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首页> 外文期刊>Dyes and Pigments >Deep blue fluorescent 2,5-bis(phenylsilyl)-substituted 3,4-diphenylsiloles: Synthesis, structure and aggregation-induced emission
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Deep blue fluorescent 2,5-bis(phenylsilyl)-substituted 3,4-diphenylsiloles: Synthesis, structure and aggregation-induced emission

机译:深蓝色荧光2,5-双(苯基甲硅烷基)取代的3,4-二苯基甲硅烷:合成,结构和聚集诱导的发射

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摘要

A series of 2,5-bis(phenylsilyl)-substituted 3,4-diphenylsiloles were synthesized by one pot reaction in moderate yields (47—66%) and characterized by NMR, Mass and elemental analysis. Their crystals were grown from THF/methanol mixtures and analyzed by single-crystal X-ray diffraction. The electronic structures and energy levels were calculated by B3LYP/6-31G(d) basis set. The results show that these new siloles possess a flexible conformation with novel σ-π~* conjugation. The absorption and fluorescence spectra were measured in the solution and aggregate states. Whereas they are weakly fluorescent in solutions, they are induced to emit strong deep blue light in solid films and crystals, demonstrating an aggregation-induced emission (A1E) characteristic.
机译:通过锅反应以中等收率(47-66%)合成了一系列2,5-双(苯基甲硅烷基)取代的3,4-二苯基甲硅烷,并通过NMR,质量和元素分析对其进行了表征。它们的晶体由THF /甲醇混合物生长而成,并通过单晶X射线衍射进行分析。电子结构和能级通过B3LYP / 6-31G(d)基集计算。结果表明,这些新的小柱具有新的σ-π〜*共轭的柔性构型。在溶液和聚集态下测量吸收光谱和荧光光谱。尽管它们在溶液中的荧光较弱,但被诱导在固体膜和晶体中发出强烈的深蓝光,这表明了聚集诱导的发射(A1E)特性。

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