Insight into the cocatalyst effect of 4A molecular sieve on Sn(II) porphyrin-catalyzed B–V oxidation of cyclohexanone

• Remarkable cocatalytic effect was obtained in the SnTPP-catalyzed B–V oxidation.
• The role of 4A-MS was to activate benzaldehyde and cyclohexanone molecules.
• The cocatalytic mechanism was tested by in situ characterization methods.

The cocatalyst effect of 4A molecular sieve (4A-MS) on the catalytic activity of tin(II) meso-tetraphenylporphyrin (SnTPP) was investigated in the aerobic Baeyer–Villiger oxidation of cyclohexanone in the presence of benzaldehyde as reductant, remarkable enhancement on the yield of ɛ-caprolactone was achieved (from 21% to 83%). The in situ Raman spectroscopy confirmed the interaction between 4A-MS and the carbonyl group of benzaldehyde and cyclohexanone molecules. The major role of 4A-MS was to active cyclohexanone and benzaldehyde molecules by the coordination between the oxygen atom of carbonyl group and the Lewis acid site of 4A-MS. The activated benzaldehyde tended to combine dioxygen easily, which resulted in the accelerated generation rate of peroxybenzoic acid and the high-valent Sn porphyrin (PorSnIVO). Accordingly, the slow generation rate of Criegee adduct intermediate by the reaction between cyclohexanone and high-valent Sn porphyrin was accelerated. A cocatalytic mechanism involving the activated cyclohexanone and benzaldehyde was proposed.

Remarkable enhancement on the yield of ɛ-caprolactone (from 21% to 83%) in the tin(II) meso-tetraphenylporphyrin (SnTPP)-catalyzed Baeyer–Villiger oxidation was obtained with 4A-molecular sieve (4A-MS) as cocatalyst.Figure optionsDownload high-quality image (199 K)Download as PowerPoint slide