Weber E M M, Vezin H, Kempf J G, Bodenhausen G, Abergél D, Kurzbach D
Département de Chimie, Ecole Normale Supérieure, PSL Research University, UPMC Univ Paris 06, CNRS, Laboratoire des Biomolécules (LBM), 24 rue Lhomond, 75005 Paris, France.
Phys Chem Chem Phys. 2017 Jun 21;19(24):16087-16094. doi: 10.1039/c7cp03242k.
We report the observation of anisotropic longitudinal electronic relaxation in nitroxide radicals under typical dynamic nuclear polarization conditions. This anisotropy affects the efficiency of dynamic nuclear polarization at cryogenic temperatures of 4 K and high magnetic fields of 6.7 T. Under our experimental conditions, the electron paramagnetic resonance spectrum of nitroxides such as TEMPOL (4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl) is only partly averaged by electronic spectral diffusion, so that the relaxation times T(ω) vary across the spectrum. We demonstrate how the anisotropy of T(ω) can be taken into account in simple DNP models.
我们报告了在典型的动态核极化条件下对氮氧化物中各向异性纵向电子弛豫的观察结果。这种各向异性在4 K的低温和6.7 T的高磁场下会影响动态核极化的效率。在我们的实验条件下,诸如TEMPOL(4-羟基-2,2,6,6-四甲基哌啶-1-氧基)等氮氧化物的电子顺磁共振谱仅通过电子光谱扩散得到部分平均,因此弛豫时间T(ω)在整个谱上会发生变化。我们展示了如何在简单的动态核极化模型中考虑T(ω)的各向异性。