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首页> 外文期刊>Angewandte Chemie >Slow Molecular Motions in Ionic Liquids Probed by Cross-Relaxation of Nuclear Spins During Overhauser Dynamic Nuclear Polarization
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Slow Molecular Motions in Ionic Liquids Probed by Cross-Relaxation of Nuclear Spins During Overhauser Dynamic Nuclear Polarization

机译:在超负荷动态核极化期间通过核自旋的交叉弛豫探测离子液体中的慢分子运动。

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摘要

Solution-state Overhauser dynamic nuclear polarization (ODNP) at moderate fields, performed by saturating the electron spin resonance (ESR) of a free radical added to the sample of interest, is well known to lead to significant NMR signal enhancements in the steady state, owing to electron-nuclear cross-relaxation. Here it is shown that under conditions which limit radical access to the molecules of interest, the time course of establishment of ODNP can provide a unique window into internuclear cross-relaxation, and reflects relatively slow molecular motions. This behavior, modeled mathematically by a three-spin version of the Solomon equations (one unpaired electron and two nuclear spins), is demonstrated experimentally on the F-19/H-1 system in ionic liquids. Bulky radicals in these viscous environments turn out to be just the right setting to exploit these effects. Compared to standard nuclear Overhauser effect (NOE) work, the present experiment offers significant improvement in dynamic range and sensitivity, retains usable chemical shift information, and reports on molecular motions in the sub-megahertz (MHz) to tens of MHz range-motions which are not accessed at high fields.
机译:众所周知,通过饱和添加到目标样品中的自由基的电子自旋共振(ESR)进行的中等状态下的溶液状态Overhauser动态核极化(ODNP)会导致稳态下NMR信号显着增强,由于电子核交叉松弛。在此表明,在限制自由基接近目标分子的条件下,ODNP建立的时间过程可以为核间交叉松弛提供独特的窗口,并反映相对较慢的分子运动。这种行为是通过Solomon方程的三旋形式(一个不成对电子和两个核自旋)数学建模的,已在离子液体中的F-19 / H-1系统上进行了实验证明。在这些粘性环境中,庞大的自由基被证明是利用这些效应的正确环境。与标准核Overhauser效应(NOE)的工作相比,本实验在动态范围和灵敏度方面有了显着改善,保留了可用的化学位移信息,并报告了亚兆赫兹(MHz)至数十MHz范围运动的分子运动。在高领域不被访问。

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