新型氧化钒配合物的合成、表征及N,N′-双(水杨基)- 1,2 -双-(对氨基苯氧基)乙烷的电导研究

H. Temel, Ü. Çakır, H. İbrahim Uğraş
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引用次数: 27

摘要

摘要采用水杨醛与1,2 -双(对氨基苯氧基)乙烷缩合反应合成了一种新的希夫碱氧钒配合物。通过元素分析、磁性测量、紫外可见光谱和红外光谱对配合物进行了表征。用电导法测定了本文方法合成的Cu(NO3)2、Zn(NO3)2·6H2O和VOSO4·5H2O盐与配体在80%二氧六烷水和纯甲醇中络合的稳定性常数和热力学值。在80%二氧六烷/水溶液中,稳定性常数(log K e)以Cu(II) > Zn(II)的顺序递减。然而,这些金属配合物在甲醇中与配体的反应正好相反(Zn(II) > (Cu(II)))。这些离子缔合常数的大小与阳离子和络合阳离子的溶剂化性质有关。配合物的流动性也部分取决于溶剂化效应。由于VO(IV)L络合物的迁移率高于VO(IV)离子的迁移率,假设VO(IV)‐L体系中的络合物-溶剂相互作用相对较弱。络合的一个主要后果是络合物的摩尔电导率的增加和相应的κ值的大幅下降。因此,在两种类型的溶剂中,没有得到VO(IV)‐L体系的稳定常数值。
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Synthesis and Characterization of a Novel Oxovanadium(IV) Complex and Conductometric Studies with N,N′‐bis(Salicylidene)‐1,2‐bis‐(p‐aminophenoxy)ethane
Abstract A new oxovanadium complex of the Schiff base obtained by the condensation of 1,2‐bis(p‐aminophenoxy)ethane with salicylaldehyde was synthesized. The complex has been characterized by elemental analyses, magnetic measurements, UV‐VIS and IR spectra. Stability constants and thermodynamic values for complexation between Cu(NO3)2, Zn(NO3)2 · 6H2O, and VOSO4 · 5H2O salts and the ligand synthesized by the method described in the literature in 80% dioxane–water and pure methanol were determined by conductance measurements. The stability constants (log K e) in 80% dioxane/water decrease in the order Cu(II) > (Zn(II). However, just the opposite behavior has been obtained for these metal complexes with the ligand in methanol (Zn(II) > (Cu(II)). The magnitudes of these ion association constants are related to the nature of solvation of the cation and of the complexed cation. The mobility of the complexes is also dependent, in part, upon solvation effects. Since the mobility of the VO(IV)L complex has been found to be higher than that of VO(IV) ion, assuming that the complex–solvent interaction in the VO(IV)‐L systems is comparatively weak. A major consequence of the complexation is the increase in the molar conductivity of the complex and a corresponding large decrease in κ values. For this reason, it was not obtained any stability constant values for VO(IV)‐L systems in two type of solvents.
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