质子高频耦合和奥弗豪斯 DNP。

Michael Mardini, Christy George, Ravi Shankar Palani, Xizi Du, Kong Ooi Tan, Ivan Sergeyev, Yangping Liu, Robert G Griffin
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引用次数: 0

摘要

我们制备了质子位于苯基环中-COOH 基团位置的三苯甲基自由基,并研究了它们的 EPR 光谱(显示出较大的超线性耦合)及其动态核极化(DNP)泽曼场剖面。通过评估这些极化剂的高场和奥弗霍瑟效应 DNP,我们深入了解了这些超线性耦合和其他分子特性在这些自由基的 DNP 性能中所起的作用。有趣的是,在我们研究的三种分子中,我们没有观察到 OE DNP。这表明超精细耦合本身不足以支持 OE DNP。在这种情况下,电子自旋密度的 75% 都集中在中心碳原子上,而不是均匀地分布在芳香环上。这与 BDPA 形成鲜明对比,在 BDPA 中,电子自旋分布是分散的。我们的研究结果并不表明这些自由基中的任何一种特别适合高场 DNP。此外,我们还强调,极化剂对其溶剂环境极为敏感,甚至会掩盖自由基的内在磁性。
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Proton hyperfine couplings and Overhauser DNP.

We have prepared trityl radicals with protons at the positions of the -COOH group in the phenyl rings and examined their EPR spectra, which show large - hyperfine couplings, and their dynamic nuclear polarization (DNP) Zeeman field profiles . By assessing these polarizing agents for high-field and Overhauser effect DNP, we gain insight into the roles that these hyperfine couplings and other molecular properties play in the DNP performance of these radicals. Interestingly, we do not observe OE DNP in any of the three molecules we examined. This suggests that hyperfine couplings by themselves are not sufficient to support OE DNP. In this case the electron spin density is ∼75 % localized on the central carbon atom rather than being distributed uniformly over the aromatic rings. This is in contrast to BDPA where the distribution is delocalized. Our findings do not suggest that any of these radicals are particularly well-suited to high-field DNP. Furthermore, we emphasize that polarizing agents can be extremely sensitive to their solvent environment, even obscuring the intrinsic magnetic properties of the radical.

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A Tribute to a Friend, a Mentor, a Spin Master, and a Mensch - Eriks Kupce. Proton hyperfine couplings and Overhauser DNP.
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