EventsThe 24th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session A. General Organic Synthesis of the event The 24th International Electronic Conference on Synthetic Organic Chemistry
Published date
14 Nov, 2020
Citation
Sónia C. S. Pinto, Raquel C. R. Gonçalves, Susana P. G. Costa, M. Manuela M. Raposo, Synthesis and characterization of a meso-anthracene-BODIPY derivative for colorimetric recognition of Cu²⁺ and Fe³⁺, in Proceedings of The 24th International Electronic Conference on Synthetic Organic Chemistry, 15 November–15 December 2020, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-24-08292
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Synthesis and characterization of a meso-anthracene-BODIPY derivative for colorimetric recognition of Cu2+ and Fe3+

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1. Centre of Chemistry, University of Minho
2. Centre of Chemistry, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.
Abstract

Ions exist widely in biological and environmental media, and the scarcity or excess of these species can have adverse consequences for these media. BODIPY dyes appear as heterocyclic organic compounds capable of recognizing metal ions in solution and in cells, through optical signals (colorimetric and/or fluorimetric), and its photophysical properties can be adjusted through the functionalization of the BODIPY core. In continuation of the work developed recently, our research group reports the synthesis of a meso-anthracene-BODIPY derivative and the respective characterization by 1H and 13C nuclear magnetic resonance (NMR) and UV-Vis. spectroscopies. The preliminary study of the chemosensory capacity of the BODIPY derivative was also carried out in the presence of several cations in acetonitrile solution which shows a selective colorimetric response for Cu2+ and Fe3+.

Keywords
Synthesis
BODIPY
metal ions
optical chemosensor
colorimetric signal
Manuscript
meso-Triphenylamine-BODIPY derivative for optical chemosensing of metal ions
Uncommon coordination modes of a potential heptadentate aminophenol donor