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2-aryloxybenzo[d]oxazoles as deep blue solid-state emitters: Synthesis, aggregation-induced emission properties and crystal structure

机译:2-芳氧基苯并[D]恶唑作为深蓝色固态发射器:合成,聚集诱导的发射性能和晶体结构

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The design and exploration of efficient organic fluorophores have attracted significant scientific interest for their various potential applications. As blue fluorescent materials are essential for the achievement of a full-color display and white emission, the development of new efficient organic blue-emitting materials is of great importance. In this work, we found that simple organic molecules 2-aryloxybenzo [d]oxazoles could act as novel organic fluorophores with special AIE properties and efficient blue fluorescent emission in the solid states. Compounds 3 and 4 possess moderately high quantum yields at 10.3% and 11.4%, respectively. The CIE coordinates indicate that most of these compounds are deep-blue emitters. The single crystal structure of compound 3 shows that it has a twisted V-shape molecular structure with J-type aggregation. Noncovalent interactions widely exist in the crystal structures, while pi-pi stacking interactions are not observed between adjacent aromatic rings. The special fluorescent properties of these new emitters could ascribe to the unique molecular packing mode in the crystal structure. This work provides a new strategy to access organic solid-state fluorophores with deep-blue emission.
机译:高效有机荧光团的设计和探索因其各种潜在的应用而引起了极大的科学兴趣。由于蓝色荧光材料对于实现全彩显示和白色发射至关重要,因此开发新型高效有机蓝色发光材料具有重要意义。在这项工作中,我们发现简单的有机分子2-芳氧基苯并[d]恶唑可以作为新型有机荧光团,具有特殊的AIE性质和高效的固态蓝色荧光发射。化合物3和4具有较高的量子产率,分别为10.3%和11.4%。CIE坐标表明,这些化合物中的大多数是深蓝色发光体。化合物3的单晶结构表明,它具有扭曲的V形分子结构和J型聚集。非共价相互作用广泛存在于晶体结构中,而相邻芳环之间未观察到π-π堆积相互作用。这些新发光体的特殊荧光性质可以归因于晶体结构中独特的分子堆积模式。这项工作为获得具有深蓝色发射的有机固态荧光团提供了一种新的策略。

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