Selective and pH‐Independent Detection of Ba2+ in Water by a Benzo‐21‐crown‐7‐Functionalized BODIPY

Author:

Sprenger Tobias1,Schwarze Thomas2ORCID,Müller Holger2,Sperlich Eric2,Holdt Hans‐Jürgen2,Nazaré Marc3,Hentsch Axel3,Eidner Sascha4,Kraft Ronja4,Kumke Michael U.4

Affiliation:

1. Medizinische Fakultät HMU Potsdam Olympischer Weg 1 14471 Potsdam Germany

2. Institut für Chemie, Anorganische Chemie Universität Potsdam Karl-Liebknecht-Str. 24–25 14476 Golm Germany

3. Leibniz-Institut für Molekulare Pharmakologie (FMP) Robert-Rössle-Str. 10 13125 Berlin-Buch Germany

4. Institut für Chemie, Physikalische Chemie Universität Potsdam Karl-Liebknecht-Str. 24–25 14476 Golm Germany

Abstract

AbstractHerein, we report on highly Ba2+ selective fluorescence sensing in water by a fluorescent probe consisting of a benzo‐21‐crown‐7 as a Ba2+ binding unit (ionophore) and a tetramethylated BODIPY fluorophore as a fluorescence reporter. This fluorescent probe showed a Ba2+ induced fluorescence enhancement (FE) by a factor of 12±1 independently of the pH value and a high Ba2+ sensitivity with a limit of detection (LOD) of (17.2±0.3) μM. Moreover, a second fluorescent probe consisting of the same BODIPY fluorophore, but a benzo‐18‐crown‐6 as a cation‐responsive binding moiety, showed an even higher FE upon Ba2+ complexation by a factor of 85±3 and a lower LOD of (13±3) μM albeit a lower Ba2+ selectivity. The fluorescence sensing mechanism of Ba2+ was further investigated by time‐resolved fluorescence as well as transient absorption spectroscopy (TAS) and it turned out that within these probes a blocking of a photoinduced electron transfer (PET) by Ba2+ is very likely responsible for the FE.

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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