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Ruthenium(II) Complexes Containing Lutidine-derived Pincer CNC Ligands: Synthesis, Structure and Catalytic Hydrogenation of C=N bonds

机译:含卢替丁衍生的钳式CNC配体的钌(II)配合物:C = N键的合成,结构和催化加氢

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摘要

A series of Ru complexes 3-5 containing lutidine-derived pincer CNC ligands have been prepared by transmetallation with the corresponding silver-carbene derivatives 2. Characterization of these derivatives shows both mer and fac coordination of the CNC ligands depending on the wingtips of the N-heterocyclic carbene fragments. Ru-CNC complexes 3-4 are active, in the presence of tBuOK, in the hydrogenation of a series of imines. In addition, these complexes also catalyze the reversible hydrogenation of phenantridine. Detailed NMR studies have shown the capability of the CNC ligand to be deprotonated and get involved in ligand-assisted activation of dihydrogen. More interestingly, upon deprotonation, Ru-CNC complex 5e(BF4) is able to add aldimines to the\udmetal-ligand framework to yield amido complexes 10. Finally, investigation of the mechanism of the hydrogenation of imines has been carried out by means of DFT calculations. The calculated mechanism involves outer-sphere stepwise hydrogen transfer to the C=N bond assisted either by the pincer ligand or a second coordinated H2 molecule.
机译:通过与相应的银-卡宾衍生物2进行金属转移,已制备了一系列含卢剔啶衍生的钳型CNC配体的Ru配合物3-5。这些衍生物的表征显示CNC配体的mer和fac配位取决于N的翼尖-杂环卡宾片段。在tBuOK存在下,Ru-CNC配合物3-4在一系列亚胺的氢化中具有活性。另外,这些配合物还催化菲啶的可逆氢化。详细的NMR研究表明,CNC配体具有去质子化能力并参与了配体辅助的二氢活化。更有趣的是,在去质子化后,Ru-CNC络合物5e(BF4)能够向\ udmetal-配体骨架中添加醛亚胺以生成酰胺基络合物10。最后,通过以下方法对亚胺的氢化机理进行了研究: DFT计算。计算的机理包括通过钳形配体或第二个配位的H2分子协助外球逐步将氢转移至C = N键。

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