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231224s2011 xx |||||o 00| ||eng c |
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|a 10.1021/la200316b
|2 doi
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|a pubmed24n0691.xml
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|a DE-627
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|e rakwb
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|a eng
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|a Schwarze, Michael
|e verfasserin
|4 aut
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|a Quasi-homogeneous hydrogenation with platinum and palladium nanoparticles stabilized by dendritic core-multishell architectures
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|c 2011
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 30.08.2011
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|a Date Revised 10.05.2011
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a Platinum and palladium nanoparticles, supported and stabilized by polymeric core-shell architectures, proved to be active catalysts for hydrogenation reactions. Here, two different reactions were used as probes to investigate the influence of the polymeric support: the hydrogenation of α-methyl styrene (AMS) to cumene and the partial hydrogenation of 1,5-cyclooctadiene (COD). We found that the stability of the nanoparticles and the rate of reaction are higher in the presence of a hydrophobic octadecyl shell within a three-shell polymer system. The kinetic study of AMS hydrogenation showed much higher activities for palladium nanoparticles than for platinum nanoparticles, and the obtained results (e.g., 35 kJ/mol for the activation energy) are of the same order of magnitude as reported earlier for palladium supported on alumina. A methanol/n-heptane biphasic mixture was tested for catalyst recycling and allowed for highly efficient catalyst separation with very low metal leaching
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|a Journal Article
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|a Keilitz, Juliane
|e verfasserin
|4 aut
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|a Nowag, Sabrina
|e verfasserin
|4 aut
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|a Parapat, Riny Y
|e verfasserin
|4 aut
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|a Haag, Rainer
|e verfasserin
|4 aut
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|a Schomäcker, Reinhard
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 27(2011), 10 vom: 17. Mai, Seite 6511-8
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|x 1520-5827
|7 nnns
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|g volume:27
|g year:2011
|g number:10
|g day:17
|g month:05
|g pages:6511-8
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|u http://dx.doi.org/10.1021/la200316b
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