Silicon nanostructure-doped polymer/nematic liquid crystal composites for low voltage-driven smart windows.

In this work, two silicon nanostructures were doped into polymer/nematic liquid crystal composites to regulate the electric-optical performance. Commercial SiO2nanoparticles and synthesized thiol polyhedral oligomeric silsesquioxane (POSS-SH) were chosen as the dopants to afford the silicon nanostructures. SiO2nanoparticles were physically dispersed in the composites and the nanostructure from POSS-SH was implanted into the polymer matrix of the composites via photoinduced thiol-ene crosslinking. Scanning electron microscopy results indicated that the implantation of POSS microstructure into the polymer matrix was conducive to obtaining the uniform porous polymer microstructures in the composites while the introduction of SiO2nanoparticles led to the loose and heterogeneous polymer morphologies. The electric-optical performance test results also demonstrated that the electric-optical performance regulation effect of POSS microstructure was more obvious than that of SiO2nanoparticles. The driving voltage was reduced by almost 80% if the concentration of POSS-SH in the composite was nearly 8 wt% and the sample could be completely driven by the electric field whose voltage was lower than the safe voltage for continuous contact (24 V). This work could provide a creative approach for the regulation of electric-optical performance for polymer/nematic liquid crystal composites and the fabrication of low voltage-driven PDLC films for smart windows.

Downregulation of long noncoding RNA SNHG7 protects against inflammation and apoptosis in Parkinson's disease model by targeting the miR-425-5p/TRAF5/NF-κB axis.

Accumulated evidence has manifested that long noncoding RNA (lncRNA) is involved in the progress of Parkinson's disease (PD). SNHG7, a novel lncRNA, has been found to be involved in tumorigenesis. However, SNHG7 expression and its functional effects on PD remain uncharted. Rotenone (Rot) was adopted to construct PD models in Sprague-Dawley (SD) rats and SH-SY5Y cells, respectively. The expression levels of caspase 3, tyrosine hydroxylase (TH), ionized calcium-binding adapter molecule 1 (Iba1) in SD rat striatum were measured via immunohistochemistry and western blot. Additionally, the expressions of inflammatory cytokines (interleukin 1ß [IL-1ß], IL-6, tumor necrosis factor α) and oxidative stress factors (malondialdehyde, superoxide dismutase, and glutathione peroxidase) in the brain tissues were examined using real-time polymerase chain reaction and enzyme-linked immunosorbent assay, respectively. Moreover, the protein levels of tumor necrosis factor receptor-associated factor (TRAF5), I-κB, nuclear factor-κB (NF-κB), HO-1, Nrf2 were detected via western blot. Bioinformatics was applied to predict the targeting relationship between SNHG7, miR-425-5p, and TRAF5. Dual-luciferase activity assay and RNA immunoprecipitation assays were conducted to verify their interactions. In comparison to healthy donors, SNHG7 was found upregulated while miR-425-5p expression was downregulated in PD patients. Functional experiments confirmed that SNHG7 downregulation or miR-425-5p overexpression attenuated neuronal apoptosis in the Rot-mediated PD model, TH-positive cell loss, and microglial activation by mitigating inflammation and oxidative stress. Mechanistically, SNHG7 served as a competitive endogenous RNA by sponging miR-425-5p and promoted TRAF5 mediated inflammation and oxidative stress. Inhibition of SNHG7 ameliorated neuronal apoptosis in PD through relieving miR-425-5p/TRAF5/NF-κB signaling pathway modulated inflammation and oxidative stress, and similar results were observed in the Rot-mediated rat model of PD.

Photoinduced Multiple Effects to Enhance Uranium Extraction from Natural Seawater by Black Phosphorus Nanosheets.

Based on the photoinduced photothermal, photoelectric, and photocatalytic effects of black phosphorus (BP) nanosheets, a BP-PAO fiber with enhanced uranium extraction capacity and high antibiofouling activity is fabricated by compositing BP nanosheets into polyacrylamidoxime (PAO). The photothermal effect increases the coordination interaction between UO2 2+ and the functional amidoxime group, and the photoelectric effect produces the surface positive electric field that exhibits electrostatic attraction to the negative [UO2 (CO3 )3 ]4- , which all increase the capacity for uranium adsorption. The photocatalytic effect endows the adsorbent with high antibiofouling activity by producing biotoxic reactive oxygen species. Owing to these three photoinduced effects, the photoinduced BP-PAO fiber shows a high uranium adsorption capacity of 11.76 mg g-1 , which is 1.50 times of the PAO fiber, in bacteria-containing natural seawater.

Preparation of Cyano-Substituted Tetraphenylethylene Derivatives and Their Applications in Solution-Processable OLEDs.

