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Polyolefin–polar block copolymers from versatile new macromonomers
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Kay, Christopher, Goring, Paul D., Burnett, Connah A., Hornby, Ben, Lewtas, Kenneth, Morris, Shaun N., Morton, Colin, McNally, Tony, Theaker, Giles W., Waterson, Carl, Wright, Peter M. and Scott, Peter (2018) Polyolefin–polar block copolymers from versatile new macromonomers. Journal of the American Chemical Society, 140 (42). pp. 13921-13934. doi:10.1021/jacs.8b09039
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WRAP-polyolefin-polar-block-copolymers-versatile-macromonomers-Scott-2018.pdf - Accepted Version Embargoed item. Restricted access to Repository staff only until 27 September 2019. Contact author directly, specifying your specific needs. - Requires a PDF viewer. Download (4Mb) |
Official URL: http://dx.doi.org/10.1021/jacs.8b09039
Abstract
A new metallocene-based polymerization mechanism is elucidated in which a zirconium hydride center inserts α-methylstyrene at the start of a polymer chain. The hydride is then regenerated by hydrogenation to release a polyolefin containing a single terminal α-methylstyrenyl group. Through the use of the difunctional monomer 1,3-diisopropenylbenzene, this catalytic hydride insertion polymerization is applied to the production of linear polyethylene and ethylene–hexene copolymers containing an isopropenylbenzene end group. Conducting simple radical polymerizations in the presence of this new type of macromonomer leads to diblock copolymers containing a polyolefin attached to an acrylate, methacrylate, vinyl ester, or styrenic segments. The new materials are readily available and exhibit interfacial phenomena, including the mediation of the mixing of immiscible polymer blends.
| Item Type: | Journal Article | ||||||||||||
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| Subjects: | T Technology > TP Chemical technology | ||||||||||||
| Divisions: | Faculty of Science > Chemistry Faculty of Science > WMG (Formerly the Warwick Manufacturing Group) |
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| Library of Congress Subject Headings (LCSH): | Polyolefins, Copolymers | ||||||||||||
| Journal or Publication Title: | Journal of the American Chemical Society | ||||||||||||
| Publisher: | American Chemical Society | ||||||||||||
| ISSN: | 0002-7863 | ||||||||||||
| Official Date: | 24 October 2018 | ||||||||||||
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| Date of first compliant deposit: | 23 October 2018 | ||||||||||||
| Volume: | 140 | ||||||||||||
| Number: | 42 | ||||||||||||
| Page Range: | pp. 13921-13934 | ||||||||||||
| DOI: | 10.1021/jacs.8b09039 | ||||||||||||
| Status: | Peer Reviewed | ||||||||||||
| Publication Status: | Published | ||||||||||||
| Publisher Statement: | “This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/page/policy/articlesonrequest/index.html.” | ||||||||||||
| Access rights to Published version: | Restricted or Subscription Access | ||||||||||||
| RIOXX Funder/Project Grant: |
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