dc.creatorPeoples, Brian C.
dc.creatorVega, Gala De la
dc.creatorValdebenito, Carolina
dc.creatorQuijada Abarca, Juan
dc.creatorIbañez, Andrés
dc.creatorValderrama, Mauricio
dc.creatorRojas Cortés, René
dc.date.accessioned2012-06-27T15:31:44Z
dc.date.accessioned2019-04-25T23:50:46Z
dc.date.available2012-06-27T15:31:44Z
dc.date.available2019-04-25T23:50:46Z
dc.date.created2012-06-27T15:31:44Z
dc.date.issued2012
dc.identifierJournal of Organometallic Chemistry 700 (2012) 147-153
dc.identifierdoi:10.1016/j.jorganchem.2011.11.035
dc.identifierhttp://www.repositorio.uchile.cl/handle/2250/125658
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/2429985
dc.description.abstractIn this contribution the synthesis and polymerization activity of the nickel complexes [NiBr2{N0-(2,6- diisopropylphenyl)-N-[1-(2,6-diisopropylphenylimine)ethyl]-N-(2,3,4,5,6-pentafluorophenyl)acetam idine}] (2), [NiBr2{N0-(2,6-diisopropylphenyl)-N-[1-(2,6-diisopropylphenylimine)ethyl]-N-(2,3,4,5,6- pentafluorophenylimine)ethylacetamidine}] (2a) and [NiBr2{N-(2,6-diisopropylphenyl)-N-[1-(2,6- diisopropylphenylimine)]-N-(pyridin-4-yl)acetamidine}] (3) are reported. The variation of the phenyl substituents on the b amine was found to influence the polymerization activity of the complexes. The electron withdrawing/donating capacity of the substituted ring was found to be correlated with the polymerization activity, with the pentafluoro substituted ring increasing the polymerization activity and the pyridine ring decreasing the activity. The ligands and complexes were characterized using standard techniques and the polymer properties analyzed.
dc.languageen
dc.publisherElsevier
dc.subjectNi polymerization catalysts
dc.titleNickel pre-catalysts bearing [(N)-imidoylamidine] ligands; influence of the presence of pyridine and pentafluorophenyl groups in ligand backbone on the reactivity in ethylene polymerizations
dc.typeArtículos de revistas


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