Binary Complexes of Zirconium(IV) Naphthylideneamino Acids and their Ternary Complexes with Some Imidazoles. Synthesis, Characterization, and Electrochemical Studies

M. K. Rabia, Gamila Y. Aly, Maha A. F. Al‐Mohanna
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引用次数: 5

Abstract

Abstract A new series of binary and ternary complexes of zirconium(IV) with N‐naphthylideneamino acids and some imidazoles has been synthesized. The complexes were characterized on the basis of elemental analyses, 1H NMR, IR and electronic spectra, conductivity, and thermal analytical data. It was found that N‐naphthylideneamino acids act as divalent tridentate (ONO) Schiff bases, whereas the imidazoles behave as monodentate ligands. The involvement of anions (OAc− and Cl−) in coordination was explored. The apparent formation constant values of Zr(IV)–Schiff base binary complexes were determined by a continous‐variation spectrophotometric method. Voltammetric results indicate that some of the prepared complexes underwent two successive, irreversible and reversible one‐electron charge transfer steps coupled with a follow‐up chemical reaction. The stability and redox properties of complexes are discussed in relation to the ligand molecular structure.
锆(IV)萘基氨基酸二元配合物及其与咪唑的三元配合物。合成、表征和电化学研究
摘要合成了一系列新的锆(IV)与N -萘基氨基酸和咪唑的二元和三元配合物。根据元素分析、1H NMR、IR和电子能谱、电导率和热分析数据对配合物进行了表征。发现N -萘基氨基酸作为二价三齿(ONO)席夫碱,而咪唑作为单齿配体。探讨了阴离子(OAc−和Cl−)在配位中的作用。用连续变化分光光度法测定了Zr(IV) -希夫碱二元配合物的表观形成常数。伏安结果表明,某些制备的配合物经历了两个连续的、不可逆的和可逆的单电子电荷转移步骤,并伴有后续的化学反应。讨论了配合物的稳定性和氧化还原性能与配体分子结构的关系。
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