Friishoffmann0975

As a validation of the MALDI-MSI analysis, a differentially expressed protein (GFAP) was verified using immunohistochemical staining. Furthermore, since several proteins detected in this study have previously been associated with neuronal loss, neuronal loss in the cortical region was demonstrated using an anti-NeuN immunohistochemical staining method. In conclusion, the findings of this research have provided insights into the spatial proteomic changes between HD transgenic and non-transgenic littermates and therefore, we suggest that MALDI-MSI is a powerful technique to determine spatial proteomic alterations between biological samples, and the data processing that we present here can be employed as a complementary tool for the data analysis.We report the thinnest copper sulfur atomic monolayer in an organic copper chalcogenide [Cu(CMP)]n (CMP = 5-chloro-2-mercaptopyridine). The layer features a new type of copper sulfur structure woven by both covalent bond and cuprophilic interaction and shows an intriguing oriented photoconductivity.The late stage photochemical hydroxylation of biaryl sulfonium salts was enabled with a TEMPO derivative as a simple oxygen source, in metal free conditions. The scope and mechanism of this exceptionally simple synthetic method, which constructs important arylated phenols from aromatic C-H bonds, are herein discussed.We report the synthesis of a tantalum phosphate catalyst with abundant strong acid sites, which is very active for the catalytic conversion of acetone into mesitylene. Characterizations, kinetic studies, and theoretical results show a relationship between the acidic sites and catalytic performance in this reaction.Self-targeting antimicrobial platforms have yielded new possibilities for the treatment of infectious biofilms. Self-targeting involves stealth transport through the blood circulation towards an infectious biofilm, where the antimicrobial platform penetrates and accumulates in a biofilm in response to a change in environmental conditions, such as local pH. In a final step, nano-antimicrobials need to be activated or the antimicrobial cargo of nanocarriers released. Zwitterions possess both cationic and anionic groups, allowing full reversal in zeta potential from below to above zero in response to a change in environmental conditions. Electrolyte-based platforms generally do not have the ability to change their zeta potentials from below to above zero. Zwitterions for use in self-targeting platforms are usually hydrophilic and have a negative charge under physiological conditions (pH 7.4) providing low adsorption of proteins and assisting blood circulation. However, near or in the acidic environment of a biofilm, they become positively-charged yielding targeting, penetration and accumulation in the biofilm through electrostatic double-layer attraction to negatively-charged bacteria. Response-times to pH changes vary, depending on the way the zwitterion or electrolyte is built in a platform. Self-targeting zwitterion-based platforms with a short response-time in vitro yield different accumulation kinetics in abdominal biofilms in living mice than platforms with a longer response-time. In vivo experiments in mice also proved that self-targeting, pH-responsive zwitterion-based platforms provide a feasible approach for clinical control of bacterial infections. Clinically however, also other conditions than infection may yield an acidic environment. Therefore, it remains to be seen whether pH is a sufficiently unique recognition sign to direct self-targeting platforms to an infectious biofilm or whether (additional) external targeting through e.g. near-infrared irradiation or magnetic field application is needed.We report for the first time the coupling of activated thioamides with alcohols to efficiently form thionoesters via a palladium-catalyzed C-N cleavage strategy. The new approach employs thioamides as a thioacylating reagent to give thionoesters in moderate to good yields. Notably, this methodology demonstrates a broad substrate scope, as alkyl/aryl alcohols are well tolerated, and this process might facilitate the synthesis of sulfur-containing compounds under simple and mild conditions.The distinct nanosized cluster Gd22Ni21 was isolated using a mixture of anions (SO32- and SO42-) as templates, and to the best of our knowledge, this was the first such 3d-4f cluster to have been developed. Additionally, of a number of 3d-4f heterometallic clusters, Gd22Ni21 showed the largest low-field magnetic entropy change (26.1 J kg-1 K-1) at 2.0 K and ΔH = 2.0 T.Although the origin and assignment of the complex XPS features of the cations in ionic compounds has been the subject of extensive theoretical work, agreement with experimental observations remains insufficient for unambiguous interpretation. This paper presents a rigorous ab initio treatment of the main and satellite features in the Fe 2p XPS of Fe2O3. This has been possible using a unique methodology for the selection of orbitals that are used to form the ionic wavefunctions. This orbital selection makes it possible to treat both the angular momentum coupling of the open shell core and valence electrons as well the shake excitations from the closed shell orbitals associated with the O ligands into the valence open shell orbitals associated with the Fe 3d shell. This allows the character of the ionic states in terms of the occupations of the open shell core and valence orbitals and of the contributions of 2p1/2 and 2p3/2 ionization to the XPS intensities to be determined. Our analysis gives strong evidence tbe relevant for other ionic compounds as well.Red, green and blue emitting materials, the three primary colors, are very important in lighting and display. Red-emitting Eu(III) complexes and green-emitting Tb(III) complexes exhibit high color purity and photoluminescence (PL) efficiency. However, it is difficult to realize efficient blue emission based on f-f