光谱学与光谱分析
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铒有机配合物的合成、表征与近红外发光性能研究
王怀善1 ,钱国栋1* ,王民权1 ,骆永石2 ,林久令2
1. 浙江大学材料科学与工程系,硅材料国家重点实验室,浙江 杭州 310027 2. 中国科学院长春光学精密机械与物理研究所,激发态物理重点实验室,吉林 长春 130021
Synthesis, Characterization and NIR Luminescence Properties of Erbium Organic Complexes
WANG Huai-shan1 , QIAN Guo-dong1 * , WANG Min-quan1 ,LUO Yong-shi2 , LIN Jiu-ling2
1. Department of Materials Science & Engineering, State Key Lab of Silicon Materials, Zhejiang University, Hangzhou 310027,China 2. Key Laboratory of Excited State Processes, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun 130021, China
摘要 : 合成了乙酰基丙酮(AcAc)和二苯甲酰基甲烷(DBM)的水合二元铒配合物以及乙酰基丙酮、二苯甲酰基甲烷和三氟乙酰基丙酮(TFA)分别与1,10-邻菲罗啉(Phen)的三元铒配合物,并经元素分析确认;表征了配合物的紫外-可见吸收光谱和红外吸收光谱;探讨了铒配合物的近红外发光性能,并对不同配体对发光性能的影响进行分析比较。结果表明Er(AcAc)3 Phen三元配合物是所研究的几种配合物中近红外发光性能最优的。
关键词 :铒有机配合物;近红外发光;光谱表征
Abstract :Several erbium organic complexes, hydrated erbium binary complexes with acetylacetone (AcAc) or dibenzoylmethane (DBM), erbium ternary complexes derived from 1,10-phenanthroline (Phen) with acetylacetone (AcAc), dibenzoylmethane (DBM) or trifluoroacetylacetone (TFA), were synthesized and identified by elemental analysis. The UV-Vis absorption and FTIR spectra measurements have been employed for all the erbium complexes. Near infrared (NIR) photoluminescence properties, such as luminescence intensity and effective bandwidth, of the erbium complexes were also studied. As a result, the erbium ternary complex with AcAc and Phen exhibits the most excellent luminescence properties among those investigated complexes.
Key words :Erbium organic complex;NIR photoluminescence;Spectroscopic characterization
收稿日期: 2003-09-20
修订日期: 2004-02-06
通讯作者:
钱国栋
引用本文:
王怀善1 ,钱国栋1* ,王民权1 ,骆永石2 ,林久令2 . 铒有机配合物的合成、表征与近红外发光性能研究[J]. 光谱学与光谱分析, 2005, 25(03): 387-390.
WANG Huai-shan1 , QIAN Guo-dong1 * , WANG Min-quan1 ,LUO Yong-shi2 , LIN Jiu-ling2 . Synthesis, Characterization and NIR Luminescence Properties of Erbium Organic Complexes . SPECTROSCOPY AND SPECTRAL ANALYSIS, 2005, 25(03): 387-390.
链接本文:
https://www.gpxygpfx.com/CN/Y2005/V25/I03/387
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