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通过多元 XAS 分析提供非血红素配合物反应的直接机制证据。

Direct Mechanistic Evidence for a Nonheme Complex Reaction through a Multivariate XAS Analysis.

机构信息

Dipartimento di Chimica, Università di Roma "La Sapienza", P.le A. Moro 5, 00185 Roma, Italy.

Dipartimento di Chimica, Università degli Studi di Torino, Via P. Giuria 7, 10125 Torino, Italy.

出版信息

Inorg Chem. 2020 Jul 20;59(14):9979-9989. doi: 10.1021/acs.inorgchem.0c01132. Epub 2020 Jun 29.

Abstract

In this work, we propose a method to directly determine the mechanism of the reaction between the nonheme complex Fe(tris(2-pyridylmethyl)amine) ([Fe(TPA)(CHCN)]) and peracetic acid (AcOOH) in CHCN, working at room temperature. A multivariate analysis is applied to the time-resolved coupled energy-dispersive X-ray absorption spectroscopy (EDXAS) reaction data, from which a set of spectral and concentration profiles for the reaction key species is derived. These "pure" extracted EDXAS spectra are then quantitatively characterized by full multiple scattering (MS) calculations. As a result, structural information for the elusive reaction intermediates [Fe(TPA)(κ-OOAc)] and [Fe(TPA)(O)(X)] is obtained, and it is suggested that X = AcO in opposition to X = CHCN. The employed strategy is promising both for the spectroscopic characterization of reaction intermediates that are labile or silent to the conventional spectroscopic techniques, as well as for the mechanistic understanding of complex redox reactions involving organic substrates.

摘要

在这项工作中,我们提出了一种方法,可以直接确定非血红素配合物 Fe(三(2-吡啶甲基)胺)([Fe(TPA)(CHCN)])与过氧乙酸(AcOOH)在 CHCN 中反应的机理,在室温下进行。多元分析应用于时间分辨的能量色散 X 射线吸收光谱(EDXAS)反应数据,从中得出反应关键物种的一组光谱和浓度分布。然后,通过全多次散射(MS)计算对这些“纯”提取的 EDXAS 光谱进行定量表征。结果表明,获得了难以捉摸的反应中间体[Fe(TPA)(κ-OOAc)]和[Fe(TPA)(O)(X)]的结构信息,并且建议 X = AcO 而不是 X = CHCN。所采用的策略不仅有望对传统光谱技术不稳定或无声的反应中间体进行光谱表征,而且有望对涉及有机底物的复杂氧化还原反应的机理理解。

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