An antipyrine based fluorescence "turn-on" dual sensor for Zn2+ and Al3+ and its selective fluorescence "turn-off" sensing towards 2,4,6-trinitrophenol (TNP) in the aggregated state.

A 2,6-diformyl-p-cresol (DFC)-4-amino antipyrine (AP) based dual signaling fluorescent Schiff base ligand (DFCAP) is found to exhibit colorimetric and fluorescence turn on selective sensing towards metal ions, Zn2+ and Al3+. It also exhibits a significant aggregation induced emission (AIE) phenomenon by controlling the water-THF solvent ratio which provides robust green emissive fluorogenic aggregates with well-defined morphologies. Turn-on fluorescence enhancements as high as 195 fold and 168 fold in methanol for Al3+ and Zn2+ at 480 nm and 508 nm, respectively, were noticed. The binding constants and stoichiometry determined from the fluorescence titration data are K = 7.63 × 104 M-1 and 3.42 × 104 M-1 and 1 : 1 complexation for both Al3+ and Zn2+ respectively, supported by Job's method. DFCAP shows high sensitivity towards the detection of Zn2+ and Al3+ ions with very low detection limit values of ca. ∼21 nM and 30 nM respectively. Besides by applying its attractive AIE feature, the green emissive hydrosol functions as a good chemosensor with high sensitivity for a selected explosive TNP through ground state complexation with a LOD value of ca. ∼1.74 µM and especially a high Stern-Volmer quenching constant of ca. ∼4.14 × 105 M-1. For instant 'naked eye' response for the trace detection of TNP in the solution state, we fabricated a simple paper strip that could detect TNP on-site in a fast, inexpensive and simple way.

Rhodamine scaffolds as real time chemosensors for selective detection of bisulfite in aqueous medium.

Rhodamine and its derivatives have been widely used in designing fluorescent 'turn on' cation sensors, while very few rhodamine based fluorescent probes have been reported to date for the detection of anions in water. In this article, a new rhodamine based facile and convenient 'turn on' fluorescent chemosensor 2-(2-(1-hydroxynaphthyllideneamino)ethyl)-3',6'-bis(diethylamino)spiro [isoindoline-1,9'-xanthen]-3-one (RAHN) has been developed by Schiff base condensation and characterized by standard techniques for selective detection of bisulfite anions in water. A faintly yellow colour solution of RAHN turns pink upon addition of bisulfite. Again RAHN is weakly emissive in solution but becomes strongly emissive on addition of bisulfite and the emission intensity increases gradually in the presence of increasing concentration of bisulfite. No other analytes can cause emission enhancement of RAHN, suggesting the selectivity of the probe towards bisulfite. The detection limit for bisulfite was found to be ∼0.4 µM.

Aggregation induced emission from α-napthoflavone microstructures and its cyto-toxicity.

α-Napthoflavone (ANF) microstructures of various morphologies were synthesized using reprecipitation method. Sodium Dodecyl Sulfate (SDS) was used as morphology directing agent. The morphologies of the particles were characterized using optical and scanning electron microscopy (SEM). Single crystal data of ANF suggests that the aromatic units of ANF are in parallel slipped conformation in its aggregated form. Photophysical properties of aggregated ANF hydrosol were studied using UV-Vis absorption, steady state and time resolved spectroscopy. Red shift and broadening of UV-Vis spectra of ANF hydrosol are explained due to strong π-π and H-π interactions among the neighboring ANF molecules within the aggregated microstructures. Though ANF is non-luminescent in good solvent, a strong emission is observed in its aggregated state. This aggregation induced emission (AIE) has been explained due to restriction of intramoleculer rotation and large amplitude vibrational modes of ANF in its aggregated state. Our Photophysical study also reveals that AIE effect decreases after an optimum concentration of ANF and this has been explained due to softening of crystal lattice. Cytotoxicity of ANF hydrosol was examined to get an idea of the toxic level of this hydrosol toward cultured normal human cells. It is observed that ANF hydrosol may draw beneficial effect in biological application as it has no higher toxic activity but has antioxidant property.

Enhanced photocatalytic activity of metal coated ZnO nanowires.

A simple, facile and template free route has been described for the synthesis of ZnO nanowires. The morphology and structure of ZnO nanowires have been tuned by deposing silver and gold onto the surface of ZnO nanowire and this has been done by adding AgNO(3) and HAuCl(4) to aqueous suspension of ZnO. Our synthesized Ag and Au coated ZnO nanoparticles show different emissive property than the native ZnO nanowires. The photocatalytic degradation of Methylene Blue is also evaluated using ZnO and Ag and Au coated ZnO nanowires. It has been observed that Ag coated ZnO nano-needles exhibits significantly enhanced photocatalytic efficiency compare to ZnO nanowire and Au coated ZnO nano-leaves. Fluorescence spectra and surface structure of the samples with their photocatalytic activity indicates that surface deposited metal serves as an electron sinks to enhance the separation of photoinduced electrons from holes, leading to the formation of OH and it enhances their photocatalytic efficiency.