Metal-organic frameworks based on double-bond-coupled di-isophthalate linkers with high hydrogen and methane uptakes

Solvothermal reactions of Cu(NO3)(2) with azoxybenzene-3,3',5,5'-tetracarboxylic acid (H(4)aobtc) or trans-stilbene-3,3',5,5'-tetracarboxylic acid (H(4)sbtc) give rise to two isostructural microporous metal-organic frameworks, Cu-2(abtc)(H2O)(2)center dot 3DMA (PCN-10, abtc = azobenzene-3,3',5,5'-tetracarboxylate) and Cu-2(sbtc)(H2O)(2)center dot 3DMA (PCN-11, sbtc = trans-stilbeile-3,3',5,5'-tetracarboxylate), respectively. Both PCN-10 and PCN-11 possess significant enduring porosity with Langmuir surface areas of 1779 and 2442 m(2)/g (corresponding to BET Surface areas of 1407 or 1931 m(2)/g, respectively) and contain nanoscopic cages and coordinatively unsaturated metal centers. At 77 K, 760 Torr, the excess gravimetric (volumetric) hydrogen uptake of PCN-10 is 2.34 wt% (18.0 g/L) and that of PCN-11 can reach 2.55 wt% (19.1 g/L). Gas-adsorption studies also suggest that MOFs containing C=C double bonds are more favorable than those with N=N double bond in retaining enduring porosity after thermal activation, although N=N has slightly higher H-2 affinity. The excess gravimetric (volumetric) adsorption at 77 K saturates around 20 atm and reaches values of 4.33% (33.2 g/L) and 5.05% (37.8 g/L) for PCN-10 and PCN-11, respectively. In addition to its appreciable hydrogen uptake, PCN-11 has an excess methane uptake of 17 1 cm 3 (STP)/cm(3) at 298 K and 35 bar, approaching the DOE target of 180 v(STP)/v for methane storage at ambient temperature. Thus, PCN-11 represents one of the few materials that is applicable to both hydrogen and methane storage applications.