The direct access to dimethoxymethane (DMM) from CO2/H2 in MeOH is an attractive approach, but more active, selective and robust catalyst systems are still desirable for an application of this...

Selectivity of immobilized Triphos-type catalysts can be tuned for application in nitrile hydrogenation in batch and continuous flow processes.

In contrast to their symmetrical analogues, nonsymmetrical PNP‐type ligand motifs have been less investigated despite the modular pincer structure. However, the introduction of mixed phosphorus donor moieties provides access to a larger variety of PNP ligands. Herein, a facile solid‐phase synthesis approach towards a diverse PNP‐pincer ligand library of 14 members is reported. Contrary to often challenging workup procedures in solution‐phase, only simple workup steps are required. The corresponding supported ruthenium‐PNP catalysts are screened in ester hydrogenation. Usually, industrially applied heterogeneous catalysts require harsh conditions in this reaction (250–350 °C at 100–200 bar) often leading to reduced selectivities. Heterogenized reusable Ru‐PNP catalysts are capable of reducing esters and lactones selectively under mild conditions.