Thermo-cleavable bottlebrush polymers were synthesized by a facile grafting-to method via radical coupling and atom transfer radical polymerization (ATRP) without small-molecule synthesis involved. Bottlebrushes were achieved by coupling backbones of poly(4-methacryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl), which contain nitroxide radicals, and ATRP-synthesized side chains, which can be halogen-abstracted to generate carbon-centered radicals. Bottlebrushes were prepared using homopolymer or block copolymer side chains. Alkoxyamine covalent bonds resulting from radical coupling are thermo-reversible at high temperature, and grafting density may be tuned by annealing of post-synthesis bottlebrush, with the bottlebrush regime going from loose bottlebrush to dense comb and loose comb. The effects of confinement on the T-g and fragility of films of polystyrene bottlebrush were studied by ellipsometry; comparisons were made to thermally cleaved linear components obtained directly after annealing. Relative to linear polymer, bottlebrush topology reduces bulk fragility and suppresses T-g- and fragility-confinement effects. The correlation between the strengths of the confinement effects is consistent with other film studies of linear and non-linear polymers and supports the notion that fragility is a fundamental property underlying perturbations to T-g. Besides providing a platform for advancing fundamental scientific understanding, our synthetic strategy may afford novel applications of bottlebrushes via incorporated dynamic chemistry.
