SYNTHESIS OF COMPLEXES OF Cu(II) AND VO(IV) WITH HYDRAZIDE OF MALEIC AND HYDRAZINEDIACETIC ACID

E. Guliyeva, P. A. Fatullayeva, F. F. Jalaladdinov, T.Ya. Askerova, T.M. Akhverdiyeva, M. Mammedova, R. D. Kasumov, M. Bayramov
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Abstract

The work demonstrated that hydrazide of maleic and hydrazine diacetic acid(L-2,2'-(2-(3- carboxyacryloyl)hydrazine-1,1-diil)diacetic acid) forms mononuclear complexes [CuL(H2O)2] and [VОL(H2O)2]. The structure and physical properties of these complex compounds have been studied by IR, UV spectroscopy and thermogravimetric methods of analysis. On the basis of the data obtained, the structure of the complexes was proposed, in which the metal ion is coordinated by two oxygen atoms and one nitrogen atom of the aminodiacetic fragment. In the electronic spectra of the copper complex, there are absorption bands of the transition at ~240 nm (related to charge transfer) and one d-d transition 740 nm. In the electronic spectra of the vanadyl complex, several absorption bands are observed at 300 nm (inflection), ~625 nm (inflection), and 780 nm, which can be attributed to d–d transitions of the VO2+in the low symmetry ligand environment. The five-coordinated structure of the complex is carried out by two oxygen atoms of two water molecules. The EPR spectrum of the polycrystalline [CuL(H2O)2] complex at room temperature indicates a low symmetry of the complex and has three g -factor values: g1=2.30, g2=2.22; g3=2.11. Additionally, a hyperfine structure is observed due to 63.64Cu nuclei (nuclear spin 3/2) with a splitting constant of 80 G.
铜(II)和VO(IV)与顺丁烯二酸肼配合物的合成
研究表明,马来酸酐和肼二乙酸的肼(l -2,2'-(2-(3-羧基丙烯酰)肼-1,1-二乙酯)二乙酸)形成单核配合物[CuL(H2O)2]和[VОL(H2O)2]。用红外光谱、紫外光谱和热重分析方法研究了这些配合物的结构和物理性质。根据得到的数据,提出了配合物的结构,其中金属离子由氨基二乙酸片段的两个氧原子和一个氮原子配位。在铜配合物的电子光谱中,存在~240 nm(与电荷转移有关)的跃迁吸收带和740 nm的一个d-d跃迁吸收带。在钒基配合物的电子光谱中,在300 nm(拐点)、~625 nm(拐点)和780 nm处观察到几个吸收带,这可以归因于低对称配体环境中VO2+的d-d跃迁。配合物的五配位结构是由两个水分子的两个氧原子构成的。多晶[CuL(H2O)2]配合物在室温下的EPR谱表明配合物的对称性较低,有3个g因子值:g1=2.30, g2=2.22;g3 = 2.11。此外,由于63.64个cu原子核(核自旋为3/2),分裂常数为80 G,观察到超精细结构。
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