Abstract
The peroxometalate-based polymer immobilized ionic liquid phase catalyst [PO4{WO(O-2)(2)}(4)]@PIILP has been prepared by anion exchange of ring opening metathesis-derived pyrrolidinium-decorated norbornene/ cyclooctene copolymer and shown to be a remarkably efficient system for the selective oxidation of sulfides under mild conditions. A cartridge packed with a mixture of [PO4{WO(O-2)(2)}(4)]@PIILP and silica operated as a segmented or continuous flow process and gave good conversions and high selectivity for either sulfoxide (92% in methanol at 96% conversion for a residence time of 4 min) or sulfone (96% in acetonitrile at 96% conversion for a residence time of 15 min). The immobilized catalyst remained active for 8 h under continuous flow operation with a stable activity/selectivity profile that allowed 6.5 g of reactant to be processed (TON = 46 428) while a single catalyst cartridge could be used for the consecutive oxidation of multiple substrates giving activity-selectivity profiles that matched those obtained with fresh catalyst.
Original language | English |
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Pages (from-to) | 1559-1571 |
Number of pages | 13 |
Journal | Green Chemistry |
Volume | 17 |
Issue number | 3 |
DOIs | |
Publication status | Published - Mar 2015 |
Keywords
- LAYERED DOUBLE HYDROXIDES
- MILD OXIDATION
- ROOM-TEMPERATURE
- DEEP DESULFURIZATION
- SULFUR HETEROCYCLES
- SULFOXIDES
- H2O2
- SULFONES
- FUELS
- VANADIUM