首页> 外文期刊>Inorganica Chimica Acta >Synthesis, molecular structure, and voltammetric behaviour of unusually stable cis-dioxobis(diisobutyldithiocarbamato)tungsten(VI)
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Synthesis, molecular structure, and voltammetric behaviour of unusually stable cis-dioxobis(diisobutyldithiocarbamato)tungsten(VI)

机译:异常稳定的顺式-二氧双(二异丁基二硫代氨基甲酸酯)钨(VI)的合成,分子结构和伏安行为

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摘要

The unusually stable cis-dioxobis(diisobutyldithiocarbamato)tungsten(VI) [WO2(i-Bu(2)dtc)2] was synthesized by the reaction between WO42- and i-Bu(2)dtc(-) in water under the air. The X-ray crystal structure and voltammetric behaviour of the complex are reported. The geometry of the WO2S4 core of the complex is distorted octahedral with two terminal oxo ligands in a cis position to each other. The average W=O distance of the complex is 1.719 Angstrom and the bond angle of O-W-O is 104.7degrees, which are in the range of those of cis-dioxotungsten(VI) complexes. The structural features of [WO2(i-Bu(2)dtc)(2)] are very similar to those of corresponding cis-dioxomolybdenum(VI) analogues. The complex [WO2(i-Bu(2)dtc)(2)] undergoes one-electron quasi-reversible reduction followed by a homogeneous chemical reaction at more negative potential (-1.40 V vs. SSCE) than the corresponding molybdenum analogue [MoO2(i-Bu(2)dtc)(2)] (-0.92 V vs. SSCE) in dichloromethane. (C) 2003 Elsevier B.V. All rights reserved. [References: 24]
机译:通过WO42-和i-Bu(2)dtc(-)在空气中在水中反应,合成了异常稳定的顺式-二氧杂双(二异丁基二硫代氨基甲酸酯)钨(VI)[WO2(i-Bu(2)dtc)2] 。报道了配合物的X射线晶体结构和伏安行为。配合物的WO2S4核心的几何形状是八面体变形的,两个末端的oxo配体彼此处于顺式位置。配合物的平均W = O距离为1.719埃,O-W-O的键角为104.7度,在顺式-二氧钨(VI)配合物的范围内。 [WO2(i-Bu(2)dtc)(2)]的结构特征与相应的顺式-二氧钼(VI)类似物的结构特征非常相似。络合物[WO2(i-Bu(2)dtc)(2)]经历单电子准可逆还原,然后以比相应的钼类似物[MoO2更多的负电势(-1.40 V vs. SSCE)发生均相化学反应。 (i-Bu(2)dtc)(2)](-0.92 V vs. SSCE)在二氯甲烷中。 (C)2003 Elsevier B.V.保留所有权利。 [参考:24]

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