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Preparation of titanocene and zirconocene dichlorides bearing bulky 1,4-dimethyl-2,3-diphenylcyclopentadienyl ligand and their behavior in polymerization of ethylene

  1. 1.
    SYSNO ASEP0336710
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitlePreparation of titanocene and zirconocene dichlorides bearing bulky 1,4-dimethyl-2,3-diphenylcyclopentadienyl ligand and their behavior in polymerization of ethylene
    TitlePříprava titanocen a zirkonocen dichloridů obsahujících objemný 1,4-dimethyl-2,3-difenylcyklopentadienylový ligand a jejich chování při polymerizaci ethylenu
    Author(s) Horáček, Michal (UFCH-W) RID, ORCID
    Pinkas, Jiří (UFCH-W) RID, ORCID
    Merna, J. (CZ)
    Gyepes, R. (CZ)
    Meunier, P. (FR)
    Source TitleJournal of Organometallic Chemistry. - : Elsevier - ISSN 0022-328X
    Roč. 694, č. 2 (2009), s. 173-178
    Number of pages6 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordssubstituted cyclopentadienes ; titanocene ; zirconocene
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsKAN100400701 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000262010200006
    DOI10.1016/j.jorganchem.2008.10.019
    AnnotationNew metallocene dichlorides [eta(5)-(1,4-Me-2-2,3-Ph-2-C5H)(2)TiCl2] (2), [eta(5)-(1,4-Me-2-2,3-Ph-2-C5H)(2)ZrCl2] (3) and [eta(5)-(1,4-Me-2-2,3-Ph-2-C5H)eta(5)-(C5H5)ZrCl2] (4) were prepared from lithium salt of 1,4-dimethyl-2,3-diphenylcyclopentadiene (1) and [TiCl3(THF)(3)], [ZrCl4] and [eta(5)-(C5H5)ZrCl3(DME)], respectively. Compounds 2-4 were characterized by NMR spectroscopy, EI-MS and IR spectroscopy, and the solid state structure of 3 was determined by single crystal X-ray crystallography. The catalytic systems 3/MAO and 4/MAO were almost inactive in polymerization of ethylene at 30-50 degrees C, however, they exhibited high activity at temperature 80 degrees C. The catalyst formed from 2 and excess of MAO was practically inactive at all temperatures.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2010
Number of the records: 1  

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