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Abstract The master thesis include aim of the work and three main chapter I- Aim of the work the work aimed to prepare and characterize a new dihydrazone ether ligand and its metal complexes aiming to study their effects in the treatment of tumor diseases. II- Introduction This chapter includes an overview of previous researches for complexes of di-hydrazone ligands and their application. III- Experimental This chapter contains the chemical and instruments used in Practical part of thesis as follow: 1) Preparation of di-hydrazone ligand and its metal complexes. 2) characterization of the ligand and its complexes using: Physical techniques such as molar conductance and magnetic susceptibility Elemental analyses (C, H, N, Cl and M). Spectral techniques as IR, UV- Vis., 1HNMR, mass spectra and ESR measurements. Thermal techniques as DTA. and TGA 3) Measurement of antitumor activity iv. Results and discussion This chapter includes characterization of the ligand and its complexes. The ligand (E)-N’-(2-hydroxybenzylidene)-4-(4-(((E)-2-(2- hydroxybenzylidene)hydrazinyl)oxy)phenoxy)benzohydrazide ( H2L)was prepared as follow: 1- Condensation of parachlorophenol with of methoxy-para-hydroxy benzoate sodium salt (1:1) for one hour to obtain methyl 4-(4- hydroxyphenoxy)benzoate 2- Condensation of methyl 4-(4-hydroxyphenoxy)benzoate with hydrazine hydrate for two hours (1:2) to obtain 4-(4- hydrazinylphenoxy)benzohydrazide. 3- Condensation of 4-(4-hydrazinylphenoxy)benzohydrazide with salicyaldehyde for 30 minutes (1:2) to obtain The ligand (H2L) (E)- N’-(2-hydroxybenzylidene)-4-(4-(((E)-2-(2- hydroxybenzylidene)hydrazinyl)oxy) phenoxy)benzohydrazide. The reaction of the ligand (H2L) with Cu(II), Ni(II), Fe(III), Co(II), Zn(II), Pb(II), Ca(II), Mg(II), AL(III), and Ba(II) complexes have been synthesized and characterized by (1H-NMR, mass, IR, UV-VIS, ESR) spectroscopy, (magnetic moments, conductance) measurements, (elemental and thermal) analyses. The IR spectral data show that, the Schiff base behaves as a neutral tetra dentate ligand bonded to the metal ions through the azomethine nitrogen atom and oxygen atom in hydroxyl group which protonated or deprotonated form adopting either octahedral or tetragonally distorted octahedral geometries. Molar conductance in DMF solution indicates that, the complexes are non-electrolytes. The ESR spectra of solid of copper(II) complexes (8,9 and 11) are characteristic of species d9 configuration having axial type of a d(x2-y2) ground state which is the most common for copper(II) complexes. However, Fe (III) complex (4), show isotropic type indicating an English summary iii octahedral geometry. Cytotoxic evolution of the ligand and its complexes have been carried out. Complexes show enhanced activity in comparison to the parent ligand. Metal complexes (9), (13),(17) and (18) were evaluated against HEPG-2 cell line showed better chemotherapeutic effect against HEPG- 2 cell line than the standard drug used. Also, the Cd(II) complex (17) shows the highest potency of inhibition at 500 μg/ml against HEPG-2, compared with the standard drug. |