Abstract Amphiphilic graft copolymers were prepared via a grafting through approach to yield materials with a hydrophilic backbone and hydrophobic arms. The thermally responsive macromonomers were designed to contain a Diels–Alder adduct such that cyclo‐reversion would cleave the arms from the backbone thus altering polymer topology, composition and solubility. The macromonomers were prepared via light‐inducted atom transfer radical polymerization followed by post‐polymerization modification to install a polymerizable functionality. Next, free radical polymerization was employed to yield thermally responsive amphiphilic graft copolymers, whose solution state characteristics were extensively characterized by UV/Vis spectroscopy and fluorimetry. Due to the amphiphilic nature of the graft copolymer, some unexpected results occurred because of aggregation and solubility limitations. Furthermore, it was discovered that poly(N‐isopropyl acrylamide) exhibited distinct and unique aggregation properties by itself. 
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                            Thermal, mechanical, and morphological studies of a depolymerizable graft copolymer thermoplastic
                        
                    
    
            Graft polymers are gaining increasing interest because of their unique architectural characteristics. We recently reported a novel type of depolymerizable graft polymer based on poly(trans-cyclobutane fused cyclooctene), in an effort to address the trade-off between depolymerizability and controlled grafting-through polymerization. In this work, we examine the thermal, mechanical, and morphological properties of a graft copolymer thermoplastic material prepared by copolymerizing poly(L-lactide) and margaric acid-based macromonomers. A copolymerization kinetics study reveals that the two macromonomers are incorporated almost randomly and that the domain spacing measured from small-angle X-ray scattering is consistent with the random distribution. An investigation of the crystallization behavior suggests that proper thermal treatment is required to maximize, or to even observe crystallinity. The physical states of the soft and hard domains, whether melt, glassy, or semicrystalline, significantly impact the tensile properties of the resulting copolymer materials. Finally, the rheological properties and morphological features are discussed. 
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                            - Award ID(s):
- 2042494
- PAR ID:
- 10508370
- Publisher / Repository:
- Springer Nature
- Date Published:
- Journal Name:
- Polymer Journal
- Volume:
- 55
- Issue:
- 11
- ISSN:
- 0032-3896
- Page Range / eLocation ID:
- 1171 to 1178
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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