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es for imaging saturable targets of the body.MXenes are a recently discovered class of two-dimensional materials that have shown great potential as electrodes in electrochemical energy storage devices. Despite their promise in this area, MXenes can still suffer limitations in the form of restricted ion accessibility between the closely spaced multistacked MXene layers causing low capacities and poor cycle life. Pillaring, where a secondary species is inserted between layers, has been used to increase interlayer spacings in clays with great success but has had limited application in MXenes. We report a new amine-assisted pillaring methodology that successfully intercalates silica-based pillars between Ti3C2 layers. Using this technique, the interlayer spacing can be controlled with the choice of amine and calcination temperature, up to a maximum of 3.2 nm, the largest interlayer spacing reported for an MXene. Another effect of the pillaring is a dramatic increase in surface area, achieving BET surface areas of 235 m2 g-1, a sixty-fold increase over the unpillared material and the highest reported for MXenes using an intercalation-based method. The intercalation mechanism was revealed by different characterization techniques, allowing the surface chemistry to be optimized for the pillaring process. The porous MXene was tested for Na-ion battery applications and showed superior capacity, rate capability and remarkable stability compared with those of the nonpillared materials, retaining 98.5% capacity between the 50th and 100th cycles. These results demonstrate the applicability and promise of pillaring techniques applied to MXenes providing a new approach to optimizing their properties for a range of applications, including energy storage, conversion, catalysis, and gas separations.We numerically study the droplet coalescence of an oil-in-water (O/W) emulsion permeating through a fibrous filter. Our numerical simulation method is based on the phase-field model for capturing a free interface, the immersed boundary method used to calculate fluid-solid interactions, and the wetting model that assigns an order parameter to the solid surface according to the wettability. To represent realistic flow inside the filter during simulation, the voxel data obtained from X-ray computed tomography (CT) images of the filter microstructure are used in the simulation. learn more The effects of the filter microstructure, such as fiber arrangement and orientation of the droplet coalescence, are investigated by using several filter domains. Our simulations demonstrate that the arrangement of closely attached fibers placed at the permeate-side surface enhances droplet coalescence. In addition, the parallel orientation of the fiber to the main flow direction suppresses droplet enlargement due to the coalescence but reduces the number of droplet passages without coalescence in the filter.Nucleation phenomena play an important role in our world and understanding them is of major interest. However, we lack analytical methods with the sufficient temporal and spatial resolution to analyze nucleation processes. In this work we used CTAB stabilized gold nanocubes as a model system for nucleation, meaning the nanoparticles act like ions or atoms and built up bigger superstructures comparable to normal nucleation phenomena. Thereby we analyzed the heterogeneous nucleation of the gold nanocubes on hydrophobized and negatively charged mica surfaces with a combination of UV-Vis-NIR spectroscopy and light microscopy. With the plasmon resonance of the gold nanocubes we gained valuable information about the early nucleation of the particles and their concentration in solution via UV-Vis-NIR spectroscopy. The combination with a light microscope enabled the simultaneous detection of nucleated species on the surfaces and opened the possibility to analyze the kinetics of the heterogeneous nucleation process. With this, we were able to determine the nucleation rates. While the hydrophobized surfaces did not influence the nucleation of the gold nanocubes, the negatively charged surfaces greatly promoted the nucleation. Thereby, we could demonstrate that the combination of light microscopy and optical spectroscopies in general is a suitable and easy to handle system to analyze heterogeneous nucleation processes in-situ directly in solution on a relevant statistical basis with simple and commonly available equipment.Thin polymer films have found many important applications in organic electronics, such as active layers, protective layers, or antistatic layers. Among the various experimental methods suitable for studying the thermo-optical properties of thin polymer films, temperature-dependent spectroscopic ellipsometry plays a special role as a nondestructive and very sensitive optical technique. In this Review Article, issues related to the physical origin of the dependence of ellipsometric angles on temperature are surveyed. In addition, the Review Article discusses the use of temperature-dependent spectroscopic ellipsometry for studying phase transitions in thin polymer films. The benefits of studying thermal transitions using different cooling/heating speeds are also discussed. Furthermore, it is shown how the analysis and modeling of raw ellipsometric data can be used to determine the thermal properties of thin polymer films.Deregulation of the transcriptional repressor BCL6 enables tumorigenesis of germinal center B-cells, and hence BCL6 has been proposed as a therapeutic target for the treatment of diffuse large B-cell lymphoma (DLBCL). Herein we report the discovery of a series of benzimidazolone inhibitors of the protein-protein interaction between BCL6 and its co-repressors. A subset of these inhibitors were found to cause rapid degradation of BCL6, and optimization of pharmacokinetic properties led to the discovery of 5-((5-chloro-2-((3R,5S)-4,4-difluoro-3,5-dimethylpiperidin-1-yl)pyrimidin-4-yl)amino)-3-(3-hydroxy-3-methylbutyl)-1-methyl-1,3-dihydro-2H-benzo[d]imidazol-2-one (CCT369260), which reduces BCL6 levels in a lymphoma xenograft mouse model following oral dosing.The preparation of phthalazinone derivatives is pivotal for their utilization as pharmaceutical agents and other entities. Herein, we report the phthalazinone-assisted carbon-nitrogen bond forming reaction using dioxazolones as robust amidation sources under Rh(III) catalysis. The broad functional group tolerance and complete site-selectivity are observed. Notably, a series of transformations of synthesized compounds into biologically relevant N-heterocycles demonstrates the applicability of the developed methodology.
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