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完善图景:通过光化学诱导动态核极化光谱法测定黄素半醌自由基的C超精细偶合常数

Completing the Picture: Determination of C Hyperfine Coupling Constants of Flavin Semiquinone Radicals by Photochemically Induced Dynamic Nuclear Polarization Spectroscopy.

作者信息

Pompe Nils, Illarionov Boris, Fischer Markus, Bacher Adelbert, Weber Stefan

机构信息

Institute of Physical Chemistry, University of Freiburg, 79104 Freiburg im Breisgau, Germany.

Hamburg School of Food Science, University of Hamburg, 20146 Hamburg, Germany.

出版信息

J Phys Chem Lett. 2022 Jun 5:5160-5167. doi: 10.1021/acs.jpclett.2c00919.

Abstract

We investigate the electronic structure of flavin semiquinone radicals in terms of their C hyperfine coupling constants. Photochemically induced dynamic nuclear polarization (photo-CIDNP) spectroscopy was used to study both the neutral and anionic radical species of flavin mononucleotide (FMN) in bulk aqueous solution. Apart from universally C-labeled FMN, partially labeled isotopologues are used to increase sensitivity for nuclei exhibiting very small hyperfine couplings and to cope with spectral overlap. In addition, experimental findings are supported by quantum chemical calculations, and implications for the spin density distribution in free flavin radicals are discussed.

摘要

我们根据黄素半醌自由基的碳超精细偶合常数研究其电子结构。利用光化学诱导动态核极化(光化学诱导动态核极化)光谱研究了黄素单核苷酸(FMN)在本体水溶液中的中性和阴离子自由基物种。除了普遍用碳标记的FMN外,还使用了部分标记的同位素异构体来提高对具有非常小的超精细偶合的原子核的灵敏度,并应对光谱重叠。此外,量子化学计算支持实验结果,并讨论了对游离黄素自由基中自旋密度分布的影响。

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