Walaszek, B. ; Xu, Y. P. ; Adamczyk, A. ; Breitzke, H. ; Pelzer, K. ; Limbach, H. H. ; Huang, J. L. ; Li, H. X. ; Buntkowsky, G. (2009)
H-2-solid-state-NMR study of hydrogen adsorbed on catalytically active ruthenium coated mesoporous silica materials.
In: Solid State Nuclear Magnetic Resonance, 35 (3)
Artikel, Bibliographie
Kurzbeschreibung (Abstract)
H-2 solid-state NMR measurements were performed on three samples of ruthenium nanoparticles synthesized inside two different kinds of mesoporous silica, namely SBA-3 silica materials and SBA-15 functionalized with -COOH groups and loaded with deuterium gas. The line-shape analyses of the spectra reveal the different deuteron species. In all samples a strong -OD signal is found, which shows the catalytic activity of the metal, which activates the D-D bond and deuterates the -SiOH groups through the gas phase, corroborating their usability as catalysts for hydrogenation reactions. At room temperature the mobility of the -Si-OD groups depends on the sample preparation. In addition to the -Si-OD deuterons, the presence of different types of deuterons bound to the metal is revealed. The singly coordinated -Ru-D species exhibit several different quadrupolar couplings, which indicate the presence of several non-equivalent binding sites with differing binding strength. In addition to the dissociated hydrogen species there is also a dihydrogen species -Ru-D-2, which is attributed to defect sites on the surface. It exhibits a fast rotational dynamics at all temperatures. Finally there are also indications of three-fold coordinated surface deuterons and octahedrally coordinated deuterons inside the metal. (c) 2009 Elsevier Inc. All rights reserved.
Typ des Eintrags: | Artikel |
---|---|
Erschienen: | 2009 |
Autor(en): | Walaszek, B. ; Xu, Y. P. ; Adamczyk, A. ; Breitzke, H. ; Pelzer, K. ; Limbach, H. H. ; Huang, J. L. ; Li, H. X. ; Buntkowsky, G. |
Art des Eintrags: | Bibliographie |
Titel: | H-2-solid-state-NMR study of hydrogen adsorbed on catalytically active ruthenium coated mesoporous silica materials |
Sprache: | Englisch |
Publikationsjahr: | 2009 |
Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Solid State Nuclear Magnetic Resonance |
Jahrgang/Volume einer Zeitschrift: | 35 |
(Heft-)Nummer: | 3 |
URL / URN: | http://apps.webofknowledge.com/full_record.do?product=WOS&se... |
Kurzbeschreibung (Abstract): | H-2 solid-state NMR measurements were performed on three samples of ruthenium nanoparticles synthesized inside two different kinds of mesoporous silica, namely SBA-3 silica materials and SBA-15 functionalized with -COOH groups and loaded with deuterium gas. The line-shape analyses of the spectra reveal the different deuteron species. In all samples a strong -OD signal is found, which shows the catalytic activity of the metal, which activates the D-D bond and deuterates the -SiOH groups through the gas phase, corroborating their usability as catalysts for hydrogenation reactions. At room temperature the mobility of the -Si-OD groups depends on the sample preparation. In addition to the -Si-OD deuterons, the presence of different types of deuterons bound to the metal is revealed. The singly coordinated -Ru-D species exhibit several different quadrupolar couplings, which indicate the presence of several non-equivalent binding sites with differing binding strength. In addition to the dissociated hydrogen species there is also a dihydrogen species -Ru-D-2, which is attributed to defect sites on the surface. It exhibits a fast rotational dynamics at all temperatures. Finally there are also indications of three-fold coordinated surface deuterons and octahedrally coordinated deuterons inside the metal. (c) 2009 Elsevier Inc. All rights reserved. |
Freie Schlagworte: | silica ruthenium immobilized catalysts deuteron nmr solid-state nmr transition-metal dihydrides selective hydrogenation catalysts complexes surface sba-15 oxidation nanoparticles dynamics |
Zusätzliche Informationen: | Sp. Iss. SI 445OE Times Cited:11 Cited References Count:65 |
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 07:42 |
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