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硼碳稳定的“19 电子”钼金属自由基。

Carborane Stabilized "19-Electron" Molybdenum Metalloradical.

机构信息

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.

出版信息

J Am Chem Soc. 2021 Jul 7;143(26):9842-9848. doi: 10.1021/jacs.1c03568. Epub 2021 Jun 23.

Abstract

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.

摘要

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。

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