Five new supramolecular metal-organic coordination polymers (MOCPs), {[Ni(bipy) 5) (bipy = 4,4 0 -bipyridyl; 2,6-nds = 2,6-naphthalenedisulphonate) have been synthesized and structurally characterized. Compounds 1 and 5 were synthesized at room temperature in H 2 O/EtOH medium, whereas 2-4 were isolated under hydrothermal conditions. Compounds 1-4 were synthesized maintaining the same stoichiometric ratio of metal and ligand under different reaction temperatures, and the different structures of the compounds indicate that the temperature plays a significant role in the construction of the coordination polymers. Structural characterization reveals that the one-dimensional [M(bipy)(H 2 O) 4 ] 2þ cationic chain is a basic building unit for all of the MOCPs, while 2,6-nds remains as a counteranion. In all cases, 2,6-nds counteranions interact with water and bipy molecules through strong hydrogen-bonding and π-π interactions to afford threedimensional supramolecular structures. Compounds 1-4 have the same building unit with different network superstructures and are related as supramolecular isomers. Supramolecular isomerism in 3 and 4 is very interesting since they have the same molecular formula, {[Ni(bipy)(H 2 O) 4 ](2,6-nds)}, and are polymorphs. Compounds 4 and 5 are isomorphous. The thermogravimetric study suggests that the dehydrated compounds are stable up to 300 °C. Furthermore, sorption studies suggest that dehydrated compounds of 1 and 2 are permanently porous.

1D, 2D, and 3D three metal-organic hybrid frameworks of Mg (II) have been synthesized using 4,5-imidazoledicarboxylic acid (H 3idc) with control of the temperature and stoichiometry in a hydrothermal technique. All of the frameworks show high thermal stability, and frameworks 1D and 3D provide highly hydrophilic pore surfaces, correlated by the selective sorption of water molecules over the organic vapor and other gases like N 2 and CO 2.

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A 2D noninterpenetrated flexible metal-organic porous solid, {[Cu(2)(cis-chdc)(2)(bpee)] x H(2)O}(n) (1) based on a paddle-wheel building unit has been constructed using a mixed-ligand system. Guest-induced irreversible internetwork displacements of the 2D grids result in permanent porosity in the framework, as realized by the selective CO(2) sorption over N(2). The different affinity and selectivity of the solvent molecules was correlated with the internal polarity of the pore surfaces.