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Chain‐growth polymerization of azide–alkyne difunctional monomer: Synthesis of star polymer with linear polytriazole arms from a core
Author(s) -
Gan Weiping,
Cao Xiaosong,
Shi Yi,
Gao Haifeng
Publication year - 2020
Publication title -
journal of polymer science
Language(s) - English
Resource type - Journals
eISSN - 2642-4169
pISSN - 2642-4150
DOI - 10.1002/pola.29440
Subject(s) - monomer , polymer chemistry , polymerization , polymer , dispersity , chain transfer , chemistry , reversible addition−fragmentation chain transfer polymerization , living polymerization , kinetic chain length , step growth polymerization , molar mass distribution , materials science , solution polymerization , radical polymerization , organic chemistry
This article reports a chain‐growth coupling polymerization of AB difunctional monomer via copper‐catalyzed azide–alkyne cycloaddition (CuAAC) reaction for synthesis of star polymers. Unlike our previously reported CuAAC polymerization of AB n ( n ≥ 2) monomers that spontaneously demonstrated a chain‐growth mechanism in synthesis of hyperbranched polymer, the homopolymerization of AB monomer showed a common but less desired step‐growth mechanism as the triazole groups aligned in a linear chain could not effectively confine the Cu catalyst in the polymer species. In contrast, the use of polytriazole‐based core molecules that contained multiple azido groups successfully switched the polymerization of AB monomers into chain‐growth mechanism and produced 3‐arm star polymers and multi‐arm hyperstar polymers with linear increase of polymer molecular weight with conversion and narrow molecular weight distribution, for example, M w / M n ~ 1.05. When acid‐degradable hyperbranched polymeric core was used, the obtained hyperstar polymers could be easily degraded under acidic environment, producing linear degraded arms with defined polydispersity. © 2019 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58 , 84–90