4.7 Article

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

期刊

MACROMOLECULES
卷 52, 期 3, 页码 1210-1219

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AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.8b01520

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  1. Region Nord-Pas-de-Calais
  2. University of Lille 1
  3. Chevreul Institute in Lille [FR 2638]
  4. Ministere de l'Enseignement Superieur et de la Recherche
  5. FEDER

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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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