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David Sander posted an update 6 months, 2 weeks ago
Tetraphenylborate (TPB) anions traverse membranes but are excluded from mitochondria by the membrane potential (Δψ). TPB-conjugates also distributed across membranes in response to Δψ, but surprisingly, they rapidly entered cells. They accumulated within lysosomes following endocystosis. This pH-independent targeting of lysosomes makes possible new classes of probe and bioactive molecules.Nitrosoarenes (ArNOs) are toxic metabolic intermediates that bind to heme proteins to inhibit their functions. Although much of their biological functions involve coordination to the Fe centers of hemes, the factors that determine N-binding or O-binding of these ArNOs have not been determined. We utilize X-ray crystallography and density functional theory (DFT) analyses of new representative ferrous and ferric ArNO compounds to provide the first theoretical insight into preferential N-binding versus O-binding of ArNOs to hemes. Our X-ray structural results favored N-binding of ArNO to ferrous heme centers, and O-binding to ferric hemes. Results of the DFT calculations rationalize this preferential binding on the basis of the energies of associated spin-states, and reveal that the dominant stabilization forces in the observed ferrous N-coordination and ferric O-coordination are dπ-pπ* and dσ-pπ*, respectively. Our results provide, for the first time, an explanation why in situ oxidation of the ferrous-ArNO compound to its ferric state results in the observed subsequent dissociation of the ligand.The mechanism of the low-temperature water-gas shift (LT-WGS) reaction over Au/CeO2 catalysts with different ceria terminations, i.e., (111), (110), and (100) facets, was investigated. Using combined operando Raman and UV-Vis spectroscopy as well as isotope exchange experiments, we are able to draw conclusions about the reducibility behaviour and the exchange of surface oxygen. Additional density functional theory (DFT) calculations facilitate the vibrational bands assignments and enhance the interpretation of the results on a molecular level. A facet-dependent role of gold is observed with respect to the oxygen dynamics, since for the CeO2(111) facet the presence of gold is required to exchange surface oxygen, whereas the CeO2(110) facet requires no gold, as rationalized by the low defect formation energy of this facet. This behaviour suggests that surface properties (termination, stepped surface) may have a strong effect on the reactivity. AdipoRon supplier While the reduction of the support accompanies the reaction, its extent does not directly correlate with activity, highlighting the importance of other properties, such as the dissociative adsorption of water and/or CO2/H2 desorption. The results of our facet-dependent study are consistent with a redox mechanism, as underlined by H218O isotopic exchange experiments demonstrating the ready exchange of surface oxygen.Theranostic platforms that combine therapy with diagnosis not only prevent the undesirable biological responses that may occur when these processes are conducted separately, but also allow individualized therapies for patients. Polymer hydrogels have been employed to provide well-controlled drug release and targeted therapy in theranostics, where injectable hydrogels enable non-invasive treatment and monitoring with a single injection, offering greater patient comfort and efficient therapy. Efforts have been focused on applying injectable polymer hydrogels in theranostic research and clinical use. This review highlights recent progress in the design of injectable polymer hydrogels for cancer theranostics, particularly focusing on the elements/components of theranostic hydrogels, and their cross-linking strategies, structures, and performance with regard to drug delivery/tracking. Therapeutic agents and tracking modalities that are essential components of the theranostic platforms are introduced, and the design strategies, properties and applications of the injectable hydrogels developed via two approaches, namely chemical bonds and physical interactions, are described. The theranostic functions of the platforms are highly dependent on the architecture and components employed for the construction of hydrogels. Challenges currently presented by theranostic platforms based on injectable hydrogels are identified, and prospects of acquiring more comfortable and personalized therapies are proposed.Photon upconversion is a fascinating phenomenon that can convert low-energy photons to high-energy photons efficiently. However, most previous relevant research has been focused on upconversion systems with a sufficiently low lanthanide emitter concentration, such as 2 mol% for Er3+ in an Er-Yb coupled system. Realizing the upconversion from lanthanide heavily doped systems in particular, the emitter sublattice is still a challenge. Here, we report a mechanistic strategy to achieve the intense upconversion of the holmium sublattice in a core-shell-based nanostructure design through interfacial energy transfer channels. This design allowed a spatial separation of Ho3+ and sensitizers (e.g., Yb3+) into different regions and unwanted back energy transfers between them could then be minimized. By taking advantage of the dual roles of Yb3+ as both a migrator and energy trapper, a gradual color change from red to yellowish green was achievable upon 808 nm excitation, which could be further markedly enhanced by surface attaching indocyanine green dyes to facilitate the harvesting of the incident excitation energy. Moreover, emission colors could be tuned by applying non-steady state excitation. Such a fine-tunable color behavior holds great promise in anti-counterfeiting. Our results present a facile but effective conceptual model for the upconversion of the holmuim sublattice, which is helpful for the development of a new class of luminescent materials toward frontier applications.Recent in situ works have shown extensive evidence of the dramatic and reversible structure reconstructions of metal and alloy materials in reaction conditions. The reconstructions are of primary interest because they could lead to alternative catalytic mechanisms during real reactions. However, how the catalyst structure evolves under the pressures relevant to industrial applications (>1 atm) is so far unexplored. In our recent works, we have developed multiscale theoretical models to give reliable and precise predictions of the equilibrium shapes of metal nanoparticles and of the segregation properties of alloy surfaces at a given temperature and gas pressure. The theoretical predictions have been successfully used in interoperations of various in situ experimental observations. In this work, we applied these methods to study the detailed structural information of metal NPs and of bimetallic alloys at the temperature from 300 to 1000 K and the gas pressure from 10 to 107 Pa. The results show, in some cases, both the gas-induced shape change and the gas-induced segregation change are maximized when the gas adsorption is ‘just right’.
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