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首页> 外文期刊>Angewandte Chemie >K beta X-Ray Emission Spectroscopic Study of a Second-Row Transition Metal (Mo) and Its Application to Nitrogenase-Related Model Complexes
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K beta X-Ray Emission Spectroscopic Study of a Second-Row Transition Metal (Mo) and Its Application to Nitrogenase-Related Model Complexes

机译:kβX射线发射光谱研究二行过渡金属(MO)及其在氮酶相关模型复合物中的应用

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摘要

In recent years, X-ray emission spectroscopy (XES) in the K beta (3p-1s) and valence-to-core (valence-1s) regions has been increasingly used to study metal active sites in (bio)inorganic chemistry and catalysis, providing information about the metal spin state, oxidation state and the identity of coordinated ligands. However, to date this technique has been limited almost exclusively to first-row transition metals. In this work, we present an extension of K beta XES (in both the 4p-1s and valence-to-1s [or VtC] regions) to the second transition row by performing a detailed experimental and theoretical analysis of the molybdenum emission lines. It is demonstrated in this work that K beta(2) lines are dominated by spin state effects, while VtC XES of a 4d transition metal provides access to metal oxidation state and ligand identity. An extension of Mo K beta XES to nitrogenase-relevant model complexes shows that the method is sufficiently sensitive to act as a spectator probe for redox events that are localized at the Fe atoms. Mo VtC XES thus has promise for future applications to nitrogenase, as well as a range of other Mo-containing biological cofactors. Further, the clear assignment of the origins of Mo VtC XES features opens up the possibility of applying this method to a wide range of second-row transition metals, thus providing chemists with a site-specific tool for the elucidation of 4d transition metal electronic structure.
机译:近年来,Kβ(3P-1S)和核心至核(价1S)区的X射线发射光谱(XES)越来越多地用于研究(生物)无机化学和催化的金属活性位点,提供有关金属旋转状态,氧化状态和配位配体的特性的信息。然而,迄今为止,该技术几乎完全限制为一行过渡金属。在这项工作中,我们通过对钼排放线进行详细的实验和理论分析,向第二过渡行呈现Kβxes(在4p-1s和价达1s [或VTC]区域中)的延伸。在这项工作中证明了Kβ(2)线以旋转状态效应支配,而4D过渡金属的VTC XES提供对金属氧化状态和配体同一性的访问。 MoKβXes对氮酶相关的模型复合物的延伸表明,该方法足够敏感,以充当氧化还原事件的销售探针,该redox事件在Fe原子下定位。因此,Mo VTC Xes承诺将来应用于氮酶,以及一系列含MO的生物辅因子。此外,Mo VTC XES特征的起源的明确分配开辟了将该方法应用于各种二排过渡金属的可能性,从而提供具有用于阐明4D过渡金属电子结构的特定场地工具的化学家。

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