Synthesis, characterization, equilibrium study and biological activity of Cu(II), Ni(II) and Co(II) complexes of polydentate Schiff base ligand

Author(s):  
Ahmed A. El-Sherif ◽  
Mohamed R. Shehata ◽  
Mohamed M. Shoukry ◽  
Mohammad H. Barakat
2017 ◽  
Vol 30 (3) ◽  
pp. 114
Author(s):  
Hasan A. Hasan

 The precursor [W] [2-(2-(naphthalen-5-yl) diazenyl)-4-amino-3-hydroxynaphthalene-1sulfonic acid] was synthesized from reaction of diazonium salt with 1-amino-2-naphtol-4sulfonic acid. Then the tridentate Schiff base ligand type ONO was synthesized from the reaction of the precursor with salicyaldehyde in 1:1 mole ratio to produce the ligand H2L [2-(2-(naphthalen5-yl) diazenyl)-4-(2-hydroxynaphthalen-3-yl)methyleneamino)-3-hydroxy salicyalene-1-sulfonic acid],the reaction achieved in methanol as a solvent under reflux. Spectroscopic methods IR, U.V, 1H,13C-NMR was used to characterize the ligand. Complexes of [CrIII, CoII, NiII and CdII] ions were also prepared through reaction of ligand with metal salts in 2:1 mole ratio at reflux, using KOH as a base, ethanol as a solvent. Chloride content, molar conductivity and melting point measurements along with I.R and U.V-Vis, atomic absorption (A.A) spectroscopy were used to characterize the complexes.1H-NMR spectroscopy was used to characterize Cd complex. Thermal analysis was used to insure the presence of crystallized H2O molecule in the complexes structure. The following formula was proposed for Cr complex: K[Cr(L)2]. H2O, while CoII, NiII and CdII complexes have the K2[M(L)2].H2O formula. The biological activity of the prepared compounds was studied. Fluorescence properties of the prepared compounds were studied (at room temperature) which indicate that the ligand may behave as strong fluorescent emitter. The complexes also showed fluorescence characteristic with the ligand. The ligand revealed high relative intensity and its fluorescence peak were also shifted to the lower or higher wavelength when compared with the complexes.


2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Riyadh M. Ahmed ◽  
Enaam I. Yousif ◽  
Hasan A. Hasan ◽  
Mohamad J. Al-Jeboori

A new macrocyclic multidentate Schiff-base ligand Na4L consisting of two submacrocyclic units (10,21-bis-iminomethyl-3,6,14,17-tricyclo[17.3.1.18,12]tetracosa-1(23),2,6,8,10,12(24),13,17,19,21,-decaene-23,24-disodium) and its tetranuclear metal complexes with Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) are reported. Na4L was prepared via a template approach, which is based on the condensation reaction of sodium 2,4,6-triformyl phenolate with ethylenediamine in mole ratios of 2 : 3. The tetranuclear macrocyclic-based complexes were prepared from the reaction of the corresponding metal chloride with the ligand. The mode of bonding and overall geometry of the compounds were determined through physicochemical and spectroscopic methods. These studies revealed tetrahedral geometries about Mn, Co, and Zn atoms. However, square planar geometries have been suggested for NiIIand CuIIcomplexes. Biological activity of the ligand and its metal complexes against Gram positive bacterial strainStaphylococcus aureusand Gram negative bacteriaEscherichia colirevealed that the metal complexes become more potentially resistive to the microbial activities as compared to the free ligand. However, these metal complexes do not exhibit any effects on the activity ofPseudomonas aeruginosabacteria. There is therefore no inhibition zone.


2021 ◽  
Vol 20 (2) ◽  
pp. 193-202
Author(s):  
Çiğdem Yörür-Göreci ◽  
Nilay Altaş-Puntar ◽  
Abdullah Toraman ◽  
Nebahat Demirhan

The new salicylaldimine, as O,N-bidentate ligand (HL), containing amino acide ester and its Ru(II) complex [Ru(bpy)2(HL)]Cl2 have been prepared. Synthesized compounds have been structurally characterized by IR, 1H NMR, LC-MS, fluorescence spectroscopy, elemental and thermal (TGA-DSC) analyses. The metal to the ligand ratio of the Ru(II) complex was found to be 1:1. Antifungal activities of the ligand and complex have been investigated. The Ru(II) complex have strong antifungal activity than the ligand against Aspergillus niger.


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