Centre de RMN à Très Hauts Champs, Université de Lyon (CNRS/ENS Lyon/UCBL), 69100 Villeurbanne, France.
Department of Chemistry and Applied Biosciences, Eidgenössische Technische Hochschule Zürich, CH-8093 Zürich, Switzerland.
J Phys Chem B. 2021 Dec 9;125(48):13329-13338. doi: 10.1021/acs.jpcb.1c07307. Epub 2021 Nov 24.
Pairing the spectral resolution provided by high magnetic fields at ambient temperature with the enhanced sensitivity offered by dynamic nuclear polarization (DNP) is a major goal of modern solid-state NMR spectroscopy, which will allow one to unlock ever-challenging applications. This study demonstrates that, by combining HyTEK2, a hybrid BDPA-nitroxide biradical polarizing agent, with -terphenyl (OTP), a rigid DNP matrix, enhancement factors as high as 65 can be obtained at 230 K, 40 kHz magic angle spinning (MAS), and 18.8 T. The temperature dependence of the DNP enhancement and its behavior around the glass transition temperature () of the matrix is investigated by variable-temperature EPR measurements of the electron relaxation properties and numerical simulations. A correlation is suggested between the decrease in enhancement at the passage of the and the concomitant drop of both transverse electron relaxation times in the biradical.
将环境温度下高磁场提供的光谱分辨率与动态核极化 (DNP) 提供的增强灵敏度相结合,是现代固态 NMR 光谱学的主要目标,这将允许人们解锁更具挑战性的应用。本研究表明,通过将混合 BDPA-氮氧自由基双自由基极化剂 HyTEK2 与刚性 DNP 基质 -三联苯 (OTP) 结合,可以在 230 K、40 kHz 魔角旋转 (MAS) 和 18.8 T 下获得高达 65 的增强因子。通过电子弛豫性质的变温 EPR 测量和数值模拟研究了 DNP 增强的温度依赖性及其在基质玻璃化转变温度 (Tg) 周围的行为。在通过玻璃化转变温度 (Tg) 时,增强的降低与双自由基中横向电子弛豫时间的同时下降之间存在相关性。