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9.4特斯拉下卤素键介导的碳奥弗豪泽动态核极化

Halogen-Bond-Mediated C Overhauser Dynamic Nuclear Polarization at 9.4 T.

作者信息

Yang Luming, Orlando Tomas, Bennati Marina

机构信息

Research Group ESR Spectroscopy, Max Planck Institute for Multidisciplinary Sciences, Am Fassberg 11, 37077 Göttingen, Germany.

Institute of Physical Chemistry, Department of Chemistry, Georg-August-University, Tammanstr. 6, 37077 Göttingen, Germany.

出版信息

J Phys Chem Lett. 2025 May 8;16(18):4505-4514. doi: 10.1021/acs.jpclett.5c00798. Epub 2025 Apr 28.

Abstract

Overhauser dynamic nuclear polarization (OE-DNP) is capable of enhancing solution C NMR signals of analytes by 1-2 orders of magnitude through spin polarization transfer from paramagnetic polarizing agents, usually nitroxide radicals, at magnetic fields relevant for high-resolution NMR spectroscopy (≳9 T). While some halogen atoms have been revealed to mediate OE-DNP on adjacent C, methods of promoting OE-DNP through halogen bond (XB) design were not well-understood. Here we investigate OE-DNP of selected halogenated compounds by tuning their XB strengths to the nitroxide radicals through molecular design. Up to 10-fold boosts in OE-DNP enhancements were achieved by increasing the analyte XB donor strength in selected iodinated and brominated derivatives. Furthermore, we observed strong correlation between OE-DNP performance and XB properties for compounds sharing similar XB binding sites. Our results suggest new possibilities for designing hyperpolarized probes and labels for biosensors and the study of biomolecular processes.

摘要

奥弗豪泽动态核极化(OE-DNP)能够通过顺磁极化剂(通常是氮氧自由基)在与高分辨率核磁共振光谱相关的磁场(≳9 T)下的自旋极化转移,将分析物的溶液¹³C核磁共振信号增强1 - 2个数量级。虽然已经发现一些卤素原子可介导相邻¹³C上的OE-DNP,但通过卤键(XB)设计促进OE-DNP的方法尚未得到充分理解。在此,我们通过分子设计调整选定卤代化合物与氮氧自由基之间的XB强度,研究其OE-DNP。通过增加选定碘化和溴化衍生物中分析物的XB供体强度,OE-DNP增强倍数提高了10倍。此外,我们观察到对于具有相似XB结合位点的化合物,OE-DNP性能与XB性质之间存在强相关性。我们的结果为设计用于生物传感器的超极化探针和标记以及生物分子过程的研究提供了新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9272/12067439/4cbe804ede53/jz5c00798_0005.jpg

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