The development of high-efficient catalysts for the oxidation reaction of sulfides received much attention in recent years due to the extensive applications of such reactions from the utility in pharmaceutical chemistry and biology to the detoxification of chemical warfare agents in war. Herein, we report two innovative polyoxometalate-based metal−organic frameworks (POMOFs) {(1-α and 1-β), which were characterized by elemental analysis, UV−vis diffuse reflectance spectroscopy, X-ray single-crystal and powder diffraction, X-ray photoelectron spectroscopy, and Fourier-transform infrared spectroscopy techniques in detail. Single-crystal X-ray diffraction analysis indicates that 1-α and 1-β are polymorphic with the identical compositions and analogical structures. Compounds 1-α and 1-β are both connected by Zn 4 -ε-Keggin polyoxoanions and 4,4′-bipyridine (bpy) ligands to form twofold interpenetrated three-dimensional POMOF structures. 1-β can be seen as a rotational polymorph of 1-α, that is, 1-α takes the b axis as the rotation axis and rotates ∼39°clockwise to obtain 1-β. Both compounds 1-α and 1-β can be used as heterogeneous catalysts to catalyze the selective oxidation of multitudinous sulfides with H 2 O 2 as an oxidant. When the oxidation of methyl phenyl sulfide was used as the template reaction, the yield of methyl phenyl sulfoxide is close to 100% within 30 min by 1-α and 1-β and the oxidant utilization efficiency is more than 93%. Gratifying catalytic effects have also been achieved in the selective oxidation of phenyl and aliphatic sulfide derivatives. Simultaneously, both 1-α and 1-β showed an extraordinary degradation efficiency of 2-chloroethyl ethyl sulfide and have a half lifetime (t 1/2 ) approximately 2.5 or 3 min, respectively, with 100% selectivity toward the nontoxic product 2-chloroethyl ethyl sulfoxide and an abnormally high oxidant utilization efficiency (94.5% for 1-α and 94.3% for 1-β) at room temperature. In addition, after seven cycles and continuous cycle catalytic experiments, their structures remained and catalytic activities did not decrease obviously, revealing their outstanding recyclability and structural stability.