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Moore, E.G., Bernhardt, P.V., Fuerstenberg, A., Riley, M.J., Smith, T.A. and Vauthey, E. (2005) Tuning the Photophysical Behavior of Luminescent Cyclam Derivatives by Cation Binding and Excited State Redox Potential. Journal of Physical Chemistry A, 109, 3788-3796. https://doi.org/10.1021/jp044221t

has been cited by the following article:

• TITLE: Study of the Double Fluorescence of a New Anthracene (13)aneN4

  AUTHORS: Rim Zaari Jabri, Alla Lemeune, Abdellah Zrineh, Franck Denat

  KEYWORDS: Tetraazacycloalcane, Fluorescence, Charge Transfer, pH Sensor, Double Fluorescence, Anthracene, Metals Coordination

  JOURNAL NAME: Open Access Library Journal, Vol.10 No.9, September 13, 2023

  ABSTRACT: In this work, a new ligand (13)aneN4 with anthracene was synthesized and characterized by mass spectrometry, NMR, UV-Vis and fluorescence spectroscopies. The ligand has a double fluorescence explained by the presence of a photoinduced charge transfer. The fluorescence spectra in various solvents show an increase in the intensity of the band charge transfer with solvent polarity and a decrease in the intensity of the band of the locally excited state of anthracene. The fluorescence studies was also performed in order to study the influence of pH on the charge transfer band, therefore, the ligand can be considered as “pH sensor” in the pH range (10 - 11). Finally, we show that the dual fluorescence intensity of the complex L-metal could be influenced by the coordination of the exocyclic nitrogen atom to the central metal.