Synthesis and structural characterization of copper(II) complexes with a tetradentate semicarbazone ligand derived from 2,5-hexadione

被引:1
|
作者
Vafazadeh, Rasoul [1 ]
Ehsani, Mahboobeh [1 ]
Willis, Anthony C. [2 ]
机构
[1] Yazd Univ, Dept Chem, Yazd, Iran
[2] Australian Natl Univ, Res Sch Chem, Canberra, ACT 2601, Australia
关键词
Copper complex; Semicarbazone; 2; 5-Hexadione; Disorder; Tetradentate; SCHIFF-BASE LIGAND; CRYSTAL-STRUCTURE; DNA-BINDING; MAGNETIC-PROPERTIES; EXCHANGE REACTION; CU(II) COMPLEXES; ANION; SALICYLALDEHYDE; DERIVATIVES; MONONUCLEAR;
D O I
10.1007/s13738-019-01721-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Four Cu(II) complexes [CuLH2O](ClO4)(2), 1; [CuLCl]Cl.H2O, 2; [CuLBr](2)(Cu3Br5), 3; and [CuLH2O](NO3)(2), 4; where L = tetradentate semicarbazone ligand, have been synthesized and characterized by elemental analysis, FT-IR and UV-Vis. The structures of compounds 1 and 3 have been determined by single-crystal X-ray diffraction analyses. In mononuclear 1, the semicarbazone, L acts as a tetradentate neutral ligand and a water molecule also coordinates to the Cu atom. There are two independent [CuL(H2O)](2+) cations and four perchlorate anions in the crystallographic asymmetric unit. One of the cations has a weak interaction between its Cu atom and a O atom of an adjacent perchlorate anion. The structure of 3 contains two independent [CuLBr](+) cations and a (Cu3Br5)(2-) anion. The coordination geometry around the cation's Cu(II) ion is five-coordinated square pyramidal, with L acting as a tetradentate neutral ligand and with a Br at the apical position. The Cu(3)Br52- anions link to one another to form an infinite one-dimensional (Cu(3)Br52-)(n) chain. Furthermore, the Hirshfeld surface analyses and the 2D fingerprint plot have been discussed.
引用
收藏
页码:2509 / 2518
页数:10
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