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通过结合光谱学和多元曲线重建简化中间体搜索:以[Cu(6,6'-二甲基-2,2'-联吡啶)]PF氧化为例。

Easing Intermediates Search by Combining Spectroscopy and Multivariate Curve Reconstruction: [Cu(6,6'-dimethyl-2,2'-bipyridyl)]PF Oxidation as Case Study.

作者信息

Deplano Gabriele, Gerz Isabelle, Demirbas Derya, Centrella Barbara, Bonomo Matteo, DeBeer Serena, Bordiga Silvia, Signorile Matteo, Jannuzzi Sergio A V

机构信息

Department of Chemistry, NIS and INSTM Reference Centre, Università di Torino, Via P. Giuria 7, 10125 and Via G. Quarello 15/A, 10135 Torino, Italy.

Department of Inorganic Spectroscopy, Max Planck Institute for Chemical Energy Conversion, Stiftstraße 34-36, 45470 Mülheim an der Ruhr, Germany.

出版信息

J Phys Chem Lett. 2025 Feb 20;16(7):1652-1659. doi: 10.1021/acs.jpclett.4c03467. Epub 2025 Feb 6.

DOI:10.1021/acs.jpclett.4c03467
PMID:39913620
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11849003/
Abstract

Despite their prevalence in catalysis, complex reaction mixtures are not trivial to investigate and disentangle. Different approaches can be applied to characterize them, even featuring low-dimensionality data sets. The liquid-phase reaction of [Cu(6,6'-dimethyl-2,2'-bipyridyl)]PF () with -butyl hydroperoxide is investigated: two Cu species are found upon oxidation of the pristine complex, characterized by different spectroscopic and kinetics fingerprints. Coupling EPR and UV-vis spectroscopies with chemometric methods (namely, multivariate curve reconstruction, MCR) allowed for easily retrieving pure spectral features and concentration profiles. Spectrokinetic analysis independently showed an optimal agreement with kinetic outcomes from MCR. Finally, hypotheses on the nature of the Cu species are drawn on the basis of EPR fitting and quantum chemistry computations on a series of candidate structures. Beyond the accurate characterization of a model system, this study demonstrates the potential of coupling multivariate statistical techniques, experiments, and computations toward a quantitative understanding of electronic and kinetic information on complex chemical systems.

摘要

尽管复杂反应混合物在催化中普遍存在,但对其进行研究和解析并非易事。可以采用不同的方法对其进行表征,甚至包括低维数据集。本文研究了[Cu(6,6'-二甲基-2,2'-联吡啶)]PF()与叔丁基过氧化氢的液相反应:在原始配合物氧化后发现了两种铜物种,其具有不同的光谱和动力学特征。将电子顺磁共振(EPR)和紫外可见光谱与化学计量学方法(即多元曲线重建,MCR)相结合,能够轻松获取纯光谱特征和浓度分布。光谱动力学分析独立显示与MCR的动力学结果具有最佳一致性。最后,基于对一系列候选结构的EPR拟合和量子化学计算,对铜物种的性质提出了假设。除了对模型系统进行准确表征外,本研究还展示了将多元统计技术、实验和计算相结合,以定量理解复杂化学系统中电子和动力学信息的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/2927efbcddc7/jz4c03467_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/3866f9984d4c/jz4c03467_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/d835a46b01ba/jz4c03467_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/303f8f3bd3ec/jz4c03467_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/2927efbcddc7/jz4c03467_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/3866f9984d4c/jz4c03467_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/d835a46b01ba/jz4c03467_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/303f8f3bd3ec/jz4c03467_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e372/11849003/2927efbcddc7/jz4c03467_0004.jpg

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A Conserved Second Sphere Residue Tunes Copper Site Reactivity in Lytic Polysaccharide Monooxygenases.一种保守的第二配位层残基调节溶菌多糖单加氧酶中的铜活性位点。
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A multi-technique approach to unveil the redox behaviour and potentiality of homoleptic Cu complexes based on substituted bipyridine ligands in oxygenation reactions.
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A Combined Spectroscopic and Computational Study on the Mechanism of Iron-Catalyzed Aminofunctionalization of Olefins Using Hydroxylamine Derived N-O Reagent as the "Amino" Source and "Oxidant".铁催化烯烃的氨官能化反应机理的光谱和计算联合研究:以羟胺衍生的 N-O 试剂作为“氨基”源和“氧化剂”。
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