Turkish Journal of Chemistry
DOI
-
Abstract
Multidentate N-ligands (Schiff bases) were prepared by the condensation of 2-acetylpyridine or 2-benzoylpyridine, and 1,2-diaminoethane or 1,6-diaminohexane (2:1 ratio) in ethanol. These ligands were reacted with Mo(CO)_6 to obtain dinuclear metal tetracarbonyl compounds. Both terminal amine groups were seen to form imines from the reaction of mono-ketones with diamines in 2:1 or 1:1 ratios. The structures of these ligands and metal complexes were characterized by elemental analysis, and FT-IR, ^1H-NMR, ^{13}C-NMR, and LC-MS spectral techniques. N,N'-bis[1-(pyridin-2-yl)ethylidene]ethane-1, 2-diamine, which was obtained by the reaction of 2-acetylpyridine and 1,2-diaminoethane, was also characterized by single crystal X-ray structure analysis. The crystal packing is stabilized by intermolecular H-bonding and \pi-\pi interactions.
Keywords
Dinuclear, intermolecular H-bonding, molybdenum, polyimines, Schiff base, tetracarbonyl
First Page
667
Last Page
676
Recommended Citation
MENTEŞ, AYFER; SEZEK, SEDA; HANHAN, M. EMRE; and BÜYÜKGÜNGÖR, ORHAN (2007) "Dinuclear Molybdenum Tetracarbonyl Complexes of Tetradentate Nitrogen Ligands and Intermolecular Hydrogen Bonding in the Crystal Structure of N,N´-bis-[1-(pyridin-2-yl)ethylidene]-ethane-1,2-diamine," Turkish Journal of Chemistry: Vol. 31: No. 6, Article 12. Available at: https://journals.tubitak.gov.tr/chem/vol31/iss6/12
