The use of two different classes of covalent organic frameworks (covalent triazine and imine linked frameworks) as supports for molecular Ni²⁺ catalysts is presented. For COFs, a large concentration of N heteroatoms, either in the form of quasi bipyridine or as diiminopyridine moieties, allows for the coordination of NiBr₂ to the scaffold of the porous polymers. When applied as catalysts in the oligomerization of ethylene under mild reaction conditions (15 bar, 50 °C), these new catalysts display an activity comparable to those of their homogeneous counterpart and a fivefold higher selectivity to C₆ ⁺ olefins. Accumulation of long chain hydrocarbons within the porosity of the COFs leads to reversible deactivation. Full activity and selectivity of the best catalysts can be recovered upon washing with dichlorobenzene.

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A Co@N-doped carbon (Co@ NC) hybrid was synthesized by thermal decomposition of the metal–organic framework (MOF) ZIF-67 under N2 atmosphere. These hybrid materials exhibit outstanding catalytic activity and chemoselectivity for the conversion of a wide range of substituted nitroarenes to their corresponding anilines under relatively mild reaction conditions. The high catalytic performance is attributed to the formation of cobalt nanoparticles and to the presence of atomically dispersed Co species in close interaction with nitrogen-doped graphene. Both active species are formed in situ during the pyrolytic transformation of ZIF-67. The catalysts could be reused in consecutive runs, exhibiting a slightly lower activity ascribed to blockage of the active sites by strongly adsorbed reaction species. These results open up a pathway for the design of noble-metal-free solid catalysts for industrial applications.@en

Mixed-matrix membranes (MMMs) comprising Matrimid and a microporous azine-linked covalent organic frameworks (ACOF-1) were prepared and tested in the separation of CO₂ from an equimolar CO₂/CH₄ mixture. The COF-based MMMs show a more than doubling of the CO₂ permeability upon 16 wt % ACOF-1 loading together with a slight increase in selectivity compared to the bare polymer. These results show the potential of COFs in the preparation of MMMs.

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A facile one-step method to shape covalent triazine frameworks (CTFs) for catalytic applications is reported. Phase inversion of the CTF powder by using a polyimide as a binder in a microfluidic device results in the formation of composite spheres with accessible CTF porosity and a high mechanical and thermal stability. The fabricated spheres can be used to host organometallic complexes. The obtained shaped catalysts, Ir@CTF spheres, are active and fully recyclable in the direct hydrogenation of carbon dioxide into formic acid under mild reaction conditions (20 bar and 50–90 °C) and in the dehydrogenation of formic acid.

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