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Synthesis and Optical Properties of Dipolar Thiazole Derivatives Incorporating Nitro and Amino Substituents

机译:掺入硝基和氨基取代基的偶极噻唑衍生物的合成与光学性质

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We report the synthesis of two dipolar thiazole derivatives functionalized with nitro group as electron acceptor and amino group as electron donor, in order to study their optical properties in the UV-vis range. Their structures were verified by ~1H NMR, ~(13)C NMR, HRMS and FT-IR. The resulted thiazole derivatives have good thermal stability with decomposition temperature, T_d of 320.20 °C and 284 °C for compounds 1 and 2 respectively. The absorbance bands of compound 2 in the UV-vis range are more red-shifted than that of compound 1 which made compound 2 could have high potential as a great organic NLO material.
机译:我们报道了用硝基组官能化的两种双极噻唑衍生物作为电子受体和氨基作为电子供体,以研究其在UV-VIS范围内的光学性质。它们的结构〜1H NMR,〜(13)C NMR,HRMS和FT-IR验证。得到的噻唑衍生物分别具有良好的热稳定性,分解温度为320.20℃和284℃,分别为化合物1和2。在UV-VIS范围内的化合物2的吸光度带比制备化合物2的化合物1的吸光度带更加红移,这使得化合物2可以具有高潜力作为大量的有机NLO材料。

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