2009
DOI: 10.1016/j.molcata.2009.02.039
|View full text |Cite
|
Sign up to set email alerts
|

Palladium-loaded oxidized diamond catalysis for the selective oxidation of alcohols

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

2
10
0

Year Published

2011
2011
2017
2017

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 24 publications
(12 citation statements)
references
References 41 publications
2
10
0
Order By: Relevance
“…However, the cinnamaldehyde product is unstable with respect to decarbonylation (to styrene) and hydrogenation (to 3-phenylpropionaldehyde), leaving only 22 % of reactively formed cinnamaldehyde intact. [3][4][5][6][7][8][9][10][11][12][13][14][15] phenylpropionaldehyde intermediate is itself extremely unstable with respect to subsequent oxidation to the corresponding 3-phenylpropanoic acid. Interestingly, reactively-formed cinnamaldehyde does not undergo over-oxidation to cinnamic acid under our conditions, presumably because surface hydrogen 20 co-liberated during its formation from cinnamyl alcohol promotes competing hydrogenolysis/hydrogenation pathways.…”
Section: Cinnamyl Alcohol Selective Oxidationmentioning
confidence: 99%
See 1 more Smart Citation
“…However, the cinnamaldehyde product is unstable with respect to decarbonylation (to styrene) and hydrogenation (to 3-phenylpropionaldehyde), leaving only 22 % of reactively formed cinnamaldehyde intact. [3][4][5][6][7][8][9][10][11][12][13][14][15] phenylpropionaldehyde intermediate is itself extremely unstable with respect to subsequent oxidation to the corresponding 3-phenylpropanoic acid. Interestingly, reactively-formed cinnamaldehyde does not undergo over-oxidation to cinnamic acid under our conditions, presumably because surface hydrogen 20 co-liberated during its formation from cinnamyl alcohol promotes competing hydrogenolysis/hydrogenation pathways.…”
Section: Cinnamyl Alcohol Selective Oxidationmentioning
confidence: 99%
“…[7][8][9] Palladium has been extensively studied for the selective oxidation of allylic alcohols, 4,[10][11][12] wherein sophisticated in-situ/operando spectroscopic and kinetic measurements have identified surface PdO as the active site responsible for crotyl and cinnamyl alcohol. 13 22 is also effective towards allylic alcohol selox.…”
Section: Introductionmentioning
confidence: 99%
“…The XPS spectrum of the Pd 3d core level in Figure d exhibits two pronounced bands at binding energies ( BE s) of 335.7 and 340.9 eV, which are attributed to Pd 0 3d 5/2 and 3d 3/2 photoelectrons, respectively. The presence of two weak satellite peaks at BE = 337.6 and 342.8 eV, ascribed to 3d 3/2 and 3d 5/2 of PdO, suggests a weak and partial oxidation of the Pd NPs, as is often observed for Pd‐based nanocomposites . The Pd 0 /Pd II molar ratio is calculated to be ca.…”
Section: Resultsmentioning
confidence: 77%
“…291 The O-Dia supported catalyst exhibited a high catalytic activity among the support materials of Pd-loaded catalysts in the oxidation of benzyl alcohol at 358 K, showing TOFs of 850 h −1 . The addition of a small amount of CeO 2 to O-Dia supports further improved catalytic activity in the oxidation of 1-phenylethanol with molecular oxygen.…”
Section: Alcohol Oxidation Reactionsmentioning
confidence: 97%