Ablyasova Olesya S, Ugandi Mihkel, Boydas Esma B, da Silva Santos Mayara, Flach Max, Zamudio-Bayer Vicente, Roemelt Michael, Lau J Tobias, Hirsch Konstantin
Abteilung für Hochempfindliche Röntgenspektroskopie, Helmholtz-Zentrum Berlin für Materialien und Energie, Albert-Einstein-Straße 15, 12489 Berlin, Germany.
Physikalisches Institut, Universität Freiburg, Hermann-Herder-Straße 3, 79104 Freiburg, Germany.
J Am Chem Soc. 2025 Mar 5;147(9):7336-7344. doi: 10.1021/jacs.4c14543. Epub 2025 Feb 19.
In a comprehensive investigation of the dinuclear [MnO] cluster, the smallest dimanganese entity with two μ-oxo bridges and a terminal oxo ligand, and a simplified structural model of the active center in the oxygen-evolving complex, we identify antiferromagnetically coupled high-spin manganese centers in very different oxidation states of +2 and +5, but rule out the presence of a manganese(IV)-oxyl species by experimental X-ray absorption and X-ray magnetic circular dichroism spectroscopy combined with multireference calculations. This first identification of a high-spin manganese(V) center in any polynuclear oxidomanganese complex underscores the need for multireference computational methods to describe high-valent oxidomanganese species.
在对双核[MnO]簇(具有两个μ-氧桥和一个端基氧配体的最小二锰实体,以及析氧复合物活性中心的简化结构模型)进行的全面研究中,我们确定了处于非常不同氧化态(+2和+5)的反铁磁耦合高自旋锰中心,但通过实验X射线吸收和X射线磁圆二色光谱结合多参考计算排除了锰(IV)-氧基物种的存在。在任何多核氧化锰复合物中首次鉴定出高自旋锰(V)中心,这突出了使用多参考计算方法来描述高价氧化锰物种的必要性。