2,4-Dihydroxy-5-[(5-mercapto-1H-1,2,4-triazole-3-yl)diazenyl] benzaldehyde acetato, chloro and nitrato Cu(II) complexes: Synthesis, structural characterization, DNA binding and anticancer and antimicrobial activity

被引:60
|
作者
Gaber, Mohamed [1 ]
Fathalla, Shaimaa K. [2 ]
El-Ghamry, Hoda A. [1 ,3 ]
机构
[1] Tanta Univ, Chem Dept, Fac Sci, Tanta, Egypt
[2] Taif Univ, Chem Dept, Fac Sci, At Taif, Saudi Arabia
[3] Umm Al Qura Univ, Fac Appl Sci, Dept Chem, Mecca, Saudi Arabia
关键词
azo dye; biological studies; Cu complexes; DNA binding; triazole; TRANSITION-METAL-COMPLEXES; IN-VITRO ANTICANCER; SCHIFF-BASE; SPECTROSCOPIC CHARACTERIZATION; COPPER(II) COMPLEXES; CRYSTAL-STRUCTURE; DICOPPER(II) COMPLEXES; THERMAL-DECOMPOSITION; PT(II) COMPLEXES; ZN(II) COMPLEXES;
D O I
10.1002/aoc.4707
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Acetato, chloro and nitrato Cu(II) complexes of a novel azo compound, namely 2,4-dihydroxy-5-[(5-mercapto-1H-1,2,4-triazole-3-yl)diazenyl]benzaldehyde, have been prepared. The stoichiometry, stereochemistry and bonding fashion of these copper chelates were deduced via elemental analyses, spectral methods and conductivity and magnetic measurements. Infrared spectral data confirmed the participation of azo N atom and the deprotonated OH group. UV-visible spectral data and magnetic measurements indicated octahedral stereostructure for the acetato and nitrato compounds and square planer for the chloro compound. Thermogravimetric analysis was applied to investigate the thermal degradation of the metal chelates. The thermo-kinetic parameters were computed. The molecular modeling technique was used to support the predicted geometry of the prepared chelates. The interaction between the Cu(II) complexes and calf thymus DNA was studied using two techniques: absorption and viscosity measurements. The values of binding constant obtained from the absorption spectral method were calculated and found to be 4.23 x 10(4), 26.93 x 10(4), 13.01 x 10(4) and 5.36 x 10(4) M-1 for ligand and acetato, chloro and nitrato complexes, respectively. The antimicrobial activities were evaluated against various bacterial and fungi strains. The in vitro antitumor efficacy of the synthesized compounds was investigated against the HEPG2 cell line.
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页数:14
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