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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 |
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