http://www.cnr.it/ontology/cnr/individuo/prodotto/ID54591
Terpolymerization of Linear and Alicyclic ±-Olefins with Norbornene and Ethylene by ansa-Metallocene Catalysts (Articolo in rivista)
- Type
- Label
- Terpolymerization of Linear and Alicyclic ±-Olefins with Norbornene and Ethylene by ansa-Metallocene Catalysts (Articolo in rivista) (literal)
- Anno
- 2011-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/ma102515c (literal)
- Alternative label
Marconi R., Boggioni L.,. Ravasio A, Di Colo F., Tritto I., and Stehling Udo M. (2011)
Terpolymerization of Linear and Alicyclic ±-Olefins with Norbornene and Ethylene by ansa-Metallocene Catalysts
in Macromolecules (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Marconi R., Boggioni L.,. Ravasio A, Di Colo F., Tritto I., and Stehling Udo M. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://pubs.acs.org/doi/pdf/10.1021/ma102515c (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Marconi R., Boggioni L.,. Ravasio A, Di Colo F., Tritto I., Ismac-Milano,
Stehling Udo M.TICONA GmbH (literal)
- Titolo
- Terpolymerization of Linear and Alicyclic ±-Olefins with Norbornene and Ethylene by ansa-Metallocene Catalysts (literal)
- Abstract
- ABSTRACT: Ethylene-norbornene (E-N) terpolymerization experiments using the linear olefin 1-octene
(O) or the alicyclic vinylcyclohexane (VCH) were conducted with two different ansa-metallocene compounds
Zr(?5
:?5
-C5H4CPh2C13H8)Cl2] (1) and [Zr{(?5
-2,5-Me2C5H2)2CHMe}Cl2] (2). The terpolymers obtained
were investigated in detail by determining microstructure and termonomer contents by 13C NMR, molar
masses, and thermal properties. Chain end group analysis gave insight into factors that influence termonomer
insertion and chain termination. Terpolymer molar masses were lower than those of the corresponding
copolymers, those from 1 being higher than those from 2. This is related to the lower tendency of catalyst 1 to
give ?-H elimination at a last enchained E unit as revealed from the low amount of vinyl chain end groups in 1
H
NMR spectra. In VCH terpolymers from catalyst 1, only vinylene end groups, arising from 2,1 VCH insertions
after one last inserted E unit, are present. This along with the lower activity reveals that VCH insertion is more
difficult with this catalyst than with catalyst 2. Furthermore, all experiments showed that in general VCH is more
difficult to coordinate to an active catalyst than O. While catalyst 1 provides higher molar masses, catalyst 2
enables to reach higher activities, higher N and termonomer contents, and higher Tg values. Finally, it was found
that termonomer content greater than 3 mol % clearly affects Tg values. Thus, preparation of norborneneethylene-R-olefin
terpolymers with high Tg and attractive molar masses was achieved in high yield by
metallocene catalysts. (literal)
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- Autore CNR
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