4.1 Article

Telomerization of 1,3-butadiene with glycerol carbonate and subsequent ring-opening lactone co-polymerization

Journal

COMPTES RENDUS CHIMIE
Volume 19, Issue 3, Pages 299-305

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.crci.2015.11.008

Keywords

Glycerol carbonate; Butadiene telomerization; Glyceryl carbonate ethers; ROP; epsilon-Caprolactone copolymer; Bio-resources

Funding

  1. Region Nord-Pas-de-Calais
  2. University of Lille 1, Science Technology

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Glycerol carbonate, straightforwardly issued from glycerol, is functionalized by telomerization with 1,3-butadiene by means of a palladium catalyst, to selectively afford the linear octadienylglyceryl carbonate. Further hydrogenation of the double bonds gives the saturated functionalized product. The resulting glyceryl carbonate ethers are tentatively co-polymerized with lactones in the presence of a neodymium initiator. Copolymers with up to ca 4 mol % of inserted carbonate are received. The rather low amount of inserted co-monomer is found sufficient to modulate the thermal behavior of polycaprolactone. (C) 2015 Academie des sciences. Published by Elsevier Masson SAS. This is an open access article under the CC BY-NC-ND license.

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