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Spin Order Transfer from a Parahydrogen Molecule to the Counterion in the Iridium Complex under the SABRE Conditions. / Garaeva, V. V.; Spiridonov, K. A.; Nikovskii, I. A. и др.

в: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, Том 48, № 9, 09.2022, стр. 572-578.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Garaeva, VV, Spiridonov, KA, Nikovskii, IA, Peregudov, AS, Kiryutin, AS, Yurkovskaya, AV, Polezhaev, AA & Novikov, VV 2022, 'Spin Order Transfer from a Parahydrogen Molecule to the Counterion in the Iridium Complex under the SABRE Conditions', Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, Том. 48, № 9, стр. 572-578. https://doi.org/10.1134/S1070328422080036

APA

Garaeva, V. V., Spiridonov, K. A., Nikovskii, I. A., Peregudov, A. S., Kiryutin, A. S., Yurkovskaya, A. V., Polezhaev, A. A., & Novikov, V. V. (2022). Spin Order Transfer from a Parahydrogen Molecule to the Counterion in the Iridium Complex under the SABRE Conditions. Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 48(9), 572-578. https://doi.org/10.1134/S1070328422080036

Vancouver

Garaeva VV, Spiridonov KA, Nikovskii IA, Peregudov AS, Kiryutin AS, Yurkovskaya AV и др. Spin Order Transfer from a Parahydrogen Molecule to the Counterion in the Iridium Complex under the SABRE Conditions. Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2022 сент.;48(9):572-578. doi: 10.1134/S1070328422080036

Author

Garaeva, V. V. ; Spiridonov, K. A. ; Nikovskii, I. A. и др. / Spin Order Transfer from a Parahydrogen Molecule to the Counterion in the Iridium Complex under the SABRE Conditions. в: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2022 ; Том 48, № 9. стр. 572-578.

BibTeX

@article{7052372bf63247279a9a298a9b44dc1e,
title = "Spin Order Transfer from a Parahydrogen Molecule to the Counterion in the Iridium Complex under the SABRE Conditions",
abstract = "A possibility of generating spin polarization of 19F nuclei in the counterions that form no covalent bond with the metal center is shown for the first time for new iridium complexes synthesized by reversible binding with the substrate (pyridine) and parahydrogen. This makes it possible to observe the integral polarization of 19F nuclei in weakly coordinated tetrafluoroborate and hexafluorophosphate anions. The optimum parameters of the magnetic field strength for the maximum amplification of the 19F signal in two fluorine-containing anions are determined from the dependences of the signal intensity in the NMR spectra on the magnetic field strength for two synthesized iridium complexes.",
keywords = "carbene ligands, hyperpolarization, iridium complexes, NMR spectroscopy, parahydrogen, parahydrogen-induced nuclear hyperpolarization, signal amplification",
author = "Garaeva, {V. V.} and Spiridonov, {K. A.} and Nikovskii, {I. A.} and Peregudov, {A. S.} and Kiryutin, {A. S.} and Yurkovskaya, {A. V.} and Polezhaev, {A. A.} and Novikov, {V. V.}",
note = "Funding Information: This work was supported by the Russian Science Foundation (interdisciplinary projects nos. 20-63-47107 and 20-62-47038). Funding Information: Elemental analysis of the synthesized compounds was supported by the Ministry of Science and Higher Education of the Russian Federation using the equipment of the Center of Molecular Structure Investigation at the Nesmeyanov Institute of Organoelement Compounds (Russian Academy of Sciences). Publisher Copyright: {\textcopyright} 2022, Pleiades Publishing, Ltd.",
year = "2022",
month = sep,
doi = "10.1134/S1070328422080036",
language = "English",
volume = "48",
pages = "572--578",
journal = "Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya",
issn = "1070-3284",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "9",

}

RIS

TY - JOUR

T1 - Spin Order Transfer from a Parahydrogen Molecule to the Counterion in the Iridium Complex under the SABRE Conditions

AU - Garaeva, V. V.

AU - Spiridonov, K. A.

AU - Nikovskii, I. A.

AU - Peregudov, A. S.

AU - Kiryutin, A. S.

AU - Yurkovskaya, A. V.

AU - Polezhaev, A. A.

AU - Novikov, V. V.

N1 - Funding Information: This work was supported by the Russian Science Foundation (interdisciplinary projects nos. 20-63-47107 and 20-62-47038). Funding Information: Elemental analysis of the synthesized compounds was supported by the Ministry of Science and Higher Education of the Russian Federation using the equipment of the Center of Molecular Structure Investigation at the Nesmeyanov Institute of Organoelement Compounds (Russian Academy of Sciences). Publisher Copyright: © 2022, Pleiades Publishing, Ltd.

PY - 2022/9

Y1 - 2022/9

N2 - A possibility of generating spin polarization of 19F nuclei in the counterions that form no covalent bond with the metal center is shown for the first time for new iridium complexes synthesized by reversible binding with the substrate (pyridine) and parahydrogen. This makes it possible to observe the integral polarization of 19F nuclei in weakly coordinated tetrafluoroborate and hexafluorophosphate anions. The optimum parameters of the magnetic field strength for the maximum amplification of the 19F signal in two fluorine-containing anions are determined from the dependences of the signal intensity in the NMR spectra on the magnetic field strength for two synthesized iridium complexes.

AB - A possibility of generating spin polarization of 19F nuclei in the counterions that form no covalent bond with the metal center is shown for the first time for new iridium complexes synthesized by reversible binding with the substrate (pyridine) and parahydrogen. This makes it possible to observe the integral polarization of 19F nuclei in weakly coordinated tetrafluoroborate and hexafluorophosphate anions. The optimum parameters of the magnetic field strength for the maximum amplification of the 19F signal in two fluorine-containing anions are determined from the dependences of the signal intensity in the NMR spectra on the magnetic field strength for two synthesized iridium complexes.

KW - carbene ligands

KW - hyperpolarization

KW - iridium complexes

KW - NMR spectroscopy

KW - parahydrogen

KW - parahydrogen-induced nuclear hyperpolarization

KW - signal amplification

UR - http://www.scopus.com/inward/record.url?scp=85139553946&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/88aaab82-e3b8-3d5f-b009-20d9c31c76f6/

U2 - 10.1134/S1070328422080036

DO - 10.1134/S1070328422080036

M3 - Article

AN - SCOPUS:85139553946

VL - 48

SP - 572

EP - 578

JO - Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya

JF - Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya

SN - 1070-3284

IS - 9

ER -

ID: 38157886