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某些芳香羧酸盐镨配合物在紫外和可见光区域的双荧光转换

Double fluorescence conversion in ultraviolet and visible region for some praseodymium complexes of aromatic carboxylates.

作者信息

Yan Bing, Wang Wei-Jing, Song Yi-Shan

机构信息

Department of Chemistry, Tongji University, Shanghai, 200092, People's Republic of China.

出版信息

J Fluoresc. 2006 Jul;16(4):495-500. doi: 10.1007/s10895-006-0083-y. Epub 2006 Jun 15.

Abstract

Four praseodymium complexes of aromatic carboxylates (benzoate, 4-tert-butylbenzoate, 2-benzoylbe-noate, and benzimidazole-5-carboxylate) have been synthesized and characterized, whose photophysical properties have been studied with ultraviolet spectra, phosphorescence spectra, and fluorescence spectra. The fluorescent emission spectra of all praseodymium complexes show two emission peaks under the excitation band of 245 nm at about 395 and 595 nm respectively, while one peak under 415 nm at about 595 nm, which attributed to be 1S0 --> 1I6 (395 nm) transition and the characteristic emission 1D2 --> 3H4 (595 nm) transition of Pr3+ ion. The 1S0 --> 1I6 transition can be ascribed as the transition of charge transfer state, and the 1D2 --> 3H4 can be further proved that there exists an antenna effect in the fluorescence of praseodymium with aromatic carboxylic acids. In conclusion, the praseodymium complexes systems can realize the double fluorescent conversion in both ultraviolet and visible region and can be further studied the application of this conversion.

摘要

已合成并表征了四种镨的芳香羧酸盐配合物(苯甲酸盐、4-叔丁基苯甲酸盐、2-苯甲酰苯甲酸酯和苯并咪唑-5-羧酸盐),并通过紫外光谱、磷光光谱和荧光光谱对其光物理性质进行了研究。所有镨配合物的荧光发射光谱在245nm激发带分别在约395和595nm处显示两个发射峰,而在415nm激发下在约595nm处有一个峰,这归因于Pr3+离子的1S0→1I6(395nm)跃迁和特征发射1D2→3H4(595nm)跃迁。1S0→1I6跃迁可归因于电荷转移态的跃迁,1D2→3H4跃迁可进一步证明镨与芳香羧酸的荧光中存在天线效应。总之,镨配合物体系可在紫外和可见光区域实现双荧光转换,可进一步研究这种转换的应用。

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