AIE active fluorescent organic nanoparticles based optical detection of Cu ions in pure water: a case of aggregation-disaggregation reversibility

An AIE-active pyrene-terpyridine derivative, (4′-(pyren-1-yl)-2,2′:6′,2′′-terpyridine) ( 1 ) was found to form nanoaggregate in an aqueous medium. The probe involved hydrogen bonding with solvent molecules that modulated the charge transfer behavior and consequently resulted in different spectroscopic behavior due to the formation of fluorescent organic nanoparticles (FONs). In the presence of Cu 2+ ions, FONs displayed a ratiometric red shift of the absorption band (360 to 420 nm) accompanied by a prominent naked-eye color change from colorless to light yellow. With a gradual increase in water content, 1 displayed a huge red shift of the emission band (430 to 475 nm) denoting its switching from monomer to FONs. In the presence of Cu 2+ , the 475 nm emission band of FONs gradually diminished, facilitating the micromolar scale detection of Cu 2+ (LOD = 8.57 μM) in a 100% aqueous medium with a fluorogenic color change from cyan to dark. The SEM and DLS data indicated the cation-induced disaggregation of FONs, which was further confirmed by mass spectral analysis and electron paramagnetic resonance measurement. In addition, the high selectivity of FONs towards Cu 2+ ions over other potential cations and the 2 : 1 ( 1 -Cu 2+ ) binding stoichiometry were also determined. Moreover, the spectroscopic behavior of the monomeric amphiphilic probe was well supported by extensive DFT study. Such detection of Cu 2+ ions in pure aqueous medium denoting an aggregation-disaggregation event is very rare in the literature. This work highlights the development of an AIE active pyrene-terpyridine derivative turning out to be fluorescent organic nanoparticles (FONs) in an aqueous medium which undergoes disaggregation towards Cu 2+ ions in a pure water medium.