Fluxional Bis(phenoxy-imine) Zr and Ti Catalysts for Polymerization

Bis(phenoxy-imine) complexes of zirconium or titanium, a type of Fenokishi-Imin (FI) catalysts, allow the production of polyethylenes with well-defined bimodal molecular weight distributions. Interestingly, by substitution of phenyl rings in the bis(phenoxy-imine) ligands by perfluorinated phenyl ri...

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Detalles Bibliográficos
Autores: Escayola Gordils, Sílvia, Brotons Rufes, Artur, Bahri-Laleh, Naeimeh, Ragone, Francesco, Cavallo, Luigi, Solà i Puig, Miquel, Poater Teixidor, Albert
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2021
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10256/19820
Acceso en línea:http://hdl.handle.net/10256/19820
Access Level:acceso abierto
Palabra clave:Polimerització
Catalitzadors
Transferència de càrrega
Teoria del funcional de densitat
Polymerization
Catalysts
Charge transfer
Density functionals
Descripción
Sumario:Bis(phenoxy-imine) complexes of zirconium or titanium, a type of Fenokishi-Imin (FI) catalysts, allow the production of polyethylenes with well-defined bimodal molecular weight distributions. Interestingly, by substitution of phenyl rings in the bis(phenoxy-imine) ligands by perfluorinated phenyl rings, the polymerization reaches a desired unimodal behaviour. These catalysts have 3 isomers of similar energy that can be easily interconverted. It is likely that the bimodal behaviour is due to the coexistence of more than one isomer in the reaction vessel. Here, we perform static and dynamic DFT calculations to understand the isomerization of the catalytic active species. We analyze the relative Gibbs energies of the different isomers and the barriers for the isomerization processes. Further characterization of the isomers is obtained through stereo maps, aromaticity measures, and NCI plots. Our results show that by changing the phenyl group by a perfluorinated phenyl ring, one of the isomers is particularly stabilized, thus explaining the unimodal behaviour of the polyethylene production process