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Enhancing (19)F Benchtop NMR Spectroscopy by Combining para-Hydrogen Hyperpolarization and Multiplet Refocusing

[Image: see text] Benchtop NMR spectrometers provide a promising alternative to high-field NMR for applications that are limited by instrument size and/or cost. (19)F benchtop NMR is attractive due to the larger chemical shift range of (19)F relative to (1)H and the lack of background signal in most...

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Detalles Bibliográficos
Autores principales: Silva Terra, Ana I., Rossetto, Matheus, Dickson, Claire L., Peat, George, Uhrín, Dušan, Halse, Meghan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9936801/
https://www.ncbi.nlm.nih.gov/pubmed/36817010
http://dx.doi.org/10.1021/acsmeasuresciau.2c00055
Descripción
Sumario:[Image: see text] Benchtop NMR spectrometers provide a promising alternative to high-field NMR for applications that are limited by instrument size and/or cost. (19)F benchtop NMR is attractive due to the larger chemical shift range of (19)F relative to (1)H and the lack of background signal in most applications. However, practical applications of benchtop (19)F NMR are limited by its low sensitivity due to the relatively weak field strengths of benchtop NMR spectrometers. Here we present a sensitivity-enhancement strategy that combines SABRE (Signal Amplification By Reversible Exchange) hyperpolarization with the multiplet refocusing method SHARPER (Sensitive, Homogeneous, And Resolved PEaks in Real time). When applied to a range of fluoropyridines, SABRE-SHARPER achieves overall signal enhancements of up to 5700-fold through the combined effects of hyperpolarization and line-narrowing. This approach can be generalized to the analysis of mixtures through the use of a selective variant of the SHARPER sequence, selSHARPER. The ability of SABRE-selSHARPER to simultaneously boost sensitivity and discriminate between two components of a mixture is demonstrated, where selectivity is achieved through a combination of selective excitation and the choice of polarization transfer field during the SABRE step.