An infrared study of azobenzene photoisomerization in a polymer matrix

John D. Webb , Hermann H. Neidlinger , John S. Connolly
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引用次数: 9

Abstract

A technique involving in situ Fourier transform infrared spectroscopy in the reflection-absorbance mode (FTIR-RA) was used to study photoisomerization and the thermal back reaction of a solid solution of trans-azobenzene in a poly(methyl methacrylate) (PMMA) matrix. The FTIR-RA method, although inherently less sensitive than UV spectrophotometry, affords better resolution of specific isomer absorbances and permits simultaneous observation of changes in the matrix and chromophore vibrational bands. A change in the orientation of the acrylate side groups in isotactic sequences of the atactic PMMA matrix was observed to coincide with photoisomerization of the dissolved azobenzene. This orientational change is a direct confirmation of the matrix effect on isomerization reactions postulated by other researchers. The frequencies of the most intense vibrational absorption bands in the thermally unstable cis isomer were determined. With this information, the relative quantum yields φt→cφc→t for photoisomerization of azobenzene and the half-life for thermal cis→trans isomerization were obtained and compared with literature values.

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偶氮苯在聚合物基体中光异构化的红外研究
采用原位傅里叶变换红外光谱反射-吸收模式(FTIR-RA)研究了反式偶氮苯在聚甲基丙烯酸甲酯(PMMA)基体中的光异构化和热反应。FTIR-RA方法虽然固有的灵敏度低于紫外分光光度法,但提供了更好的特定异构体吸光度分辨率,并允许同时观察基质和发色团振动带的变化。观察到无规PMMA基体等规序列中丙烯酸酯侧基取向的变化与溶解的偶氮苯的光异构化相一致。这种取向变化直接证实了其他研究人员假设的基质对异构化反应的影响。测定了热不稳定顺式异构体中最强烈的振动吸收带的频率。利用这些信息,得到了偶氮苯光异构反应的相对量子产率φt→cφc→t和热顺→反异构反应的半衰期,并与文献值进行了比较。
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