偶氮苯
自由基聚合
高分子化学
胶粘剂
聚合
光异构化
部分
化学
原子转移自由基聚合
材料科学
光化学
单体
丙烯酸酯
有机化学
复合材料
聚合物
异构化
催化作用
图层(电子)
作者
Shotaro Ito,Aishi Yamashita,Haruhisa Akiyama,Hideyuki Kihara,Masaru Yoshida
出处
期刊:Macromolecules
[American Chemical Society]
日期:2018-04-16
卷期号:51 (9): 3243-3253
被引量:129
标识
DOI:10.1021/acs.macromol.8b00156
摘要
Atom transfer radical polymerization was employed to induce the living polymerization of an azobenzene-containing monomer, 10-[4-(4-hexylphenylazo)phenoxy]decyl acrylate, with the resulting polyacrylate and the corresponding polymethacrylate undergoing a reversible solid–liquid phase transition under isothermal conditions caused by the photoinduced change of the azobenzene moiety shape. Irradiation-induced property changes were investigated by nuclear magnetic resonance, ultraviolet–visible (UV–vis) absorption spectroscopy, and dynamic viscoelasticity measurements, with focus on the effects of the main chain chemical structure and molecular weight. Azobenzene moiety photoisomerization and the concomitant phase transition were faster for the polyacrylate than for the polymethacrylate, which indicated the strong influence of the main chain structure. Finally, phototuning of the adhesion strength using azopolymer-bonded glass substrates was studied by single lap shear tests, with the maximum adhesion strength of >3 MPa being comparable to that of commercial hot-melt adhesives. Irradiation with UV light for only 15 s lowered the adhesion strength to <0.2 MPa, allowing easy debonding upon the application of a small force.
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