Kursunlu, Ahmed NuriDeveci, PervinGuler, Ersin2020-03-262020-03-2620130022-23131872-7883https://dx.doi.org/10.1016/j.jlumin.2012.12.020https://hdl.handle.net/20.500.12395/29866The aryl-amine containing azacrown ether ring and alkyl-chloro boradiazaindacene (Bodipy) were synthesized by the Schiff base condensation. The absorption and emission of a novel Schiff base derivative (based on azacrown-Bodipy) were performed in presence of different cations such as Zn2+, Ga3+, Pb2+, Hg2+, NH4+ Ca2+, Cu2+, Na+, Ni2+, Cd2+ and Cr3+. The complexation property of the Schiff base was studied in dimethylformamide (DMF) by interacting azacrown-ether group and transition metal nitrates-ammonium chloride. The electrochemical behavior of the Schiff base has also been investigated by cyclic voltammetry. All experimental results indicated that the new compound acts as a selective ratiometric chemosensor for Hg2+. (C) 2012 Elsevier B.V. All rights reserved.en10.1016/j.jlumin.2012.12.020info:eu-repo/semantics/openAccessBodipyAzacrown etherChemosensorAbsorptionEmissionCyclic voltammetryArticle13643043624496245WOS:000316033000069Q1