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TinyPols:一类为在18.8和21.1特斯拉下进行动态核极化增强核磁共振光谱量身定制的水溶性双氮氧自由基。

TinyPols: a family of water-soluble binitroxides tailored for dynamic nuclear polarization enhanced NMR spectroscopy at 18.8 and 21.1 T.

作者信息

Lund Alicia, Casano Gilles, Menzildjian Georges, Kaushik Monu, Stevanato Gabriele, Yulikov Maxim, Jabbour Ribal, Wisser Dorothea, Renom-Carrasco Marc, Thieuleux Chloé, Bernada Florian, Karoui Hakim, Siri Didier, Rosay Melanie, Sergeyev Ivan V, Gajan David, Lelli Moreno, Emsley Lyndon, Ouari Olivier, Lesage Anne

机构信息

Centre de RMN à; Très Hauts Champs, Université; de Lyon (CNRS/ENS Lyon/UCB Lyon 1) 69100 Villeurbanne France

Aix Marseille Univ, CNRS, ICR Marseille France

出版信息

Chem Sci. 2020 Feb 5;11(10):2810-2818. doi: 10.1039/c9sc05384k.

DOI:10.1039/c9sc05384k
PMID:34084341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8157490/
Abstract

Dynamic Nuclear Polarization (DNP) has recently emerged as a key method to increase the sensitivity of solid-state NMR spectroscopy under Magic Angle Spinning (MAS). While efficient binitroxide polarizing agents such as AMUPol have been developed for MAS DNP NMR at magnetic fields up to 9.4 T, their performance drops rapidly at higher fields due to the unfavorable field dependence of the cross-effect (CE) mechanism and AMUPol-like radicals were so far disregarded in the context of the development of polarizing agents for very high-field DNP. Here, we introduce a new family of water-soluble binitroxides, dubbed TinyPols, which have a three-bond non-conjugated flexible amine linker allowing sizable couplings between the two unpaired electrons. We show that this adjustment of the linker is crucial and leads to unexpectedly high DNP enhancement factors at 18.8 T and 21.1 T: an improvement of about a factor 2 compared to AMUPol is reported for spinning frequencies ranging from 5 to 40 kHz, with of up to 90 at 18.8 T and 38 at 21.1 T for the best radical in this series, which are the highest MAS DNP enhancements measured so far in aqueous solutions at these magnetic fields. This work not only breathes a new momentum into the design of binitroxides tailored towards high magnetic fields, but also is expected to push the application frontiers of high-resolution DNP MAS NMR, as demonstrated here on a hybrid mesostructured silica material.

摘要

动态核极化(DNP)最近已成为一种在魔角旋转(MAS)下提高固态核磁共振波谱灵敏度的关键方法。虽然已经开发出了高效的双氮氧极化剂,如AMUPol,用于在高达9.4 T的磁场下进行MAS DNP NMR,但由于交叉效应(CE)机制对磁场的不利依赖性,它们在更高磁场下的性能会迅速下降,并且在超高场DNP极化剂的开发背景下,类似AMUPol的自由基至今未被考虑。在此,我们引入了一个新的水溶性双氮氧家族,称为TinyPols,它具有一个三键非共轭柔性胺连接基,使得两个未成对电子之间能够实现可观的耦合。我们表明,连接基的这种调整至关重要,并在18.8 T和21.1 T时导致了出乎意料的高DNP增强因子:对于5至40 kHz的旋转频率,与AMUPol相比提高了约2倍,该系列中最佳自由基在18.8 T时高达90,在21.1 T时高达38,这是迄今为止在这些磁场下的水溶液中测得的最高MAS DNP增强。这项工作不仅为针对高磁场量身定制的双氮氧设计注入了新的活力,而且有望推动高分辨率DNP MAS NMR的应用前沿,如此处对混合介孔结构二氧化硅材料所展示的那样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/c9b11f92c9df/c9sc05384k-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/89ceee942aed/c9sc05384k-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/62079c2fb5b0/c9sc05384k-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/25ea034dd868/c9sc05384k-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/f761ff529ba5/c9sc05384k-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/304a16d8d374/c9sc05384k-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/c9b11f92c9df/c9sc05384k-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/89ceee942aed/c9sc05384k-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/62079c2fb5b0/c9sc05384k-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/25ea034dd868/c9sc05384k-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/f761ff529ba5/c9sc05384k-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/304a16d8d374/c9sc05384k-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/8157490/c9b11f92c9df/c9sc05384k-f6.jpg

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