Villumsenowens0625

Practical Pd-catalyzed 2-pyridones were designed to achieve chromeno[2,3-b]pyridine-2-ones. The reaction proceeds through domino nucleophilic addition and decarboxylative arylation, respectively. This methodology offers a moderately efficient approach to construct the bioactive, fused-heterocyclic skeletons via selective C-O bond formation and decarboxylative arylation in a single step with high selectivity and good yields.Complexes with ligand-to-metal charge-transfer (LMCT) excited states involving d0 metals represent a new design for photocatalysts. Herein, the photochemistry and photophysics of d0 titanocenes of the type Cp2Ti(C2R)2, where C2R = ethynylphenyl (C2Ph), 4-ethynyldimethylaniline (C2DMA), or 4-ethynyltriphenylamine (C2TPA), have been investigated. Cp2Ti(C2Ph)2 and Cp2Ti(C2DMA)2 have also been characterized by single-crystal X-ray diffraction. The two aryl rings in Cp2Ti(C2DMA)2 are nearly face-to-face in the solid state, whereas they are mutually perpendicular for Cp2Ti(C2Ph)2. All three complexes are brightly emissive at 77 K but photodecompose at room temperature when irradiated into their lowest-energy absorption band. The emission wavelengths and photodecomposition quantum yields are as follows Cp2Ti(C2Ph)2, 575 nm and 0.65; Cp2Ti(C2TPA)2, 642 nm and 0.42; Cp2Ti(C2DMA)2, 672 nm and 0.25. Extensive benchmarking of the density functional theory (DFT) model against the structural data and of the time-dependent DFT (TDDFT) model against the absorption and emission data was performed using combinations of 13 different functionals and 4 basis sets. The model that predicted the absorption and emission data with the greatest fidelity utilized MN15/LANL2DZ for both the DFT optimization and the TDDFT. Computational analysis shows that absorption involves a transition to a 1LMCT state. Whereas the spectroscopic data for Cp2Ti(C2TPA)2 and Cp2Ti(C2DMA)2 are well modeled using the optimized structure of these complexes, Cp2Ti(C2Ph)2 required averaging of the spectra from multiple rotamers involving rotation of the Ph rings. Consistent with this finding, an energy scan of all rotamers showed a very flat energetic surface, with less than 1.3 kcal/mol separating the minimum and maximum. The computational data suggest that emission occurs from a 3LMCT state. Optimization of the 3LMCT state demonstrates compression of the C-Ti-C bond angle, consistent with the known products of photodecomposition.Per- and polyfluoroalkyl substances (PFAS) are a diverse class of synthetic chemicals that accumulate in the environment. Many proteins, including the primary human serum transport protein albumin (HSA), bind PFAS. The predictive power of physiologically based pharmacokinetic modeling approaches is currently limited by a lack of experimental data defining albumin-binding properties for most PFAS. A novel thermal denaturation assay was optimized to evaluate changes in the thermal stability of HSA in the presence of increasing concentrations of known ligands and a structurally diverse set of PFAS. Assay performance was initially evaluated for fatty acids and HSA-binding drugs ibuprofen and warfarin. Concentration-response relationships were determined and dissociation constants (Kd) for each compound were calculated using regression analysis of the dose-dependent changes in HSA melting temperature. Estimated Kd values for HSA binding of octanoic acid, decanoic acid, hexadecenoic acid, ibuprofen, and warfarin agreed with established values. The binding affinities for 24 PFAS that included perfluoroalkyl carboxylic acids (C4-C12), perfluoroalkyl sulfonic acids (C4-C8), mono- and polyether perfluoroalkyl ether acids, and polyfluoroalkyl fluorotelomer substances were determined. These results demonstrate the utility of this differential scanning fluorimetry assay as a rapid high-throughput approach for determining the relative protein-binding properties and identification of chemical structures involved in binding for large numbers of structurally diverse PFAS.A recently reported ruthenium(II) complex bearing an extended dipyridophenazine ligand exhibits unusual long-lived dual emission at room temperature. In this study, the effect of the introduction of a methyl protecting group to the imidazole moiety of this ligand (L1, 11-methyl-11H-imidazo[4,5-i]dipyrido[3,2-a2',3'-c]phenazine) on the photophysics of the respective ruthenium(II) complex [(tbbpy)2Ru(L1)]2+ (C1) is demonstrated by means of electrochemistry, UV/vis absorption and emission spectroscopy, as well as emission lifetime measurements, and transient absorption spectroscopy on the nanosecond time scale. At room temperature, C1 shows dual emission both in aprotic and in protic solvents with time constants of 1.1/34.2 and 1.2/8.4 μs, respectively. These lifetimes are assigned to the emission from 3MLCT and 3LC states. The introduction of the methyl group increases the lifetime of the 3LC state in C1 almost by a factor of 2 in acetonitrile solution compared to the previously reported compound. Accordingly, the newly introduced methyl group is described as a protecting group for the imidazole moiety of the heterocyclic ligand, which enables prolonged lifetimes of the dual emissive complex in protic solvents. The stabilization of the electronic structure is further underlined by the enhanced stability toward electrochemical reduction as evidenced by cyclic voltammetry.Breast cancer is one of the most common malignant diseases among women worldwide, and the existence of breast cancer stem cells is closely associated with poor outcomes. Herein, we report an electrochemical phenotyping method to characterize the stemlike phenotype in breast cancer, offering a low-cost but robust choice other than the