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Gas-Phase Hydrogenation with Parahydrogen Over Immobilized Vaska’s Complex Научная публикация

Журнал Zeitschrift fur Physikalische Chemie-International Journal of Research in Physical Chemistry and Chemical Physics
ISSN: 0942-9352 , E-ISSN: 2196-7156
Вых. Данные Год: 2017, Том: 231, Номер: 3, Страницы: 575-592 Страниц : 18 DOI: 10.1515/zpch-2016-0824
Ключевые слова Hydrogenation, immobilized complex, parahydrogen, PHIP
Авторы Skovpin Ivan V. 1,2 , Zhivonitko Vladimir V. 1,2 , Prosvirin Igor P. 2,3 , Khabibulin Dzhalil F. 3 , Koptyug Igor V. 1,2
Организации
1 Laboratory of Magnetic Resonance Microimaging, International Tomography Center SB RAS, 3A Institutskaya St., Novosibirsk 630090, Russia
2 Novosibirsk State University, 2 Pirogova St., Novosibirsk 630090, Russia
3 Boreskov Institute of Catalysis SB RAS, 5 Acad. Lavrentiev Pr. Novosibirsk 630090, Russia

Информация о финансировании (1)

1 Российский научный фонд 14-35-00020

Реферат: Generating parahydrogen-induced polarization (PHIP) of nuclear spins with immobilized transition metal complexes as hydrogenation catalysts allows one to produce pure hyperpolarized substances, which can open new revolutionary perspectives for PHIP applications. A major drawback of immobilized complexes is their low stability under reaction conditions. In the present work we studied an immobilized iridium complex, Ir/SiO2P, synthesized by a covalent anchoring of Vaska’s complex on phospine-modified silica gel. This complex was used to obtain hyperpolarized gasses in the phase hydrogenation of propene, propyne and 1-butyne with parahydrogen in PASADENA and ALTADENA experiments. It was found that, in contrast to other immobilized complexes, Ir/SiO2P is stable under reaction conditions at up to 140°C, and the reduction of iridium does not occur according to XPS analysis. Moreover, the application of Ir/SiO2P catalyst allowed us to generate continuous flow of hyperpolarized propene and 1-butene with (300–500)-fold NMR signal enhancement which is significantly higher than commonly observed for most supported metal catalysts. The shape of polarized propene signals in PASADENA experiment has indicated that parahydrogen addition to propyne occurs non-stereospecifically, i.e. PHIP was observed for all protons of the vinyl fragment of propene. The analysis of the polarized signals has shown that syn pairwise addition dominates, which was confirmed by spectra simulations. It was found that storage of Ir/SiO2P under Ar atmosphere leads to a decrease in PHIP amplitude and an increase in the activity of the catalyst. This observation is discussed in terms of the interaction of Ir/SiO2P with trace amounts of oxygen in Ar, leading to partial oxidation of triphenylphosphine ligand to triphenylphosphine oxide accompanied by the activation of the immobilized complex. It was also found that the interaction of Ir/SiO2P with alkenes likely leads to formation of stable monohydride complexes, decreasing the production of PHIP in hydrogenations. At the same time, stable substrate complexes are likely formed in alkyne hydrogenations, leading to a significant decrease in the monohydride complex formation and to an increased production of PHIP.
Библиографическая ссылка: Skovpin I.V. , Zhivonitko V.V. , Prosvirin I.P. , Khabibulin D.F. , Koptyug I.V.
Gas-Phase Hydrogenation with Parahydrogen Over Immobilized Vaska’s Complex
Zeitschrift fur Physikalische Chemie-International Journal of Research in Physical Chemistry and Chemical Physics. 2017. V.231. N3. P.575-592. DOI: 10.1515/zpch-2016-0824 WOS Scopus РИНЦ CAPlus OpenAlex
Даты:
Поступила в редакцию: 15 июн. 2016 г.
Принята к публикации: 26 авг. 2016 г.
Опубликована online: 24 сент. 2016 г.
Опубликована в печати: 1 мар. 2017 г.
Идентификаторы БД:
Web of science: WOS:000393583200012
Scopus: 2-s2.0-85012283229
РИНЦ: 29483800
Chemical Abstracts: 2017:302702
OpenAlex: W2524423052
Цитирование в БД:
БД Цитирований
Web of science 11
Scopus 12
РИНЦ 13
OpenAlex 15
Альметрики: