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Isolable iodosylarene and iodoxyarene adducts of Co and their O-atom transfer and C–H activation reactivity

机译:Co的可分离的碘亚芳基和碘氧基芳烃加合物及其O原子转移和CH活化反应性

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摘要

We report an unusual series of discrete iodosyl- and iodoxyarene adducts of Co. The formation of these adducts was confirmed by a suite of techniques including single crystal X-ray diffraction. The reactivity of these adducts with O-atom acceptors and an H-atom donor has been investigated with particular focus on elucidating mechanistic details. Detailed kinetic analysis allows for discrimination between proposed oxo and adduct mediated mechanisms. In particular, these reactions have been interrogated by competition experiments with isotopically labelled mixtures which shows that all of the studied adducts display a large KIE. These studies suggest different mechanisms may be relevant depending on subtle substituent changes in the adduct complexes. Reactivity data are consistent with the involvement of a transient oxo complex in one case, while the two other systems appear to react with substrates directly as iodosyl- or iodoxyarene adducts. These results support that reactivity typically ascribed to metal-oxo complexes, such as O-atom transfer and C–H activation, can also be mediated by discrete transition metal iodosyl- or iodoxyarene adducts that are frequent intermediates in the generation of oxo complexes. The influence of additional Lewis acids such as Sc3+ on the reactivity of these systems has also been investigated.
机译:我们报告了Co的一系列不寻常的离散的碘基-和碘氧基芳烃加合物。通过一系列包括单晶X射线衍射在内的技术证实了这些加合物的形成。已经研究了这些加合物与O-原子受体和H-原子供体的反应性,尤其着重于阐明机理细节。详细的动力学分析可以区分拟议的羰基合成和加合物介导的机理。尤其是,这些反应已通过竞争实验与同位素标记的混合物进行了比较,结果表明所有研究的加合物均显示出较大的KIE。这些研究表明,不同的机理可能取决于加合物中取代基的细微变化。在一种情况下,反应性数据与瞬态氧配合物的参与相一致,而另外两种系统似乎以碘代基-或碘氧基芳烃加合物的形式直接与底物反应。这些结果支持通常归因于金属-氧代络合物的反应性,例如O-原子转移和CH-H活化,也可以由离散的过渡金属碘代-碘代芳烃加合物(它们是氧代络合物生成中的常见中间体)介导。还研究了另外的路易斯酸如Sc 3 + 对这些系统反应性的影响。

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