Fluorescent “OFF–ON” Sensors for the Detection of Sn2+ Ions Based on Amine-Functionalized Rhodamine 6G
Balamurugan Rathinam, Vajjiravel Murugesan, Bo‐Tau Liu
Abstract
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.