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Unraveling the Mechanism of Polymerization with the Phillips Catalyst
The mechanism of polymer chain growth at the Phillips catalyst has been studied, with the three prevailing mechanistic proposals, the Cosee−Arlman, Green−Rooney, and metallacycle mechanisms, considered. Through analysis of low molecular weight oligomers/polymers formed during ethylene/α-olefin copol...
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Published in: | Organometallics 2010-11, Vol.29 (22), p.6111-6116 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The mechanism of polymer chain growth at the Phillips catalyst has been studied, with the three prevailing mechanistic proposals, the Cosee−Arlman, Green−Rooney, and metallacycle mechanisms, considered. Through analysis of low molecular weight oligomers/polymers formed during ethylene/α-olefin copolymerization with labeled monomers, it is shown that the isotopomer distribution is inconsistent with a metallacycle mechanism. Further analysis of polymer formed by copolymerization of labeled ethylene was used to rule out a Green−Rooney mechanism. The results support the notion of chain growth via a Cossee−Arlman process. |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om100883n |