Padhan Subrata Kumar, Mishra Vipin Kumar, Murmu Narayan, Mishra Sabyashachi, Sahu Satya Narayan
School of Chemistry, Sambalpur University Jyoti Vihar Burla-768 019 Odisha India
Department of Chemistry, Indian Institute of Technology Kharagpur - 721302 India
RSC Adv. 2020 Jul 30;10(47):28422-28430. doi: 10.1039/d0ra05357k. eCollection 2020 Jul 27.
The detection of fluoride ions in a competitive environment often poses several challenges. In this work, we have designed and synthesized a coumarin functionalized fluorescein dyad (R3) which represents an ideal through bond energy transfer (TBET) fluorophore with the coumarin unit as donor and fluorescein unit as acceptor. The bichromophoric dyad demonstrates the detection of fluoride ions in the parts per billion (ppb) concentration level (22.8 ppb) with high selectivity a TBET emission signal at 548 nm with a diagnostic bright yellow colour fluorescence output. Based on UV-visible, fluorescence, H NMR and DFT studies, it is shown that the fluoride ion induces the opening of the spirolactam ring of the fluorescein moiety and provides a π-conjugation link between the donor and acceptor units enabling a TBET phenomenon with a larger pseudo-Stokes shift of 172 nm. To the best of our knowledge, this is the first report where the fluoride ion is detected a TBET signal between the coumarin and fluorescein units in a bichromophoric dyad.
在竞争环境中检测氟离子通常会带来诸多挑战。在这项工作中,我们设计并合成了一种香豆素功能化的荧光素二元化合物(R3),它是一种理想的通过键能转移(TBET)荧光团,其中香豆素单元作为供体,荧光素单元作为受体。这种双色团二元化合物能够在十亿分之一(ppb)浓度水平(22.8 ppb)下高选择性地检测氟离子,在548 nm处有一个TBET发射信号,并伴有诊断性的亮黄色荧光输出。基于紫外可见光谱、荧光光谱、核磁共振氢谱和密度泛函理论研究表明,氟离子会诱导荧光素部分的螺内酰胺环打开,并在供体和受体单元之间提供一个π共轭连接,从而实现具有172 nm较大伪斯托克斯位移的TBET现象。据我们所知,这是首次报道在双色团二元化合物中通过香豆素和荧光素单元之间的TBET信号来检测氟离子。