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. 2020 Apr 30;10(29):17026–17036. doi: 10.1039/d0ra02728f

The electrochemical catalytic oxidation of methyl phenyl sulfide and cyclooctene.

Entry Catalyst Oxidation of methyl phenyl sulfide Oxidation of cyclooctene
Conversiona (%) Selectivityb (%) Conversionc (%) Selectivityd (%)
1 No catalyst 0 0 0 0
2 Fe3O4@SiO2 0 0 0 0
3 [MnL(OAc)] 95 100 95 100
4 Fe3O4@SiO2-[MnL(OAc)] 96 100 97 100
a

Reaction conditions: cat. (0.0017 mmol), molar ratio of cat. : imidazole : MePhS : H2O2: is 1 : 100 : 300 : 1500, solvent: EtOH (1 mL), stirred at r.t., potential: 60 V, and time: 90 s.

b

GC yield based on the starting reactant methyl phenyl sulfide. Methyl phenyl sulfoxide is the sole product.

c

Reaction conditions: cat. (0.0017 mmol), molar ratio of cat. : imidazole : cyclooctene : H2O2 is 1 : 100 : 150 : 750, solvent: EtOH (1 mL), stirred at r.t., potential: 60 V, and time: 90 s.

d

GC yield based on the starting reactant cyclooctene. Cyclooctene oxide is the sole product.