Journal of Polymer Science Part A: Polymer Chemistry, Vol.53, No.2, 239-248, 2015
Synthesis of Degradable Molecular Brushes via a Combination of Ring-Opening Polymerization and Click Chemistry
Acid-degradable molecular brushes with polycarbonate backbone and densely grafted side chains (approximate to 1.9 SCs per backbone repeating unit) were synthesized for the first time using the grafting-onto method. Extremely efficient copper-catalyzed azide-alkyne cycloaddition click reactions between the polycarbonate backbone containing two pendant azido groups per backbone unit and alkynyl-terminated poly (methyl acrylate) (ay-PMA(72), average degree of polymerization DP=72) SCs were demonstrated to finish in 10 min with a quantitative conversion of the azido groups. Similar grafting efficiencies were also achieved when using alkynyl-terminated polystyrene (ay-PS), poly(ethylene oxide) (ay-PEO), and poly (t-butyl acrylate)-b-polystyrene (ay-PtBA-b-PS) to successfully prepare molecular brushes with high grafting density (>1.8 SCs per backbone repeating unit). Under acidic condition, the polycarbonate backbones were completely degradable and the final degraded product of the molecular brushes was a linear polymer chain with molecular weight two times of the SCs. When a mixture of hydrophobic ay-PS and hydrophilic ay-PEO chains was used, amphiphilic heterobrushes PC-g-(PS-co-PEO) were synthesized, which could self-assemble into micelles or vesicles in selective solvents, depending on the ratio of the two SCs in the brush. (c) 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 239-248
Keywords:copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction;degradation;polycarbonates;ring-opening polymerization;self-assembly