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Synthesis, spectral characterization and catalytic studies of new ruthenium(II) chalcone thiosemicarbazone complexes

机译:新型钌(II)查尔酮硫半碳carb配合物的合成,光谱表征和催化研究

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A series of new hexa-coordinated ruthenium(II) complexes of the type [Ru(CO)(EPh3)(B)(L)] (E = P or As; B = PPh3, AsPh3 or Py; L = chalcone thiosemicarbazone) have been prepared by reacting [RuHCl(CO)(EPh3)2(B)] (E = P or As; B = PPh3, AsPh3 or Py) with chalcone thiosemicarbazones in benzene under reflux. The new complexes have been characterized by analytical and spectroscopic (IR, UV-vis, ~1H, ~(31)P and ~(13)C NMR) methods. On the basis of data obtained, an octahedral structure was assigned for all of the complexes. The chalcone thiosemicarbazones behave as dianionic tridentate O, N, S donors and coordinate to ruthenium via the phenolic oxygen of chalcone, the imine nitrogen of thiosemicarbazone and thienol sulfur. The new complexes exhibit catalytic activity for the oxidation of primary and secondary alcohols to their corresponding aldehydes and ketones and they were also found to be efficient catalysts for the transfer hydrogenation of carbonyl compounds.
机译:[Ru(CO)(EPh3)(B)(L)]类型的一系列新的六配位钌(II)配合物(E = P或As; B = PPh3,AsPh3或Py; L =查尔酮硫半碳carb)通过使[RuHCl(CO)(EPh3)2(B)](E = P或As; B = PPh3,AsPh3或Py)与查尔酮硫代半氨基甲酮在苯中回流制得。新的配合物已通过分析和光谱法(红外,紫外-可见,〜1H,〜(31)P和〜(13)C NMR)进行了表征。根据获得的数据,为所有配合物分配了八面体结构。查尔酮硫半脲酮作为三齿双齿O,N,S供体,并通过查尔酮的酚氧,硫代半脲的亚胺氮和噻吩硫磺与钌配位。新的配合物对伯和仲醇氧化为相应的醛和酮具有催化活性,并且还发现它们是羰基化合物转移加氢的有效催化剂。

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