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Small-Angle Neutron Scattering Analysis of Bottlebrush Polymers Prepared via Grafting-Through Polymerization

2013; American Chemical Society; Volume: 46; Issue: 17 Linguagem: Inglês

10.1021/ma401246b

1520-5835

Stacy L. Pesek, Xianyu Li, Boualem Hammouda, Kunlun Hong, Rafael Verduzco,

Dendrimers and Hyperbranched Polymers

Bottlebrush polymers are highly branched macromolecules with potential applications in antifouling coatings, rheological modifiers, and drug delivery systems. However, the solution conformation of bottlebrush polymers has been studied in only a limited set of materials made primarily by grafting-from polymerization. Here we present small-angle neutron scattering (SANS) measurements on a series of polystyrene bottlebrush polymers with varying side-chain and backbone lengths in d8-toluene to analyze their size, shape, and conformation. Bottlebrush polymers with 2–7 kg mol–1 polystyrene side chains (degree of polymerization DP = 14–54) and poly(oxanorbornene) backbones (DP = 10–264) were synthesized using reversible addition–fragmentation chain transfer (RAFT) followed by a ring-opening metathesis polymerization (ROMP) grafting-through synthesis scheme. Analysis by Guinier–Porod, rigid cylinder, and flexible cylinder models provided estimates of the bottlebrush polymer length, radius, and stiffness. The bottlebrush polymer cross-sectional area depends primarily on side-chain DP, and the radius of gyration Rg exhibits a power-law dependence with side-chain DP. We also observe a sphere-to-cylinder transition with increasing backbone DP, with the transition occurring at a backbone DP of approximately 120 for the polystyrene bottlebrush polymers studied. The maximum molecular dimension for the series studied varies from 25 to 350 nm.