Abstract
AbstractThe synthesis of various Schiff base mononuclear and binuclear ruthenium complexes, whose additional ligands around the metal core have been selected from an array of motifs, is described. These types of ruthenium complexes, conveniently prepared from commonly available ruthenium sources, are rather stable, display good tolerance towards diverse organic functionalities and also to air and moisture. Remarkably, they exhibit a high activity and chemoselectivity in a variety of catalytic processes such as ring‐closing metathesis (RCM), Kharasch addition, alkyne dimerization, enol ester synthesis, ring‐opening metathesis polymerization (ROMP) and atom‐transfer radical polymerization (ATRP). This review covers both homogeneous and heterogeneous hybrid Schiff base‐ruthenium complexes.
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