LAUSR

An AIE (aggregation induced emission) active probe DFP–AMQ was designed and synthesized as a hexa-coordinated N2O donor chelator for the selective sensing of Al3+ colorimetrically as well as fluorimetrically with a 27-fold fluorescence enhancement for CH3CN–H2O (9 : 1, v/v, pH 7.2, HEPES buffer). The fluorescence enhancement occurred through the blocking of ESIPT, chelation enhanced fluorescence effect (CHEF) arose, and as a result fluorescence enhancement was observed through 1 : 1 complexation with Al3+ ions. Detailed spectroscopic studies including UV-Vis, FTIR, 1H NMR, and HRMS studies were carried out to characterize the probable structure of DFP–AMQ including the complexation of DFP–AMQ with Al3+ ions. The spectrophotometric and spectrofluorimetric titrations revealed strong binding towards Al3+ and the Kd values were obtained from UV-Vis (3.26 × 10−5 M−1) and fluorescence titration (2.02 × 10−5 M−1). The limit of detection of Al3+ by DFP–AMQ was 1.11 μM. The quantum yields of DFP–AMQ and [DFP–AMQ–Al]+ were calculated to be 0.008 and 0.211, respectively. Dynamic light scattering (DLS) studies showed that the sizes of the particles increased with increasing water percentage due to aggregation. SEM (scanning electron microscopy) studies revealed interesting morphological changes in microstructures in which DFP–AMQ demonstrated a rod-like shape, which was converted to a spherical-like shape in the presence of Al3+ and when DFP–AMQ aggregated in H2O it showed aggregated block-like shape. In the solid phase, DFP–AMQ with nitrate has no particular shape, but in the presence of acetate, it converts to stone-like shape. This probe (DFP–AMQ) could be employed for on-site Al3+ ion detection in the solid state.