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Synthesis and luminescent properties of a novel green-emitting Tb (III) complex based on amino-modified fluorine silicone oil and isophorone diisocyanate

机译:基于氨基改性氟硅油和异佛尔酮二异氰酸酯的新型绿色发射Tb(III)配合物的合成和发光性能

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摘要

The novel luminescent polymer-rare earth complexes, denoted as (PFSi-IPDI)-Tb(III)-Phen, have been successfully synthesized and can be made into flexible films. Amino-modified fluorine silicone oil-isophorone diisocyanate (PFSi-IPDI) was used as the host macromolecular ligand, and 1, 10-Phenanthroline (Phen) as the secondary small-molecular co-ligand. The luminescent lanthanide complexes were characterized by fourier transform infrared (FITR), scanning electron microscope (SEM), thermogravimetric analysis (TGA). The luminescent properties were investigated through photoluminescence excitation (PLE) and emission (PL) spectroscopy. FTIR analysis verifies the successful preparation and integration of PFSi-IPDI to Tb3+. The comparatively uniform morphological structure can be observed in the images of SEM. The polymer-rare earth complexes display the typical luminescence emission peaks under the excitation wavelength of 330 nm. From the decay curve, the short lifetime (about 0.89 ms) is observed for (PFSi-IPDI)-Tb(III)-Phen (0.6 mol/L). Moreover, these luminescent polymer-rare earth complexes possess superior thermal stability (T-5 > 195 degrees C). All the interesting results suggest the potential application of the luminescent polymer-rare earth complexes in green-emitting luminescent materials under high temperature. (C) 2017 Elsevier B.V. All rights reserved.
机译:已成功合成了新型发光聚合物-稀土复合物,称为(PFSi-IPDI)-Tb(III)-Phen,可制成柔性薄膜。氨基改性的氟硅油-异佛尔酮二异氰酸酯(PFSi-IPDI)被用作主体大分子配体,而1,10-邻菲咯啉(Phen)被用作次要小分子共配体。通过傅立叶变换红外(FITR),扫描电子显微镜(SEM),热重分析(TGA)对发光镧系元素进行了表征。通过光致发光激发(PLE)和发射(PL)光谱研究了发光性质。 FTIR分析验证了PFSi-IPDI与Tb3 +的成功制备和集成。在SEM图像中可以观察到相对均匀的形态结构。聚合物-稀土配合物在330 nm的激发波长下显示出典型的发光峰。从衰减曲线可以看出,(PFSi-IPDI)-Tb(III)-苯酚(0.6 mol / L)的寿命短(约0.89 ms)。而且,这些发光聚合物-稀土配合物具有优异的热稳定性(T-5> 195摄氏度)。所有有趣的结果表明,在高温下,发光聚合物-稀土配合物在绿色发光材料中的潜在应用。 (C)2017 Elsevier B.V.保留所有权利。

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