Department of Electronic Science, Fujian Provincial Key Laboratory of Plasma and Magnetic Resonance,State Key Laboratory for Physical Chemistry of Solid Surfaces, Xiamen University, Xiamen 361005, China.
Molecules. 2020 Jan 22;25(3):473. doi: 10.3390/molecules25030473.
Longitudinal spin-lattice relaxation () and transverse spin-spin relaxation () reveal valuable information for studying molecular dynamics in NMR applications. Accurate relaxation measurements from conventional 1D proton spectra are generally subject to challenges of spectral congestion caused by coupling splittings and spectral line broadenings due to magnetic field inhomogeneity. Here, we present an NMR relaxation method based on real-time pure shift techniques to overcome these two challenges and achieve accurate measurements of and relaxation times from complex samples that contain crowded NMR resonances even under inhomogeneous magnetic fields. Both theoretical analyses and detailed experiments are performed to demonstrate the effectiveness and ability of the proposed method for accurate relaxation measurements on complex samples and its practicability to non-ideal magnetic field conditions.
纵向自旋晶格弛豫(T1)和横向自旋自旋弛豫(T2)在 NMR 应用中为研究分子动力学提供了有价值的信息。从传统的一维质子谱中进行准确的弛豫测量通常受到由于耦合分裂引起的谱线拥挤和由于磁场不均匀引起的谱线展宽的影响。在这里,我们提出了一种基于实时纯位移技术的 NMR 弛豫方法,以克服这两个挑战,并从复杂样品中实现 T1 和 T2 弛豫时间的精确测量,即使在不均匀磁场下,复杂样品中的 NMR 共振也很拥挤。通过理论分析和详细实验,证明了该方法在复杂样品的精确弛豫测量中的有效性和能力,以及在非理想磁场条件下的实用性。