solution. Formation of mer-[2] proceeded via a C–H activation of the CH2 group next to the amine nitrogen atom of the ethylene arm. Reduction reactions of fac- and mer-[1] afforded a triacetonitrile complex mer-[RuII(CH3CN)3(ebpea)](PF6)2 (mer-[3](PF6)2). Five nitrosyl complexes fac-[RuX2(NO)(ebpea)]PF6 (X = Cl for fac-[4]PF6; X = ONO2 for fac-[5]PF6) and mer-[RuXY(NO)(ebpea)]PF6 (X = Cl, Y = Cl for mer-[4]PF6;
The (iminiumion)ruthenium(II) complex mer(Cl,Cl,Cl)-[RuCl3η2-NCHCH2py(C2H4py)C2H5}] was synthesized via a C−H activation of the bridging ethyl group of an ethylbis(2-pyridylethyl)amine ligand and characterized by X-ray structural analysis. Oxidations of alcohols by the (iminiumion)ruthenium(II) complex occurred with generation of mer-[RuIIICl3(ebpea)].
的(亚铵离子)钌(II)配合物聚体(氯,氯,氯) -将[RuCl 3 η 2 -NCHCH 2 PY(C 2 H ^ 4 PY)C 2 H ^ 5 }]通过C-H活化合成双(2-吡啶基乙基)胺配体的桥连乙基的结构分析,并通过X射线结构分析进行表征。由(亚铵离子)钌(II)配合物的醇的氧化反应发生以产生聚体-的[Ru III氯3(ebpea)]。