Zinc(II) complexes with thiadiazole derivatives-1,3,4

K. S. Khusenov, B. B. Umarov, K. K. Turgunov, O. Z. Bakhranova, T. B. Aliev, B. Ibragimov
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Abstract

Zn(II) complexes of the composition [ZnLn2X2] and [ZnLn3(NO3)2] were synthesized, where n = 1, 2; X=Cl, Br, I; L1=2-aminothiadiazole-1,3,4, L2=2-amino-5-methylthiadiazole-1,3,4. The obtained complexes were studied by elemental analysis methods, IR and 1H NMR spectroscopy. The structure of the [ZnL22Br2] complex was determined by the RSA method (CIF file CCDC No. 2251742). The ligand molecules of 2-amino-5-R-thiadiazoles-1,3,4 (R = –H, –CH3) are coordinated monodentately by an endocyclic nitrogen atom located in the α-position to the amino group. The polyhedron of the central atom of halide complexes is a slightly distorted tetrahedron, in the coordination sphere of which two halide atoms and two endocyclic nitrogen atoms are located. During complexation in the spectrum of the solution of the [ZnL22Br2] complex, coordinated L2 ligands undergo amino-imine tautomerization into a heterocyclic amine with a nitrogen atom in a heterocycle. The polyhedron of the central atom for nitrate complexes is a slightly distorted trigonal bipyramide, in the coordination sphere of which three nitrogen atoms of ligands are located in the equatorial plane and two oxygen atoms of two nitrate anions in the axial position.
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锌(II)与噻二唑衍生物-1,3,4 的配合物
合成了成分为[ZnLn2X2]和[ZnLn3(NO3)2]的锌(II)配合物,其中 n = 1,2;X=Cl,Br,I;L1=2-氨基噻二唑-1,3,4,L2=2-氨基-5-甲基噻二唑-1,3,4。研究人员通过元素分析方法、红外光谱和 1H NMR 光谱对获得的配合物进行了研究。用 RSA 方法确定了 [ZnL22Br2] 复合物的结构(CIF 文件 CCDC 编号 2251742)。配体分子中的 2-氨基-5-R-噻二唑-1,3,4(R = -H,-CH3)通过位于氨基 α 位的内环氮原子单端配位。卤化物络合物中心原子的多面体是一个略微畸变的四面体,在其配位层中有两个卤化物原子和两个内环氮原子。在[ZnL22Br2]配合物溶液的光谱中,配位的 L2 配体在络合过程中会发生氨基-亚胺同素异形反应,变成杂环胺,其中的氮原子位于杂环中。硝酸根配合物中心原子的多面体是一个略微变形的三叉二棱锥,在其配位层中,配体的三个氮原子位于赤道面,两个硝酸根阴离子的两个氧原子位于轴向位置。
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