SABRE-enhanced real-time pure shift NMR spectroscopy

Daniel A Taylor, Louise S Natrajan, Mathias Nilsson, Ralph W Adams*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)1244-1252
Number of pages9
JournalMAGNETIC RESONANCE IN CHEMISTRY
Volume59
Issue number12
Early online date25 Aug 2021
DOIs
Publication statusPublished - 14 Nov 2021
Externally publishedYes

Bibliographical note

© 2021 John Wiley & Sons, Ltd.

Keywords

  • Hydrogen
  • Magnetic Resonance Imaging
  • Magnetic Resonance Spectroscopy
  • Protons

Cite this