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Using 2 H labelling to improve the NMR detectability of pyridine and its derivatives by SABRE.
Norcott, Philip; Burns, Michael J; Rayner, Peter J; Mewis, Ryan E; Duckett, Simon B.
Affiliation
  • Norcott P; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Burns MJ; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Rayner PJ; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Mewis RE; Department of Chemistry, University of York, York, YO10 5DD, UK.
  • Duckett SB; Division of Chemistry and Environmental Science, Manchester Metropolitan University, Manchester, Greater Manchester, UK.
Magn Reson Chem ; 56(7): 663-671, 2018 07.
Article in En | MEDLINE | ID: mdl-29274294
ABSTRACT
By introducing a range of 2 H labels into pyridine and the para-substituted agents, methyl isonicotinate and isonicotinamide, we significantly improve their NMR detectability in conjunction with the signal amplification by reversible exchange process. We describe how the rates of T1 relaxation for the remaining 1 H nuclei are increased and show how this leads to a concomitant increase in the level of 1 H and 13 C hyperpolarization that can ultimately be detected.
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