'-联吡啶(bpy)和4,4'-二甲基-2,2'-联吡啶(dmbpy)]。 Dmbpy衍生物的晶体结构

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The electrochemical behaviour of the iron(III) complexes [Fe(L)(2)Cl-2](+) and [Fe2O(L)(4)Cl-2](2+) [L = 2,2'-bipyridine (bpy) and 4,4'-dimethyl-2,2'-bipyridine (dmbpy)] has been investigated in acetonitrile. Their reduction leads to the iron(II) complex ion [Fe(L)(3)](2+), accompanied by the release of Cl- ions and the formation of [FeCl4](-) ions or by the formation of an unidentified Fe(III) chloro oxide, depending on the starting complex. These two new chloro complexes can be further reduced into Fe(II) species at a more negative potential. In addition, it has been shown that [Fe(L)(2)Cl-2](+) can be obtained in good yield via the electrochemical oxidation of [Fe(L)(3)](2+) in the presence of free Cl- anions, at least for L = dmbpy. The crystal structure of the new mono- and binuclear dmbpy complexes has been determined by X-ray diffraction. [References: 25]
机译:铁(III)配合物[Fe(L)(2)Cl-2](+)和[Fe2O(L)(4)Cl-2](2+)[L = 2,2'-已在乙腈中研究了联吡啶(bpy)和4,4'-二甲基-2,2'-联吡啶(dmbpy)]。它们的还原导致铁(II)络合物离子[Fe(L)(3)](2+),伴随着Cl-离子的释放和[FeCl4](-)离子的形成,或取决于起始配合物,未确定的三氧化二铁(III)。这两个新的氯配合物可以进一步以负电势还原成Fe(II)物种。另外,已经表明,在存在下,通过[Fe(L)(3)](2+)的电化学氧化,可以高收率获得[Fe(L)(2)Cl-2](+)。至少在L = dmbpy的情况下含有游离氯离子。新的单核和双核dmbpy配合物的晶体结构已通过X射线衍射确定。 [参考:25]

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