Through rational chemical design, and thanks to the hybrid nature of metal-organic frameworks (MOFs), it is possible to prepare molecule-based 2D magnetic materials stable at ambient conditions. Here, we illustrate the versatility of this approach by changing both the metallic nodes and the ligands in a family of layered MOFs that allows the tuning of their magnetic properties. Specifically, the reaction of benzimidazole-type ligands with different metal centers (MII = Fe, Co, Mn, Zn) in a solvent-free synthesis produces a family of crystalline materials, denoted as MUV-1(M), which order antiferromagnetically with critical temperatures that depend on M. Furthermore, the incorporation of additional substituents in the ligand results in a novel system, denoted as MUV-8, formed by covalently bound magnetic double layers interconnected by van der Waals interactions, a topology that is very rare in the field of 2D materials and unprecedented for 2D magnets. These layered materials are robust enough to be mechanically exfoliated down to a few layers with large lateral dimensions. Finally, the robustness and crystallinity of these layered MOFs allow the fabrication of nanomechanical resonators that can be used to detect-through laser interferometry-the magnetic order in thin layers of these 2D molecule-based antiferromagnets.

Separation of propylene/propane is one of the most challenging and energy consuming processes in the chemical industry. Propylene demand is increasing and a 99.5% purity is required for industrial purposes. Adsorption based solutions are the most promising alternatives to improve the economical/energetic efficiency of the process. Zeolitic Imidazolate Frameworks (ZIFs) combine the desired characteristics from both MOFs and zeolites: tunability and flexibility from metal organic frameworks, and exceptional thermal and chemical stability from zeolites. In order to enlighten the role of the cation in the sodalite ZIF-8 framework for propane/propylene separation, dynamic breakthrough measurements have been performed over ZIF-8(Zn), ZIF-67 (i.e. ZIF-8(Co)) and MUV-3 (i.e. ZIF-8(Fe)), all isostructural materials based on the same linker (2-methylimidazole). Cation substitution has a remarkable influence in the framework flexibility, and, consequently, in SOD-ZIF selectivity for light hydrocarbons. The differences between the crystallographic pore sizes of the material and the molecular dimensions of propane and propylene are so small, that the slightest change in the framework causes notable advantages/disadvantages in the final application. While cobalt is known to promote a more rigid framework resulting in an adsorption selectivity towards propane, iron presents the inverse effect yielding selectivity to propylene. Zinc has an intermediate effect. A threshold pressure in the isotherm is observed for propylene uptake by ZIF-67 at 273 and 298 K, and only at the lower temperature for ZIF-8. Inlet mixture composition does not highly influence the adsorptive selectivity, although it clearly affects the pure hydrocarbon recovery. Over ZIF-67 breakthrough experiments at 298 K yield a temporary pure propylene flow representing 10–15% of the amount fed. ZIF-67 is a promising candidate for propylene/propane adsorptive separation.