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Stimuli-responsive luminescent materials, which are dependent on changes in physical molecular packing modes, have attracted more and more interest over the past ten years. In this study, 2,2-dihydroxy-1,1-naphthalazine was synthesized and shown to exhibit different fluorescence emission in solution and solid states with characteristic aggregation-induced emission (AIE) properties. A remarkable change in the fluorescence of 2,2-dihydroxy-1,1-naphthalazine occurred upon mechanical grinding, heating, or exposure to solvents. According to the characterization by solid-state fluorescence spectroscopy, X-ray crystallography, differential scanning calorimetry, and X-ray powder diffraction, the fluorescence change could be attributed to transitions between two structurally different polymorphs. These significant properties could also give 2,2-dihydroxy-1,1-naphthalazine more potential applications as a multifunctional material. [ABSTRACT FROM AUTHOR]

A new chromene pyrazoline derivatives fluorescent probe L was designed and synthesized. The probe L appears in a 55-fold fluorescence enhancement after 5 equiv. Zn 2+ was added, and it also exhibits high sensitivity and selectivity for response to Zn 2+ in ethanol-water (V:V = 1:1) solution through “OFF-ON” type process and a possible photoinduced electron transfer (PET). Notably, the probe L distinguishes between Zn 2+ and Cd 2+ . The association constant was considered as 2.38 × 10 3  M −1 via fluorescence titration experiments. The probe L-Zn 2+ complex forms a 1:1 binding stoichiometry which was discussed by Job’s plot. The probe is very highly sensitive with fluorometric detection limit of 1.603 × 10 −10  M. It also shows good reversibility upon addition of EDTA. Furthermore, the viability of L to Zn 2+ has practical application in live cell imaging. [ABSTRACT FROM AUTHOR]

Abstract: A new fluorescent chemosensor, sodium 2-(2-(1H-benzo[d]imidazol-2-yl)quinolin-8-yloxy)acetate (HL), based on 8-hydroxyquinoline derivative has been designed, synthesized and characterized. Once combined with Hg2+ in aqueous solution, HL displays a fluorescence quenching effect to form the compound mercury(II) 2-(2-(1H-benzo[d]imidazol-2-yl)quinolin-8-yloxy)acetate chloride (LHg), which could be fast dissociated by the addition of cyanide in this system so that “ON–OFF–ON” type fluorescence change can be achieved. Cyanide induces the revival of fluorescence of LHg and results in “OFF–ON” type sensing with high sensitivity and rapid response in 100% aqueous system. Furthermore, the fluorescence microscopic imaging also indicates that LHg is suitable for the detection of CN− in biological environment. [Copyright &y& Elsevier]