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  Ethene co- and terpolymerizations with TIBA-protected norbornenemethanol and TIBA-protected norbornenecarboxylic acid using homogeneous metallocene/MAO catalyst systems

Wendt, R. A., & Fink, G. (2002). Ethene co- and terpolymerizations with TIBA-protected norbornenemethanol and TIBA-protected norbornenecarboxylic acid using homogeneous metallocene/MAO catalyst systems. Macromolecular Chemistry and Physics, 203(8), 1071-1080. doi:10.1002/1521-3935(20020501)203:8<1071:AID-MACP1071>3.0.CO;2-0.

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 Urheber:
Wendt, R. A.1, Autor           
Fink, G.1, Autor           
Affiliations:
1Research Department Fink, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445583              

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Schlagwörter: copolymerization; kinetics; metallocene catalysts; NMR; polar norbornene derivatives
 Zusammenfassung: Full Paper: Ethene copolymerizations were carried out with triisobutylaluminum (TTBA)-protected norbornenemethanol and norbornenecarboxylic acid, respectively, using homogeneous metallocene/MAO catalyst systems. Moreover, ethene terpolymerizations with both polar norbornene derivatives were investigated for the first time, The metallocenes utilized, such as iPr[CpInd]ZrCl2, iPR[(3-iPr-Cp)Ind]ZrCl2, and iPr[(3- tert-But-Cp)Ind]ZrCl2 contain ligand frameworks of various sterical demands. The incorporation of polar monomers into the polymer chain was determined by NMR spectroscopic investigations. Kinetic and analytical results of the polymerization experiments revealed increasing activities and a decreasing comonomer incorporation into the polymer chain with an increasing sterical demand of the metallocene ligand. Additionally, the TIBA-protected norbornenecarboxylic acid shows a lower incorporation rate into the copolymer chain in comparison with the TIBA-protected norbornenemethanol.

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Sprache(n): eng - English
 Datum: 2002-06-10
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Art des Abschluß: -

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Titel: Macromolecular Chemistry and Physics
  Alternativer Titel : Macromol. Chem. Phys.
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 203 (8) Artikelnummer: - Start- / Endseite: 1071 - 1080 Identifikator: ISSN: 1022-1352