Tezin Türü: Yüksek Lisans
Tezin Yürütüldüğü Kurum: Orta Doğu Teknik Üniversitesi, Fen Edebiyat Fakültesi, Kimya Bölümü, Türkiye
Tezin Onay Tarihi: 2005
Tezin Dili: İngilizce
Öğrenci: Fatma Sanem Koçak
Danışman: SAİM ÖZKAR
Özet:In this study a bidentate ligand containing two ferrocenyl moieties, N,N'-bis(ferrocenylmethylene)ethylenediamine, was prepared by condensation reaction of ferrocenecarboxyaldehyde and ethylenediamine on refluxing in benzene. The molecule was identified by IR, Raman, UV-Vis, 1H-, 13C-NMR spectroscopies. Then, this bidentate molecule was reacted with tetracarbonyl(bicyclo[2.1.1] hepta-2,5-diene)molybdenum(0). The ligand substitution reaction in toluene yielded the new complex, tetracarbonyl[N,Ń-bis(ferrocenylmethylene)ethylenediamine] molybdenum(0). This new complex could be isolated from the reaction solution in the form of orange crystals and fully characterized by elemental analysis, IR, UV-Vis, MS, 1H- and 13C-NMR spectroscopies. As a bidentate ligand, N,Ń-bis(ferrocenylmethylene)ethylenediamine binds the metal atom in the two cis positions in the pseudooctahedral geometry of the molybdenum-complex. Electrochemistry of the tetracarbonyl[N,Ń-bis(ferrocenylmethylene) ethylenediamine]molybdenum(0) was studied by cyclic voltammetry, chronoamperometry and controlled potential electrolysis combined with the UV-Vis or infrared spectroscopy. One irreversible oxidation and three reversible oxidations were observed in the cyclic voltammogram. Irreversible and a reversible oxidations are attributed to molybdenum and the other two reversible oxidation to iron centers. It is found that the two ferrocene groups started communication with each other after formation of molybdenum-complex.