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The Influence of Deuterium Isotope Effects on Structural Rearrangements, Ensemble Equilibria, and Hydrogen Bonding in Protic Ionic Liquids Научная публикация

Журнал ChemPhysChem
ISSN: 1439-4235 , E-ISSN: 1439-7641
Вых. Данные Год: 2022, Том: 23, Номер: 23, Номер статьи : e202200557, Страниц : 6 DOI: 10.1002/cphc.202200557, 10.1002/cphc.202200828, 10.1002/cphc.202200827
Ключевые слова isotope effects, ionic liquids, hydrogen bonding, solid state NMR spectroscopy, thermodynamics
Авторы Khudozhitkov Alexander E. 1,2 , Stange Peter 3 , Paschek Dietmar 3 , Stepanov Alexander G. 1 , Kolokolov Daniil I. 1,2 , Ludwig Ralf 3,4
Организации
1 Boreskov Institute of Catalysis, Siberian Branch of Russian Academy of Sciences, Prospekt Akademika Lavrentieva 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova Street 2, Novosibirsk 630090, Russia
3 Universität Rostock, Institut für Chemie, Abteilung für Physikalische Chemie, AlbertEinstein-Straße 27, 18059 Rostock, Germany
4 Leibniz-Institut für Katalyse an der Universität Rostock e.V., Albert-Einstein-Str. 29a, 18059 Rostock, Germany

Информация о финансировании (3)

1 Российский научный фонд 21-13-00047
2 German Research Foundation LU 506/15 (401427621)
3 Alexander von Humboldt Foundation

Реферат: We report strong isotope effects for the protic ionic liquid triethylammonium methanesulfonate [TEA][OMs] by means of deuterium solid-state NMR spectroscopy covering broad temperature ranges from 65 K to 313 K. Both isotopically labelled PILs differ in non-deuterated and fully deuterated ethyl groups of the triethyl ammonium cations. The N-D bond of both cations is used as sensitive probe for hydrogen bonding and structural ordering. The 2 H NMR line shape analysis provides the deuteron quadrupole coupling constants and the characteristics of a broad heterogeneous phase with simultaneously present static and mobile states indicating plastic crystal behavior. The temperatures where both states are equally populated differ by about 80 K for the two PILs, showing that deuteration of the ethyl groups in the trialkylammonium cations tremendously shifts the equilibrium towards the static state. In addition, it leads to a significant less cooperative transition, associated with a significantly reduced standard molar transition entropy.
Библиографическая ссылка: Khudozhitkov A.E. , Stange P. , Paschek D. , Stepanov A.G. , Kolokolov D.I. , Ludwig R.
The Influence of Deuterium Isotope Effects on Structural Rearrangements, Ensemble Equilibria, and Hydrogen Bonding in Protic Ionic Liquids
ChemPhysChem. 2022. V.23. N23. e202200557 :1-6. DOI: 10.1002/cphc.202200557, 10.1002/cphc.202200828, 10.1002/cphc.202200827 WOS Scopus РИНЦ РИНЦ РИНЦ CAPlusCAPlus PMID OpenAlex
Даты:
Поступила в редакцию: 28 июл. 2022 г.
Принята к публикации: 8 авг. 2022 г.
Опубликована online: 9 авг. 2022 г.
Опубликована в печати: 5 дек. 2022 г.
Идентификаторы БД:
Web of science: WOS:000849808100001
Scopus: 2-s2.0-85137356034
РИНЦ: 50783470 | 59515893 | 58673988
Chemical Abstracts: 2022:2322774 | 2022:3012097
PMID (PubMed): 35944124
OpenAlex: W4292457893
Цитирование в БД:
БД Цитирований
Scopus 3
Web of science 1
OpenAlex 2
РИНЦ 1
Альметрики: