Lanthanide Coordination Polymer Nanoparticles for Sensing of Mercury(II) by Photoinduced Electron Transfer

被引:239
作者
Tan, Hongliang [1 ]
Liu, Baoxia [1 ]
Chen, Yang [1 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Jiangsu, Peoples R China
关键词
coordination polymer nanoparticles; photoinduced electron transfer; Hg2+; sensors; METAL-ORGANIC FRAMEWORKS; COLORIMETRIC DETECTION; LUMINESCENT PROBES; IONS; HG2+; RECOGNITION;
D O I
10.1021/nn304469j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The metal-organic coordination polymers at the nanoscale have emerged as attractive nanomaterials due to their tunable nature. In this work, we for the first time prepared an adenine-based lanthanide coordination polymer nanoparticle (CPNP) with fluorescence sensing function. This kind of CPNP was composed of adenine, terbium ion (Tb3+), and dipicolinic acid (DPA) as an auxiliary linking molecule that can sensitize the fluorescence of Tb3+. The fluorescence of the CPNPs is very weak due to the existence of photoinduced electron transfer (PET) from adenine to DPA, which prevents the intramolecular energy transfer from DPA to Tb3+, leading to the quench of fluorescence of the CPNPs. In the presence of Hg2+, however, significant enhancement in the fluorescence of CPNPs was observed because of the suppression of the PET process by the coordination of Hg2+ with adenine. As a kind of Hg2+ nanosensor, the CPNPs exhibit excellent selectivity and ultrahigh sensitivity up to the 0.2 nM detection limit. The CPNPs also possess an approximately millisecond-scale-long fluorescence lifetime due to the inclusion of Tb3+ ions. We envision that the CPNPs could find great potential applications in ultrasensitive time-resolved fluorometric assays and biomedical imaging in the future owing to their long emission lifetimes, excellent dispersion, and stability in aqueous solution.
引用
收藏
页码:10505 / 10511
页数:7
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