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氘代TEKPol双自由基与MAS DNP中的自旋扩散势垒

Deuterated TEKPol Biradicals and the Spin-Diffusion Barrier in MAS DNP.

作者信息

Venkatesh Amrit, Casano Gilles, Rao Yu, De Biasi Federico, Perras Frédéric A, Kubicki Dominik J, Siri Didier, Abel Sébastien, Karoui Hakim, Yulikov Maxim, Ouari Olivier, Emsley Lyndon

机构信息

Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.

Aix Marseille Université, CNRS, Institut de Chimie Radicalaire, UMR 7273, 13013, Marseille, France.

出版信息

Angew Chem Int Ed Engl. 2023 Aug 1;62(31):e202304844. doi: 10.1002/anie.202304844. Epub 2023 Jun 22.

Abstract

The sensitivity of NMR spectroscopy is considerably enhanced by dynamic nuclear polarization (DNP). In DNP polarization is transferred from unpaired electrons of a polarizing agent to nearby proton spins. In solids, this transfer is followed by the transport of hyperpolarization to the bulk via H- H spin diffusion. The efficiency of these steps is critical to obtain high sensitivity gains, but the pathways for polarization transfer in the region near the unpaired electron spins are unclear. Here we report a series of seven deuterated and one fluorinated TEKPol biradicals to probe the effect of deprotonation on MAS DNP at 9.4 T. The experimental results are interpreted with numerical simulations, and our findings support that strong hyperfine couplings to nearby protons determine high transfer rates across the spin diffusion barrier to achieve short build-up times and high enhancements. Specifically, H DNP build-up times increase substantially with TEKPol isotopologues that have fewer hydrogen atoms in the phenyl rings, suggesting that these protons play a crucial role transferring the polarization to the bulk. Based on this new understanding, we have designed a new biradical, NaphPol, which yields significantly increased NMR sensitivity, making it the best performing DNP polarizing agent in organic solvents to date.

摘要

通过动态核极化(DNP),核磁共振光谱的灵敏度得到了显著提高。在DNP过程中,极化从极化剂的未成对电子转移到附近的质子自旋上。在固体中,这种转移之后是通过H-H自旋扩散将超极化传输到主体中。这些步骤的效率对于获得高灵敏度增益至关重要,但未成对电子自旋附近区域的极化转移途径尚不清楚。在此,我们报告了一系列七个氘代和一个氟化的TEKPol双自由基,以探究去质子化对9.4 T下的MAS DNP的影响。实验结果通过数值模拟进行解释,我们的研究结果支持与附近质子的强超精细耦合决定了跨越自旋扩散势垒的高转移速率,从而实现短的极化建立时间和高增强效果。具体而言,随着苯环中氢原子较少的TEKPol同位素异构体,H DNP的极化建立时间大幅增加,这表明这些质子在将极化转移到主体中起着关键作用。基于这一新认识,我们设计了一种新的双自由基NaphPol,它能显著提高核磁共振灵敏度,使其成为迄今为止在有机溶剂中性能最佳的DNP极化剂。

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