Haaninglawrence2913

Likewise, the ratiometric sensing of solution alkalinity and tris(2-carboxyethyl)phosphine can be achieved using blue-emitted diTyr residues and red-emitted AuNCs as the responsive units, respectively, and the corresponding other two fluorophores as the reference signals. This study addresses a concept of trinity fluorescence ratiometric sensing system with multiple targets and optional references, which should be a promising pathway to meet the challenges from complexing biochemical environments and multivariate analysis. Copyright © 2020 American Chemical Society.Overall performance of composite calcium silicate boards (CCSBs) was investigated to further promote their application. The alkali activators were used to fully hydrate the calcium and silicon raw materials, which further improved the comprehensive performance of the CCSBs made of four pure industrial solid wastes. Within the range of dosage in this study, single doping of different proportions of the alkali activator improved the flexural strength of the CCSB. Based on this, the mechanical properties of the CCSB were further improved as the compounded alkali activator was optimized. Flexural strength is improved when the average pore diameter was refined. The freeze-thaw cycle test shows that a compound-doped alkali activator can effectively reduce the mass loss and strength loss, thereby improving the frost resistance of this material. This research discussed an economically affordable approach to prepare the CCSB material made of industrial solid waste. Copyright © 2020 American Chemical Society.Developing a photocatalyst system to generate hydrogen from water is a topic of great interest for fundamental and practical importance. In this study, we develop a new Z-scheme photocatalytic system for overall water splitting that consists of Rh/K4Nb6O8 for H2 evolution, Pt/BiVO4 for O2 evolution, and I-/IO3 - for an electron mediator under UV light irradiation. The oxygen evolution photocatalyst BiVO4 was prepared by the microwave-assisted hydrothermal method. The method is fast and simple, as compared to conventional hydrothermal synthesis. The catalysts were characterized by powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and UV-visible spectroscopy. The photocatalytic water splitting is investigated in (i) aqueous AgNO3 as sacrificial electron scavengers and (ii) a Z-scheme photocatalytic water splitting system. The BiVO4 photocatalysts prepared by the microwave-assisted hydrothermal method not only showed a very high oxygen evolution rate (2622 μmol g-1 h-1) of water splitting reaction in an aqueous AgNO3 solution but also achieved a high H2 evolution rate (340 μmol g-1 h-1) and O2 evolution rate (172 μmol g-1 h-1) in a Z-scheme overall water splitting system. Copyright © 2020 American Chemical Society.Realizing the diagnosis of lung cancer at an inchoate stage is significant to get valuable time to conduct curative surgery. In this work, we relied on a density functional theory (DFT)-proposed Ru-SnS2 monolayer as a novel, promising biosensor for lung cancer diagnosis through exhaled gas analysis. The results indicated that the Ru-SnS2 monolayer has admirable adsorption performance for three typical volatile organic compounds (VOCs) of lung cancer patients, which therefore results in a remarkable change in the electronic behavior of the Ru-doped surface. As a consequence, the conductivity of the Ru-SnS2 monolayer increases after gas adsorption based on frontier molecular orbital theory. This provides the possibility to explore the Ru-SnS2 monolayer as a biosensor for lung cancer diagnosis at an early stage. In addition, the desorption behavior of three VOCs from the Ru-SnS2 surface is studied as well. Our calculations aim at proposing novel sensing nanomaterials for experimentalists to facilitate the progress in lung cancer prognosis. Copyright © 2020 American Chemical Society.Herein, we report the synthesis, characterization, and catalytic performance of cationic Pd(II)-Anthraphos complexes in the intermolecular hydroamination of aromatic alkynes with aromatic amines. The reaction proceeds with 0.18 mol % of catalyst loading, at 90 °C for 4 h under neat conditions. Good to excellent yields could be obtained for a broad range of amines and alkynes. Copyright © 2020 American Chemical Society.A one-pot clean preparation procedure and catalytic performance of platinum nanoparticles (NPs) reduced and stabilized by sodium lignosulfonate in aqueous solution are reported. No other chemical reagents are needed during the metal reduction and stabilization step, thanks to the active participation of sodium lignosulfonate (SLS). UV-vis, Fourier transform infrared (FT-IR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), 1H NMR, 195Pt NMR, and two-dimensional heteronuclear single-quantum coherence (2D HSQC) NMR studies were thoroughly performed to analyze the formation, particle size, and main lattice planes of NPs, the valence-state changes of the metal, and structural changes of SLS. An ecofriendly selective synthesis of cis-pinane from an abundant renewable natural resource, α-pinene, was developed in the presence of the prepared Pt NP aqueous system. Furthermore, this catalyst system was proved to show easy recovery and stable reusability by five-run tests. The synergistic effect of SLS reduction and stabilization not only avoided the introduction of conventional reducing agents and stabilizers but also made full use of the byproducts of the pulp and paper industry. This proved to be an environmentally friendly method for converting the natural resource α-pinene