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1,2,4-三唑并[3,4-b]-1,3,4-噻二唑衍生物及其铽配合物的合成与荧光性质

Synthesis and fluorescence properties of 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazol derivatives and their terbium complexes.

作者信息

Zhang Wu, Chai Yuchao, Li Kangyun, Chen Yanwen, Yan Dong, Guo Dongcai

机构信息

School of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, China.

出版信息

Luminescence. 2014 Dec;29(8):1113-22. doi: 10.1002/bio.2668. Epub 2014 May 21.

Abstract

Eight novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazol derivatives have been designed and synthesized, and their corresponding Tb(3+) complexes were also prepared successfully. The fluorescence properties and fluorescence quantum yields of the target complexes were investigated, the results showed that the ligands were an efficient sensitizer for Tb(3+) luminescence, and the target complexes exhibited characteristic fluorescence emissions of Tb(3+) ion. The fluorescence intensity of the complex substituted by chlorine was stronger than that of other complexes. The substituents' nature has a great effect upon the electrochemical properties of the target complexes. The results showed that the introduction of the electron-withdrawing groups tended to decrease the oxidation potential and highest occupied molecular orbital energy levels of the target Tb(3+) complexes; however, introduction of the electron-donating groups can increase the corresponding complexes' oxidation potential and highest occupied molecular orbital energy levels.

摘要

设计并合成了八种新型的1,2,4-三唑并[3,4-b]-1,3,4-噻二唑衍生物,并成功制备了它们相应的Tb(3+)配合物。研究了目标配合物的荧光性质和荧光量子产率,结果表明配体是Tb(3+)发光的有效敏化剂,目标配合物表现出Tb(3+)离子的特征荧光发射。氯取代的配合物的荧光强度比其他配合物更强。取代基的性质对目标配合物的电化学性质有很大影响。结果表明,吸电子基团的引入倾向于降低目标Tb(3+)配合物的氧化电位和最高占据分子轨道能级;然而,给电子基团的引入可以提高相应配合物的氧化电位和最高占据分子轨道能级。

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