Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1312624 | Inorganica Chimica Acta | 2010 | 5 Pages |
The electrochemical oxidation of anodic metal (iron, cobalt, nickel and copper) in an acetonitrile solution of the potentially chelating Schiff base N,N(dithiodiethylenebis-(aminylydenemethylydene)-bis(1,2-phenylene)ditosylamide (H2L) afforded stable complexes of empirical formula [ML]. The compounds obtained have been characterized by microanalysis, IR spectroscopy and ES-MS mass spectrometry. The crystal and molecular structures of [FeL]·CH3CN (1) [CoL]·CH3CN (2), [NiL]·CH3CN (3) and [CuL]·CH3CN (4) have been determined by X-ray diffraction in all complexes, the metal atom is in a distorted tetrahedral environment with the Schiff base acting as a tetradentate N4 donor.
Graphical abstractHerein we report the coordination chemistry of iron, cobalt, nickel and copper with the potentially tetradentate dianionic Schiff base, N,N(dithiodiethylenebis-(aminylydenemethylydene)-bis(1,2-phenylene)ditosylamide. The crystal and molecular structures of [FeL]·CH3CN (1) [CoL]·CH3CN (2), [NiL]·CH3CN (3) and [CuL]·CH3CN (4) have been determined by X-ray diffraction. In all complexes the metal atom is in a distorted tetrahedral environment with the Schiff base acting as a tetradentate N4 donor.Figure optionsDownload full-size imageDownload as PowerPoint slide