MIL-101 promotes the efficient aerobic oxidative desulfurization of dibenzothiophenes

被引:142
作者
Gomez-Paricio, Adrian [1 ]
Santiago-Portillo, Andrea [1 ]
Navalon, Sergio [1 ]
Concepcion, Patricia [2 ]
Alvaro, Mercedes [1 ]
Garcia, Hermenegildo [2 ,3 ]
机构
[1] Univ Politecn Valencia, Dept Quim, C Camino Vera S-N, E-46022 Valencia, Spain
[2] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, Av Naranjos S-N, E-46022 Valencia, Spain
[3] King Abdulaziz Univ, Ctr Excellence Adv Mat Res, Jeddah 21413, Saudi Arabia
关键词
METAL-ORGANIC FRAMEWORK; COORDINATIVELY UNSATURATED SITES; H BOND ACTIVATION; HETEROGENEOUS CATALYST; SELECTIVE OXIDATION; ADSORPTION; NANOPARTICLES; HYDROCARBONS; ALKENES; OXYGEN;
D O I
10.1039/c5gc00862j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:508 / 515
页数:8
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