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Harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their NMR detectability
The signal amplification by reversible exchange (SABRE) approach has been used to hyperpolarise the substrates indazole and imidazole in the presence of the co‐ligand acetonitrile through the action of the precataysts [IrCl(COD)(IMes)] and [IrCl(COD)(SIMes)]. (2)H‐labelled forms of these catalysts w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599957/ https://www.ncbi.nlm.nih.gov/pubmed/28497481 http://dx.doi.org/10.1002/mrc.4607 |
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author | Fekete, Marianna Rayner, Peter J. Green, Gary G. R. Duckett, Simon B. |
author_facet | Fekete, Marianna Rayner, Peter J. Green, Gary G. R. Duckett, Simon B. |
author_sort | Fekete, Marianna |
collection | PubMed |
description | The signal amplification by reversible exchange (SABRE) approach has been used to hyperpolarise the substrates indazole and imidazole in the presence of the co‐ligand acetonitrile through the action of the precataysts [IrCl(COD)(IMes)] and [IrCl(COD)(SIMes)]. (2)H‐labelled forms of these catalysts were also examined. Our comparison of the two precatalysts [IrCl(COD)(IMes)] and [IrCl(COD)(SIMes)], coupled with (2)H labelling of the N‐heterocyclic carbene and associated relaxation and polarisation field variation studies, demonstrates the critical and collective role these parameters play in controlling the efficiency of signal amplification by reversible exchange. Ultimately, with imidazole, a 700‐fold(1)H signal gain per proton is produced at 400 MHz, whilst for indazole, a 90‐fold increase per proton is achieved. The co‐ligand acetonitrile proved to optimally exhibit a 190‐fold signal gain per proton in these measurements, with the associated studies revealing the importance the substrate plays in controlling this value. Copyright © 2017 The Authors. Magnetic Resonance in Chemistry published by John Wiley & Sons Ltd. |
format | Online Article Text |
id | pubmed-5599957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55999572017-10-02 Harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their NMR detectability Fekete, Marianna Rayner, Peter J. Green, Gary G. R. Duckett, Simon B. Magn Reson Chem Research Articles The signal amplification by reversible exchange (SABRE) approach has been used to hyperpolarise the substrates indazole and imidazole in the presence of the co‐ligand acetonitrile through the action of the precataysts [IrCl(COD)(IMes)] and [IrCl(COD)(SIMes)]. (2)H‐labelled forms of these catalysts were also examined. Our comparison of the two precatalysts [IrCl(COD)(IMes)] and [IrCl(COD)(SIMes)], coupled with (2)H labelling of the N‐heterocyclic carbene and associated relaxation and polarisation field variation studies, demonstrates the critical and collective role these parameters play in controlling the efficiency of signal amplification by reversible exchange. Ultimately, with imidazole, a 700‐fold(1)H signal gain per proton is produced at 400 MHz, whilst for indazole, a 90‐fold increase per proton is achieved. The co‐ligand acetonitrile proved to optimally exhibit a 190‐fold signal gain per proton in these measurements, with the associated studies revealing the importance the substrate plays in controlling this value. Copyright © 2017 The Authors. Magnetic Resonance in Chemistry published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2017-06-20 2017-10 /pmc/articles/PMC5599957/ /pubmed/28497481 http://dx.doi.org/10.1002/mrc.4607 Text en Copyright © 2017 The Authors. Magnetic Resonance in Chemistry published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Fekete, Marianna Rayner, Peter J. Green, Gary G. R. Duckett, Simon B. Harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their NMR detectability |
title | Harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their NMR detectability |
title_full | Harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their NMR detectability |
title_fullStr | Harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their NMR detectability |
title_full_unstemmed | Harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their NMR detectability |
title_short | Harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their NMR detectability |
title_sort | harnessing polarisation transfer to indazole and imidazole through signal amplification by reversible exchange to improve their nmr detectability |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599957/ https://www.ncbi.nlm.nih.gov/pubmed/28497481 http://dx.doi.org/10.1002/mrc.4607 |
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