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

TY - JOUR

T1 - Ring opening metathesis polymerisation of a new bio-derived monomer from itaconic anhydride and furfuryl alcohol

AU - Bai, Yinjuan

AU - De Bruyn, Mario

AU - Clark, James H.

AU - Dodson, Jennifer R.

AU - Farmer, Thomas J.

AU - Honoré, Mathilde

AU - Ingram, Ian D V

AU - Naguib, Mohamed

AU - Whitwood, Adrian C.

AU - North, Michael

N1 - © 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.

PY - 2016/6/1

Y1 - 2016/6/1

N2 - 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).

AB - 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).

UR - http://www.scopus.com/inward/record.url?scp=84978924695&partnerID=8YFLogxK

U2 - 10.1039/C6GC00623J

DO - 10.1039/C6GC00623J

M3 - Article

AN - SCOPUS:84978924695

SN - 1463-9262

VL - 18

SP - 3945

EP - 3948

JO - Green Chemistry

JF - Green Chemistry

IS - 14

ER -