77Se Hyperpolarization Enabled by Reversible Parahydrogen Exchange and Audio-Frequency Magnetic Fields at 0.1 mT Full article
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The Journal of Physical Chemistry Letters
ISSN: 1948-7185 |
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| Output data | Year: 2025, Volume: 16, Number: 41, Pages: 10621-10626 Pages count : 6 DOI: 10.1021/acs.jpclett.5c02693 | ||||||
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Abstract:
Nuclear spin hyperpolarization boosts NMR sensitivity but typically requires complex infrastructure. Signal Amplification by Reversible Exchange (SABRE), a parahydrogen-based hyperpolarization technique, can be conducted using a remarkably low-cost polarizer (<$100) comprising only magnetic coils and a standard PC sound card, avoiding magnetic shielding. However, under these conditions, SABRE requires direct spin-coupling between parahydrogen and the target nucleus, limiting its application to distant heteronuclear spins such as 77Se in biologically relevant selenium−nitrogen heterocycles (e.g., antioxidant, antiviral, and anticancer agents). Here, we overcome the distance restrictions by developing 15N-mediated polarization transfer driven by oscillating magnetic fields of the audio frequency. As a proof-of-concept, we achieve a 11600-fold enhancement of the 77Se NMR signal (>6% net polarization) at 9.4 T in a shielding-free setup using a selenadiazole derivative. These results suggest that selenadiazole-based compounds are particularly well suited for this strategy and provide a basis for extending it to other selenium-containing molecules.
Cite:
Markelov D.A.
, Kiryutin A.S.
, Borisov A.V.
, Kosenko I.D.
, Godovikov I.A.
, Yurkovskaya A.V.
77Se Hyperpolarization Enabled by Reversible Parahydrogen Exchange and Audio-Frequency Magnetic Fields at 0.1 mT
The Journal of Physical Chemistry Letters. 2025. V.16. N41. P.10621-10626. DOI: 10.1021/acs.jpclett.5c02693 WOS OpenAlex
77Se Hyperpolarization Enabled by Reversible Parahydrogen Exchange and Audio-Frequency Magnetic Fields at 0.1 mT
The Journal of Physical Chemistry Letters. 2025. V.16. N41. P.10621-10626. DOI: 10.1021/acs.jpclett.5c02693 WOS OpenAlex
Dates:
| Submitted: | Aug 29, 2025 |
| Accepted: | Oct 1, 2025 |
| Published online: | Oct 6, 2025 |
| Published print: | Oct 16, 2025 |
Identifiers:
| Web of science: | WOS:001588962500001 |
| OpenAlex: | W4414848049 |
Citing:
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