transition. Alternatively, Ce3+ with d-f transition can be used to construct blue-emitting lanthanide complexes. Herein, we synthesized two heteroleptic Ce(III) complexes Ce-1Me-OTf and Ce-2Me-OTf based on hydrotris(3-methylpyrazolyl)borate (TpMe) and hydrotris(3,5-dimethylpyrazolyl)borate (TpMe2) ligands, respectively, in which triflate is used as the ancillary ligand. Ce-1Me-OTf and Ce-2Me-OTf exhibit strong blue emission in dichloromethane and as powder with maximum emission wavelengths in the range of 424-436 nm. Both complexes demonstrate near-unity photoluminescence quantum yields (PLQYs) in powder and good sublimation properties. In particular, Ce-1Me-OTf emits deep blue light both in dichloromethane and as powder with Commission Internationale de l'Eclairage (CIE) coordinates of (0.15, 0.07) and (0.15, 0.06), respectively, which are close to the standard blue points recommended by the National Television System Committee (NTSC) and the European Broadcast Union (EBU).By experiment and simulation, we report that viscoelastic liquid bridges made of constant viscosity elastic liquids, a.k.a. Boger fluids, can be effectively destabilized by torsion. Under torsion, the deformation of the liquid bridge depends on the competition between elastocapillarity and torsion-induced normal stress effects. When the elastocapillary effect dominates, the liquid bridge undergoes elastocapillary instability and thins into a cylindrical thread, whose length increases and whose radius decays exponentially over time. When the torsion-induced normal stress effect dominates, the liquid bridge deforms in a way similar to edge fracture, a flow instability characterized by the sudden indentation of the fluid's free surface when a viscoelastic fluid is sheared at above a critical deformation rate. The vertical component of the normal stress causes the upper and lower portions of the liquid bridge to approach each other, and the radial component of the normal stress results in the liquid bridge thinning more quickly than under elastocapillarity. Whether such quick thinning continues until the bridge breaks depends on both the liquid bridge configuration and the level of torsion applied.Biological mercaptans, also known as biothiols, play their own roles in a number of important physiological processes, and the abnormal levels of biothiols are closely associated with a variety of diseases. Therefore, the selective detection of biothiols in biological systems is crucial for understanding their roles in physiological processes and the early diagnosis of diseases. In this article, we developed a coumarin-based fluorescent probe (CouSePh) with 4-phenylselenium as the active site for the discriminative detection of all three biothiols. By introducing 4-phenylselenium as the active group, the probe CouSePh exhibits a rapid and sensitive response to three biothiols. For all three biothiols, the first-step sensing reaction is the nucleophilic substitution of 4-phenylselenium by the thiol group of biothiols, and they subsequently undergo three distinct intramolecular reactions to form three sensing products with different fluorescence emissions. The sensing mechanisms of the three biothiols have been demonstrated by spectral measurements and the analysis of high resolution mass spectrometry as well as the separation and characterization of the sensing product. selleck kinase inhibitor Furthermore, by two-channel fluorescence imaging, probe CouSePh has been successfully applied in the discriminative detection of endogenous biothiols in living cells.Bacterial infection has received substantial attention and poses a serious threat to human health. Although antibiotics can effectively fight against bacterial infection, the occurrence of antibiotic resistance has become increasingly serious in recent years, which tremendously hinders its clinical application. Consequently, it is urgent to explore novel strategies to achieve efficacious treatment of bacterial diagnosis and detection. Manganese dioxide (MnO2) nanomaterial has been extensively reported in tumor therapy. Nevertheless, there are few antibacterial reviews of MnO2. Herein, we will discuss the applications of MnO2 in the detection and treatment of bacterial infection, including photodynamic therapy, immunotherapy, improvement of hypoxia, dual-modal combination therapy, reactive oxygen species scavenging, magnetic resonance imaging, optical application of acoustic imaging, and so forth. This review is expected to provide meaningful guidance on further research of MnO2 nanomaterial for antibacterial applications.Correction for 'Synthesis and characterization of diacylgermanes persistent derivatives with superior photoreactivity' by Sabrina D. Püschmann et al., Dalton Trans., 2021, 50, 11965-11974, DOI 10.1039/D1DT02091A.Tailored to the special tumor microenvironment (TME), chemodynamic therapy (CDT) has been introduced to generate hydroxyl radicals (˙OH) primarily for the tumor via Fenton and Fenton-like reactions. However, deficient hydrogen peroxide (H2O2) levels and low reaction efficiency severely limit the development of CDT, which have attracted tremendous efforts to alleviate. Inspired by the H2O2 homeostasis in cancer cells, here, hollow Cu2-xS nanocatalysts (CS NCs) loaded with doxorubicin (DOX) (named CSD NCs) are engineered. As biometric enzyme-like reactive oxygen species (ROS) regulators, the CS NCs were fabricated to cyclically take advantage of H2O2 for enhanced CDT and synergistic photothermal therapy (PTT) and photodynamic therapy (PDT). According to the conception here, CDT is strengthened due to the H2O2 generation step, which is dependent on superoxide radical (O2˙-) conversion by the superoxide dismutase-mimicking activity of the nanoparticles. Meanwhile, catalase-like activity promotes O2 levels, which overcome the hypoxia limitation in the TME and further promote ˙OH and O2˙- creation and augmentation through PDT/PTT under NIR II laser stimulation.