Vanadium Imido NHC Complexes for Ring-Closing Olefin Metathesis Reactions

Vanadium bis-phosphine imido and oxo chloride alkylidenes have been extensively applied in the ring-closing metathesis of various acyclic olefins. However, their reactions involving ethylene have shown limited productivity due to rapid decomposition. The primary degradation pathway involving V bis-p...

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Detalles Bibliográficos
Autores: Tejeda, Gabriela, Belov, Dmitry S., Fenoll, Didac A.|||0000-0003-1141-8114, Rue, Kelly L., Tsay, Charlene, Solans-Monfort, Xavier|||0000-0002-2172-3895, Bukhryakov, Konstantin V.|||0000-0002-8425-9671
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:280615
Acceso en línea:https://ddd.uab.cat/record/280615
https://dx.doi.org/urn:doi:10.1021/acs.organomet.2c00013
Access Level:acceso abierto
Descripción
Sumario:Vanadium bis-phosphine imido and oxo chloride alkylidenes have been extensively applied in the ring-closing metathesis of various acyclic olefins. However, their reactions involving ethylene have shown limited productivity due to rapid decomposition. The primary degradation pathway involving V bis-phosphine imido complexes is β-H elimination at an unsubstituted metallacyclobutane. In contrast, β-H elimination is disfavored for V oxo species, but bimolecular decomposition precludes its high productivity. Herein, we present the synthesis of V imido NHC complexes that are the most productive V catalysts toward various terminal olefins in ring-closing metathesis reactions. Experimental and computational studies suggest that β-H elimination and bimolecular decomposition are disfavored for V imido NHC complexes.