The development of polyoxometalates for olefin oxidation is critical to achieving the green chemical process of the C5 fraction further processing. Di-lacunary silicotungstic anions were easily obtained by continuously adjusting the pH instead of the traditional step-by-step method

which exhibited excellent performance in the catalytic oxidation of cyclopentene (CPE) to aldehydes or alcohols. The 93.69% CPE conversion and 97.15% total product selectivity (41.38% for glutaraldehyde (GA) and 55.77% for 1

2-cyclopentanediol (1

2-diol) were achieved by using H

2

O

2

as the oxidant and acetonitrile as the solvent. Through complementary characterization

it was found that the optimized di-lacunary silicotungstic polyoxometalate retained a complete Keggin structure

and exhibited better catalytic activity and stability than the mono-lacunary or saturated silicodecatungstate because it exposed more catalytic active centers. Furthermore

in situ

FT-IR spectra was utilized to monitor the reaction process

revealing the formation of the active species W(O

2

) on the di-lacunary silicotungstic polyoxometalate and the intermediate epoxycyclopentane during the catalytic oxidation of cyclopentene.