Stabilization of single metal atoms is a persistent challenge in heterogeneous catalysis. Especially supported late transitions metals are prone to undergo agglomeration to nanoparticles under reducing conditions. In this study, nitrogen‐rich covalent triazine frameworks (CTFs) are used to immobilize iridium complexes. Upon reduction at 400 °C, immobilized Ir(acac)(COD) on CTF does not form nanoparticles but transforms into a highly active Ir single atom catalyst. The resulting catalyst systems outperforms both the immobilized complex and supported nanoparticles in the dehydrogenation of formic acid as probe reaction. This superior performance could be traced back to decisive changes of the coordination geometry positively influencing activity, selectivity and stability. Spectroscopic analysis reveals an increase of electron density on the cationic iridium site by donation from the CTF macroligand after removal of the organic ligand sphere from the Ir(acac)(COD) precursor complex upon reductive treatment. This work demonstrates the ability of nitrogen moieties to stabilize molecular metal species against agglomeration and opens avenues for catalysts design using isolated sites in high‐temperature applications under reducing atmosphere.

Heterogeneous single-site and single-atom catalysts potentially enable combining the high catalytic activity and selectivity of molecular catalysts with the easy continuous operation and recycling of solid catalysts. In recent years, covalent triazine frameworks (CTFs) found increasing attention as support materials for particulate and isolated metal species. Bearing a high fraction of nitrogen sites, they allow coordinating molecular metal species and stabilizing particulate metal species, respectively. Dependent on synthesis method and pretreatment of CTFs, materials resembling well-defined highly crosslinked polymers or materials comparable to structurally ill-defined nitrogen-containing carbons result. Accordingly, CTFs serve as model systems elucidating the interaction of single-site, single-atom and particulate metal species with such supports. Factors influencing the transition between molecular and particulate systems are discussed to allow deriving tailored catalyst systems.

Glycerol can be converted to propylene glycol via metal and base catalyzed hydrogenolysis. The nature of the base has a profound influence on the outcome of the reaction. We have tested a range of alkaline (LiOH, NaOH and CsOH) and alkaline earth (Mg(OH) 2 , Ca(OH) 2 , Sr(OH) 2 and Ba(OH) 2 ) metal hydroxides in combination with Pt/C. The data reveal that alkaline earth metal hydroxides exhibit a much higher activity and improved selectivity. DFT calculations confirm that the coordination of reactive intermediates to divalent cations is responsible for the observed behavior. In the study, the effect of the cation on hydrogenolysis was elucidated for the first time.