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This decoration method also expands the wide range of application fields of PPy@MoS2. As a proof of application, the ternary PPy@MoS2@Au hybrids reveal excellent enzyme-like catalytic performance. Owing to the high coverage of Au NPs as well as one dimensional hierarchical MoS2-based ternary unique structures, the resultant PPy@MoS2@Au hybrid composites exhibited synergistically enhanced peroxidase-like catalytic activity relative to MoS2, MoS2@Au, and PPy@MoS2 alone, demonstrating the remarkable prospects of MoS2-based hybrids in chemical/biological molecule sensing application.Reflective assemblies of high refractive index organic crystals are used to produce striking optical phenomena in organisms based on light reflection and scattering. In aquatic animals, organic crystal-based reflectors are used both for image-formation and to increase photon capture. Here we report the characterization of a poorly-documented reflector in the eye of the shrimp L. vannamei lying 150 μm below the retina, which we term the proximal reflective layer (PR-layer). The PR-layer is made from a dense but disordered array of polycrystalline isoxanthopterin nanoparticles, similar to those recently reported in the tapetum of the same animal. Each spherical nanoparticle is composed of numerous isoxanthopterin single crystal plates arranged in concentric lamellae around an aqueous core. The highly reflective plate faces of the crystals are all aligned tangentially to the particle surface with the optical axes projecting radially outwards, forming a birefringent spherulite which efficiently scatters light. The nanoparticle assemblies form a broadband reflective sheath around the screening pigments of the eye, resulting in pronounced eye-shine when the animal is viewed from a dorsal-posterior direction, rendering the eye pigments inconspicuous. We assess possible functions of the PR-layer and conclude that it likely functions as a camouflage device to conceal the dark eye pigments in an otherwise largely transparent animal.A feasible analytical method based on high performance liquid chromatography-quadrupole/electrostatic field orbitrap high-resolution mass spectrometry (HPLC-Q/orbitrap MS) has been established for the identification and characterization of anticancer constituents in ethyl acetate components from Hedyotis diffusa in our work. The mass spectrometer provided significant fragment information both in the full MS scan and data-dependent MS2 modes. Sixty-two possible compounds were analyzed and identified from the above results. Of the above 62 compounds, 12 have good separation in the positive ion mode, and 27 compounds have good separation in the anion mode. Currently, 39 have been reported in the literature related to the chemical composition of the plant, while the other 23 of the 62 compounds have not been reported. Fifteen tentatively identified compounds were given detailed descriptions. Four representative compounds from the ethyl acetate extract among the fifteen were actually isolated in good yield with sir the rapid detection of the potential anticancer compounds from Hedyotis diffusa.Correction for 'H2 as a fuel for flavin- and H2O2-dependent biocatalytic reactions' by Ammar Al-Shameri et al., Chem. Commun., 2020, DOI 10.1039/d0cc03229h.Electrostatic interactions between a quaternary pyridyl-β-diketonate and anionic charged nanosheets were observed to produce a highly emissive dispersion in a rich water solution. A greater fluorescence quantum yield of approximately 50% was obtained when a luminogenic β-diketonate, 1-(4-methoxyphenyl)-3-(3-hydroxyethyl-pyridinium bromide)-1,3-propandione (prepared by the Claisen condensation reaction and subsequent quaternization), was molecularly dispersed and enclosed by a couple of atomically flat ultrathin (approximately 1.0 nm) silicate sheets of anionic layered clay. By accommodating β-diketonate into a narrow interlamellar space (approximately 0.4 nm distance), the molecular motion was suppressed, as confirmed by a smaller non-radiative relaxation rate constant, which was obtained by time-resolved luminescence and quantum yield measurements. Because the dense packing of β-diketonate quenched the excited state, the isolation of luminogens by the co-adsorption of photochemical inert cations (tetramethylammonium and benzylammonium) was prevented by concentration quenching. A lower quantum yield was obtained by expanding the interlayer distance above 1.0 nm by co-adsorbing a photo-inactive water-soluble polymer, poly(vinylpyrrolidone). Therefore, the fixation and spatial separation of β-diketonate in the narrow interlayer space was determined to be essential for obtaining strong emission.In the modern era, the escalation of heavy metal discharges, especially from the industrial sector, is causing an enormous threat to nature. This article explores the dual sensing of heavy metals (Cr6+ and Fe3+) using a naturally formed microcline based sensor. A nano-sized microcline (M) was obtained via a facile top-down synthesis. In order to enhance the fluorescence property of the material, nitrogenous carbon-dots were loaded into the porous structure of the microcline (MCD) causing a bright blue fluorescence with remarkable stability. Detailed analysis of the composition and structure of the natural nano-sensor was carried out using X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, and BET analysis. This sensor material is highly selective towards Cr6+ and Fe3+, demonstrating a "turn-off" response in aqueous Fe3+ and a radical red shift of the fluorescence maxima for aqueous Cr6+. Density functional studies suggest that photoinduced electron transfer (PET) based quenching of fluorescence is responsible for these types of fluorescence alteration mechanisms. selleck chemicals Efficient sensing of both Cr6+ and Fe3+ in various real-life water samples along with a real wastewater sample is also reported herein. A few studies have previously reported on efficient, natural material-based sensors, but they lack real-life applications due to their complicated synthesis and restricted functionalities. This work manages to overcome those drawbacks in its own fashion, providing a tremendously selective and sensitive (4 μM for Cr6+ and 19 μM for Fe3+) dual fluorescent probe.