4.7 Article

Precise Synthesis of Bottlebrush Block Copolymers from omega-End-Norbornyl Polystyrene and Poly(4-tert-butoxystyrene) via Living Anionic Polymerization and Ring-Opening Metathesis Polymerization

期刊

MACROMOLECULES
卷 51, 期 2, 页码 447-455

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AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.7b02447

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资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning [NRF-2015R1A2A1A01002493]
  2. GIST Research Institute (GRI) - GIST

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A facile and efficient synthetic grafting-through strategy for preparing well-defined bottlebrush block copolymers (BBCPs). was developed through a combination of-living anionic polymerization (LAP) and ring-opening metathesis polymerization (ROMP). co-End-norbornyl polystyrene (NPSt) and poly(4-tert-butoxystyrene) (NPtBOS) were synthesized by LAP using terminator of chlorine moiety containing silane-protecting amine and coupled with a subsequent amidation using norbornyl activated ester. Bottlebrush homopolymers of NPSt were obtained by ROMP with ultrahigh molecular weights (MWs, M-w, = 2928 kDa) and narrow molecular weight distributions (MWDs, D = 1.07) at high degre of polymerizations (DPw = 1084). Welldefined BBCPS with ultrahigh MWs (M-w similar to 3055 kDa) and narrow MWDs (D similar to 1.13) were synthesized through sequential ROMP of NPSt with NPtBOS. The effect of ultrahigh MWs was investigated by self-assembly of the BBCPs in which the phase separated BBCPs presented periodic lamellar structures and exhibited structural colors from blue to pink.

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