Chemosensors (Feb 2022)

Fluorescent “OFF–ON” Sensors for the Detection of Sn<sup>2+</sup> Ions Based on Amine-Functionalized Rhodamine 6G

  • Balamurugan Rathinam,
  • Vajjiravel Murugesan,
  • Bo-Tau Liu

DOI
https://doi.org/10.3390/chemosensors10020069
Journal volume & issue
Vol. 10, no. 2
p. 69

Abstract

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These structurally isomeric rhodamine 6G-based amino derivatives are designed to detect Sn2+ ions. The receptors exhibit rapid fluorescent “turn-on” responses towards Sn2+. The absorption (530 nm) and fluorescent intensity (551 nm) of the receptors increase when increasing the concentration of Sn2+. The hydrazine derivative exhibits more rapid sensitivity towards Sn2+ than the ethylene diamine derivative, indicating that the presence of an alkyl chain in the diamine decreases the sensitivity of the receptors towards Sn2+. The presence of carbonyl groups and terminal amino groups strongly influences the sensitivity of the chemosensors toward Sn2+ by a spirolactam ring-opening mechanism. The receptors exhibit 1:1 complexation with Sn2+ as evidenced by Job plot, and the corresponding limit of detection was found to be 1.62 × 10−7 M. The fluorescence images of the receptors and their complexes reveal their potential applications for imaging of Sn2+ in real/online samples.

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