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A new AIE-based luminogen TPES, as a ratiometric fluorescence probe for mercury(II) was readily synthesized. The probe combined the advantages of the outstanding specificity of Hg 2+ -triggered deprotection reaction of thioketal and the brilliant emission of AIEgens in aggregated state. Once encountered aqueous Hg 2+ , fluorescent color of TPES in THF-H 2 O (f w  = 98%) altered from blue to green rapidly, while other metal cations gave no interference to the probe. And the mechanism of this chemosensor was carefully verified by 1 H NMR analysis, FTIR and MS spectra. As expected, TPES exhibits excellent selectivity and sensitivity towards Hg 2+ in the solid state. When using filter paper as the solid medium, the fabricated test strips could signify Hg 2+ ions with the LOD as 1 × 10 -5 M (Hg 2+ in aqueous solution), accompanied with a distinct emitting altered from blue to green. Furthermore, by changing the medium from filter paper to silica gel plate, a more significant fluorescence alteration from blue to yellow was achieved, and the LOD was further optimized to 1 × 10 -6 M as discerned by naked-eye., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

A copper (I) polymer, [Cu 2 Mg(pzdc) 2 (H 2 O) 5 •2H 2 O] n (pzdc = 2,3-Pyrazinedicarboxylic acid), was synthesized by solvothermal method. The complex was characterized using X-ray diffraction (XRD), fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible spectrophotometry (UV-Vis), and element analysis. X-ray crystal structure analysis reveals that the complex is a two-dimensional coordination polymer. The photophysical and luminescent properties of the complex were investigated. At room temperature, the complex exhibits reversible double strands cyclic voltammogram and displays efficient blue emission with peak maxima at 468 nm. Catalytic liquid phase oxidation of dyes and glyphosate was carried out using the copper (I) polymer as catalyst and H 2 O 2 as oxidant. Degradation efficiencies were evaluated by varying the reaction conditions (i.e. illumination and oxidant). In the degradation reactions, the polymer exhibits high degradation efficiency within a short reaction time under the optimum reaction conditions. Furthermore, the reusability of the catalyst is excellent, showing no activity loss in four repeated cycles. The possible reaction mechanism catalyzed by the polymer was inferred on the basis of the results of electron spin resonance (ESR), electrochemical and ion chromatography analyses (IC).

The title compound, [Cu4(C11H13NO4)4]·CH3CH2OH·2.5H2O, is an electronically neutral tetra-nuclear copper(II) complex with a cubane-like Cu4O4 core. The complete molecule has point group symmetry 2. The phenol hy-droxy group and one of the three alcohol hy-droxy groups of each 2-{[tris-(hy-droxy-meth-yl)meth-yl]imino-meth-yl}phenol ligand are depro-ton-ated, while the secondary amine and the other two hy-droxy groups remain unchanged. The Cu(II) atoms in the Cu4O4 core are connected by four μ3-O atoms from the deprotonated alcohol hy-droxy groups. Each of the penta-coordinated Cu(II) ions has an NO4 distorted square-pyramidal environment through coordination to the tridentate Schiff base ligands. The Cu-N/O bond lengths span the range 1.902 (4)-1.955 (4) Å, similar to values reported for related structures. There are O-H⋯O hydrogen-bond inter-actions between the complex molecules and the ethanol and water solvent molecules, leading to the formation of a three-dimensional network. The ethanol solvent molecule is disordered about a twofold rotation axis. One of the two independent water molecules is also located on this twofold rotation axis and shows half-occupancy.