SYNTHESIS AND PHOTOVOLTAIC PROPERTIES OF SYMMETRIC BIS-AZOMETHINES WITH ACCEPTOR SUBSTITUENTS IN THE 4,4'-POSITION

V. Ovdenko, D. Vyshnevskyi, S. Studzinsky, N. Davidenko
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Abstract

Two new symmetric azomethine dyes capable of photoinduced isomerization were synthesized by condensing symmetric bis-aldehyde (obtained by the reaction of epichlorohydrin with 4-oxybenzaldehyde) with 4-nitroaniline and 4-chloroaniline, respectively. The yield of the target products decreases with the transition from nitro-substituted azomethine to chlorine-substituted. This is due to the greater basicity of the starting amines with nitro-substitution when increasing the acceptor force of the substituent complicates the course of the reaction. Azomethines are characterized by absorption with a maximum at 400–410 nm, which makes them sensitive to radiation with a blue component of the spectrum. The photoelectric properties of azomethines upon irradiation were investigated by the method of measuring the surface potential with the help of a Kelvin dynamic probe. The maximum value of the electric potential of the photosensitive films free surface during irradiation with white LED at I = 60 W/m2 is about 270 mV in the case of azomethine with a nitro group in the 4,4' position and about 125 mV in the case of azomethine with chlorine as a substituent. That is, the magnitude of the electric potential of the free surface decreases approximately twice during the transition from nitro substituent to chlorine. This may be explained by the fact that the photoinduced changes in azomethine with a higher acceptor substituent flow more quickly and with greater efficiency. But at the same time, the reverse changes when turning off the light are just as fast. For chlorine substituted azomethine samples, the reverse process proceeds rather slowly, which may indicate greater stability over time of the photochemically modified form in case of chlorine substitution compared to the nitro-substituted analogue. Thus, the synthesized azomethines can be used in the development of new photovoltaic media and recording media for optical information recording.
具有4,4'位受体取代基的对称双偶氮亚胺的合成及光伏性质
以对称二醛(由环氧氯丙烷与4-氧苯甲醛反应得到)与4-硝基苯胺和4-氯苯胺分别缩合,合成了两种新的光致异构化对称亚甲基染料。目标产物的产率随着硝基取代亚甲基向氯取代亚甲基的转变而降低。这是由于当增加取代基的受体力使反应过程复杂化时,以硝基取代的起始胺的碱度更大。偶氮亚胺的特点是在400-410 nm处具有最大的吸收,这使得它们对光谱中蓝色成分的辐射敏感。采用开尔文动态探针测量表面电位的方法研究了辐照后偶氮亚胺的光电性质。在I = 60 W/m2的白光LED照射下,具有4,4'位硝基的亚甲基光敏膜自由表面电势最大值约为270 mV,具有氯取代基的亚甲基光敏膜自由表面电势最大值约为125 mV。也就是说,在从硝基取代基到氯基的转变过程中,自由表面的电势大小减小了大约两倍。这可以解释为具有较高受体取代基的亚甲基的光致变化流动更快,效率更高。但与此同时,当关灯时,相反的变化也一样快。对于氯取代的亚甲基样品,相反的过程进行得相当缓慢,这可能表明,在氯取代的情况下,与硝基取代的类似物相比,光化学修饰形式随着时间的推移具有更大的稳定性。因此,所合成的偶氮亚胺可用于开发新型光电介质和光信息记录介质。
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