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Activating a Peroxo Ligand for C-O Bond Formation

机译:用于C-O键形成的过氧配体

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摘要

Dioxygen activation for effective C-O bond formation in the coordination sphere of a metal is a long-standing challenge in chemistry for which the design of catalysts for oxygenations is slowed down by the complicated, and sometimes poorly understood, mechanistic panorama. In this context, olefin-peroxide complexes could be valuable models for the study of such reactions. Herein, we showcase the isolation of rare "Ir(cod)(peroxide)" complexes (cod=1,5-cyclooctadiene) from reactions with oxygen, and then the activation of the peroxide ligand for O-O bond cleavage and C-O bond formation by transfer of a hydrogen atom through proton transfer/electron transfer reactions to give 2-iradaoxetane complexes and water. 2,4,6-Trimethylphenol, 1,4-hydroquinone, and 1,4-cyclohexadiene were used as hydrogen atom donors. These reactions can be key steps in the oxy-functionalization of olefins with oxygen, and they constitute a novel mechanistic pathway for iridium, whose full reaction profile is supported by DFT calculations.
机译:金属配位球体中有效C-O键形成的二恶英激活是一种在化学中的长期挑战,其中氧合的催化剂的设计被复杂,有时是理解的机械全景的复杂性。在这种情况下,烯烃 - 过氧化物复合物可以是用于研究这种反应的有价值的模型。在此,我们展示稀有“IR(COD)(过氧化物)”复合物(COD = 1,5-环辛基)与氧的反应分离,然后通过转移激活过氧化物配体并通过转移的CO键形成通过质子转移/电子转移反应的氢原子得到2- aradaOxetane络合物和水。使用2,4,6-三甲基苯酚,1,4-羟基醌和1,4-环己二烯作为氢原子供体。这些反应可以是烯烃的氧官能化的关键步骤,其具有氧气的氧氟丝,它们构成了铱的新机制途径,其全反应谱通过DFT计算支持。

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