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Synthesis and characterization of azobenzene based compounds for their photo-induced effects

机译:偶氮苯类化合物的光诱导作用及其合成与表征

摘要

Photonics, in which photo-induced effect can be controlled by light as stimulus has attracted a lot of attentions due to their variety of applications ranging from photonic industries to electronic computer technologies. Among them, optical storage system is a unique subject in which light illumination can alter the molecular structure drastically. These tuning structural property relations are extremely important to fabricate the optical storage devices. Although various light sensitive azobenzene derivatives are available in literature, no detail investigation has been carried out in terms of their controllable photo-induced effects with respect to structure-property relationship. Organic synthesis is a perfect tool, which can manipulate the molecular structure easily to get the desired compounds of azobenzene derivatives by incorporating several functional groups in the molecular architecture. This study gives an idea about the molecular structure and functional groups in azobenzene compounds to vary the time duration of photo-induced effects. Then, evaluated the photo-induced effects and liquid crystalline properties of the synthesized azobenzene compounds such as amides, aliphatic/aromatic spacers, phenol/anisol, fluorine with esters, isoflavones, halogens and siloxanes. The variation observed in the photo-induced effects of the respective compounds in terms of physical and chemical properties such as hydrogen bonding , electron withdrawing effect, hyper conjugation, flexibility, polarity, molecular symmetry, asymmetric effect, photo-crosslinking and electropositive nature. Particularly, amides, aliphatic/aromatic spacers, phenol/anisol, fluorine substituted esters, halogens and siloxane substituted azobenzene derivatives showed long duration of thermal back relaxation due to the action of hydrogen bonding effect, flexibility, polarity, molecular symmetry, photo-crosslinking and electropositive nature. These compounds with long duration of thermal back relaxation are suitable for optical storage technology. On the other hand, isoflavone based azobenzene compounds showed fast photo-response, due to the presence of asymmetric effect in the molecular system. Hence, these isoflavone based azobenzene derivatives are useful to fabricate molecular switches. However, other light sensitive compounds such as, chalcones, stilbenes and imines exhibited lack of photo-induced effects compare to azobenzene compounds. Tacitly, chalcones, stilbenes and imine did not show interesting photo-induced effects as compared to azobenzene compounds. Thus, azobenzene derivatives with various molecular structures and functional groups are suitable to evaluate the photo-induced effects. Also, azobenzene compounds are suitable for optical storage device fabrication. Nevertheless, amides, aliphatic/aromatic spacers, fluorine substituted esters and halogens substituted azobenzene derivatives were liquid crystals. Particularly, these compounds showed nematic and smectic liquid crystal phases. But, chalcones, stilbenes and imine derivatives did not showed liquid crystallinity. The optical storage device was fabricated using 20a, azobenzene compound substituted by olefinic group. The resolution and sharp edges of the letters and pattern, which are stored in the fabricated optical storage device, are showing the novelty of this work. Thus, azobenzene derivatives can be extensively useful for photo-induced optical storage technology.
机译:在光子学中,由于光的刺激,可以通过光来控制光致效应,这是由于光子学的应用范围广泛,从光子工业到电子计算机技术,引起了人们的广泛关注。其中,光学存储系统是一个独特的主题,其中光照射可以极大地改变分子结构。这些调整结构特性关系对于制造光存储装置非常重要。尽管在文献中可获得各种光敏偶氮苯衍生物,但尚未就其关于结构-性质关系的可控制的光诱导效应进行详细研究。有机合成是一种完美的工具,通过在分子结构中引入多个官能团,可以轻松地控制分子结构以获得所需的偶氮苯衍生物化合物。这项研究给出了关于改变偶氮苯化合物光诱导作用持续时间的分子结构和官能团的想法。然后,评估了合成的偶氮苯化合物(如酰胺,脂族/芳族间隔基,苯酚/苯酚,氟与酯,异黄酮,卤素和硅氧烷)的光诱导效应和液晶性能。在诸如氢键,吸电子效应,超共轭,柔韧性,极性,分子对称,不对称效应,光交联和正电性等物理和化学性质方面,观察到的各化合物在光诱导作用中的变化。特别是,酰胺,脂族/芳族间隔基,苯酚/苯甲醚,氟取代的酯,卤素和硅氧烷取代的偶氮苯衍生物由于氢键作用,柔韧性,极性,分子对称性,光交联以及正电性质。这些化合物具有长时间的热反向弛豫,适用于光学存储技术。另一方面,基于异黄酮的偶氮苯化合物由于在分子系统中存在不对称作用而显示出快速的光响应。因此,这些基于异黄酮的偶氮苯衍生物可用于制造分子开关。然而,与偶氮苯化合物相比,其他光敏化合物(如查耳酮,丁苯甲醚和亚胺)表现出缺乏光诱导作用。显然,与偶氮苯化合物相比,查耳酮,丁苯醚和亚胺没有表现出有趣的光诱导作用。因此,具有各种分子结构和官能团的偶氮苯衍生物适用于评估光致效应。同样,偶氮苯化合物也适用于光学存储设备的制造。然而,酰胺,脂族/芳族间隔基,氟取代的酯和卤素取代的偶氮苯衍生物是液晶。特别地,这些化合物显示出向列和近晶液晶相。但是,查耳酮,丁苯醚和亚胺衍生物没有显示出液晶性。使用被烯烃基取代的20a偶氮苯化合物制造光存储装置。存储在制造的光学存储设备中的字母和图案的分辨率和锐利边缘显示了这项工作的新颖性。因此,偶氮苯衍生物可广泛用于光诱导光存储技术。

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    Yuvaraj A. R.;

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  • 年度 2016
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