SABRE-enhanced real-time pure shift NMR spectroscopy

被引:7
作者
Taylor, Daniel A. [1 ]
Natrajan, Louise S. [1 ]
Nilsson, Mathias [1 ]
Adams, Ralph W. [1 ]
机构
[1] Univ Manchester, Dept Chem, Oxford Rd, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会;
关键词
parahydrogen; pure shift NMR; SABRE; POLARIZATION TRANSFER; REVERSIBLE INTERACTIONS; HYPERPOLARIZATION; RESOLUTION; COMPLEXES; ANALYTES;
D O I
10.1002/mrc.5206
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pure shift nuclear magnetic resonance (NMR) methods suppress the effect of homonuclear scalar couplings to produce NMR spectra consisting solely of a single signal for each chemically distinct site. They are increasingly relied upon for analysis of complex molecules and mixtures as they overcome the extensive signal overlap that complicates proton NMR spectra of all but the simplest species. Current broadband pure shift methodologies for 1D proton spectra suffer from reduced sensitivity compared with their conventional counterparts and typically require a large amount of instrument time for low concentration samples. In this study, we demonstrate how the sensitivity limitation may be overcome by transiently increasing the bulk polarization using signal amplification by reversible exchange (SABRE) hyperpolarization. We utilize para-enriched dihydrogen to enhance the pure shift NMR resonances of pyridine by up to a factor of 60 in a single-scan experiment and extend this to propose a method to unambiguously determine mixture components based on the enhancement of their pure shift NMR signals.
引用
收藏
页码:1244 / 1252
页数:9
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