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Updated: Sep 21, 2025

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization
Published on: February 18, 2022
Tunable Assembly of Block Copolymer Tethered Particle Brushes by Surface-Initiated Atom Transfer Radical
Zongyu Wang1, Jaejun Lee2, Zhenhua Wang1,3,4
1Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States.
Abstract:
A strategy to synthesize SiO2-g-PMMA/PMMA-b-PS mono- and bimodal block copolymer particle brushes by surface-initiated atom transfer radical polymerization (SI-ATRP) from silica particles is presented. First, PMMA blocks were prepared by normal ATRP with controlled degree of polymerizations and grafting density. In a second step, the PS block was synthesized through a chain extension using low parts per million of Cu catalyst. Variation of the SiO2-g-PMMA-Br macroinitiator concentration had a pronounced effect on the modality of the chain extension product. In the limit of small concentration, partial termination resulted in bimodal brush architectures, while more uniform brush architectures were observed with increasing concentration of macroinitiator. Brush nanoparticles with bimodal architectures assembled into string-like aggregates that bore a resemblance to structures found in systems comprised of sparse (homopolymer) brush particles. The unexpected effect of modality on structure formation points to opportunities in controlling microstructures in brush particle materials.
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