Hydrocarbon Oxidation over Fe- and Cr-Containing Metal-Organic Frameworks MIL-100 and MIL-101– A Comparative Study
Full article
| Общее |
Language:
Английский,
Genre:
Full article,
Status:
Published,
Source type:
Original
|
| Conference |
7th World Congress on Oxidation Catalysis
09-12 Jun 2013
,
Saint Louis
|
| Journal |
Catalysis Today
ISSN: 0920-5861
, E-ISSN: 1873-4308
|
| Output data |
Year: 2014,
Volume: 238,
Pages: 54-61
Pages count
: 8
DOI:
10.1016/j.cattod.2014.01.010
|
| Tags |
Alkenes, Anthracene, Heterogeneous catalysis, MIL-100, MIL-101, Selective oxidation |
| Authors |
Kholdeeva Oxana A.
1,2
,
Skobelev Igor Y.
1
,
Ivanchikova Irina D.
1
,
Kovalenko Konstantin A.
2,3
,
Fedin Vladimir P.
2,3
,
Sorokin Alexander B.
4
|
| Affiliations |
| 1 |
Boreskov Institute of Catalysis, Lavrentiev ave. 5, Novosibirsk 630090, Russia
|
| 2 |
Novosibirsk State University, Pirogova st. 2, Novosibirsk 630090, Russia
|
| 3 |
Nikolaev Institute of Inorganic Chemistry, Lavrentiev ave. 3, Novosibirsk 630090, Russia
|
| 4 |
Institut de Recherches sur la Catalyse et l’Environnement de Lyon (IRCELYON), UMR 5256, CNRS-Université Lyon 1, 2, av. A. Einstein, 69626 Villeurbanne Cedex, France
|
|
Funding (3)
|
1
|
Russian Foundation for Basic Research
|
13-03-00413
|
|
2
|
The Ministry of Education and Science of the Russian Federation
|
|
|
3
|
French Embassy in Moscow
|
|
Catalytic properties of Fe- and Cr-based metal-organic frameworks (MOFs) MIL-100 and MIL-101 have been assessed in two liquid-phase reactions: solvent-free allylic oxidation of alkenes (cyclohexene, α- and β-pinenes) with molecular oxygen and oxidation of anthracene (AN) with tert-butyl hydroperoxide (TBHP). In the oxidation of alkenes, the product selectivity strongly depends on the nature of metal (Fe or Cr) but, for the same metal, only slightly differs for the MIL-100 and MIL-101 structures. The Fe-containing MOFs afford the formation of unsaturated alcohols while Cr-based MOFs give mainly unsaturated ketones. Both Cr-MIL-100 and Cr-MIL-101 favor decomposition of cyclohexenyl hydroperoxide to produce 2-cyclohexen-1-one with 67–69% selectivity. Stability toward destruction reduced in the order Cr-MIL-101, Cr-MIL-100 > Fe-MIL-100 > Fe-MIL-101. In the oxidation of anthracene over both Cr-MOFs and Fe-MIL-101, the selectivity toward 9,10-anthraquinone (AQ) attained 100% at 92–100% AN conversion. The turnover frequency (TOF) decreased in the order Cr-MIL-101 > Fe-MIL-101 > Cr-MIL-100 > Fe-MIL-100. Cr-MIL-101 revealed superior catalytic performance in terms of AN conversion, AQ selectivity and TOF. Nearly quantitative yield of AQ was obtained after 1.5 h at 100 °C in chlorobenzene as solvent. No leaching of active metal occurred under optimal reaction conditions and the MOFs could be recycled several times without deterioration of the catalytic properties.