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Synthesis, Liquid Crystal Characterization and Photo-Switching Studies on Fluorine Substituted Azobenzene based Esters

机译:氟取代的偶氮苯基酯的合成,液晶表征和光开关研究

摘要

A series offluorinated azobenzene esters have been synthesized and studied by polarized optical microscopy (POM) and UV-Vis spectrophotometry. The–CO2C2H5group with monofluoro-substituted azobenzene exhibited nematic and smectic phases whereas difluoro-substituted azobenzene showed only the nematic phase. The addition of the electronegativefluorine atom plays an important role inudphotoisomerization of the azobenzene molecules. The monofluoro-substituted azobenzene gave strong photoisomerization in solution as compared with its diflouro counterparts. In these systems,trans–cis isomerization occurred after 4 minutes and cis–trans isomerization occurred after 22 hours which is much longer than expected forfluorine-substituted azobenzene systems. The presented results might have an influence on creating optical data storage devices.
机译:合成了一系列的氟化偶氮苯酯,并通过偏振光学显微镜(POM)和紫外可见分光光度法进行了研究。具有一氟取代的偶氮苯的–CO2C2H5基团显示向列相和近晶相,而二氟取代的偶氮苯仅显示向列相。负电性氟原子的添加在偶氮苯分子的光致异构化中起重要作用。与二氟取代偶氮苯相比,单氟取代的偶氮苯在溶液中具有很强的光异构化作用。在这些系统中,反式-顺式异构化发生在4分钟后,而顺式-反式异构化发生在22小时后,这比氟取代的偶氮苯系统的预期长得多。呈现的结果可能会对创建光学数据存储设备产生影响。

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