School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Department of Organic Chemistry, Weizmann Institute of Science, Rehovot 7610001, Israel.
J Am Chem Soc. 2021 Jul 7;143(26):9842-9848. doi: 10.1021/jacs.1c03568. Epub 2021 Jun 23.
Paramagnetic metal complexes gained a lot of attention due to their participation in a number of important chemical reactions. In most cases, these complexes are dominated by 17-e metalloradicals that are associatively activated with highly reactive paramagnetic 19-e species. Molybdenum paramagnetic complexes are among the most investigated ones. While some examples of persistent 17-e Mo-centered radicals have been reported, in contrast, 19-e Mo-centered radicals are illusive species and as such could rarely be detected. In this work, the photodissociation of the [Cp(CO)Mo] dimer () in the presence of phosphines was revisited. As a result, the first persistent, formally 19-e Mo radical with significant electron density on the Mo center (22%), Cp(CO)MoPPh(-CBH) (), was generated and characterized by EPR spectroscopy and MS as well as studied by DFT calculations. The stabilization of was likely achieved due to a unique electron-withdrawing effect of the -carboranyl substituent at the phosphorus center.
由于参与了许多重要的化学反应,顺磁金属配合物引起了广泛关注。在大多数情况下,这些配合物主要由 17 电子金属茂自由基组成,这些自由基通过高反应性的顺磁 19 电子物种协同活化。钼顺磁配合物是研究最多的配合物之一。虽然已经报道了一些持久的 17 电子 Mo 中心自由基的例子,但相反,19 电子 Mo 中心自由基是难以捉摸的物种,因此很少被检测到。在这项工作中,重新研究了膦存在下 [Cp(CO)Mo]二聚体 () 的光解。结果,首次生成了具有 Mo 中心上显著电子密度(22%)的持久的、形式上为 19 电子 Mo 自由基 Cp(CO)MoPPh(-CBH) (),并用 EPR 光谱、MS 以及 DFT 计算进行了表征。磷中心的 -碳硼烷取代基的独特吸电子效应可能导致了的稳定。