顺势排列
锚固
共聚物
聚丙烯酸
聚电解质
丙烯酸
水溶液
块(置换群论)
聚合物
化学
化学工程
高分子化学
材料科学
液晶
有机化学
光电子学
几何学
结构工程
数学
工程类
作者
Dong-Yul Lee,Jungmin Seo,Waliullah Khan,Julia A. Kornfield,Zuleikha Kurji,Soo‐Young Park
出处
期刊:Soft Matter
[Royal Society of Chemistry]
日期:2010-01-01
卷期号:6 (9): 1964-1964
被引量:62
摘要
Block copolymers that combine a side-group liquid crystalline polymer (SGLCP) block and a pH-responsive hydrophilic block, poly(acrylic acid) (PAA), are shown to confer pH-dependent anchoring of the director orientation at the aqueous/LC interface. The SGLCP block, poly(4-cyanobiphenyl-4-oxyundecylacrylate), was chosen based on its ability to influence the director field of the 5CB (4-cyano-4′-pentylbiphenyl). At low pH the PAA block collapses and the inherent, planar alignment tendency of 5CB at a water interface prevails. As pH increases, the polyelectrolyte block becomes increasingly charged and expands, producing a change to homeotropic anchoring. The change in anchoring occurs as quickly as the buffer can be changed (within ∼2 s) and is reversible, with a response that is repeatable over as many cycles as were tested (approximately 20 cycles). The polymer-mediated anchoring persists for 6 days, indicating that the SGLCP block secures the self-assembled layer on the 5CB, even under conditions that cause repulsive interactions among the PAA blocks. Thus, SGLCP blocks can translate conformational changes of a responsive hydrophilic block into rapid, reversible changes in the director field.
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