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Methacrylate copolymers with substituted azobenzene side groups: synthesis, characterization and photo-induced birefringence properties

机译:具有取代的偶氮苯侧​​基的甲基丙烯酸酯共聚物:合成,表征和光致双折射性能

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摘要

Well-defined copolymer of methyl methacrylate (MMA) and 2-methylacrylic- acid-2-{ethyl-[4-(4-methoxy-phenylazo)-3-methyl-phenyl]-amino}-ethyl ester (MAMP) bearing pendent azobenzene groups, was synthesized via reversible addition-fragmentation chain transfer polymerization (RAFT). Copolymers with different contents of azobenzene moieties, e. g. from 12 mol % to 100 mol %, were obtained by varying the feed molar ratios of MAMP and MMA. The reactivity ratios of these two monomers were measured and calculated via the modified Kelen- Tüdos method. Glass transition temperature of the copolymers was measured by differential scanning calorimetry (DSC). Photoinduced trans-cis isomerization of azobenzene moieties in the copolymer was studied at room temperature. Films cast from the functional copolymers were characterized by photo-induced birefringence and surface relief grating (SRG).
机译:甲基丙烯酸甲酯(MMA)和2-甲基丙烯酸-2- {乙基-[4-(4-甲氧基-苯基偶氮)-3-甲基-苯基]-氨基}-乙酯(MAMP)的明确定义的共聚物偶氮苯基是通过可逆的加成-断裂链转移聚合(RAFT)合成的。具有不同含量的偶氮苯部分的共聚物,例如。 G。通过改变MAMP和MMA的进料摩尔比,获得从12mol%到100mol%的摩尔比。通过改良的Kelen-Tüdos方法测量和计算这两种单体的反应率。通过差示扫描量热法(DSC)测量共聚物的玻璃化转变温度。在室温下研究了共聚物中偶氮苯部分的光诱导反式-顺式异构化。由功能共聚物浇铸的薄膜的特征在于光致双折射和表面起伏光栅(SRG)。

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