MIL-101 promotes the efficient aerobic oxidative desulfurization of dibenzothiophenes
MIL-101 promotes aerobic oxidation in n -dodecane of dibenzothiophene (DBT) and its methyl-substituted derivatives to their corresponding sulfones with complete selectivity, without observation of the sulfoxide. DBT sulfones can be completely separated from n -dodecane by water extraction. MIL-101(C...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2016-01, Vol.18 (2), p.58-515 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | MIL-101 promotes aerobic oxidation in
n
-dodecane of dibenzothiophene (DBT) and its methyl-substituted derivatives to their corresponding sulfones with complete selectivity, without observation of the sulfoxide. DBT sulfones can be completely separated from
n
-dodecane by water extraction. MIL-101(Cr) without the need of pre-activation was found to be more convenient than the also-active MIL-101(Fe) analog. The reaction exhibits an induction period due to the diffusion inside the pore system of the solvent or oxygen and it is not observed if the MIL-101 sample is first in contact with the solvent at the reaction temperature for a sufficiently long time. MIL-101 is reusable for at least five times without any sign of deactivation according to the time-conversion plots. Evidence by electron paramagnetic resonance spectroscopy detecting the hydroperoxide radical adduct with a spin trapping agent and Raman spectroscopy detection of superoxide supports that the process is an auto-oxidation reaction initiated by MIL-101 following the expected radical chain mechanism inside the MIL-101 cages.
MIL-101(Cr) promotes the oxidative desulfurization of dibenzothiophenes by air. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/c5gc00862j |