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Design, Synthesis, Investigation, and Application of a Macromolecule Photoswitch

机译:高分子光电开关的设计,合成,研究与应用

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摘要

Azobenzene (AZO) has attracted increasing interest due to its reversible structural change upon a light stimulus. However, poor fatigue durability and the photobleaching phenomenon restricts its further application. Herein, the AZO domain as a pendent group, was incorporated into copolymers, which was synthesized by radical copolymerization in the research. Structure-properties of synthesized copolymer can be adjusted by monomer ratios. Emphatically, responsive properties of copolymer in different solutions were investigated. In the DMSO solution, copolymer exhibited effective structural change, stable rapid responsive time (1 min) upon UV light at room temperature, stable relative acceptable recovery time (100 min) upon white light at room temperature, and good fatigue resistance property. In an aqueous solution, even more controllable responsive properties and fatigue resistance properties for copolymer were verified by results. More pervasively, the recovery process could be controlled by light density and temperature. In order to clarify reasons for the difference between the AZO molecule and the AZO domain of copolymer, energy barrier or interactions between single atoms or even structural units was calculated using the density functional theory (DFT). Furthermore, the status of copolymer was characterized by dynamic light scattering (DLS) and transmission electron microscope (TEM). Finally, copolymer was further functionalized with bioactive protein (concanavalin, ConA) to reduce the cytotoxicity of the AZO molecule.
机译:偶氮苯(AZO)由于在光刺激下可逆的结构变化而引起了越来越多的兴趣。但是,疲劳耐久性差和光漂白现象限制了其进一步的应用。在此,将AZO结构域作为侧基引入到共聚物中,该共聚物是通过自由基共聚在研究中合成的。合成共聚物的结构性质可以通过单体比例来调节。着重研究了共聚物在不同溶液中的响应性能。在DMSO溶液中,共聚物表现出有效的结构变化,在室温下紫外光下具有稳定的快速响应时间(1分钟),在室温下白光下具有相对稳定的相对可接受的恢复时间(100分钟),并且具有良好的抗疲劳性能。结果证明,在水溶液中,共聚物的响应性能和耐疲劳性能甚至更可控。更普遍地,可以通过光密度和温度来控制恢复过程。为了阐明AZO分子与共聚物AZO域之间差异的原因,使用密度泛函理论(DFT)计算了能垒或单个原子甚至结构单元之间的相互作用。此外,通过动态光散射(DLS)和透射电子显微镜(TEM)来表征共聚物的状态。最后,将共聚物进一步用生物活性蛋白(伴刀豆球蛋白,ConA)功能化,以减少AZO分子的细胞毒性。

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