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Article dans une revue

Efficient One-Pot Synthesis of End-Functionalized trans-Stereoregular Polydiene Macromonomers

Abstract : End-functionalized 1,4-trans-polydienes (isoprene and myrcene) were prepared by means of a neodymium-mediated continuous polymerization–functionalization process. A chain transfer stage was essential to get a high level of functionalization of the polymer. The living 1,4-trans-stereoregular polymer chain was reacted with benzophenone to afford up to 97% −CPh2OH end-group with isoprene, while in the case of myrcene, using the same strategy afforded 1,4-trans-polymyrcene with a functionalization rate of 83%. The strategy was validated with complementary functionalization experiments using benzaldehyde and styrene oxide, both affording 95% end-capped trans-stereoregular polydienes.
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https://hal.univ-lille.fr/hal-02309293
Contributeur : Lilloa Université de Lille <>
Soumis le : mercredi 2 juin 2021 - 09:17:46
Dernière modification le : mercredi 2 juin 2021 - 09:25:37

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Sébastien Georges, Obaid-Hasan Hashmi, Marc Bria, Philippe Zinck, Yohan Champouret, et al.. Efficient One-Pot Synthesis of End-Functionalized trans-Stereoregular Polydiene Macromonomers. Macromolecules, American Chemical Society, 2019, 52 (3), pp.1210-1219. ⟨10.1021/acs.macromol.8b01520⟩. ⟨hal-02309293⟩

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