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H-2 and F-19 solid-state NMR studies of the ionic liquid C2PyBTA-d(10) confined in mesoporous silica materials

Waechtler, M. ; Sellin, M. ; Stark, A. ; Akcakayiran, D. ; Findenegg, G. ; Gruenberg, A. ; Breitzke, H. ; Buntkowsky, G. (2010)
H-2 and F-19 solid-state NMR studies of the ionic liquid C2PyBTA-d(10) confined in mesoporous silica materials.
In: Physical Chemistry Chemical Physics, 12 (37)
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

Ionic liquids confined in porous materials are important solvents which allow a simple heterogenization of homogenous liquids. The perdeuterated ionic liquid N-ethylpyridiniumbis(trifluoromethanesulfonyl) amide (C2PyBTA-d(10)) was prepared and its bulk phase behavior was studied by differential scanning calorimetry (DSC) and temperature-resolved H-2 and F-19 solid-state NMR spectroscopy. Its bulk properties were compared to C2PyBTA-d(10) confined in a mesoporous silica support material as model material usable in SILP catalysts. The line shape analysis of the temperature-dependent NMR spectra of the bulk material reveals two phase transitions, one at 287-289 K (solid II/solid I) and one extending over a temperature range of 298-306 K (solid I/liquid). While the first phase transition is caused by the onset of an intramolecular rotation of the ethyl group of the cation, the second is due to the melting of the ionic liquid. In the bulk material, a hysteresis between the transition temperatures in heating and cooling scans occurs. In confinement, the dynamics of the ionic liquid changes considerably: no hysteresis is observed for C2PyBTA-d(10) confined in the mesopores. Instead, only a broad transition from solid II to the liquid state, which spans the temperature range of 215-245 K, is observed. This transition is identified as the result of a broad distribution of molecular environments of the confined ionic liquid, which thus forms an amorphous phase inside the pores. Hence, the behavior of the ionic liquid in confinement is similar to the behavior of non-ionic guest molecules in the mesoporous silica. Finally, it was found that the anion and cation of the ionic liquid exhibit the same dynamic behavior in confinement.

Typ des Eintrags: Artikel
Erschienen: 2010
Autor(en): Waechtler, M. ; Sellin, M. ; Stark, A. ; Akcakayiran, D. ; Findenegg, G. ; Gruenberg, A. ; Breitzke, H. ; Buntkowsky, G.
Art des Eintrags: Bibliographie
Titel: H-2 and F-19 solid-state NMR studies of the ionic liquid C2PyBTA-d(10) confined in mesoporous silica materials
Sprache: Englisch
Publikationsjahr: 2010
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Physical Chemistry Chemical Physics
Jahrgang/Volume einer Zeitschrift: 12
(Heft-)Nummer: 37
URL / URN: http://apps.webofknowledge.com/full_record.do?product=WOS&se...
Kurzbeschreibung (Abstract):

Ionic liquids confined in porous materials are important solvents which allow a simple heterogenization of homogenous liquids. The perdeuterated ionic liquid N-ethylpyridiniumbis(trifluoromethanesulfonyl) amide (C2PyBTA-d(10)) was prepared and its bulk phase behavior was studied by differential scanning calorimetry (DSC) and temperature-resolved H-2 and F-19 solid-state NMR spectroscopy. Its bulk properties were compared to C2PyBTA-d(10) confined in a mesoporous silica support material as model material usable in SILP catalysts. The line shape analysis of the temperature-dependent NMR spectra of the bulk material reveals two phase transitions, one at 287-289 K (solid II/solid I) and one extending over a temperature range of 298-306 K (solid I/liquid). While the first phase transition is caused by the onset of an intramolecular rotation of the ethyl group of the cation, the second is due to the melting of the ionic liquid. In the bulk material, a hysteresis between the transition temperatures in heating and cooling scans occurs. In confinement, the dynamics of the ionic liquid changes considerably: no hysteresis is observed for C2PyBTA-d(10) confined in the mesopores. Instead, only a broad transition from solid II to the liquid state, which spans the temperature range of 215-245 K, is observed. This transition is identified as the result of a broad distribution of molecular environments of the confined ionic liquid, which thus forms an amorphous phase inside the pores. Hence, the behavior of the ionic liquid in confinement is similar to the behavior of non-ionic guest molecules in the mesoporous silica. Finally, it was found that the anion and cation of the ionic liquid exhibit the same dynamic behavior in confinement.

Freie Schlagworte: phase silp catalysis heck reaction molten-salts organic-synthesis guest molecules glass formers n-hexane hydroformylation dynamics benzene
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648XD Times Cited:9 Cited References Count:63

Fachbereich(e)/-gebiet(e): 07 Fachbereich Chemie
07 Fachbereich Chemie > Eduard Zintl-Institut > Fachgebiet Physikalische Chemie
Hinterlegungsdatum: 27 Okt 2014 20:52
Letzte Änderung: 31 Mai 2019 07:27
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