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  4. Tuning the Chemoselectivity of Rh Nanoparticle Catalysts by Site-Selective Poisoning with Phosphine Ligands: The Hydrogenation of Functionalized Aromatic Compounds
 
research article

Tuning the Chemoselectivity of Rh Nanoparticle Catalysts by Site-Selective Poisoning with Phosphine Ligands: The Hydrogenation of Functionalized Aromatic Compounds

Snelders, Dennis J. M.  
•
Yan, Ning  
•
Gan, Weijia  
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2012
Acs Catalysis

The hydrogenation of phenylacetone to cyclohexylacetone, in which the aromatic ring is selectively reduced in preference to the carbonyl group, has been achieved with chemoselectivities exceeding 90%. The catalyst (precatalyst) used to achieve this transformation comprises PVP-stabilized Rh nanoparticles dispersed in water with some phosphine ligand additives. Phosphine ligands with different steric and electronic properties and polarities were investigated for this purpose, and several clear trends were observed, showing the potential of well-defined phosphine ligands as modifiers in nanocatalysis.

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Type
research article
DOI
10.1021/cs200575r
Web of Science ID

WOS:000299967500001

Author(s)
Snelders, Dennis J. M.  
Yan, Ning  
Gan, Weijia  
Laurenczy, Gabor  
Dyson, Paul J.  
Date Issued

2012

Published in
Acs Catalysis
Volume

2

Start page

201

End page

207

Subjects

nanoparticles

•

nanocatalysis

•

hydrogenation

•

selectivity

•

phosphine ligands

•

poisoning

•

Nuclear-Magnetic-Resonance

•

Heterogeneous Catalysis

•

Heteroarylphosphorus Compounds

•

Rhodium Nanoparticles

•

Metal Nanoparticles

•

Arene Hydrogenation

•

Phase

•

Nanoclusters

•

Chemistry

•

Benzene

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCOM  
Available on Infoscience
March 8, 2012
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/78540
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