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A CuI /CuIII prototypical organometallic mechanism for the deactivation of an active pincer-like CuI catalyst in Ullmann-type couplings

机译:CuI / CuIII原型有机金属机制,用于钝化Ullmann型偶联中的活性钳状CuI催化剂

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摘要

Unraveling the mechanistic details of copper-catalyzed arylation of nucleophiles (Ullmann-type couplings) is a very challenging task. It is a matter of intense debate whether it is a radical-based process or an organometallic redox- based process. The ancillary ligand choice in Ullmann-type couplings plays a key role in such transformations and can strongly influence the catalytic efficiency as well as the mechanism. Here, we show how a predesigned tridentate pincer-like catalyst undergoes a deactivation pathway through a Cu I /Cu III prototypical mechanism as demonstrated by helium-tagging infrared photodissociation (IRPD) spectroscopy and DFT studies, lending a strong support to the existence of an aryl-Cu III species in the Ullmann couplings using this tridentate ligand
机译:阐明亲核试剂的铜催化芳基化(Ullmann型偶联)的机理细节是一项非常具有挑战性的任务。无论是基于自由基的过程还是基于有机金属氧化还原的过程,都引起了激烈的争论。乌尔曼型偶联中辅助配体的选择在这种转化中起关键作用,并且可以强烈影响催化效率及其机理。在这里,我们展示了预先设计的三齿钳状催化剂如何通过Cu I / Cu III原型机制经历失活途径,如氦标记红外光解离(IRPD)光谱法和DFT研究所证明的那样,为存在一种使用该三齿配体的Ullmann偶联中的芳基-Cu III物种

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