Photoinduced Increase in the Conjugation Length of Polymer Chains in Blue-Phase Polydiacetylene Films based on Diacetylene Alcohol Derivatives

A. S. Alekseev, A. B. Ivanov, V. V. Klechkovskaya, M. S. Lukasov, R. M. Sarimov, T. O. Teplyakova
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Abstract

Photoinduced polymerization of Langmuir–Schaefer monolayers of four unsymmetrical hydroxyalkadiynyl N-arylcarbamate derivatives, prepared on the basis of diynes solutions with an extremely low concentration, was studied under prolonged UV irradiation. The kinetics of these diacetylene (DA) molecules films transition to the blue phase of polydiacetylenes (PDA) films, which is not characteristic of any other DA alcohol derivatives, has been studied by light absorption spectroscopy and scanning electron microscopy. The structure homogeneity of DA and PDA films was demonstrated. A continuous shift of the optical absorption band of each PDA film to the long-wavelength region of the spectrum during 60 min of UV light irradiation was found. That indicated an increase of the chains conjugation length in blue-phase PDA samples.

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光诱导增加基于二乙炔醇衍生物的蓝相聚二乙炔薄膜中聚合物链的共轭长度
摘要 在长时间紫外线照射下,研究了以浓度极低的二炔溶液为基础制备的四种不对称羟基烷二炔 N-芳基氨基甲酸酯衍生物的朗缪尔-谢弗单层的光诱导聚合。通过光吸收光谱学和扫描电子显微镜研究了这些二乙炔(DA)分子薄膜过渡到聚二乙烯(PDA)薄膜蓝相的动力学,这是其他任何二乙炔醇衍生物所不具备的。结果表明,DA 和 PDA 薄膜的结构是均匀的。在紫外光照射 60 分钟期间,发现每种 PDA 薄膜的光吸收带持续向光谱的长波长区移动。这表明蓝相 PDA 样品的链共轭长度增加了。
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