Redox-switchable α-diimine palladium catalysts for control of polyethylene topology
File(s)POLYMER-19-920 cmnt19515.doc (28.5 KB)
Accepted version
Author(s)
Type
Journal Article
Abstract
A series of palladium complexes bearing ferrocene substituted α-diimine ligands was synthesized and investigated for ethene polymerization at different conditions to modulate the extent of “chain-walking” mechanism and regulate branching and topology of resulting polyethylenes. All ferrocene substituted complexes catalyzed living/controlled ethene polymerization. The ability of ferrocene substituted palladium complexes to provide polyethylenes with dendritic topology was proved by measuring their Mark-Houwink plots. In-situ chemical oxidation of ferrocene moieties via silver triflate was used to affect the catalyst electronic structure and support the “chain-walking” mechanism. Oxidation of palladium catalyst led to its destabilization while the catalytic activity of newly formed sites was substantially increased. It was demonstrated that catalyst oxidation is a powerful tool to regulate the topology of resulting polyethylenes.
Date Issued
2019-09-28
Date Acceptance
2019-06-28
Citation
Polymer, 2019, 179
ISSN
0032-3861
Publisher
Elsevier BV
Journal / Book Title
Polymer
Volume
179
Copyright Statement
© 2019 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0/
Subjects
Polymers
03 Chemical Sciences
09 Engineering
Publication Status
Published
Article Number
ARTN 121619
Date Publish Online
2019-06-30