Nanotubular Metal−Organic Frameworks with High Porosity Based on T-Shaped Pyridyl Dicarboxylate Ligands

Abstract

Two nanotubular metal-organic frameworks (MOFs), {Cu(L1)·2H(2)O·1.5DMF}(∞) (1) and {Cu(2)(L2)(2)(H(2)O)(2)·7H(2)O·3DMF}(∞) (2), with novel topologies have been constructed based on Cu(2+), 5-(pyridin-4-yl)isophthalic acid (L1) and 5-(pyridin-3-yl)isophthalic acid (L2), respectively. Two MOFs were characterized by IR spectroscopy, thermogravimetry, single-crystal, and powder X-ray diffraction methods. Network analysis reveals a two-nodal (3,6)-connected (4·6(2))(2)(4(2)·6(10)·8(3)) net and a three-nodal (3,4)-connected (4·8(2))(4)(4(2)·8(2)·10(2))(2)(8(4)·12(2)) net. Interpenetration is inherently prevented by both of the topologies of the frameworks. The porosity of MOF 1 was confirmed by N(2) and CO(2) gas adsorption investigations. MOF 1 exhibits remarkable hydrogen sorption hysteresis at low pressure and a H(2) uptake capacity of 1.05 wt% at 77 K and 1 atm.