Abstract − Analytical Sciences, 32(11), 1223 (2016).
A Rhodamine-based Dual Chemosensor for the Simultaneous Detection of Fe3+ and Cu2+
  Tao LAN,*1,*2,*3 Feng-He WANG,*1,*2 Xing-Jun XI,*3 Chun-Wen CHENG,*1,*2,*4 Wu LEI,*4 Ming-Zhu XIA,*4 and Feng-Yun WANG*4
  *1 Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, School of Environment, Nanjing Normal University, Nanjing 210023, PR China
*2 Jiangsu Center for Collaborative Innovation in Geographical Information Resource Development and Application, School of Geography Science, Nanjing 210023, PR China
*3 China National Institute of Standardization, Beijing 100191, PR China
*4 Industrial Chemical Institute, Nanjing University of Science and Technology, Nanjing 210094, PR China
  *2 Jiangsu Center for Collaborative Innovation in Geographical Information Resource Development and Application, School of Geography Science, Nanjing 210023, PR China
*3 China National Institute of Standardization, Beijing 100191, PR China
*4 Industrial Chemical Institute, Nanjing University of Science and Technology, Nanjing 210094, PR China
A Rhodamine-based dual chemosensor L1 for simultaneously detecting Fe3+ and Cu2+ was designed and synthesized.  The spectroscopic properties of L1 were analyzed, and its recognition mechanism was speculated.  We found that the addition of Fe3+ induced a great fluorescence enhancement, while Cu2+ induced a strong UV-Vis absorption enhancement.  The results revealed that L1 was highly selective for recognizing Fe3+ and Cu2+ in UV-Vis spectroscopy in CH3OH–H2O (1/1, v/v, pH 7.2) with the interference of other metal ions.  A good linear relationship between the fluorescence intensities of L1 and the concentration of Fe3+, as well as the UV-Vis absorption intensities of L1 and the concentration of Cu2+ was observed, respectively.  The detection limit was 9.2  ×  10−8 M (5.5 μg/L) for Fe3+ and 3.8  ×  10−8 M (2.4 μg/L) for Cu2+, respectively.  The detection capacity for targeted metal ions of Fe3+ and Cu2+ were studied, which are less than 5 min.  Job’s plot method for L1 with Fe3+ and ESI-MS for L1 with Cu2+ indicated a 1:1 stoichiometry in the complex.  The results may provide an effective strategy for the design of new dual chemosensors for the rapid detection of targeted metal ions.
  
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