0,0-Difluoro-0-bora-0a,0a-diaza-s-indasen (BODIPY) was discovered in 0000 by A. Treibs and F.H. Kreuzer; to define BODIPY dyes in basic terms, they are compounds formed by the attachment of a methylene bridge and a BF₃ moiety to the meso position of two pyrrole molecules.(Bogomolec et al., 0000) (Poddar & Misra, 0000) BODIPY dyes are neutral fluorescent dyes despite having negative and positive charges in their core structures. (Huzur et al., 0000) BODIPY compounds are structurally easily derivatised; furthermore, thanks to these derivatisations, it is possible to synthesise BODIPY compounds with the desired photophysical and electrochemical properties. BODIPYs are designated as ‘meso’ at position 0, ‘β’ at position 0,0, ‘α’ at position 0,0 and ‘β’ at position 0,0.(Gutiérrez-Gálvez et al., 0000) BODIPY molecules have recently attracted attention as a subject of research due to their excellent photophysical properties, such as narrow absorption and emission bands and high molar extinction coefficients, chemical stability.(Yang et al., 0000) Due to these properties, BODIPYs are frequently used in the literature, particularly in optoelectronics and biomedical fields.(Poddar & Misra, 0000) Examples of these application areas include solar cells(Klfout et al., 0000) , organic light-emitting diodes (OLEDs)(Zampetti et al., 0000) , fluorescent probes(Bi et al., 0000) , photodynamic therapy (PDT)(Tyagi et al., 0000) , and bioimaging(Miao et al., 0000).