Pillared-Layer Microporous Metal--Organic Frameworks Constructed by Robust Hydrogen Bonds. Synthesis, Characterization, and Magnetic and Adsorption Properties of 2,2′-Biimidazole and Carboxylate Complexes.

Two new isostructural complexes [M(H2biim)3][M(btc)(Hbiim)]•2H2O (M = Co, (1); M = Ni, (2)) (btc = 1,3,5-benzenetricarboxylate; H2biim = 2,2′-biimidazole) have been synthesized and characterized by single-crystal X-ray diffraction. They present a unique structure consisting of two distinct units: the monomeric cations [M(H2biim)3]2+ and the two-dimensional (2D) anionic polymer [M(Hbiim)(btc)]2-. In the anionic moiety, the Hbiim monoanion is simultaneously coordinated to one metal atom in a bidentate mode and further to another metal atom in a monodentate mode. The imidazolate groups bridge the two adjacent metal ions into a helical chain which is further arranged in left- and right-handed manners. These chains are bridged by btc ligands into a 2D brick wall structure. The most interesting aspect is that the [M(H2biim)3]2+ cations act as pillars and link the anionic layers via robust heteromeric hydrogen-bonded synthons R²2(9) and R¹2(7) formed by the uncoordinated oxygen atoms of carboxylate groups and the H2biim ligands, resulting in a microporous metal-organic framework with one-dimensional (1D) channels (ca. 11.85 Å ⊗ 11.85 Å for 1 and 11.43 Å ⊗ 11.43 Å for 2). Magnetic properties of these two complexes have also been studied in the temperature range of 2–300 K, and their magnetic susceptibilities obey the Curie-Weiss law in the temperature range of 20–300 K (for 1) and 2–300 K (for 2), respectively, showing anti-ferromagnetic coupling through imidazolate bridging. Taking into consideration the Heisenberg infinite chain model as well as the possibility of chain-to-chain and chain-to-cation interactions, the anti-ferromagnetic exchange of 2 is analyzed via a correction for the molecular field, giving the values of gcat = 2.296, gNi = 2.564, J = -13.30 cm-1, and zJ′ = -0.017 cm-1. The microporous frameworks are stable at ca. 350 °C. They do not collapse after removal of the guest water molecules in the channels, and they adsorb methanol molecules selectively. [ABSTRACT FROM AUTHOR]