未成对电子
旋转
超精细结构
电子顺磁共振
分子内力
自旋极化
核磁共振波谱
自旋扩散
核磁共振
电子核双共振
脉冲电子顺磁共振
极化(电化学)
光谱学
超极化(物理学)
化学
电子
密度泛函理论
核过剩效应
自旋回波
原子物理学
物理
扩散
计算化学
凝聚态物理
物理化学
磁共振成像
核物理学
医学
立体化学
热力学
量子力学
放射科
作者
Zhenfeng Pang,Kirill Sheberstov,Bogdan A. Rodin,J. B. Lumsden,Utsab Banerjee,Daniel Abergel,Frédéric Mentink‐Vigier,Geoffrey Bodenhausen,Kong Ooi Tan
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-12-11
卷期号:10 (50)
标识
DOI:10.1126/sciadv.adr7160
摘要
Dynamic nuclear polarization (DNP) enhances nuclear magnetic resonance (NMR) sensitivity by transferring polarization from unpaired electrons to nuclei, but nearby nuclear spins are difficult to detect or “hidden” due to strong electron-nuclear couplings that hypershift their NMR resonances. Here, we detect these hypershifted spins in a frozen glycerol-water mixture doped with TEMPOL at ~1.4 K using spin diffusion enhanced saturation transfer (SPIDEST), which indirectly reveals their spectrum. Additionally, we directly observe 1 H NMR lines spanning 10 MHz. The spectrum is confirmed by simulations and density functional theory (DFT) calculations, which verify that the signals originate from intramolecular protons on TEMPOL. Using two-dimensional NMR, we demonstrate polarization transfer from hypershifted to bulk nuclei across a spin diffusion barrier. This methodology provides new insights into the structures of radicals and could aid in designing more efficient DNP polarizing agents. It also complements information on hyperfine interaction accessible by electron paramagnetic resonance (EPR).
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