highly expensive and experience-dependent flow cytometry. Specially, after immune-magnetic beads-assisted enrichment, an in situ programmable DNA circuit is designed using capture probes to bring in the toeholds for DNA assembly and effector probes to accelerate the removal of background signals. The electrochemical phenotyping method could sensitively determine breast cancer stem cells in a wide linear range and exhibit desirable accuracy and reliability. The method can not only monitor the phenotypic transition of breast cancer cells and the drug-reversed effect but also determinate stemlike phenotype in the mice bearing breast cancer xenograft tumor. Overall, the electrochemical phenotyping method may provide promising technical support for precise management of breast tumors.Regulation of fast three-electron-transfer processes for electrocatalytic oxidation of ammonia to nitrogen by achieving efficient generation and utilization of active sites is the optimal strategy in ammonia-containing wastewater treatment. However, the limited number of accessible active sites and sluggish interfacial mass transfer are two main bottlenecks restricting conventional ammonia oxidation configurations. Herein, we develop a macroporous Ni foam electrode integrated with vertically aligned two-dimensional mesoporous Ni2P nanosheets to create sufficient exposure of active centers. A novel ammonia oxidation reactor with the developed hierarchical porous-structured electrodes was assembled to construct an intensified microfluidic process with flow-through operation to mitigate macroscopic mass transport limitations. The confined microreaction space in the hierarchical porous reactor further promotes spontaneous nanoscale diffusion/convection of the target contaminant to high-valence Ni sites and enhances the microscopic mass transfer. The combined results of electrochemical measurements and in situ Raman spectra showed that the ammonia degradation mechanism results from direct oxidation by the high-valence Ni, significantly different from the conventional indirect active-chlorine-species-mediated oxidation. The optimized reactor achieves high-efficiency three-electron-transfer ammonia conversion with an ammonia removal efficiency of ∼70% from an initial concentration of ∼1400 mg/L and byproduct production of ∼4%, significantly superior to a conversion unit comprising a featureless Ni-based electrode in the immersed configuration, which had >50% byproduct yield. 20 days of continuous operation under variable conditions achieved >90% ammonia degradation performance and an energy consumption of 25.42 kW h kg-1 N (1 order of magnitude lower than the active-chlorine-mediated process), showing the potential of the reactor in medium-concentration ammonia-containing wastewater treatment.The dynamics of complex topological defects in ferroelectric materials is explored using automated experimentation in piezoresponse force microscopy. Specifically, a complex trigger system (i.e., "FerroBot") is employed to study metastable domain-wall dynamics in Pb0.6Sr0.4TiO3 thin films. Several regimes of superdomain wall dynamics have been identified, including smooth domain-wall motion and significant reconfiguration of the domain structures. We have further demonstrated that microscopic mechanisms of the domain-wall dynamics can be identified; i.e., domain-wall bending can be separated from irreversible domain reconfiguration regimes. In conjunction, phase-field modeling was used to corroborate the observed mechanisms. As such, the observed superdomain dynamics can provide a model system for classical ferroelectric dynamics, much like how colloidal crystals provide a model system for atomic and molecular systems.Sensitive and reliable analysis of telomerase activity is important for clinical diagnosis, therapy, and prognosis of osteosarcoma. Telomerase activity is a complicated concept including both the amount of active telomerases and the length of the telomerases extension product. Still, few of the strategies formerly proposed distinguish the two aspects of telomerase activity. Herein, we propose a novel CRISPR-Cas12a-based fluorescent sensing platform that can output signals of both the amounts of telomerase and length of telomerase extension products with the assistance of an elegantly designed stem-loop probe and CRISPR-Cas12a system. On this basis, we induced a novel index, average telomerase activity, for accurate cancer reporting. Through systematic laboratory and clinical experiments, we have demonstrated that average telomerase activity can accurately distinguish cancer cells and has the potential for osteosarcoma staging.With the depletion of nonrenewable resources such as oil/coal/gas, more and more research studies began to focus on the high-value utilization of residual biomass resources. Herein, for the first time, honeycomb nanoporous microspheres fabricated from renewable biomass resources of cellulose were used as a carrier to fabricate a highly dispersed palladium (Pd) nanocatalyst. Various physicochemical characterizations presented convincing pieces of evidence for the good dispersion of Pd clusters with a mean diameter of 1.6 nm. As the carrier, cellulose microspheres with an interconnected nanoporous structure contributed to the adhesion and dispersion of Pd particles, and their rich hydroxyl groups could fix the Pd particles. Importantly, the cellulose matrix could in situ induce the formation of metallic Pd(0) during calcination without a reductant. buy MLN7243 The cellulose/Pd catalyst was applied to the Suzuki coupling reaction, which exhibited promising catalytic activity compared to commercial Pd/C and unsupported homogeneous Pd(OAc)2 catalysts, as well as good stability.