DOI: 10.1021/acs.macromol.6c02209 ISSN: 0024-9297

One-Pot, Dual-Wavelength 3D Printing of Bottlebrush-Based Multimaterials

Justin J. Yun, Nadia Chapple, Divya J. Iyer, Andrew Rhode, Juan Manuel Urueña, Craig J. Hawker, Christopher M. Bates

Abstract

Multimaterial 3D printing requires resin platforms that independently control softness, stiffness, and interfacial integrity within a single printed object. Here we demonstrate that crosslinkable bottlebrush polymers provide a versatile architecture for dual-wavelength printing of elastomers with mechanical contrast. UV irradiation (365 nm) efficiently crosslinks pendant 1,2-dithiolanes attached to the ends of polyethylene glycol side chains to form supersoft, dynamic bottlebrush networks with a tunable tensile modulus from 2 to 200 kPa by varying the lipoate content or acrylate comonomer concentration. Incorporation of an acrylate–epoxy hybrid monomer enables a second, orthogonal curing step: blue-light irradiation (460 nm) activates cationic epoxide polymerization to install a reinforcing network and increase the modulus into the MPa range, with post-cured materials reaching up to 200 MPa. This sequential radical/cationic strategy produces stiff–soft multimaterials from a single resin with high gel fractions, robust interfaces, and diffuse fracture behavior. Importantly, dual-cured networks have a higher stiffness than those obtained by curing acrylate-free resins, demonstrating that crosslinker chemistry controls network topology and mechanical properties. Together, these results establish lipoate-functional bottlebrush polymers as a modular platform for single-resin multimaterial 3D printing, where polymer architecture and temporally controlled photochemistry combine to program kPa-to-MPa mechanical contrast, degradability, and interfacial toughness.

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