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各向异性核间弛豫效应对超极化靶 NMR 光谱的影响。

Heteronuclear cross-relaxation effects in the NMR spectroscopy of hyperpolarized targets.

机构信息

Chemical Physics Department, Weizmann Institute of Science, Rehovot (Israel), Fax: (+972) 8-934-4903.

出版信息

Chemphyschem. 2014 Feb 24;15(3):436-43. doi: 10.1002/cphc.201300857. Epub 2014 Jan 8.

DOI:10.1002/cphc.201300857
PMID:24403222
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5040509/
Abstract

Dissolution dynamic nuclear polarization (DNP) enables high-sensitivity solution-phase NMR experiments on long-lived nuclear spin species such as (15)N and (13)C. This report explores certain features arising in solution-state (1)H NMR upon polarizing low-γ nuclear species. Following solid-state hyperpolarization of both (13)C and (1)H, solution-phase (1)H NMR experiments on dissolved samples revealed transient effects, whereby peaks arising from protons bonded to the naturally occurring (13)C nuclei appeared larger than the typically dominant (12)C-bonded (1)H resonances. This enhancement of the satellite peaks was examined in detail with respect to a variety of mechanisms that could potentially explain this observation. Both two- and three-spin phenomena active in the solid state could lead to this kind of effect; still, experimental observations revealed that the enhancement originates from (13)C→(1)H polarization-transfer processes active in the liquid state. Kinetic equations based on modified heteronuclear cross-relaxation models were examined, and found to well describe the distinct patterns of growth and decay shown by the (13)C-bound (1)H NMR satellite resonances. The dynamics of these novel cross-relaxation phenomena were determined, and their potential usefulness as tools for investigating hyperpolarized ensembles and for obtaining enhanced-sensitivity (1)H NMR traces was explored.

摘要

溶解态动态核极化(DNP)可实现对(15)N 和(13)C 等长寿命核自旋物种的高灵敏度溶液相 NMR 实验。本报告探讨了在溶液态(1)H NMR 中出现的某些特征,这些特征是通过极化低γ核物种产生的。在对(13)C 和(1)H 进行固态超极化之后,对溶解样品进行的溶液相(1)H NMR 实验揭示了瞬态效应,由此,与天然存在的(13)C 核结合的质子产生的峰比通常占主导地位的(12)C 键合(1)H 共振更大。详细研究了各种可能解释这一观察结果的机制,考察了这些卫星峰的增强情况。在固态中活跃的双自旋和三自旋现象都可能导致这种效应;尽管如此,实验观察表明,增强源自在液态中活跃的(13)C→(1)H 极化转移过程。考察了基于改进的异核交叉弛豫模型的动力学方程,并发现它们很好地描述了(13)C 结合(1)H NMR 卫星共振的生长和衰减的独特模式。确定了这些新的交叉弛豫现象的动力学,并探索了它们作为研究超极化系综和获得增强灵敏度(1)H NMR 谱的工具的潜在用途。