1998
DOI: 10.1039/a705175a
|View full text |Cite
|
Sign up to set email alerts
|

EPR characterisation of (CeO2)1-y(La2CuO4)y oxide mixtures and their catalytic activity for NO reduction by CO

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
5
0

Year Published

1998
1998
2016
2016

Publication Types

Select...
4
2

Relationship

0
6

Authors

Journals

citations
Cited by 14 publications
(8 citation statements)
references
References 17 publications
(6 reference statements)
1
5
0
Order By: Relevance
“…However, also with the former sample just one EPR pattern dominated after catalytic use in reaction Eq. (1) (Sample S2U), while no significant change was observed during the catalytic reaction with S4, as already reported in [3]. This suggested that some structural changes occurred with the oxygen-poorer S2 during that reaction.…”
Section: Resultssupporting
confidence: 64%
See 2 more Smart Citations
“…However, also with the former sample just one EPR pattern dominated after catalytic use in reaction Eq. (1) (Sample S2U), while no significant change was observed during the catalytic reaction with S4, as already reported in [3]. This suggested that some structural changes occurred with the oxygen-poorer S2 during that reaction.…”
Section: Resultssupporting
confidence: 64%
“…In fact, a broad and intense low-field EPR line was observed with the former sample, in the spectrum recorded at 135, 293, and 373 K. In these cases, the Lorentzian shape fits better than the Gaussian shape. The other parameters, obtained by spectral simulation, are compared in Table 1 to the ones already reported [3] for S2U.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…[8] These studies implied that the Si dangling bonds can be alternatively viewed as reactive ªfree radicalsº involved in the surface-attachment reactions. On the other hand, organic radical based CÀC bond formation [9] was recently shown to be highly selective in enantioselective synthesis [10] or preparation of controlled macromolecular architectures. [11] Therefore, it is of significant interest to investigate whether this radical-based CÀC formation is feasible on silicon surfaces in association with Si dangling bonds.…”
Section: Methodsmentioning
confidence: 99%
“…[6,7] Recently, we showed that the radical nature of the electrondeficient Si dangling bonds plays an essential role in the [42] cycloaddition of thiophene to the Si(111)-(7 Â 7) surface. On the other hand, organic radical based CÀC bond formation [9] was recently shown to be highly selective in enantioselective synthesis [10] or preparation of controlled macromolecular architectures. On the other hand, organic radical based CÀC bond formation [9] was recently shown to be highly selective in enantioselective synthesis [10] or preparation of controlled macromolecular architectures.…”
Section: Methodsmentioning
confidence: 99%