苯扎尔多肟类钒(V)、钒(IV)化合物的合成与表征

H. Slaouti, S. Boutamine, Z. Hank, O. Zekri, M. Meklati, O. Vittori
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引用次数: 3

摘要

摘要研究了苯甲醛肟乙醇溶液C6H5-CH˭NOH (HL)与V(V)或V(IV)水溶液的相互作用。这些反应生成了一系列化合物:(1)一种化学式为H4Na2V10O27(OH)·6H2O的绿十氰酸盐;(2)一种黄绿色二聚体配位配合物,化学式为V2O3(OH)(L*)2(HL)2,其中L*是苯甲氧肟氧化态(C6H5C(H−)NO2)的去质子化产物;(3)化学式[VO(H2O)2(L)2]·2H2O的绿色单体配合物,其中L为苯甲氧肟的去质子化形式(C6H5-CH˭NO−)。元素分析、电导法、红外光谱法、紫外可见光谱法、核磁共振(NMR)、电子顺磁共振(ESR)和质谱法已被用于阐明合成化合物的结构。磁测量、ESR光谱和紫外可见光谱显示,这些化合物中存在较低氧化态的钒。V(V)还原为V(IV)是由配-金属氧化还原反应引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Characterisation of Some Vanadium(V) and (IV) Compounds with Benzaldoxime
Abstract The interaction of an ethanolic solution of benzaldoxime, C6H5–CH˭NOH (HL), with aqueous solutions of V(V) or V(IV) has been studied. These reactions lead to the formation of a series of compounds: (1) a green decavanadate salt of the formula H4Na2V10O27(OH) · 6H2O; (2) a yellow‐green dimeric coordination complex of the formula V2O3(OH)(L*)2(HL)2 in which L* is the deprotonated species of the oxidized form of benzaldoxime, (C6H5C(H−)NO2); and (3) a green monomeric complex of the formula [VO(H2O)2(L)2] · 2H2O in which L is the deprotonated form of benzaldoxime, (C6H5–CH˭NO−). Elemental analyses, conductometry, infrared spectroscopy, UV‐Visible spectrometry, nuclear magnetic resonance (NMR), electronic paramagnetic resonance (ESR), and mass spectroscopy have been used to elucidate the structures of the resultant compounds. Magnetic measurements, ESR spectroscopy, and UV‐Visible spectrometry have shown the existence of a lower oxidation state of vanadium in some of these compounds. The reduction of V(V) to V(IV) was due to a ligand–metal redox reaction.
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