Wi Sungsool, Giannouli Angeliki, Butbul Korin, Lumata Jenica, Dubroca Thierry, Scott Faith, Dowdell Zachary, Schurko Robert W, Van Tol Hans, Frydman Lucio
National High Magnetic Field Laboratory, Tallahassee, Florida 32304, United States.
Department of Chemical and Biological Physics, Weizmann Institute of Science, 7610001 Rehovot, Israel.
J Phys Chem Lett. 2025 Jun 26;16(25):6627-6636. doi: 10.1021/acs.jpclett.5c01398. Epub 2025 Jun 20.
This study discusses a potential route for enhancing H NMR signals in the liquid phase at high magnetic fields for samples on the 100 μL volume scale using dynamic nuclear polarization (DNP). The approach involves dispersing an inert powder that is both rich in protons and capable of undergoing DNP with good efficiency at noncryogenic temperatures, and letting the solid H polarization thus enhanced pass from the dispersed particles onto the surrounding liquid via spontaneous cross relaxation effects. To this end, BDPA-doped polystyrene (PS) particles in the μm range were suspended in 30 μL of heptane, loaded into 3.2 mm sapphire rotors, and spun at ≈500 Hz for homogeneity purposes in a 14.1 T magnet. Irradiation with ≈13 W at 395 GHz while maintaining temperature in the 185-220 K range thus enhanced the PS proton polarization ≈12-fold within ≈2 s; after ca. 6 s of irradiation, this resulted in ca. 3-fold enhancements of the heptane proton resonances, while preserving their ≤2 Hz line widths. The conditions over which such particle-mediated transfer occurs were explored over a range of sample composition, deuteration and molecular weight; best results were obtained when polarizing a ball-milled powder made of deuterated-PS/PS/BDPA = 86.4/9.6/4.0 suspended on perdeuterated heptane-. While the solution-state enhancements provided by this approach are still relatively modest, its generality could open new avenues in DNP-enhanced H NMR that do not sacrifice on the volumes, on the high-resolution conditions, or on the multiscan averaging that is customary in contemporary applications.
本研究探讨了一种利用动态核极化(DNP)在高磁场下增强液相中100μL体积规模样品的¹H NMR信号的潜在途径。该方法包括分散一种富含质子且能在非低温温度下高效进行DNP的惰性粉末,并通过自发交叉弛豫效应使如此增强的固体¹H极化从分散颗粒传递到周围液体中。为此,将微米级的BDPA掺杂聚苯乙烯(PS)颗粒悬浮在30μL庚烷中,装入3.2mm蓝宝石转子中,并在14.1T磁体中以约500Hz旋转以实现均匀性。在395GHz下用约13W照射,同时将温度保持在185 - 220K范围内,从而在约2s内使PS质子极化增强约12倍;照射约6s后,这导致庚烷质子共振增强约3倍,同时保持其线宽≤2Hz。在一系列样品组成、氘代和分子量范围内探索了这种颗粒介导转移发生的条件;当极化由氘代PS/PS/BDPA = 86.4/9.6/4.0制成并悬浮在全氘代庚烷上的球磨粉末时获得了最佳结果。虽然这种方法提供的溶液态增强仍然相对较小,但其通用性可能会在DNP增强的¹H NMR中开辟新途径,这些途径在体积、高分辨率条件或当代应用中常用的多扫描平均方面不会做出牺牲。