A series of three new isostructural metalorganic frameworks (MOFs) of nickel(II), [{Ni(muco)(bpa)(2H(2)O)}2H(2)O] (1), [{Ni(muco)(bpe)(2H(2)O)}2.5H(2)O] (2), and [{Ni(muco)(azopy)(2H(2)O)}2H(2)O] (3) [where muco = trans,trans-muconate dianion, bpa = 1,2-bis(4-pyridyl)ethane, bpe = 1,2-bis(4-pyridyl)ethylene, and azopy = 4,4'-bis(azobipyridine)], have been synthesized and characterized by single-crystal X-ray diffraction analysis and other physicochemical methods. Compounds 13 exhibit an interesting 3-fold-interpenetrated three-dimensional pillar-layered framework structure constituted of 4-coordinating (4-c) Ni-II nodes with {6(6)}-neb net topology. Remarkably, in spite of 3-fold interpenetration, the structures possess one-dimensional channels with dimensions of similar to 8.05 x 5.25 angstrom(2). Gas (N-2, Ar, H-2, and CO2) adsorption studies of compounds 2 and 3 revealed selective adsorption properties for CO2 over other gases. In all three structures, the 4-c Ni-II node has two coordinated H2O molecules that can be reversibly removed by high-temperature treatment to generate a dehydrated framework composed of highly unsaturated, Lewis acidic Ni-II ions. Further, the activated compounds of 13 act as efficient recyclable catalysts for heterogeneous cycloaddition of CO2 with styrene oxide, resulting in cyclic carbonate with high conversion and selectivity. Interestingly, the cycloaddition reactions of CO2 with bulky epoxides show a decrease in the activity with an increase in the alkyl chain length of the substrate due to confinement of the pore size of the MOF. The high catalytic efficiency and size-dependent selectivity for smaller epoxides show the potential utility of 1 as a promising heterogeneous catalyst for the cycloaddition of CO2. Furthermore, the catalyst can be easily separated and reused for several cycles without significant reduction in the catalytic activity as well as structural rigidity. Compounds 13 represent rare examples of interpenetrated MOFs exhibiting selective storage and conversion of CO2 at mild conditions.