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العنوان
Synthesis and characteristic studies of metal complexes of some Schiff bases derived from o-acetoacetylphenol./
الناشر
جامعة عين شمس . كلية التربية. قسم الكيمياء.
المؤلف
مهدي ، محمد علي ناجي حسن .
هيئة الاعداد
باحث / محمد علي ناجي حسن مهدي
مشرف / سعيد محمد السيد خليل
مشرف / علي محمود طه
مناقش / مجدي شبل صالح السيد
مناقش / أميمة محمد ابراهيم عدلي
تاريخ النشر
1/1/2017
عدد الصفحات
342 ص ،
اللغة
العربية
الدرجة
ماجستير
التخصص
Biochemistry, Genetics and Molecular Biology (miscellaneous)
تاريخ الإجازة
1/1/2017
مكان الإجازة
جامعة عين شمس - كلية التربية - الكيمياء
الفهرس
يوجد فقط 14 صفحة متاحة للعرض العام

from 142

from 142

المستخلص

New three Schiff base ligands, (H3L1, H3L2, H3L3) resulting from condensation of o-acetoacetylphenol with salicylaldehyde hydrazone , 2-hydroxybenzohydrazide and benzoylhydrazide, respectively were synthesized. Reactions of the ligands with alkaline earth metals such as: magnesium(II), calcium(II), strontium(II) and barium(II) in the presence of LiOH; and some transition metal ions such as chromium(III), manganese(II), iron(III), cobalt(II), nickel(II), copper(II), zinc(II), cadmium(II) and dioxouranium(VI) ions yielded mono-, bi- and trinuclear complexes. The complexes were characterized by elemental, thermal analyses, IR, electronic, 1H NMR, ESR and mass spectra as well as conductivity and magnetic susceptibility measurements. Different geometrical structures were proposed for the metal complexes of the Schiff base ligands. Molecular orbital calculations were carried out on the free ligands and their complexes using HyperChem 7.5 program at semiempirical PM3 level. The calculated structural parameters data are found to be linearly correlated with some of the experimental data such as: TGA, IR frequencies and biological activity results. The Schiff base ligands and some of their complexes showed antibacterial activity towards some of Gram–positive, Gram–negative bacteria, yeast (C. albicans) and fungus (A. fumigatus). The antitumor activity of the ligands H3L1 and H3L2 and their Ni(II) and Cu(II) complexes was investigated against HepG2 cell line.