Research output: Contribution to journal › Article › peer-review
19F Hyperpolarization of 15N-3-19F-Pyridine via Signal Amplification by Reversible Exchange. / Chukanov, Nikita V.; Salnikov, Oleg G.; Shchepin, Roman V. et al.
In: Journal of Physical Chemistry C, Vol. 122, No. 40, 11.10.2018, p. 23002-23010.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - 19F Hyperpolarization of 15N-3-19F-Pyridine via Signal Amplification by Reversible Exchange
AU - Chukanov, Nikita V.
AU - Salnikov, Oleg G.
AU - Shchepin, Roman V.
AU - Svyatova, Alexandra
AU - Kovtunov, Kirill V.
AU - Koptyug, Igor V.
AU - Chekmenev, Eduard Y.
PY - 2018/10/11
Y1 - 2018/10/11
N2 - We report synthesis of 15N-3-19F-pyridine via Zincke salt formation with overall 35% yield and 84% 15N isotopic purity. Hyperpolarization studies of signal amplification by reversible exchange (SABRE) and SABRE in SHield Enables Alignment Transfer to Heteronuclei (SABRE-SHEATH) were performed to investigate the mechanism of polarization transfer from parahydrogen-derived hydride protons to 19F nucleus in millitesla and microtesla magnetic-field regimes in 15N-3-19F-pyridine and 14N-3-19F-pyridine. We found the mismatch between 15N and 19F magnetic-field hyperpolarization profiles in the microtesla regime indicating that the spontaneous hyperpolarization process likely happens directly from parahydrogen-derived hydride protons to 19F nucleus without spin-relaying via 15N site. In the case of SABRE magnetic-field regime (millitesla magnetic-field range), we found that magnetic-field profiles for 1H and 19F hyperpolarization are very similar and 19F polarization levels are significantly lower than 1H SABRE polarization levels and lower than 19F SABRE-SHEATH (i.e., obtained at microtesla magnetic field) polarization levels. Our findings support the hypothesis that in millitesla magnetic-field regime, the process of 19F nuclei hyperpolarization is relayed via protons of the substrate and therefore is very inefficient. These findings are important in the context of improvement of the hyperpolarization hardware and rational design of the hyperpolarized molecular probes.
AB - We report synthesis of 15N-3-19F-pyridine via Zincke salt formation with overall 35% yield and 84% 15N isotopic purity. Hyperpolarization studies of signal amplification by reversible exchange (SABRE) and SABRE in SHield Enables Alignment Transfer to Heteronuclei (SABRE-SHEATH) were performed to investigate the mechanism of polarization transfer from parahydrogen-derived hydride protons to 19F nucleus in millitesla and microtesla magnetic-field regimes in 15N-3-19F-pyridine and 14N-3-19F-pyridine. We found the mismatch between 15N and 19F magnetic-field hyperpolarization profiles in the microtesla regime indicating that the spontaneous hyperpolarization process likely happens directly from parahydrogen-derived hydride protons to 19F nucleus without spin-relaying via 15N site. In the case of SABRE magnetic-field regime (millitesla magnetic-field range), we found that magnetic-field profiles for 1H and 19F hyperpolarization are very similar and 19F polarization levels are significantly lower than 1H SABRE polarization levels and lower than 19F SABRE-SHEATH (i.e., obtained at microtesla magnetic field) polarization levels. Our findings support the hypothesis that in millitesla magnetic-field regime, the process of 19F nuclei hyperpolarization is relayed via protons of the substrate and therefore is very inefficient. These findings are important in the context of improvement of the hyperpolarization hardware and rational design of the hyperpolarized molecular probes.
KW - PARAHYDROGEN-INDUCED POLARIZATION
KW - MAGNETIC-RESONANCE
KW - N-15 HYPERPOLARIZATION
KW - PARA-HYDROGEN
KW - SABRE
KW - METRONIDAZOLE
KW - PYRIDINE
KW - MRI
KW - SPECTROSCOPY
KW - NICOTINAMIDE
UR - http://www.scopus.com/inward/record.url?scp=85054408878&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.8b06654
DO - 10.1021/acs.jpcc.8b06654
M3 - Article
C2 - 31435456
AN - SCOPUS:85054408878
VL - 122
SP - 23002
EP - 23010
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
SN - 1932-7447
IS - 40
ER -
ID: 17035528