Univ. Grenoble Alpes, CNRS, UMR 5250, DCM, 38000, Grenoble, France.
Univ. Grenoble Alpes, CNRS, UMR 5249, LCBM, 38000, Grenoble, France.
Angew Chem Int Ed Engl. 2017 Jul 3;56(28):8211-8215. doi: 10.1002/anie.201703215. Epub 2017 Jun 9.
This study deals with the unprecedented reactivity of dinuclear non-heme Mn -thiolate complexes with O , which dependent on the protonation state of the initial Mn dimer selectively generates either a di-μ-oxo or μ-oxo-μ-hydroxo Mn complex. Both dimers have been characterized by different techniques including single-crystal X-ray diffraction and mass spectrometry. Oxygenation reactions carried out with labeled O unambiguously show that the oxygen atoms present in the Mn dimers originate from O . Based on experimental observations and DFT calculations, evidence is provided that these Mn species comproportionate with a Mn precursor to yield μ-oxo and/or μ-hydroxo Mn dimers. Our work highlights the delicate balance of reaction conditions to control the synthesis of non-heme high-valent μ-oxo and μ-hydroxo Mn species from Mn precursors and O .
这项研究涉及双核非血红素 Mn -硫醇配合物与 O 的前所未有的反应性,这取决于初始 Mn 二聚体的质子化状态,选择性地生成二 μ-氧合或 μ-氧合-μ-羟合 Mn 配合物。这两个二聚体都通过不同的技术进行了表征,包括单晶 X 射线衍射和质谱。用标记的 O 进行的氧合反应明确表明,Mn 二聚体中存在的氧原子来自 O 。基于实验观察和 DFT 计算,提供了证据表明这些 Mn 物种与 Mn 前体comproportionate 以生成 μ-氧合和/或 μ-羟合 Mn 二聚体。我们的工作强调了反应条件的微妙平衡,以控制非血红素高价 μ-氧合和 μ-羟合 Mn 物种从 Mn 前体和 O 的合成。