Literature DB >> 31168901

Terminal Diazirines Enable Reverse Polarization Transfer from 15 N2 Singlets.

Guannan Zhang1, Johannes F P Colell1, Thomas Glachet2, Jacob R Lindale1, Vincent Reboul2, Thomas Theis3, Warren S Warren1,4.   

Abstract

Diazirine moieties are chemically stable and have been incorporated into biomolecules without impediment of biological activity. The 15 N2 labeled diazirines are appealing motifs for hyperpolarization supporting relaxation protected states with long-lived lifetimes. The (-CH15 N2 ) diazirine groups investigated here are analogues to methyl groups, which provides the opportunity to transfer polarization stored on a relaxation protected (-CH15 N2 ) moiety to 1 H, thus combining the advantages of long lifetimes of 15 N polarization with superior sensitivity of 1 H detection. Despite the proximity of 1 H to 15 N nuclei in the diazirine moiety, 15 N T1 times of up to (4.6±0.4) min and singlet lifetimes Ts of up to (17.5±3.8) min are observed. Furthermore, we found terminal diazirines to support hyperpolarized 1 H2 singlet states in CH2 groups of chiral molecules. The singlet lifetime of 1 H singlets is up to (9.2±1.8) min, thus exceeding 1 H T1 relaxation time (at 8.45 T) by a factor of ≈100.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  NMR spectroscopy; hyperpolarization; imaging agents; polarization transfer; singlet states

Mesh:

Substances:

Year:  2019        PMID: 31168901     DOI: 10.1002/anie.201904026

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  7 in total

1.  Quasi-Resonance Fluorine-19 Signal Amplification by Reversible Exchange.

Authors:  Nuwandi M Ariyasingha; Jacob R Lindale; Shannon L Eriksson; Grayson P Clark; Thomas Theis; Roman V Shchepin; Nikita V Chukanov; Kirill V Kovtunov; Igor V Koptyug; Warren S Warren; Eduard Y Chekmenev
Journal:  J Phys Chem Lett       Date:  2019-07-16       Impact factor: 6.475

2.  Hyperpolarization of common antifungal agents with SABRE.

Authors:  Keilian MacCulloch; Patrick Tomhon; Austin Browning; Evan Akeroyd; Sören Lehmkuhl; Eduard Y Chekmenev; Thomas Theis
Journal:  Magn Reson Chem       Date:  2021-06-20       Impact factor: 2.447

3.  Synthesis and 15 N NMR Signal Amplification by Reversible Exchange of [15 N]Dalfampridine at Microtesla Magnetic Fields.

Authors:  Nikita V Chukanov; Oleg G Salnikov; Ivan A Trofimov; Mohammad S H Kabir; Kirill V Kovtunov; Igor V Koptyug; Eduard Y Chekmenev
Journal:  Chemphyschem       Date:  2021-04-16       Impact factor: 3.102

Review 4.  Synthetic Approaches for 15 N-Labeled Hyperpolarized Heterocyclic Molecular Imaging Agents for 15 N NMR Signal Amplification by Reversible Exchange in Microtesla Magnetic Fields.

Authors:  Nikita V Chukanov; Roman V Shchepin; Sameer M Joshi; Mohammad S H Kabir; Oleg G Salnikov; Alexandra Svyatova; Igor V Koptyug; Juri G Gelovani; Eduard Y Chekmenev
Journal:  Chemistry       Date:  2021-05-21       Impact factor: 5.020

5.  Infinite-order perturbative treatment for quantum evolution with exchange.

Authors:  Jacob R Lindale; Shannon L Eriksson; Christian P N Tanner; Warren S Warren
Journal:  Sci Adv       Date:  2020-08-07       Impact factor: 14.957

6.  Real-Time High-Sensitivity Reaction Monitoring of Important Nitrogen-Cycle Synthons by 15N Hyperpolarized Nuclear Magnetic Resonance.

Authors:  Peter J Rayner; Marianna Fekete; Callum A Gater; Fadi Ahwal; Norman Turner; Aneurin J Kennerley; Simon B Duckett
Journal:  J Am Chem Soc       Date:  2022-05-04       Impact factor: 16.383

Review 7.  Recent Advances in Chemical Biology Using Benzophenones and Diazirines as Radical Precursors.

Authors:  Muhammad Murtaza Hassan; Olasunkanmi O Olaoye
Journal:  Molecules       Date:  2020-05-13       Impact factor: 4.411

  7 in total

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