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Ruthenium(II) supported by phosphine-functionalized N-heterocyclic carbene ligands as catalysts for the transfer hydrogenation of ketones

机译:膦官能化的N-杂环卡宾配体负载的钌(II)作为酮转移加氢的催化剂

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摘要

We have prepared and characterized two ruthenium(II) complexes supported by phosphine-functionalized N-heterocyclic (NHC) ligands. One of the complexes (2a) underwent ortho-metalation of the N-phenyl moiety giving rise to a tridentate PC_(NHC)C~-coordinating ligand whereas 2b bears an N-mesityl group in order to prevent C-H activation of the aryl ring thereby enforcing a PC_(NHC) bidentate binding mode. Both 2a and 2b were shown to catalyze transfer hydrogenation of ketones at 82 °C in 2-propanol in the presence of KO Bu albeit with vasdy different catalytic activities. Catalytic transfer hydrogenation by 2b was shown to proceed at room temperature and in air using unpurifled 2-propanol as solvent and hydrogen donor. Time studies revealed unique kinetic profiles for the two precatalysts; this may shed light on the difference in their catalytic activities.
机译:我们已经制备并表征了由膦官能化的N杂环(NHC)配体支持的两种钌(II)配合物。其中一种配合物(2a)进行了N-苯基部分的邻位金属化反应,生成了三齿的PC_(NHC)C-配位配体,而2b则带有一个N-间苯甲基,以防止芳基环被CH活化强制执行PC_(NHC)双齿绑定模式。已显示2a和2b都在存在BU Bu的情况下在2-丙醇中于82°C催化酮的转移氢化,尽管具有不同的催化活性。已显示2b的催化转移氢化反应在室温和空气中进行,使用未纯化的2-丙醇作为溶剂和氢供体。时间研究揭示了两种预催化剂的独特动力学特征。这可能揭示了它们催化活性的差异。

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