Amphiphilic block copolymer poly(lactic acid)-block -(glycidylazide polymer)-block -polystyrene: synthesis and self-assembly

Abstract

The triblock energetic copolymer PLA-b-GAP-b-PS was synthesized successfully through atom-transfer radical polymerization (ATRP) of styrene and ring-opening polymerization of d,l-lactide. The energetic macroinitiator GAP-Br, which was made from reacting equimolar glycidyl azide polymer (GAP) with α-bromoisobutyryl bromide, firstly triggered the ATRP of styrene with its bromide group, and then the hydroxyl group on the GAP end of the resulting diblock copolymer participated in the polymerization of lactide in the presence of stannous octoate. The triblock copolymer PLA-b-GAP-b-PS had a narrow distribution of molecular weight. In the copolymer, the PS block was solvophilic in toluene and improved the stability of the structure, the PLA block was solvophobic in toluene and served as the sacrificial component to prepare porous materials, and GAP was the basic and energetic material. The three blocks of the copolymer were fundamentally thermodynamically immiscible, which lead to the self-assembly of the block copolymer in solution. Further studies showed that the concentration and solubility of the copolymer and the polarity of the solvent affected the morphology and size of the micelles generated from the self-assembly of the PLA-b-GAP-b-PS block copolymer. The micelles generated in organic solvents at 10 mg/mL copolymer concentration were spherical but became irregular when water was used as a co-solvent. The spherical micelles self-assembled in toluene had three distinct layers, and the diameter of the micelles increased from 60 to 250 nm as the concentration of the triblock energetic copolymer increased from 5 to 15 mg/L.