共聚物
刷子
不对称
层状结构
环氧乙烷
材料科学
相(物质)
侧链
小角X射线散射
甲基丙烯酸酯
化学物理
相图
结晶学
高分子化学
形态学(生物学)
散射
化学
聚合物
光学
物理
复合材料
有机化学
量子力学
生物
遗传学
作者
Regina J. Sánchez-Leija,Joshua A. Mysona,Juan Pablo,Paul F. Nealey
出处
期刊:Macromolecules
[American Chemical Society]
日期:2024-02-20
卷期号:57 (5): 2019-2029
被引量:8
标识
DOI:10.1021/acs.macromol.3c02180
摘要
This study explores how conformational asymmetry influences the bulk phase behavior of linear-brush block copolymers. We synthesized 60 diblock copolymers composed of poly(trifluoroethyl methacrylate) as the linear block and poly[oligo(ethylene glycol) methyl ether methacrylate] as the brush block, varying the molecular weight, composition, and side-chain length to introduce different degrees of conformational asymmetry. Using small-angle X-ray scattering, we determined the morphology and phase diagrams for three different side-chain length systems, mainly observing lamellar and cylindrical phases. Increasing the side-chain length of the brush block from three to nine ethylene oxide units introduces sufficient asymmetry between the blocks to alter the phase behavior, shifting the lamellar-to-cylindrical transitions toward lower brush block compositions and transitioning the brush block from the dense comb-like regime to the bottlebrush regime. Coarse-grained simulations support our experimental observations and provide a mapping between the composition and conformational asymmetry. A comparison of our findings to strong stretching theory across multiple phase boundary predictions confirms the transition between the dense comb-like regime and the bottlebrush regime.
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