Recognition of Hg2+ and Cr3+ in Physiological Conditions by a Rhodamine Derivative and Its Application as a Reagent for Cell-Imaging Studies

• Published in: Inorganic chemistry Vol. 51; no. 1; pp. 336 - 345
• Main Authors: Saha, Sukdeb, Mahato, Prasenjit, G, Upendar Reddy, Suresh, E, Chakrabarty, Arindam, Baidya, Mithu, Ghosh, Sudip K, Das, Amitava
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 02.01.2012
• Subjects: Cell Line, Tumor; Cell Survival; Chromium - analysis; Fluorescent Dyes - chemical synthesis; Fluorescent Dyes - chemistry; Humans; Mercury - analysis; Microscopy, Fluorescence - methods; Models, Molecular; Quinolines - chemical synthesis; Quinolines - chemistry; Rhodamines - chemical synthesis; Rhodamines - chemistry
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/ic2017243

A new rhodamine-based receptor, derivatized with an additional fluorophore (quinoline), was synthesized for selective recognition of Hg2+ and Cr3+ in an acetonitrile/HEPES buffer medium of pH 7.3. This reagent could be used as a dual probe and allowed detection of these two ions by monitoring changes in absorption and the fluorescence spectral pattern. In both instances, the extent of the changes was significant enough to allow visual detection. More importantly, the receptor molecule could be used as an imaging reagent for detection of Hg2+ and Cr3+ uptake in live human cancer cells (MCF7) using laser confocal microscopic studies. Unlike Hg(ClO4)2 or Hg(NO3)2 salts, HgCl2 or HgI2 failed to induce any visually detectable change in color or fluorescence upon interaction with L 1 under identical experimental conditions. Presumably, the higher covalent nature of HgII in HgCl2 or HgI2 accounts for its lower acidity and its inability to open up the spirolactam ring of the reagent L 1 . The issue has been addressed on the basis of the single-crystal X-ray structures of L 1 ·HgX2 (X– = Cl– or I–) and results from other spectral studies.