کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1312624 | 975472 | 2010 | 5 صفحه PDF | دانلود رایگان |

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.
Herein 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 as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 363, Issue 6, 5 April 2010, Pages 1284–1288