“…11 Factually, the mono-oxo and dioxo structures for molybdenum oxides can be modulated by temperature, gas-phase composition, and loading, 12 and also an appropriate arrangement of the molybdenum species interacting with the silica support significantly increases the epoxidation reactivity of propylene. 13 Based on robust ability of Mo-based catalysts for activation and bond breaking of C−H bond, their catalytic behaviors of the selective oxidation of methanol/DME to formaldehyde, methyl formate (MF), methylal, poly(oxymethylene) dimethyl ethers, 1,2-dimethoxyethane, etc. at low temperatures were evaluated, 2,14−16 and the oxidation of C−H bond in CH 3 O* intermediate was regarded as the rate-determining step.…”