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By functionalization of the achiral carboxylate-based pyridine-N ligand 2,2'-bipyridine-3,3'-dicarboxylate (H 2 bpda) with N-oxide groups, the axially chiral ligand 2,2'-bipyridine-3,3'-dicarboxylate 1,1'-dioxide (H 2 bpdado) has been obtained. On the basis of H 2 bpdado and auxiliary N-donor ligands, two isostructural 3D dynamic porous Cu(II) metal-organic frameworks (MOFs), {[Cu 0.5 (bpdado) 0.5 (L) 0.5 ]·3H 2 O} n (L = 1,2-bis(4-pyridyl)ethane (bpa), trans-1,2-bis(4-pyridyl)ethene (bpe) for 1 and 2, respectively), have been synthesized, which contain N-oxide "open donor sites" (ODSs) and carboxyl sites on the pore surfaces. The modification of pyridine-N into the N-oxide group not only transforms the nonporous structure into a porous framework but also endows the N-oxide group with unique charge-separated plus electron-rich character, which may provide an enhanced affinity toward CO 2 molecules. Interestingly, both 1 and 2 present reversible structural transformation upon dehydration and rehydration. The adsorption properties of 1 and 2 have been investigated by N 2 , H 2 , CH 4 , and CO 2 gases, and they reveal evident adsorption for CO 2 and CH 4 . Both MOFs have high CO 2 uptake, CO 2 sorption affinity, and sorption selectivities of CO 2 over CH 4 and N 2 . Remarkably, 1' and 2' exhibit intriguingly comparable temperature-dependent CO 2 sorption behaviors that can probably be attributed to the difference in bpa and bpe. First, at 195 K, 1' and 2' exhibit stepwise adsorption and hysteretic desorption behavior for CO 2 , but in the second step, the isotherms of 2' display a starting pressure greater than that of 1'. Then, at 298 K, their CO 2 isotherms all show nonclassical type I adsorption, while peculiarly, at 273 K, the CO 2 isotherm of 1' still exhibits uncommon stepwise adsorption but that of 2' does not. Thus, these temperature-dependent CO 2 sorption behaviors indicate that there exist different threshold temperatures and pressures of channel expansion for 1' and 2'.