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通过耦合 XAS/UV-Vis 多变量统计分析获得溶液中快速双分子化学反应的直接结构和机制见解。

Direct structural and mechanistic insights into fast bimolecular chemical reactions in solution through a coupled XAS/UV-Vis multivariate statistical analysis.

机构信息

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

出版信息

Dalton Trans. 2021 Jan 7;50(1):131-142. doi: 10.1039/d0dt03083j. Epub 2020 Dec 7.

Abstract

In this work, we obtain detailed mechanistic and structural information on bimolecular chemical reactions occurring in solution on the second to millisecond time scales through the combination of a statistical, multivariate and theoretical analysis of time-resolved coupled X-ray Absorption Spectroscopy (XAS) and UV-Vis data. We apply this innovative method to investigate the sulfoxidation of p-cyanothioanisole and p-methoxythioanisole by the nonheme Fe oxo complex [N4Py·Fe(O)] (N4Py = N,N-bis(2-pyridylmethyl)-N-bis(2-pyridyl)methylamine) in acetonitrile at room temperature. By employing statistical and multivariate techniques we determine the number of key chemical species involved along the reaction paths and derive spectral and concentration profiles for the reaction intermediates. From the quantitative analysis of the XAS spectra we obtain accurate structural information for all reaction intermediates and provide the first structural characterization in solution of complex [N4Py·Fe(OH)]. The employed strategy is promising for the spectroscopic characterization of transient species formed in redox reactions.

摘要

在这项工作中,我们通过对瞬态耦合 X 射线吸收光谱 (XAS) 和紫外-可见数据的时间分辨统计、多变量和理论分析的结合,获得了在溶液中发生的双分子化学反应的详细机制和结构信息,时间范围在第二秒到毫秒之间。我们将这种创新方法应用于室温下在乙腈中通过非血红素 Fe 氧合配合物 [N4Py·Fe(O)](N4Py = N,N-双(2-吡啶基甲基)-N-双(2-吡啶基)甲胺)对对氰基硫代苯甲醚和对甲氧基硫代苯甲醚的氧化脱硫研究。通过统计和多变量技术,我们确定了反应路径中涉及的关键化学物质的数量,并得出了反应中间体的光谱和浓度分布。从 XAS 光谱的定量分析中,我们获得了所有反应中间体的精确结构信息,并首次提供了配合物 [N4Py·Fe(OH)]在溶液中的结构特征。所采用的策略有望用于氧化还原反应中形成的瞬态物种的光谱表征。

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