Activity

01 μM), confirming the design rationale.Pickering emulsion stabilized by solid nanoparticles provides a diverse solvent microenvironment and enables to promote the phase transfer of reaction substrates/products in catalytic reactions, but the intrinsic role of solvent is still not clear. Herein, using benzyl alcohol (BA) as a model reactant, we demonstrate the nature of the water-promoted activity for alcohol oxidation over the Pd/MgAl-LDO catalyst. Depending on the water in the solvent, we observe different reactivities regarding the proportion of the water in the system. Kinetic isotope effects confirm the participation and positive effects of water for oxidation of BA. The water promotion effects are recognized and identified by the water vapor pulse adsorption coupled with temperature program desorption. Moreover, the adsorption behavior of BA or benzaldehyde at the interface of water and Pd/MgAl-LDO is also investigated by quasi-in-situ Raman spectroscopy. In addition, the mechanism of water-promoted alcohol oxidation is rationally proposed based on the Langmuir-Hinshelwood mechanism. The general applicability of the water promotion effects is further demonstrated over different supports and substrates, which well achieves excellent catalytic activity and selectivity in Pickering emulsion compared to that in the pure toluene system.A bioorthogonal reaction between N,N-dialkylhydroxylamines and cyclooctynes is described. This reaction features a highly regioselective transformation between small, easily functionalizable reaction components with second-order rate constants reaching 84 M-1 s-1. The reaction is orthogonal to the inverse-electron demand Diels-Alder reactions between tetrazine and strained alkenes, and its components exhibit exquisite stability and chemoselectivity in cell lysate. This retro-Cope elimination reaction introduces a new member to the bioorthogonal reaction compendium outside the prolific class of cycloaddition reactions.Due to the inherent mechanism limitation of photocatalytic fuel cell based self-powered biosensors (PFC-SPBs), it was difficult to distinguish the power density of various photoactive materials or recognition events in one detection process, which made it lack multitarget quantitative capacity. In order to solve this problem, we proposed an electron-transfer-regulated conversion strategy for the construction of multiplexed PFC-SPBs. Herein, the n-type CdS/Fe2O3 nanorod array (NR) heterojunction and p-type CuBr semiconductor were used as photoactive materials to prepare the photoanode and photocathode. Based on the appropriate Fermi level differentiation between these two photoelectrodes, a self-powered sensing platform driven by visible light without external energy supply was achieved. AT9283 In this design, two kinds of common and easily coexisting mycotoxins OTA and AFB1 acted as model analytes. The coupling of “signal off” and “signal on” was realized by controlling the electronic transmission on the interface between the photoanode and photocathode, so as to achieve the simultaneous detection of two mycotoxins. This work established a proof-of-concept for the integration of a dual-photoelectrode with dual-assay that could provide the innovative inspiration for the formation of a general multiplexed self-powered sensing platform.Two NIR luminescent Zn(II)/Cd(II)-Yb(III) complexes were obtained by the use of a Schiff base ligand with a binaphthyl backbone. Cd(II)-Yb(III) complex 2 has a triangular structure and exhibits interesting luminescent sensing activity to antibiotics, in particular to ciprofloxacin (CPFX) and norfloxacin (NFX) due to the inner filter effect. The limits of the detection of 2 to CPFX and NFX are 0.18 and 0.36 μM, respectively, and the fluorescence sensitivity is not changed with the existence of other antibiotics tested in this study.The ion trap is a unique type of device that is used for quantum studies in physics and mass analysis in chemistry. The space charge effect, which is due to trapping of an excessive number of ions, has long been recognized to be harmful for ion manipulation or mass spectrometry analysis. Here, we show an interesting phenomenon in which the energy exchange through collective interaction between the ion species could be effectively used for ion manipulation and high-quality mass measurement. This observation not only reveals a fundamentally interesting process in ion trap operation but also suggests a new alternative means for mass analysis.The C2-symmetric photochromic molecule 3, containing dithienylethene (DTE) and ferrocene units connected by an alkyne bridge, represents a unique probe where a metal (Hg2+) binds with the central DTE moiety. Both photoisomerized states of 3 (open, 3o; closed, 3c) are found to interact with Hg2+ ion by the S atoms of the DTE core; however, the binding constants (from a UV-vis study) and DFT calculations suggest that the open isomer (3o) binds with the metal ion more strongly than that of the closed isomer (3c). Notably, the course of metal binding does not perturb the inherent photoisomerization properties of the DTE core and the photoswitchability persists even in the metal-coordinated form of 3, however, with a comparatively slower rate. The quantum yields for photocyclization (Φo→c) and photocycloreversion (Φc→o) in the free form are 0.56 and 0.007, respectively, whereas the photocyclization quantum yield in the Hg2+ complexed species is 0.068, 8.2 times lower than the photocyclization quantum yield (Φo→c) of free 3o. Thus, the rate of photoisomerization can be modulated by a suitable metal coordination to the DTE core. The dynamics of photoswitchability in the metal-coordinated form of DTE has been explored by experimental means (UV-vis and electrochemical studies) as well as quantum chemical calculations.Petroleum products and essential oils are produced and used in large amounts and are categorized as “Substances of Unknown or Variable composition, Complex reaction products or Biological materials (UVCBs).” These UVCBs are notorious difficult-to-test substances, since they are complex mixtures of hydrophobic and volatile compounds. This study introduces two passive dosing (PD) approaches for whole UVCB toxicity testing (1) headspace PD applies the UVCB and purified lipid oil as a donor to control exposure via the headspace and (2) silicone rod PD applies UVCB-loaded silicone rods to control exposure via an aqueous test medium and headspace. Headspace gas chromatography-mass spectrometry measurements were used to cross-validate the approaches at the saturation level and to confirm exposure and maintain mixture composition at varying donor concentration levels. Both approaches were applied to whole-mixture toxicity tests of petroleum and essential oil UVCBs with daphnia and algae. Finally, the observed toxicity was linked to concentrations in the donor and in lipid membranes at equilibrium with the donors.