Norwoodbrandstrup5407

These results unravel mechanistic insights that are essential for the design of lubricating systems based on strongly hydrated NPs.For energy-saving purposes, the pursuit of ultrahigh permeance nanofiltration membranes without sacrificing selectivity is never-ending in desalination, wastewater treatment, and industrial product separation. Herein, we reported a novel facile route to engineer a highly porous and superhydrophilic nanofibrous substrate to mediate the interfacial polymerization between trimesoyl chloride and piperazine, generating an ultrathin PA active layer (∼13 nm) with a hierarchical crumpled surface. The wet laying process and subsequent plasma treatment endowed a rougher and more hydrophilic surface for ethylene vinyl alcohol copolymer (EVOH) nanofibers in the thin compact nanofibrous scaffold (∼9 μm) with a mean pore size of 210 nm, radically different from the nanofibrous membrane by other methods. Nanofibrous scaffold with these features provide abundant thin-thick alternative continuous water layers between nanofibers and organic phase, facilitating the formation of the abovementioned PA layer. As a result, an ultrahigh permeance of 42.25 L·m-2 h-1 bar-1 and a reasonably high rejection of 95.97% to 1000 ppm Na2SO4 feed solution were obtained, superior to most state-of-the-art NF membranes reported so far. Our work provides an easy and scalable method to fabricate advanced PA NF membranes with outstanding performance, highlighting its great potential in liquid separation.Dynamic light scattering (DLS) experiments and equilibrium molecular dynamics (EMD) simulations were performed in the saturated liquid phase of the binary mixture of 1-hexyl-3-methylimidazolium bis(trifluormethylsulfonyl)imide ([HMIM][NTf2]) and carbon dioxide (CO2) to access the Fick diffusion coefficient (D11). The investigations were performed within or close to saturation conditions at temperatures between (298.15 and 348.15) K and CO2 mole fractions (xCO2) up to 0.81. The DLS experiments were combined with polarization-difference Raman spectroscopy (PDRS) to simultaneously access the composition of the liquid phase. For the first time in an electrolyte-based system, D11 was directly calculated from EMD simulations by accessing the Maxwell-Stefan (MS) diffusion coefficient and the thermodynamic factor. Agreement within combined uncertainties was found between D11 from DLS and EMD simulations for CO2 mole fractions up to 0.5. In general, an increasing D11 with increasing xCO2 could be observed, with a local maximum present at a CO2 mole fraction of about 0.75. The local maximum could be explained by an increasing MS diffusion coefficient with increasing xCO2 over the entire studied composition range and a decreasing thermodynamic factor at xCO2 above 0.7. Finally, PDRS and EMD simulations were combined to investigate the influence of the fluid structure on the diffusive process.We theoretically study the dynamics of charge transfer induced by femtosecond laser-pulse excitation. AT406 Models involving coupled electronic states of symmetrically bridged organic mixed-valence molecules are investigated, where the motion proceeds along two reaction coordinates. Linear absorption spectra of two species that differ in the energetical position of the bridge, relative to acceptor and donor states, are determined and compared to experimental results. From the wave packet dynamics it emerges that relaxation dominates the charge transfer. This behavior is reflected in transient absorption spectra, which are obtained from a directional decomposition of the time-dependent polarization. Due to the nature of the coupled dynamics the extraction of the relevant contributions needs an extension of well-known techniques for the decomposition.Enantiopure (R) and (S) cyclic α,α-disubstituted amino acid derivatives displaying a δ-valerolactam side chain were prepared from a common isoxazolidine precursor. The (R)-configured δ-valerolactam 11 was converted into diastereoisomeric pseudopeptides to investigate its ability to induce secondary structures in peptidomimetics. Conformational studies of these pseudopeptides were carried out in the solid state (X-ray diffraction), in solution (NMR analyses), and in silico (computer-aided conformational analysis), which demonstrated that such quaternary amino acids induce β-turn conformations stable enough to be retained in polar media (DMSO). Incorporation of this new type of α,α-disubstituted amino acid into a representative pseudopeptidic sequence by N- then C-elongation and N-debenzylation is also described herein and could serve for the synthesis of various structured peptidomimetics.The mechanism of palladium nanoparticles (Pd NPs)-catalyzed cross-coupling reactions has been the subject of intense debate since the recognition of catalytic active sites involving a wide array of dynamic changed Pd species. Here, through the combination of the hot filtration experiment together with the recently developed identical location transmission electron microscopy (IL-TEM) method, the delicate structure evolution of highly dispersed Pd NPs supported on oxygen-functionalized carbon nanotubes (Pd/oCNTs) as well as the kinetics properties of derived dissolved species in liquid phase were systemically investigated in the Suzuki-Miyaura reaction. The result indicates that the leached Pd components caused by the strong adsorption of reactants might have a significant contribution to the coupling products, and the degree for different substrates follows the order of iodobenzene > phenylboronic acid > bromobenzene. Meanwhile, the typical three sequential behaviors of supported Pd NPs, including dissolution, deposition, and growth, along with the increase of the conversion throughout the reaction were spatiotemporally observed by tracking the evolution of individually identifiable NPs. The performed work not only provides direct evidence for the interaction between Pd NPs surface with reactants on atomic scale but also gives a valuable reference for fundamentally understanding the mechanism of the heterogeneous Pd-catalyzed Suzuki coupling process as well as rational design of next-generation catalysts with high efficiency and reusability for synthetic applications.