Qian D J, Leng W N, Zhang Y, Chen Z, Van Houten J
Institute of Colloid and Interface Chemistry, Shandong University, Jinan, PR China.
Spectrochim Acta A Mol Biomol Spectrosc. 2000 Dec;56(14):2645-51. doi: 10.1016/s1386-1425(00)00306-1.
Some europium complexes with pyrazolone derivatives and 1,10-phenanthroline were synthesized and characterized. The europium ion was found to coordinate to O atoms of the pyrazolone derivatives and to N atoms of 1,10-phenanthroline. A strongly ligand-localized UV absorption leads to the europium-centered emissions between 580 and 750 nm which were assigned as the 5D0-->7F0,1,2,3,4 and 5D1-->7F3,4 transitions. A low site symmetry for the Eu3+ ion was confirmed from the observation of 5D0-->7F0 emission and from the splitting of the other bands. In contrast to many Eu complexes that have been investigated a rather weak emission was measured by introduction of a Schiff base to form a ternary complex with the pyrazolone derivative. The long fluorescence lifetimes of these complexes suggest an energy transfer process from ligands to Eu3+ ion through the triplet state of the ligands.
合成并表征了一些铕与吡唑啉酮衍生物和1,10 - 菲咯啉的配合物。发现铕离子与吡唑啉酮衍生物的O原子以及1,10 - 菲咯啉的N原子配位。强烈的配体局域紫外吸收导致在580至750 nm之间以铕为中心的发射,这些发射被指定为5D0→7F0,1,2,3,4和5D1→7F3,4跃迁。从5D0→7F0发射的观察以及其他谱带的分裂证实了Eu3 +离子的低位点对称性。与许多已研究的铕配合物不同,通过引入席夫碱与吡唑啉酮衍生物形成三元配合物时,测得的发射相当弱。这些配合物的长荧光寿命表明存在从配体通过配体的三重态向Eu3 +离子的能量转移过程。