聚合
聚合物
氧气
原子转移自由基聚合
材料科学
化学工程
阳离子聚合
聚合物刷
自由基聚合
催化作用
烷基
光化学
高分子化学
化学
有机化学
复合材料
工程类
作者
Gianluca Gazzola,Irene Filipucci,Andrea Rossa,Krzysztof Matyjaszewski,Francesca Lorandi,Edmondo M. Benetti
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2023-08-01
卷期号:12 (8): 1166-1172
被引量:20
标识
DOI:10.1021/acsmacrolett.3c00359
摘要
Achieving tolerance toward oxygen during surface-initiated reversible deactivation radical polymerization (SI-RDRP) holds the potential to translate the fabrication of polymer brush-coatings into upscalable and technologically relevant processes for functionalizing materials. While focusing on surface-initiated photoinduced atom transfer radical polymerization (SI-photoATRP), we demonstrate that a judicious tuning of the composition of reaction mixtures and the adjustment of the polymerization setup enable to maximize the compatibility of this grafting technique toward environmental conditions. Typically, the presence of O2 in the polymerization medium limits the attainable thickness of polymer brushes and causes the occurrence of "edge effects", i.e., areas at the substrates' edges where continuous oxygen diffusion from the surrounding environment inhibits brush growth. However, the concentrations of the Cu-based catalyst and "free" alkyl halide initiator in solution emerge as key parameters to achieve a more efficient consumption of oxygen and yield uniform and thick brushes, even for polymerization mixtures that are more exposed to air. Precise variation of reaction conditions thus allows us to identify those variables that become determinants for making the synthesis of brushes more tolerant toward oxygen, and consequently more practical and upscalable.
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