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Cucurbit[8]uril-Assisted Nucleophilic Response: An original Supramolecular Approach for Cyanide Recognition as well as Treatment through Aqueous Answer.
To explore a minimal feature size of less then 100 nm with electrochemical additive manufacturing, we use a strategy originally applied to microscale electrochemical machining for the nanoscale deposition of Co on Au. The concept's essence is the localization of electrochemical reactions below a probe during polarization with ns-long voltage pulses. As shown, a confinement that exceeds that predicted by a simple model based on the time constant for one-dimensional double layer charging enables a feature size of less then 100 nm for 2D patterning. We further indirectly verify the potential for out-of-plane deposition by tracking growth curves of high-aspect-ratio deposits. Importantly, we report a lack of anodic stability of Au tips used for patterning. As an inert probe is the prerequisite for controlled structuring, we experimentally verify an increased resistance of Pt probes against degradation. Consequently, the developed setup and processes show a path towards reproducible direct 2D and 3D patterning of metals at the nanoscale.Earlier reports have discussed the manifold opportunities that arise from the use of eco-friendly organic semiconductor dispersions as inks for printed electronics and, in particular, organic photovoltaics. To date, poly(3-hexylthiophene) (P3HT) plays an outstanding role since it has been the only organic semiconductor that formed nanoparticle dispersions with sufficient stability and concentration without the use of surfactants. selleck chemicals llc This work elucidates the underlying mechanisms that lead to the formation of intrinsically stable P3HT dispersions and reveals prevailing electrostatic effects to rule the nanoparticle growth. The electrostatic dispersion stability can be enhanced by photo-generation of additional charges, depending on the light intensity and its wavelength. This facile, additive-free process provides a universal handle to also stabilize surfactant-free dispersions of other semiconducting polymers, which are frequently used to fabricate organic solar cells or other optoelectronic thin-film devices. The more generalized process understanding paves the way towards a universal synthesis route for organic nanoparticle dispersions.Novel hybrids containing silver or gold nanoparticles have been synthesized in aqueous media and at room temperature using enzymes or tailor-made enzyme-polymer conjugates, which directly induced the formation of inorganic silver or gold species. The choice of pH, protein, or bioconjugate strongly affected the final metallic nanoparticles hybrid formation. Using Candida antarctica lipase (CALB) in a solution, nanobiohybrids containing Ag2O nanoparticles of 9 nm average diameter were obtained. The use of tailor-made bioconjugates, for example, the CALB modified with dextran-aspartic acid polymer (Dext6kDa), resulted in a nanobiohybrid containing smaller Ag(0)/Ag2O nanoparticles. In the case of nanobiohybrids based on gold, Au(0) species were found in all cases. The Au-CALB hybrid contained spherical nanoparticles with 18 nm average diameter size, with a minor range of larger ones (>100 nm) while the AuNPs-CALB-Dext6kDa hybrid was formed by much smaller nanoparticles (9 nm, minor range of 22 nm), and also nanorods of 20-30/40-50 nm length. Using Thermomyces lanuginosus lipase (TLL), apart from the nanoparticle formation, nanoflowers with a diameter range of 100-200 nm were obtained. All nanobiohybrids maintained (dual) enzymatic and metallic activities. For instance, these nanobiohybrids exhibited exquisite dual-activity for hydrolysis/cycloisomerization cascades starting from allenic acetates. By merging the transition metal reactivity with the inherent lipase catalysis, allenic acetates directly converted to the corresponding O-heterocycles in enantiopure form catalysed by AgNPs-CALB-Dext6kDa, taking advantage of a kinetic resolution/cyclization pathway. These results showed the high applicability of these novel hybrids, offering new opportunities for the design of novel reaction cascades.Signal stability is crucial for an accurate diagnosis via magnetic particle imaging (MPI). However, MPI-tracer nanoparticles frequently agglomerate during their in vivo applications leading to particle interactions altering the signal. Here, we investigate the influence of such magnetic coupling phenomena on the MPI signal. We prepared Zn0.4Fe2.6O4 nanoparticles by flame spray synthesis and controlled their inter-particle distance by varying SiO2 coating thickness. The silica shell affected the magnetic properties indicating stronger particle interactions for a smaller inter-particle distance. The SiO2-coated Zn0.4Fe2.6O4 outperformed the bare sample in magnetic particle spectroscopy (MPS) in terms of signal/noise, however, the shell thickness itself only weakly influenced the MPS signal. To investigate the importance of magnetic coupling effects in more detail, we benchmarked the MPS signal of the bare and SiO2-coated Zn-ferrites against commercially available PVP-coated Fe3O4 nanoparticles in water and PBS.ese commercial tracers for MPI and illustrates the advantages of our flame-made Zn-ferrites concerning signal stability and ultimately diagnostic accuracy.The interaction of colloidal particles with a planar polymer brush immersed in a solvent of variable thermodynamic quality is studied by a numerical self-consistent field method combined with analytical mean-field theory. The effect of embedded particle on the distribution of polymer density in the brush is analyzed and the particle insertion free energy profiles are calculated for variable size and shape of the particles and sets of polymer-particle and polymer-solvent interaction parameters. In particular, both cases of repulsive and attractive interactions between particles and brush-forming chains are considered. It is demonstrated that for large particles the insertion free energy is dominated by repulsive (osmotic) contribution