para -Fluoro/thiol click chemistry-driven pentafluorostyrene-based block copolymer self-assembly: to mimic or not to mimic the solubility parameter? - Université de Pau et des Pays de l'Adour Accéder directement au contenu
Article Dans Une Revue Polymer Chemistry Année : 2022

para -Fluoro/thiol click chemistry-driven pentafluorostyrene-based block copolymer self-assembly: to mimic or not to mimic the solubility parameter?

Résumé

A block copolymer (BCP) consisting of polystyrene (PS) and polypentafluorostyrene (PPFS) blocks is synthesized by nitroxide mediated polymerization (NMP). Then nucleophilic substitution of the labile para-fluorine atom onto the PPFS platform is performed by an organo-catalyzed reaction at ambient temperature using the para-fluoro/thiol click reaction. It is observed that the effect of the substitute chemical nature induces a drastic tuning of the nano-structuration of the block copolymer. Indeed, the para-fluoro/thiol click reaction leads to PS-b-modified PPFS block copolymers with solubility parameter control and drives an order/disorder transition

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Chimie Polymères
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Dates et versions

hal-03767030 , version 1 (01-09-2022)

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Citer

Prithwiraj Mandal, Pierre Marcasuzaa, Laurent Billon. para -Fluoro/thiol click chemistry-driven pentafluorostyrene-based block copolymer self-assembly: to mimic or not to mimic the solubility parameter?. Polymer Chemistry, 2022, 13 (33), pp.4757-4762. ⟨10.1039/d2py00784c⟩. ⟨hal-03767030⟩
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