镧系元素
化学
环十二烷
铽
阳离子聚合
铕
部分
猝灭(荧光)
光化学
激发态
荧光
系统间交叉
发光
镥
碘化物
组合化学
立体化学
无机化学
单重态
离子
有机化学
钇
核物理学
物理
量子力学
光电子学
氧化物
作者
Robert A. Poole,Gabriella Bobba,Martin J. Cann,Juan C. Frías,David Parker,Robert D. Peacock
摘要
The synthesis and photophysical characterisation are reported of a series of cationic, neutral and anionic europium and terbium complexes based on structurally related, nonadentate ligands based on the cyclen macrocycle. Each complex incorporates a tetraazatriphenylene moiety and overall absolute emission quantum yields are in the range 15–40% in aerated aqueous media. Dynamic quenching of the lanthanide excited state occurs with electron-rich donors, e.g. iodide, ascorbate and urate, and a mechanistic interpretation is put forward involving an electron transfer process. The cationic lanthanide complexes are taken up by NlH/3T3 cells and tend to localise inside the cell nucleus.
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