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Synthesis, characterisation and electrochemistry of some stable ruthenium(II) complexes of the bidentate NS chelating ligand 1-amino-2-thiomethylbenzene

机译:二齿NS螯合配体1-氨基-2-硫代甲基苯的一些稳定的钌(II)配合物的合成,表征和电化学

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Ruthenium(II) complexes of the bidentate aminothioether ligand, 1-amino-2-thiomethylbenzene (atb), have been synthesised by the direct reaction of atb with different ruthenium-containing starting materials. The complexes are of the type Ru(atb)(2)X-2 [X=Cl (1), X=Br (2)], [Ru(atb)(2)(PPh3)Cl]Cl (3) and Ru(atb)(bpy)Cl-2 (4), and have been characterised by elemental analysis, IR, UV-VIS and NMR spectroscopy. Contrary to the corresponding Ni-II, Pd-II, Pt-II and Cu-II complexes with the same ligand, these Ru-II complexes do not suffer demethylation on refluxing in DMF. Their electrochemical behaviour was examined by cyclic voltammetry using a glassy carbon working elctrode and an Ag/AgCl electrode as reference. [References: 28]
机译:二齿氨基硫醚配体1-氨基-2-硫代甲基苯(atb)的钌(II)配合物是通过atb与不同的含钌原料直接反应合成的。络合物的类型为Ru(atb)(2)X-2 [X = Cl(1),X = Br(2)],[Ru(atb)(2)(PPh3)Cl] Cl(3)和Ru(atb)(bpy)Cl-2(4),并已通过元素分析,IR,UV-VIS和NMR光谱进行了表征。与具有相同配体的相应的Ni-II,Pd-II,Pt-II和Cu-II配合物相反,这些Ru-II配合物在DMF中回流时不会脱甲基。通过循环伏安法,使用玻璃碳工作电极和Ag / AgCl电极作为参考,检查了它们的电化学行为。 [参考:28]

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