4.7 Article

Synthesis and evaluation of the chromo-fluorogenic recognition ability of imidazoquinoline derivatives toward ions

Journal

DYES AND PIGMENTS
Volume 122, Issue -, Pages 50-58

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2015.06.011

Keywords

Imidazoquinolines; Cation recognition; Anion recognition; Colour; Fluorescence; Proton transfer

Funding

  1. Spanish Government [MAT2012-38429-C04]
  2. Generalitat Valenciana [PROMETEO/2009/016]
  3. Spanish Ministry of Economy and Competitiveness
  4. Fundacion Carolina
  5. UPNFM-Honduras
  6. Fundacao para a Ciencia e Tecnologia (Portugal)
  7. FEDER-COMPETE through the Centro de Quimica - Universidade do Minho [PEst-C/QUI/UI0686/2013 (FCOMP-01-0124-FEDER-037302)]
  8. FCT
  9. [SFRH/BPD/79333/2011]

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Four imidazoquinolines functionalized with different carbocycles and heterocycles have been synthesized and characterized. Acetonitrile solutions of the four receptors presented absorption bands in the 330-370 nm range. The four probes were also emissive with fluorescence bands in the 390-460 nm interval. In a first step, the chromo-fluorogenic behaviour of the four probes was evaluated in the presence of selected anions. Addition of F- induced the appearance of a new red-shifted absorption band together with a moderate quenching of the fluorescence in all four receptors. In a second step, the UV-visible and emission behaviour of the four receptors in the presence of cations was tested. Addition of Hg2+, Cu2+, Co2+, Fe3+, Fe2+, Zn2+, Pb2+, Cd2+, Cr3+ and Al3+ induced a similar optical change in all four receptors (appearance of a broad red-shifted absorption band together with a remarkable quenching of the emission band). (C) 2015 Published by Elsevier Ltd.

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