Simple hybrid silica-imidazolium based ILs as highly active and selective catalysts for the carbonation of epoxides in batch and continuous flow systems under mild reaction conditions.

Ionic liquids (ILs) have been extensively explored in controlling the selectivity and stability of metal nanoparticles and/or classical heterogeneous catalysts for the hydrogenation of aromatics. ILs provide a protective layer to metal surface catalysts and a physical barrier controlling the access of substrates/intermediates/products on the nanoconfined catalysts, acting as an electronic and geometrical modifier of the catalytic active sites. As a result, this allows the stability and electronic/geometrical properties of the catalyst to be modulated. The IL layers also allow nano‐environments to be designed for encapsulation and to change the kinetic/thermodynamic of the process compared to those reactions performed in classical heterogeneous catalysis. We will focus on the physical, geometric and electronic effects imposed by the IL on metal nanoparticles and classical heterogeneous catalysts on activity and selectivity in the hydrogenation of arenes, in particular benzene.

A series of new triazolium-based supported ionic liquids (SILPs), decorated with Cu NPs, were successfully prepared and applied to the N-arylation of aryl halides with anilines.

The systems prepared in situ by addition of the corresponding equivalents of the respective phosphine (mono-, di-and tridentated), called M 2 Cl 2 (COE) 4 /n phosphine (M = Rh, Ir; and COE = cyclooctene), are efficient and regioselective precatalysts for the hydrogenation of quinoline, isoquinoline, 5,6-and 7,8-benzoquinoline and acridine. The Rh systems were more active than the corresponding Ir ones, being the systems with 1,1,1-tris(diphenylphosphinomethyl)ethane (triphos) more active than those with 1,2-bis(diphenylphosphino)ethane (dppe), except for the case of acridine, where the inversed tendencies were observed (Ir > Rh and dppe > triphos). The systems with triphenylphosphine showed the lowest activities.

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