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Two-photon absorption properties of (N-carbazolyl)-stilbenes

机译:(N-咔唑基)-Stilbenes的双光子吸收性能

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We have studied the two-photon absorption (TPA) and fluorescence properties of a series of phenylpolyenes with N-carbazolyl as donor end-groups in symmetric positions. The symmetric substitution of carbazole end-groups enhances the photostability of the molecules and maintains high TP coefficients. High fluorescence quantum efficiencies have been measured. The results suggest that TP chromophores with carbazole donors are promising materials for applications in two-photon imagin and sensitization. The study covers a broad excitation spectrum from 580nm to 820nm using a picosecond optical parametric source. We take advantage of the correlation between idler and signal waves emerging from the parametric generator and calibrate our results against Rhodamine B for which reliable data is available in the long wave range.
机译:我们已经研究了一系列苯基聚解的双光子吸收(TPA)和荧光性质,其用N-咔唑基作为对称位置的供体末端基团。咔唑末端基团的对称取代增强了分子的光稳定性并保持高TP系数。已经测量了高荧光量子效率。结果表明,具有咔唑供体的TP发色团是在两光子Imagin和敏化中的应用的有希望的材料。该研究涵盖了使用Pic秒光学参数源的580nm至820nm的宽激励光谱。我们利用来自参数发生器出现的惰轮和信号波之间的相关性,并校准我们对罗达胺B的结果,用于长波范围内可靠的数据。

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