to cis-pinane. Copyright © 2020 American Chemical Society.A porphyrin cis tautomer, where the two central NH protons are on adjacent pyrrole rings, has long been invoked as an intermediate in porphyrin tautomerism. Only recently, however, has such a species been isolated and structurally characterized. Thus, single-crystal X-ray structure determinations of two highly saddled free-base porphyrins, β-heptakis(trifluoromethyl)-meso-tetrakis(p-fluorophenyl)porphyrin, H2[(CF3)7TFPP], and β-octaiodo-5,10,15,20-tetrakis(4'-trifluoromethylphenyl)porphyrin, H2[I8TCF3PP], unambiguously revealed cis tautomeric structures, each stabilized as a termolecular complex with a pair of ROH (R = CH3 or H) molecules that form hydrogen-bonded N-H···O-H···N straps connecting the central NH groups with the antipodal unprotonated nitrogens. The unusual substitution patterns of these two porphyrins, however, have left open the question how readily such supramolecular assemblies might be engineered, which prompted us to examine the much more synthetically accessible β-octabromo-meso-tetraphenylporphyrins. Herein, single-crystal X-ray structures were obtained for two such compounds, 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetrakis(4'-trifluoromethylphenyl)porphyrin, H2[Br8TCF3PP], and 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-tetrakis(4'-fluorophenyl)porphyrin, H2[Br8TFPP], and although the central hydrogens could not all be located unambiguously, the electron density could be convincingly modeled as porphyrin cis tautomers, existing in each case as a bis-methanol adduct. In addition, a perusal of the Cambridge Structural Database suggests that there may well be additional examples of porphyrin cis tautomers that have not been recognized as such. We are therefore increasingly confident that porphyrin cis tautomers are readily accessible via supramolecular engineering, involving the simple stratagem of crystallizing a strongly saddled porphyrin from a solvent system containing an amphiprotic species such as water or an alcohol. Copyright © 2020 American Chemical Society.Electrospun materials made from biodegradable polycaprolactone are used widely in various tissue engineering and regenerative medicine applications because of their morphological similarity to the extracellular matrix. However, the main prerequisite for the use of such materials in clinical practice consists of the selection of the appropriate sterilization technique. This study is devoted to the study of the impact of traditional sterilization and disinfection methods on a nanofibrous polycaprolactone layer constructed by means of the needleless electrospinning technique. It was determined that hydrogen peroxide plasma treatment led to the loss of fibrous morphology and the creation of a foil. However, certain sterilization (ethylene oxide, gamma irradiation, and peracetic acid) and disinfection techniques (ethanol and UV irradiation) were found not to lead to a change in morphology; thus, the study investigates their impact on thermal properties, molecular weight, and interactions with a fibroblast cell line. It was determined that the surface properties that guide cell adhesion and proliferation were affected more than the bulk properties. The highest proliferation rate of fibroblasts seeded on nanofibrous scaffolds was observed with respect to gamma-irradiated polycaprolactone, while the lowest proliferation rate was observed following ethylene oxide sterilization. Copyright © 2020 American Chemical Society.The Wenzel model, commonly used for predicting the equilibrium contact angle (CA) of drops which penetrate the asperities of a rough surface, does not account for the liquid volume stored in the asperities. Interestingly, many previous experimental and molecular dynamics studies have noted discrepancies between observed CAs and those predicted by the Wenzel model because of this neglected liquid volume. Here, we apply a thermodynamic model to wetting of periodically patterned surfaces to derive a volume-corrected Wenzel equation in the limit of small pattern wavelength (compared to drop size). We show that the corrected equilibrium CA is smaller than that predicted by the Wenzel equation and that the reduction in CA can be significant when the liquid volume within the asperities becomes non-negligible compared to the total droplet volume. In such cases, the corrected CAs agree reasonably well with experimental observations and results of molecular dynamics simulations reported in previous studies. Copyright © 2020 American Chemical Society.The Ca-based sorbent cyclic calcination/carbonation reaction (CCCR) is a high-efficiency technique for capturing CO2 from combustion processes. Omipalisib nmr The CO2 capture ability of CaO modified with sodium humate (HA-Na) (HA-Na/CaO) in long-term calcination/carbonation cycles was investigated. The enhancement mechanism of HA-Na on CCCR was proposed and demonstrated. The effects of carbonation temperature, reaction duration, and the addition amount of HA-Na on the carbonation rate of the CaO adsorbent were also studied. HA-Na/CaO is allowed to react 20 min at the optimum conditions for calcination (920 °C, 100% N2) and for carbonation (700 °C, 15% CO2, 85% N2), respectively. HA-Na plays a key role in the CCCR process, and the carbonation conversion rate is lifted obviously. The maximum conversion rate of HA-Na/CaO is 23% higher than that of CaO in the first cycle. After 20 cycles, the conversion rate of HA-Na/CaO is still 0.28, while that of CaO is only 0.15. The carbonation conversion rate for HA-Na/CaO is improved by 86% compared to CaO.