In this paper, the complexes of Shiff base of Methyl -6-[2-(diphenylmethylene)amino)-2-(4hydroxyphenyl)acetamido]-2,2-dimethyl-5-oxo-1-thia-4-azabicyclo[3.2.0]heptane-3-carboxylate (L) with Cobalt(II), Nickel(II), Cupper(II) and Zinc(II) have been prepared. The compounds have been characterized by different means such as FT-IR, UV-Vis, magnetic moment, elemental microanalyses (C.H.N), atomic absorption, and molar conductance. It is obvious when looking at the spectral study that the overall complexes obtained as monomeric structure as well as the metals center moieties are two-coordinated with octahedral geometry excepting Co complexes that existed as a tetrahedral geometry. Hyper Chem-8.0.7 program was employed, after calculating the heat of formation (ΔH°f ) , binding energy (ΔE b ), dipole moment( µ ), and FT-IR frequencies are carried out in gas phase, the geometric shape is suggested. The compounds have been also screened for their bioactivity to antibacterial and antifungal.

New metal complexes of the ligand 2-[5-(Pyridin-2-ylmethylene)-amino] 1,3,4-thiadiazol-2-ylphenol (L) with the metal ions Co(II), Ni(II), Cu(II) and Zn(II) were prepared in alcoholic medium. The Schiff base was condensed [2-pyridine carbxaldehyde] with [2-amino-5-(phenyl-1,3,4oxadiazole] in alcoholic medium. Two tetradentate Schiff bases ligand were used for complexation upon two metal ions of Co 2+, Ni 2+, Cu 2+ and Zn 2+ as dineucler formula M2L2. The synthesized compound and their metal complexes were characterized by FTIR Spectroscopy, electronic spectroscopy, Elemental analysis, magnetic susceptidbility measurements, thermal analysis , 1 H-NMR spectra, and mass spectra. The activation thermodynamic parameters such as ΔE * , ΔH * , ΔS * and ΔG * were calculated from the TGA curve using Coats-Red fern method. From the measurements, structures of the complexes were proposed.

Green synthesis of bimetallic nanoparticles of Fe/Ni (G-Fe/Ni-NPs) and zeolite-5A supported (G-Z-Fe/Ni-NPs) as heterogeneous Fenton-like oxidation for the decolourisation of reactive red 120-dye (RR120) from the aqueous medium using green tea extract as a reducing agent. Zeolite-5A from local kaolin is prepared and characterised using the hydrothermal method and is used as a supporting material for Fe/Ni-NPs. (SEM), (EDX), (AFM), (XRD), (FT-IR), (BET). Its zeta potential were used to characterise G-Fe/Ni-NPs and G-Z-Fe/Ni-NPs. The decolourisation efficiency (Ed) of the RR120-dye using a heterogeneous Fenton-like for G-Fe/Ni-NPs and G-Z-Fe/Ni-NPs is 99.8% and 99.9%, respectively, under the optimum conditions: [H2O2] = 20 and 1 mmol/L, respectively, by G-Fe/Ni-NPs, NPs dosage = 0.1 g/L, [RR120-dye] = 25 mg/L and pH = 3. The results show that the reactivity of Fe/Ni-NPs was improved when zeolite-5A was used as support, showing fast removal. Three kinetic models (first-order, second-order, and Behnajady–Modirshahla–Ghanbary, BMG) were evaluated. The first-order, (econd-order and BMG models were found to be the best models representing the experimental kinetic data of RR120-dye in the state of G-Fe/Ni-NPs and G-Z-Fe/Ni-NPs, respectively. The study of the thermodynamic parameters (ΔG°, ΔH°, and ΔS°) for the removal of RR120-dye at 30°C, 40°C and 50°C indicates an appropriate, spontaneous, and endothermic reaction. The Ed using Fenton-like and adsorption processes are compared.

Schiff base (methyl 6-(2-(4-hydroxyphenyl) -2-(1-phenyl ethyl ideneamino) acetamido) -3, 3dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0] heptane-2-carboxylate)Co(II), Ni(II), Cu (II), Zn (II), and Hg(II)] ions were employed to make certain complexes. Metal analysis M percent, elemental chemical analysis (C.H.N.S), and other standard physico-chemical methods were used. Magnetic susceptibility, conductometric measurements, FT-IR and UV-visible Spectra were used to identified. Theoretical treatment of the generated complexes in the gas phase was performed using the (hyperchem-8.07) program for molecular mechanics and semi-empirical computations. The (PM3) approach was used to determine the heat of formation (ΔH˚f), binding energy (ΔEb), and total energy (ET) for ligands and metal complexes at 298 ᴼK. To explore the reactive sites of the compounds, the electrostatic potential of the ligand (L) was computed. PM3 was used to calculate the vibrational frequencies of the ligand (L) and its metal complexes, which were then compared to experimental data. The antibacterial activity of (L) and its metal complexes against three harmful microorganisms were examined: Staphylococcus aureus (gram positive), Echerchia coli (gram negative), and Candida albicans.

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