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NMR SLIC Sensing of Hydrogenation Reactions Using Parahydrogen in Low Magnetic Fields
[Image: see text] Parahydrogen-induced polarization (PHIP) is an NMR hyperpolarization technique that increases nuclear spin polarization by orders of magnitude, and it is particularly well-suited to study hydrogenation reactions. However, the use of high-field NMR spectroscopy is not always possibl...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5204359/ https://www.ncbi.nlm.nih.gov/pubmed/28066517 http://dx.doi.org/10.1021/acs.jpcc.6b07555 |
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author | Barskiy, Danila A. Salnikov, Oleg G. Shchepin, Roman V. Feldman, Matthew A. Coffey, Aaron M. Kovtunov, Kirill V. Koptyug, Igor V. Chekmenev, Eduard Y. |
author_facet | Barskiy, Danila A. Salnikov, Oleg G. Shchepin, Roman V. Feldman, Matthew A. Coffey, Aaron M. Kovtunov, Kirill V. Koptyug, Igor V. Chekmenev, Eduard Y. |
author_sort | Barskiy, Danila A. |
collection | PubMed |
description | [Image: see text] Parahydrogen-induced polarization (PHIP) is an NMR hyperpolarization technique that increases nuclear spin polarization by orders of magnitude, and it is particularly well-suited to study hydrogenation reactions. However, the use of high-field NMR spectroscopy is not always possible, especially in the context of potential industrial-scale reactor applications. On the other hand, the direct low-field NMR detection of reaction products with enhanced nuclear spin polarization is challenging due to near complete signal cancellation from nascent parahydrogen protons. We show that hydrogenation products prepared by PHIP can be irradiated with weak (on the order of spin–spin couplings of a few hertz) alternating magnetic field (called Spin-Lock Induced Crossing or SLIC) and consequently efficiently detected at low magnetic field (e.g., 0.05 T used here) using examples of several types of organic molecules containing a vinyl moiety. The detected hyperpolarized signals from several reaction products at tens of millimolar concentrations were enhanced by 10000-fold, producing NMR signals an order of magnitude greater than the background signal from protonated solvents. |
format | Online Article Text |
id | pubmed-5204359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-52043592017-10-26 NMR SLIC Sensing of Hydrogenation Reactions Using Parahydrogen in Low Magnetic Fields Barskiy, Danila A. Salnikov, Oleg G. Shchepin, Roman V. Feldman, Matthew A. Coffey, Aaron M. Kovtunov, Kirill V. Koptyug, Igor V. Chekmenev, Eduard Y. J Phys Chem C Nanomater Interfaces [Image: see text] Parahydrogen-induced polarization (PHIP) is an NMR hyperpolarization technique that increases nuclear spin polarization by orders of magnitude, and it is particularly well-suited to study hydrogenation reactions. However, the use of high-field NMR spectroscopy is not always possible, especially in the context of potential industrial-scale reactor applications. On the other hand, the direct low-field NMR detection of reaction products with enhanced nuclear spin polarization is challenging due to near complete signal cancellation from nascent parahydrogen protons. We show that hydrogenation products prepared by PHIP can be irradiated with weak (on the order of spin–spin couplings of a few hertz) alternating magnetic field (called Spin-Lock Induced Crossing or SLIC) and consequently efficiently detected at low magnetic field (e.g., 0.05 T used here) using examples of several types of organic molecules containing a vinyl moiety. The detected hyperpolarized signals from several reaction products at tens of millimolar concentrations were enhanced by 10000-fold, producing NMR signals an order of magnitude greater than the background signal from protonated solvents. American Chemical Society 2016-10-26 2016-12-29 /pmc/articles/PMC5204359/ /pubmed/28066517 http://dx.doi.org/10.1021/acs.jpcc.6b07555 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Barskiy, Danila A. Salnikov, Oleg G. Shchepin, Roman V. Feldman, Matthew A. Coffey, Aaron M. Kovtunov, Kirill V. Koptyug, Igor V. Chekmenev, Eduard Y. NMR SLIC Sensing of Hydrogenation Reactions Using Parahydrogen in Low Magnetic Fields |
title | NMR SLIC Sensing of Hydrogenation Reactions Using
Parahydrogen in Low Magnetic Fields |
title_full | NMR SLIC Sensing of Hydrogenation Reactions Using
Parahydrogen in Low Magnetic Fields |
title_fullStr | NMR SLIC Sensing of Hydrogenation Reactions Using
Parahydrogen in Low Magnetic Fields |
title_full_unstemmed | NMR SLIC Sensing of Hydrogenation Reactions Using
Parahydrogen in Low Magnetic Fields |
title_short | NMR SLIC Sensing of Hydrogenation Reactions Using
Parahydrogen in Low Magnetic Fields |
title_sort | nmr slic sensing of hydrogenation reactions using
parahydrogen in low magnetic fields |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5204359/ https://www.ncbi.nlm.nih.gov/pubmed/28066517 http://dx.doi.org/10.1021/acs.jpcc.6b07555 |
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