Three microporous metal–organic frameworks assembled from dodecanuclear {Ni II6Ln III6} subunits: synthesis, structure, gas adsorption and magnetism

Abstract

Three isostructural heterometallic metal–organic frameworks (MOFs) {[Ln₂Ni(OAc)₅(HL)(L)]·solvent molecules}_n (H₂L = 2-hydroxyimino-N-[1-(2-pyrazinyl)ethylidene]-propanohydrazone, Ln = Dy for 1, Tb for 2 and Gd for 3) were solvothermally synthesized by varying rare-earth metal ions with different electron configurations. Their crystal structures, gas adsorption and magnetic behaviors were fully investigated. The three isomorphous MOFs exhibit three-dimensional microporous frameworks with two different orientated dodecane metallic {Ni^IILn^III(HL)}₆ metallomacrocycles alternately connected by {Ln^III(L)} connectors, in which an empty one-dimensional channel decorated by the basic hydrazone interior is generated. Due to their Ln^III-independent microporous nature, the activated sample of 1 as a representative example has a significant CO₂ uptake up to 42.2 cm³ g⁻¹ and an unusually high CO₂/N₂ and CO₂/CH₄ adsorption selectivity of up to 98.8 and 16.8 at 298 K and 100 kPa. Magnetically, apparent antiferromagnetic interactions for both 1 and 2 as well as ferromagnetic coupling for 3 are respectively observed at low temperature resulting from the competition of magnetic anisotropy and intermetallic ferromagnetic superexchange. Additionally, 1 with highly anisotropic Dy^III spin shows slow magnetization relaxation under zero dc field, whereas 3 possessing isotropic Gd^III ions displays a significant cryogenic magnetocaloric effect with a maximum entropy change of 26.6 J kg⁻¹ K⁻¹ at 3.0 K and 70 kOe. These interesting results can provide valuable information on gas separation-based multifunctional 3d–4f MOF materials.