Stoichiometry, temperature, solvent, metal-directed syntheses of metal-organic frameworks based on flexible V-shaped methylenebis(3,5-dimethylpyrazole) and various aromatic dicarboxylate acids

Seven new metal-organic frameworks (MOFs), namely, {[Cd-2(NDC) 2(H2MDP)](H2O)} (1), [Cd(NDC)(H2MDP)] (2), {[ Cd2(NDC)(HNDC) 2(H2MDP) 2](H2O)(0.5)} (3), [ Cd(NH2-BDC)(H2MDP) 2] (4), [ Cd(NH2-BDC)(H2MDP) 2] (5), [ Cd(H2MDP)(Br-BDC) 0.5(Br-HBDC)] (6), {[Co(H2MDP)(Br-BDC)](H2O) 0.5} (7) (H 2 MDP =methylenebis(3,5dimethylpyrazole), H2NDC = 1,4-naphthalenedicarboxylic acid, NH2-H2BDC = 2-amino-1,4-benzenedicarboxylic acid, Br-H2BDC = 2,5-dibromo-1,4-benzenedicarboxylic acid) have been controllably synthesized with H2MDP and different aromatic dicarboxylic acids by tuning metal-to-ligand molar ratios, temperature, solvents and metal ions. Compound 1 is a 3D 2-fold interpenetrated pcu framework of 412 ? 63 topology constructed from paddle-wheel SBUs and trans-conformation H2MDP pillars, while compound 2 exhibits a 3D 3-fold interpenetrated diamondoid framework formed by single metal nodes via linear NDC2- and trans-conformation H2MDP ligands. Interestingly, compound 3 contains two different types of binuclear subunits formed by a pair of Cd(II) ions with partly deprotonated HNDC- ligands, and these subunits are further linked by completely deprotonated NDC2- and cis-conformation H2MDP ligands to form a 2D (4,4) network. Compounds 4 and 5 are solvent-induced structural isomers based on 2D (4,4) layers, and therefore have different solvent-accessible voids. Compounds 6 and 7, synthesized with different metal salts under similar solvothermal conditions, are characteristic of a 3D hydrogen-bonded supramolecular network, and a 3D 3-fold interpenetrated diamondoid network with equal number of left-and righthanded helical {Cd(H2MDP)}(n) chains further bridged together by linear Br-BDC2- ligands, respectively. In addition, the luminescent properties of solids 1-6 have been investigated at room temperature.