Bai, Yinjuan, De Bruyn, Mario orcid.org/0000-0002-9687-1606, Clark, James H. orcid.org/0000-0002-5860-2480 et al. (7 more authors) (2016) Ring opening metathesis polymerisation of a new bio-derived monomer from itaconic anhydride and furfuryl alcohol. Green Chemistry. pp. 3945-3948. ISSN 1463-9262
Abstract
A new oxa-norbornene bio-based lactone obtained from the 100% atom economic reaction of furfuryl alcohol and itaconic anhydride via a tandem Diels-Alder addition and lactonisation is presented. Esterification of the resulting acid gives a monomer for the production of a bio-based polymer with low polydispersity and well controlled molecular weight via ring-opening metathesis polymerisation (ROMP).
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © The Royal Society of Chemistry 2016. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details. |
Dates: |
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Institution: | The University of York |
Academic Units: | The University of York > Faculty of Sciences (York) > Chemistry (York) |
Funding Information: | Funder Grant number EPSRC EP/L017393/1 |
Depositing User: | Pure (York) |
Date Deposited: | 15 Jun 2016 10:30 |
Last Modified: | 29 Jan 2025 00:05 |
Published Version: | https://doi.org/10.1039/C6GC00623J |
Status: | Published |
Refereed: | Yes |
Identification Number: | 10.1039/C6GC00623J |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:100943 |