Lamontvangsgaard8011

In bioimaging, bioorthogonal chemistry is most often used to visualize chemical reporters by fluorescence in their native environment. Herein, we show that TEMPO-based probes can be ligated to monolignol reporters by Diels-Alder chemistry in plant cell walls, paving the way for the study of lignification by EPR spectroscopy and imaging.The electric field modulation of photoluminescence in ferroelectric-optical materials as a novel in situ, non-damaging and real-time controllable method has drawn much research focus. Ruxolitinib molecular weight The broad bandwidth emission of 33 nm and a tuneable luminescence contrast of 28% were achieved in Nd-doped Pb(Mg1/3Nb2/3)O3-PbTiO3 (NdPMNT) tetragonal ferroelectric-optical crystals arising from spontaneous polarization. The study of NdPMNT ferroelectric crystals under a cyclic, triangular alternating current voltage wave showed that the change in the photoluminescence intensity subjected to an electric field is mainly related to the 180° domain distribution, rather than the 90° domain. The physical process of electric field tuning luminescence is to control the 180° domain distribution using the external electric field, which thereby effectively tunes the luminescence. This finding restricts the limitation of a specific phase change region, which greatly increases the range of materials used and has guiding significance for research in the electric field modulation of luminescent technology.Replacing coenzyme F430, an Ni(i) F430-like cofactor derived from vitamin B12 (F430-B12) is revealed by DFT calculations to be able to catalyze methane formation in methyl-coenzyme M reductase with a barrier of 13.3 kcal mol-1, demonstrating the correctness of the route starting from vitamin B12. The structure-activity relationships of F430 and F430-B12 (especially the roles of the F ring) are discovered and several sources of inspiration promoting the application of F430-B12 are also obtained, coming closer to using F430 chemistry in man-made catalysis.A novel water-soluble near-infrared fluorescent probe named QX-P with simple synthesis is developed. QX-P has high sensitivity and selectivity to ALP. Moreover, the probe can not only visualize ALP activity in four cell lines, but also real-time image ALP activity during the diagnosis and treatment of diabetes in mice.The absorption and emission properties of various diphenyl-dibenzofulvene (DP-DBF) derivatives were investigated, and their crystallization-induced emission enhancement (CIEE) performances were found to show a clear correlation with the twist angle around the C[double bond, length as m-dash]C bond of the DP-DBF structure.Two iridium-based catalysts (namely IrSn and IrNi) are synthesised via a polyol route involving capping agents. The capping agents are removed according to a time-consuming multistep heat-treatment protocol described in the literature (N2 → N2/O2 → H2). In this work the effect of each of these steps on the structural composition and catalytic activity is investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and electrochemistry. It is shown that heating in nitrogen is not required, whereas air is the most effective for the removal of the capping agents. Besides FT-IR, the analysis of sp3 carbon (from XPS) turned out to give reasonable insights into capping agent removal. Induced by hydrogen treatment no further change of the surface occurs, while particles tend to grow and become more crystalline. While structural changes are similar for both catalysts, the impact of each of the steps on the catalysis is different the activity per gram of iridium becomes even lower for IrSn (an electrochemical cleaning agent that was used as reference measurements, seems best suited) while the activity is doubled for the IrNi case. Our results illustrate that the selection of the cleaning procedure strongly depends on the investigated system and should be optimised individually.A heterogeneous hydrocarboxylation process of olefins to obtain carboxylic acids with one more carbon was first realized using a single-Rh-site catalyst formed on porous organic polymer (Rh1/POPs). The in situ formation of hydrophilic porous ionic polymer from hydrophobic POPs with the help of CH3I led to high activity and superb stability.Here we report a highly stable 16π-electron antiaromatic system based on the ligand-oxidized Cu(ii)-tetrabenzocorrole. The antiaromaticity of the monocationic corrole complex was elucidated with the unique bond length alternation pattern of the crystal structure and the spectral diagnostic features. The NICS and GIMIC calculations clearly depicted its inner 15-membered-ring main pathway with a strong paratropic ring current.TMSCFX2 (X = Cl, Br; TMS = trimethylsilyl) have been developed as halofluorocarbene (CFX, X = Cl, Br) precursors for [2+1] cyclopropanation with alkenes. Structurally diverse halofluorocyclopropanes were obtained in good to excellent yields. It was found that the reactivity order of the three halofluorocarbene reagents (TMSCF2Br, TMSCFCl2, and TMSCFBr2) in halofluorocyclopropanation with 1,1-diphenylethylene can be very different under different reaction conditions.Bismuth was introduced as an intermediate to produce Au-X (X = Pt and Pd) bimetallic nanoalloys using the galvanic replacement reaction. The results showed that the Au-X nanoalloys have good activity for electrocatalytic reactions in alkaline media. This strategy can provide an option for the formation of multimetal nanoalloys with similar electrochemical potentials and compositions.A typical multicyclic branched-topology polystyrene (c-BPS) with high molecular weight (30 K ≤ Mw MALLS ≤ 300 K g mol-1) and narrow dispersity (1.2 ≤ Đ ≤ 1.3) was efficiently synthesized by combining atom transfer radical polymerization (ATRP) and atom transfer radical coupling (ATRC) techniques. The topological constraints imposed by the presence of cyclic units and branch points had a marked influence on the entanglement behaviors of the polymer chains in solution. Therefore, c-BPS possesses the lowest loss modulus (G) and viscosity (η), the highest diffusion coefficient (D0), the largest mesh size (ξ) and the fastest terminal relaxation (TR), compared with branched and linear precursors.