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Magnetic field dependence of the para-ortho conversion rate of molecular hydrogen in SABRE experiments Научная публикация

Журнал Journal of Magnetic Resonance
ISSN: 1090-7807
Вых. Данные Год: 2024, Том: 360, Номер статьи : 107630, Страниц : DOI: 10.1016/j.jmr.2024.107630
Авторы Snadin Alexander V. 1,2 , Chuklina Natalia O. 3 , Kiryutin Alexey S. 3,2 , Lukzen Nikita N. 3,2 , Yurkovskaya Alexandra V. 3
Организации
1 Nesmeyanov Institute of Organoelement Compounds RAS, Moscow 119991, Russia
2 Novosibirsk State University, Novosibirsk 630090, Russia
3 International Tomography Center, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia

Информация о финансировании (1)

1

Реферат: The use of parahydrogen – the isomer of molecular hydrogen with zero nuclear spin – is important for promising and actively developing methods for spin hyperpolarization of nuclei called parahydrogen induced polarization (PHIP). However, the dissolved parahydrogen in PHIP experiments quickly loses its spin order, resulting in the formation of orthohydrogen and reduction of the overall nuclear polarization of the substrate. This process is due to the difference of chemical shifts of hydride protons, as well as spin–spin couplings between nuclei, in the intermediate catalytic complexes, and it has not been rigorously explained so far. We proposed a new experimental technique based on magnetic field cycling for measuring the rate of molecular hydrogen para–ortho conversion in solution and applied it for non-hydrogenative PHIP Signal Amplification By Reversible Exchange (SABRE) experiments. The para–ortho conversion rate was measured over a wide range of magnetic field from 0.5 mT to 9.4 T. It was found that the conversion rate strongly depends on the magnetic field in which the reaction occurs, as well as on the concentrations of reactants. The rate decreases with increasing the concentration of pyridine ligand and increases with increasing the concentration of iridium catalyst. The model, which takes into account the reversible exchange of molecular hydrogen with the catalyst, nuclear spin–spin interaction of hydride protons with nuclei of ligands within catalytic complex and nuclear Zeeman interactions, qualitatively describes the experimental data. Two types of complexes with different spin system symmetry contribute to the molecular hydrogen conversion. In asymmetric complexes possessing hydride protons with different chemical shifts due to the presence of chlorine anion ligand the para–ortho conversion rate increases with magnetic field, while for symmetric complexes this mechanism is not operable. In the magnetic field where level anti-crossing occurs the resonant feature for the rate of para–ortho conversion is found. The results of this work can be utilized for finding the optimal conditions for obtaining the maximum hyperpolarization in the experiments employing parahydrogen.
Библиографическая ссылка: Snadin A.V. , Chuklina N.O. , Kiryutin A.S. , Lukzen N.N. , Yurkovskaya A.V.
Magnetic field dependence of the para-ortho conversion rate of molecular hydrogen in SABRE experiments
Journal of Magnetic Resonance. 2024. V.360. 107630 . DOI: 10.1016/j.jmr.2024.107630 WOS РИНЦ OpenAlex
Даты:
Поступила в редакцию: 12 сент. 2023 г.
Принята к публикации: 29 янв. 2024 г.
Опубликована online: 15 февр. 2024 г.
Опубликована в печати: 1 мар. 2024 г.
Идентификаторы БД:
Web of science: WOS:001188412100001
РИНЦ: 66623748
OpenAlex: W4391870937
Цитирование в БД:
БД Цитирований
Web of science 2
OpenAlex 5
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