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Synthesis and Light Induced Characteristics of Siloxane Substituted Azobenzene: An Application for Optical Storage Device

机译:硅氧烷取代的偶氮苯的合成及光诱导特性:在光存储器件中的应用

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摘要

The light induced behaviour of siloxane substituted azobenzene compounds in the presence of alkylene spacers is reported for the first time. Firstly, these photosensitive compounds were synthesized and elucidated the molecular structure by spectral analysis such as NMR, FTIR, and UV/Vis. Photoisomerization effect was evaluated in solution and also in nematic phase. The photosaturation occurred exactly at 29 seconds, whereas thermal back relaxation was observed ranging from 19.8 to 23.8 hours. Long duration of the thermal back relaxation is due to the presence of sterically hindered siloxane group substituted to the azobenzene molecules. Decrease in the duration of cis-trans isomerization was found when the number of alkylene spacers was increased. These siloxane based azobenzene derivatives are useful for the fabrication of optical storage device and molecular switches.
机译:首次报道了在亚烷基间隔基存在下硅氧烷取代的偶氮苯化合物的光诱导行为。首先,合成这些光敏化合物并通过光谱分析(例如NMR,FTIR和UV / Vis)阐明分子结构。在溶液中和向列相中评估了光异构化作用。光饱和恰好在29秒时发生,而观察到的热回驰时间为19.8至23.8小时。热背驰的持续时间长是由于存在取代有偶氮苯分子的位阻硅氧烷基团。当亚烷基间隔基的数目增加时,发现顺反异构化的持续时间减少。这些基于硅氧烷的偶氮苯衍生物可用于制造光学存储设备和分子开关。

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