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Tytuł pozycji:

Correlated Dynamics in Ionic Liquids by Means of NMR Relaxometry: Butyltriethylammonium bis(Trifluoromethanesulfonyl)imide as an Example

Tytuł :
Correlated Dynamics in Ionic Liquids by Means of NMR Relaxometry: Butyltriethylammonium bis(Trifluoromethanesulfonyl)imide as an Example
Autorzy :
Roksana Markiewicz
Sylwia Lotarska
Stefan Jurga
Elzbieta Masiewicz
Danuta Kruk
Pokaż więcej
Temat :
Relaxometry
Magnetic Resonance Spectroscopy
Materials science
Hydrocarbons, Fluorinated
QH301-705.5
Diffusion
Thermodynamics
Imides
Article
Catalysis
Ion
ionic liquids
Inorganic Chemistry
chemistry.chemical_compound
relaxation
Biology (General)
Physical and Theoretical Chemistry
Imide
QD1-999
Molecular Biology
Spectroscopy
Rotational correlation time
diffusion
Organic Chemistry
Relaxation (NMR)
dynamics
General Medicine
Atmospheric temperature range
Computer Science Applications
Chemistry
nuclear magnetic resonance
chemistry
Ionic liquid
Źródło :
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 9117, p 9117 (2021)
Volume 22
Issue 17
Opis pliku :
application/pdf
Język :
English
ISSN :
1422-0067
DOI :
10.3390/ijms22179117
Dostęp URL :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38c1c59a131a55b87243ba09ed8af05d
Prawa :
OPEN
Numer akcesji :
edsair.doi.dedup.....38c1c59a131a55b87243ba09ed8af05d
1H and 19F spin-lattice relaxation experiments have been performed for butyltriethylammonium bis(trifluoromethanesulfonyl)imide in the temperature range from 258 to 298 K and the frequency range from 10 kHz to 10 MHz. The results have thoroughly been analysed in terms of a relaxation model taking into account relaxation pathways associated with 1H–1H, 19F–19F and 1H–19F dipole–dipole interactions, rendering relative translational diffusion coefficients for the pairs of ions: cation–cation, anion–anion and cation–anion, as well as the rotational correlation time of the cation. The relevance of the 1H–19F relaxation contribution to the 1H and 19F relaxation has been demonstrated. A comparison of the diffusion coefficients has revealed correlation effects in the relative cation–anion translational movement. It has also turned out that the translational movement of the anions is faster than of cations, especially at high temperatures. Moreover, the relative cation–cation diffusion coefficients have been compared with self-diffusion coefficients obtained by means of NMR (Nuclear Magnetic Resonance) gradient diffusometry. The comparison indicates correlation effects in the relative cation–cation translational dynamics—the effects become more pronounced with decreasing temperature.

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