| Literature DB >> 33401624 |
Abstract
Reactions of cyclometalated compounds are numerous. This account is focused on one of such reactions, the exchange of cyclometalated ligands, a reaction between a cyclometalated compound and an incoming ligand that replaces a previously cyclometalated ligand to form a new metalacycle: + H-C*~Z ⇄ + H-C~Y. Originally discovered for PdII complexes with Y/Z = N, P, S, the exchange appeared to be a mechanistically challenging, simple, and convenient routine for the synthesis of cyclopalladated complexes. Over four decades it was expanded to cyclometalated derivatives of platinum, ruthenium, manganese, rhodium, and iridium. The exchange, which is also questionably referred to as transcyclometalation, offers attractive synthetic possibilities and assists in disclosing key mechanistic pathways associated with the C-H bond activation by transition metal complexes and C-M bond cleavage. Both synthetic and mechanistic aspects of the exchange are reviewed and discussed.Entities:
Keywords: C−H bond activation; cyclometalation; exchange of cyclometalated ligands; iridium; manganese; palladium; platinum; reaction mechanism; rhodium; ruthenium; transcyclometalation
Year: 2021 PMID: 33401624 PMCID: PMC7795987 DOI: 10.3390/molecules26010210
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411