and is approximately proportional to the particle volume in accordance with earlier theoretical predictions [Halperin et al., Macromolecules, 2011, 44, 3622]. For the particles of smaller size or/and large shape asymmetry the adsorption or depletion of a polymer from the particle surface essentially contributes to the insertion free energy balance. As a result, depending on the set of polymer-solvent and polymer-particle interaction parameters and brush grafting density the insertion free energy profile may exhibit complex patterns, i.e., from a pure repulsive effective potential barrier to an attractive well. The results of our study allow for predicting equilibrium partitioning and controlling diffusive transport of (bio)nanocolloids across (bio)polymer brushes of arbitrary geometry including polymer-modified membranes or nanopores.In the present study, the effects of the Supercritical Anti-Solvent (SAS) process and food models on the antioxidant capacity, bioaccessibility and transport dynamics of flavonol-loaded polyvinylpyrrolidone (PVP) based microparticles were investigated using a combined in vitro gastrointestinal digestion/Caco-2 cell culture model. SAS-processed and unprocessed flavonols were supplied in two different food models 10% ethanol for an aqueous hydrophilic food simulant and 3% acetic acid for an acidic food simulant. The SAS processing of quercetin and rutin resulted in a much higher recovery of these bioactives as well as greater retention of antioxidant capacity after gastrointestinal digestion in both hydrophilic and acidic food models. The present study also demonstrates that SAS coprecipitation has a positive effect on the stability and transport of bioactives across the epithelial cell layer. It can be deduced from the results that the SAS process can be a useful method in pharmaceutical and nutraceutical applications with high stability, bioaccessibility, bioavailability and thus enhanced nutritional value.Herein, we demonstrate that a thiophene-modified quinoxaline core small molecule can be applied in Sb2(S,Se)3 solar cells. We reveal that the interaction between thiophene and Sb2(S,Se)3 through the Sb-S bond essentially improves the interfacial hole-extraction ability. This study provides a cost-effective dopant-free hole-transporting material for inorganic thin film solar cell applications with excellent stability.Intermetallic CaPt2 nanoparticles, supported on titanium group oxides, were prepared using a molten salt method with CaH2 as both the reducing agent and the calcium source. The nanoparticles exhibited superior catalytic activity compared to a commercial Pt/C catalyst in the hydrogenation of ketones to alcohols, which could be promoted by electron-rich Pt sites in CaPt2.H2 has been comprehensively deemed a promising potential candidate to replace traditional fossil fuel-based energy. Typically, the hydrolysis of most hydrogen-rich boron hydrides (e.g. NaBH4, NH3BH3 and Me2NHBH3) catalyzed by nanomaterials generates H2 with only one H atom supplied by water and the other one by a hydrogen-rich boron hydride. Interestingly, both H atoms of produced H2 are provided by water upon hydrolysis of B2(OH)4. Herein, the catalytic mechanisms of H2 evolution upon water splitting at the expense of B2(OH)4 in its hydrolysis reactions catalyzed by acid, base or metal nanoparticles have been investigated by density functional theory (DFT) calculations. By computational studies, the mechanisms of catalysis by base and metal nanoparticles are basically the same as those speculated from our previous experiments. The previously proposed acid catalytic mechanism has been overturned, however. This study not only provides important insights into the catalytic mechanism for water splitting at the expense of B2(OH)4, but also opens up an exciting opportunity to use water to store H2.The zinc hydride compound, [Tptm]ZnH, may achieve the reduction of CO2 by (RO)3SiH (R = Me, Et) to the methanol oxidation level, (MeO)xSi(OR)4-x, via the formate species, HCO2Si(OR)3. However, because insertion of CO2 into the Zn-H bond is more facile than insertion of HCO2Si(OR)3, conversion of HCO2Si(OR)3 to the methanol level only occurs to a significant extent in the absence of CO2.Ab initio molecular orbital theory is used to study the structures of six and eight π-electron bare rings of group-XIV elements, and even larger [n]annulenes up to C18H18, including some of their mono-, di-, tri-, and tetra-anions. While some of the above rings are planar, others are nonplanar. A much spotlighted case is cyclo-octatetraene (C8H8), which is predicted to be nonplanar together with its heavier group-XIV analogues Si8H8 and Ge8H8, with the solely planar members of its family having the stoichiometric formulas C4Si4H8 and C4Ge4H8. A similar situation arises with the six π-electron bare rings, where benzene and substituted ones up to C3Si3H6 or so are planar, while others are not. However, the explanations encountered in the literature find support in ab initio calculations for such species, often rationalized from distinct calculated features. Using second-order Møller-Plesset perturbation theory and, when affordable (particularly tetratomics, which may allow even higher levels), the coupled-cluster method including single, double, and perturbative triple excitations, a common rationale is suggested based on a novel concept of quasi-molecules or the (3+4)-atom partition scheme. Any criticism of tautology is therefore avoided. The same analysis has also been successfully applied to even larger [n]annulenes, to their mixed family members involving silicon and germanium atoms, and to the C18 carbon ring. Furthermore, it has been extended to annulene anions to check the criteria of the popular Hückel rule for planarity and aromaticity. Exploratory work on cycloarenes is also reported. Besides a partial study of the involved potential energy surfaces, equilibrium geometries and harmonic vibrational frequencies have been calculated anew, for both the parent and the actual prototypes of the quasi-molecules.
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