Details

Autor(en) / Beteiligte

• Tsurugi, Hayato
• Mashima, Kazushi

Titel

Renaissance of Homogeneous Cerium Catalysts with Unique     Ce(IV/III) Couple: Redox-Mediated Organic Transformations Involving Homolysis of Ce(IV)–Ligand Covalent Bonds

Ist Teil von

• Journal of the American Chemical Society, 2021-06, Vol.143 (21), p.7879-7890

Ort / Verlag

United States: American Chemical Society

Erscheinungsjahr

2021

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Recent advances in the catalytic application of cerium complexes were achieved through controlling the Ce­(IV/III) redox couple. Although Ce­(IV) complexes have been extensively investigated as stoichiometric oxidants in organic synthesis on the basis of their highly positive redox potentials, these complexes can be used as catalysts, not only by introducing supporting ligands around the coordination sphere of cerium, but also by taking advantage of the photoresponsive properties of Ce­(IV) and Ce­(III) species. Cerium is highly abundant, comparable to that of some first-row transition metals such as copper, nickel, and zinc. Cerium complexes are new and promising homogeneous catalyst candidates for a variety of organic transformations under mild reaction conditions. They are typically used to activate dioxygen to oxidize organic compounds and applied for organic radical generation using the photoresponsive character of Ce­(IV) carboxylates and alkoxides as well as electronic transition of Ce­(III), in which homolysis of Ce­(IV)–ligand covalent bonds is an important step for the overall catalytic cycle. In this Perspective, we first review the early discovery of Ce­(OAc)4-mediated oxidative transformations to emphasize the importance of Ce­(IV)–OAc bond homolysis in various C–C bond-forming reactions and its relation to recent developments. We then focus on the fundamental importance of Ce­(IV) reactivity involving thermal and photoassisted homolysis of the Ce­(IV)–ligand covalent bond and the developments regarding Ce­(IV/III) redox changes in catalytic reactions together with our recent findings on cerium-based catalysis.