Abstract
A series of core−shell molecular bottlebrushes with helical polypeptide backbone and polylactide-b-poly(ethylene glycol) block copolymer side chains [PPLG-g-(PLA-b-PEG)] have been synthesized via a grafting-to method. The structurally well-defined side chains with low molecular weight distribution (PDI < 1.03) have been synthesized by ring-opening polymerization (ROP) of dl-lactides using PEG-OH macroinitiator and AlEt3 catalyst. Postpolymerization modification by esterification enables the quantitative installation of an alkynyl functionality at the block polymer chain ends. Grafting of alkynyl-terminated PLA-b-PEG onto poly(γ-azidopropyl-l-glutamate) (PAPLG) via copper-mediated [2 + 3] alkyne−azide 1,3-dipolar cycloaddition yields the targeted molecular bottlebrushes with high grafting density under mild conditions. A combination of the Langmuir−Blodgett (LB) technique with atomic force microscopy (AFM) has allowed for direct imaging of the synthesized molecular brushes and characterization of their mol...
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