UniSa - IRIS Institutional Research Information System
IRIS è la soluzione IT che facilita la raccolta e la gestione dei dati relativi alle attività e ai prodotti della ricerca. Fornisce a ricercatori, amministratori e valutatori gli strumenti per monitorare i risultati della ricerca, aumentarne la visibilità e allocare in modo efficace le risorse disponibili.
EnglishThe polyethylene obtained in the presence of the catalyst constituted by the meso isomer of the prototypical zirconocene complex (ethylene)bis(1-indenyl)zirconium dichloride activated by methylalumoxane is characterized by the presence of ethyl branches. The intensities of the 13C NMR signals associated with these branches indicate that there are about 1-2 ethyl groups per 100 monomer units. As a consequence, the melting temperature is 10-15 °C lower than the linear polyethylene obtained with the rac mixture of the same zirconocene complex. On the basis of kinetic evidence, a branching mechanism that involves a beta-H transfer to the coordinated ethylene is proposed.
| Titolo: | Branched Polyethylene by Ethylene Homopolymerization with meso-Zirconocene Catalyst |
| Autori: | |
| Data di pubblicazione: | 1999 |
| Rivista: | |
| Abstract: | The polyethylene obtained in the presence of the catalyst constituted by the meso isomer of the prototypical zirconocene complex (ethylene)bis(1-indenyl)zirconium dichloride activated by methylalumoxane is characterized by the presence of ethyl branches. The intensities of the 13C NMR signals associated with these branches indicate that there are about 1-2 ethyl groups per 100 monomer units. As a consequence, the melting temperature is 10-15 °C lower than the linear polyethylene obtained with the rac mixture of the same zirconocene complex. On the basis of kinetic evidence, a branching mechanism that involves a beta-H transfer to the coordinated ethylene is proposed. |
| Handle: | http://hdl.handle.net/11386/1060851 |
| Appare nelle tipologie: | 1.1.2 Articolo su rivista con ISSN |
File in questo prodotto:
http://hdl.handle.net/11386/1060851
Copyright © 2020