Photocontrolled Reversible Luminescent Lanthanide Molecular Switch Based on a Diarylethene-Europium Dyad

被引:42
作者
Cheng, Hong-Bo [1 ]
Hu, Guo-Fei [2 ]
Zhang, Zhan-Hui [2 ]
Gao, Liang [1 ]
Gao, Xingfa [1 ]
Wu, Hai-Chen [1 ]
机构
[1] Chinese Acad Sci, Inst High Energy Phys, Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100049, Peoples R China
[2] Hebei Normal Univ, Coll Chem & Mat Sci, Shijiazhuang 050024, Peoples R China
基金
中国国家自然科学基金;
关键词
RESPONSIVE MATERIALS; METAL COORDINATION; ENERGY-TRANSFER; LIVING CELLS; LOGIC GATES; PHOTOCHROMISM; COMPLEXES; DERIVATIVES; NANOPARTICLES; MODULATION;
D O I
10.1021/acs.inorgchem.6b01009
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new europium complex coordinated between a Eu(III) ion and an unsymmetrical diarylperfluorocyclopentene yields a light-controlled diarylethene europium dyad, DAE@TpyEu(tta)(3), whose photophysical properties can be reversibly switched by optical stimuli. When DAE@TpyEu(tta)3 is exposed to 365 nm UV light, an efficient intramolecular photochromic fluorescence resonance energy transfer (pc-FRET) occurs between the emission of the Eu3+ donor (D) and the absorption of the diarylethene acceptor (A) in closed-form DAE@TpyEu(tta)3 accompanied by luminescence quenching. However, the pc-FRET process could be effectively inhibited by visible light (lambda > 600 nm) irradiation, and the lanthanide emission of DAE@TpyEu(tta)3 is rapidly recovered. Furthermore, this luminescent lanthanide molecular switch could serve as a highly reliable and sensitive "turn on" fluorescent marker in living cells irradiated by red light without any optical interference.
引用
收藏
页码:7962 / 7968
页数:7
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