Synthesis, characterization and reactivity studies in ethylene polymerization of cyclometalated palladium(II) complexes containing terdentate ligands with a N,C,N-donor set

dc.contributor.authorJohn, Hurtado
dc.contributor.authorPortaluppi, Mariana
dc.contributor.authorQuijada, Raúl
dc.contributor.authorRojas, René
dc.contributor.authorValderrama, Mauricio
dc.date.accessioned2019-08-08T06:05:57Z
dc.date.available2019-08-08T06:05:57Z
dc.date.issued2009
dc.description.abstractThe reaction of [Na2PdCl4] with 3,5-bis(2-pyridoxy)toluene (LpyH) in acetic acid yields the cyclometalated complex [PdCl(Lpy-N, C, N)] (1). Complex 1 can be further converted into neutral species by metathesis reaction exchange of chloride by either iodide or thiocyanate to yield [PdX(Lpy-N, C, N)] (X = I (2), SCN (3)). The chloride can be replaced by neutral ligands like pyridine or acetonitrile in the presence of silver tetrafluoroborate to give the corresponding cationic compounds [PdL(Lpy-N, C, N)]BF4 (L = Py (4), MeCN (5)). In contrast, the reaction of [Na2PdCl4] with 3,5-bis(3, 5-dimethylpyrazol-1-ylmethyl)toluene (LpzH) under analogous conditions yields the neutral complex [PdCl2(LpzH-N, N)](6) with the ligand bidentate N,N-donor. The cyclometalated palladium complex [PdCl(Lpz-N, C, N)] (7) was prepared by the reaction of Pd(OAc)2 with LpzH in acetic acid followed by a metathetic reaction with lithium chloride in acetone/water. Complexes 1, 6, and 7 in the presence of methylaluminoxane (MAO) lead to an active catalyst for the polymerization of ethylene.en_US
dc.identifier.issn0095-8972
dc.identifier.urihttps://repositorio.usc.edu.co:8443/xmlui/handle/123456789/525
dc.language.isoenen_US
dc.publisherJournal of Coordination Chemistryen_US
dc.subjectPalladiumen_US
dc.subjectEthylene polymerizationen_US
dc.subjectCyclometalated complexesen_US
dc.titleSynthesis, characterization and reactivity studies in ethylene polymerization of cyclometalated palladium(II) complexes containing terdentate ligands with a N,C,N-donor seten_US
dc.typeArticleen_US

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