Ring opening metathesis polymerisation of a new bio-derived monomer from itaconic anhydride and furfuryl alcohol

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From the same journal

Green Chemistry (Journal)
Thomas James Farmer (Referee)
2012 → …
Activity: Publication peer-review and editorial work › Journal peer review

Research output: Contribution to journal › Article › peer-review

Full text download(s)

c6gc00623j
349 KB, PDF document

Published copy (DOI)

10.1039/C6GC00623J

Author(s)

Yinjuan Bai
Mario De Bruyn
James H. Clark
Jennifer R. Dodson
Thomas J. Farmer
Mathilde Honoré
Ian D V Ingram
Mohamed Naguib
Adrian C. Whitwood
Michael North

Department/unit(s)

Chemistry

Publication details

Journal	Green Chemistry
Date	Accepted/In press - 1 Jun 2016
Date	Published (current) - 1 Jun 2016
Issue number	14
Volume	18
Number of pages	4
Pages (from-to)	3945-3948
Original language	English

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).

Bibliographical note

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