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High Molecular Weight Polyester Obtained by Polymerization of Dimethylketene Using Metallocene Initiators: A Step toward Ziegler-Natta Supporting Application in Non-Olefin Systems.

Authors
  • Jiang, Bo1
  • Desilles, Nicolas1
  • Burel, Fabrice1
  • 1 Normandie Université, INSA Rouen Normandie, CNRS UMR 6270, 685 Avenue de l'Université, Saint Etienne du Rouvray, 76800, France. , (France)
Type
Published Article
Journal
Macromolecular rapid communications
Publication Date
Oct 01, 2019
Volume
40
Issue
20
Identifiers
DOI: 10.1002/marc.201900293
PMID: 31454131
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

In this report, highly active metallocene initiators are used for the polymerization of a ketene monomer, dimethylketene, which typically contains two adjacent double bonds (R2 CCO). By using the methylzirconocene methyltriarylborate complex (Cp2 ZrMe+ MeB(C6 F5 )3 - ) as the activation system, associated with the possible cleavage of CC and CO bonds in ketene monomers, a structure-specific and high-molecular-weight polyester ( M n ¯ > 300 000 g mol-1 ) can be afforded. The resulting polyester structure, comprehensively characterized by NMR, indicates a significant reactive selectivity of the "bent-sandwich" cationic site Cp2 ZrMe+ . It reveals that the positively charged zirconium (Zr+ ) prefers to coordinate with a negatively charged oxygen (O- ) when it is already bonded to the carbon, while a negatively charged carbon (C- ) will be assigned in priority if the oxygen-zirconium bond exists. This report allows for broadening the application field of metallocene initiators in non-olefin reactions and deepening our insight into the mechanism of the living insertion/Ziegler-Natta polymerization. © 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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