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Synthesis of Carbazole-Based Monolithic and Fully Functional Polymeric Photorefractive Materials

机译:咔唑基单块全功能聚合物光折变材料的合成

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Several carbazole-based monolithic and fully functional polymeric photorefractive materials were synthesized using simple synthetic approaches. In the design and synthesis of polymers, a post-azo-coupling reaction was selected for introducing the azo chromophore to the carbazole group. Without any plasticizer, TBC energy transfer could be observed in all polymers with Tg below 100℃. The best photorefractive performance was observed with polymer 12 showing 140cm~(-1) of TBC gain and 8.3% of diffraction efficiency at zero applied electric field without any extra sensitizer. Based on the principles for organic molecules exhibiting photorefractive response, six monolithic organic compounds with push-pull structure were designed and prepared via Vilsmeier and Knovenagel reactions. All of these six monolithic compounds can form glassy state. Most of them can form films with good optical quality. Compound M2 showed the best photorefractive performance, its gain coefficient was as high as 372cm~(-1) at an external electric field of 50 V/μm.
机译:使用简单的合成方法合成了几种基于咔唑的整体式和全功能聚合物光折变材料。在聚合物的设计和合成中,选择了偶氮后偶联反应以将偶氮发色团引入咔唑基团。如果没有任何增塑剂,Tg低于100℃的所有聚合物都可以观察到TBC能量转移。聚合物12在没有任何额外的敏化剂的情况下,在零电场下表现出140cm〜(-1)的TBC增益和8.3%的衍射效率,观察到了最好的光折变性能。根据有机分子表现出光折变反应的原理,通过Vilsmeier和Knovenagel反应设计并制备了六种具有推挽结构的整体式有机化合物。所有这六个整体式化合物都可以形成玻璃态。它们中的大多数可以形成具有良好光学质量的膜。化合物M2表现出最好的光折变性能,在50 V /μm的外部电场下其增益系数高达372cm〜(-1)。

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