Creation of organic luminescent materials with high solid-state efficiency is of vital importance for their applications in optoelectronic fields. Here, a series of AIE luminogens (AIE gens), (Z)-2,3-bis(4-(9,9-bis(6-(9H-carbazol-9-yl)hexyl)-9H-fluoren-2-yl)phenyl)-3-phenylacrylonitrile (SFC), and 2,3-bis(4-(9,9-bis(6-(9H-carbazol-9-yl)hexyl)-9H-fluoren-2-yl)phenyl)fumaronitrile (DFC), utilizing 2,3,3-triphenylacrylonitrile and 2,3-diphenylfumaronitrile as respective centers, are designed and synthesized by Suzuki coupling reactions with high yields. The cis- and trans-isomers of DFC are also successfully obtained. All of them are thermally stable and show good solubility in common organic solvents. They all emit weakly in solution, but become strong emitters when fabricated into solid films. It is found introduction of one additional cyano group in DFC induced a big red-shift in solid-state emission, owing to its high electron-withdrawing ability. The cis- and trans-DFC show similar photophysical and Cyclic voltammogram (CV) behaviors. Non-doped solution-processed organic light-emitting diodes (OLEDs) using the three compounds as light-emitting layers are fabricated. SFC gives the best device performance with a maximum luminance of 5201 cd m-2, a maximum current efficiency of 3.67 cd A-1 and a maximum external quantum efficiencies (EQE) of 1.37%. Red-shifted EL spectra are observed for cis- and trans-DFC-based device, and the OLED using trans-DFC as active layer exhibits better performance, which might derive from their different conformation in film state.

Investigation on Fluorescence Quenching Mechanism of Perylene Diimide Dyes by Graphene Oxide.

Perylene diimide derivatives were used as probes to investigate the effect of the molecular structures on the fluorescence quenching mechanism in a perylene diimide/graphene oxide system. The electrons transferred from the excited state of dyes to the conductive band of graphene oxide with different concentrations were determined by fluorescence spectra. The results indicated that the quenching efficiency of perylene diimides by graphene oxide was not only dependent on the difference between the lowest unoccupied molecular orbital level of dyes and the conduction band of the graphene oxide, but also mainly on the difference in the molecular structures.

Effectiveness of traditional herbal Kampo medicine Goreisan on chronic subdural hematoma recurrence: a meta-analysis.

Objectives: Our objective was to compare the effectiveness of Traditional Chinese herbal Kampo medicine Goreisan in improving recurrence in patients with chronic subdural hematoma (CSDH). Methods: Eligible randomized controlled trials prospective trials, and retrospective cohort studies were systematically identified through searches of PubMed, Cochrane Library, and CNKI from inception to March 2024. Following the application of predetermined inclusion and exclusion criteria to screen the available studies, main outcome measures were rigorously extracted. RevMan v5.4 software was utilized to evaluate the overall recurrence rate, employing a random-effects model to calculate pooled odds ratios with the Mantel-Haenszel estimation method. Inter-study heterogeneity was assessed using the Cochran Q (Chi-square) test and I2 statistics. Funnel plots were used to evaluate publication bias. Results: Among the 48 articles initially screened for citation, eight were ultimately selected for inclusion in the study. The results of our network meta-analysis indicate that patients with newly diagnosed Chronic subdural hematoma experienced a significantly reduced recurrence rate when treated with Goreisan compared to standard neurosurgical treatment (OR: 0.72; 95% CI 0.61-0.86; p = 0.00003). There was no statistically significant difference in the incidence rates of complications, including general fatigue, allergic reactions, hepatic dysfunction, and interstitial pneumonia (OR: 7.21; 95% CI 0.37-141.29; p = 0.19). Conclusion: Traditional medicine Goreisan was effective in reducing CDSH recurrence rates. For clinical treatment, it provides a high level of evidence-based medicine. It is also necessary to conduct multicenter randomized controlled trials with dose adjustments to determine whether Goreisan interventions improve neurological function or prognosis.

Thermal-Responsive Smart Windows with Passive Dimming and Thermal Energy Storage.

Chromogenic smart windows are one of the key components in improving the building energy efficiency. By simulation of the three-dimensional network of polymer hydrogels, thermal-responsive phase change materials (TRPCMs) are manufactured for energy-saving windows. For simulated polymer hydrogels, tetradecanol (TD) and a color changing dye (CCD) are filled in situ in poly(n-butyl isobutyrate) (PBB) networks. TRPCMs convert solar energy into thermal energy through a dark blue CCD. The TD phase change material (PCM) absorbs heat energy to become a transparent liquid. Simultaneously, the CCD changes from blue to colorless and transparent at around 45 °C. As a result, as-prepared TRPCMs transform from an opaque state at room temperature to a high-transparency state after melting (74.5%). TRPCMs also show a good thermal storage capacity, with a phase transition enthalpy exceeding 161.9 J g-1. As-prepared smart materials can simultaneously achieve photothermal conversion, thermal energy diffusion, latent heat storage, and resistance to liquid leakage at the phase interface between opaque and transparent states, providing more options for the design of energy-saving buildings.

Microstructure Evolution at Ni/Fe Interface in Dissimilar Metal Weld between Ferritic Steel and Austenitic Stainless Steel.

The formation and evolution of microstructures at the Ni/Fe interface in dissimilar metal weld (DMW) between ferritic steel and austenitic stainless steel were investigated. Layered martensitic structures were noted at the nickel-based weld metal/12Cr2MoWVTiB steel interface after welding and post-weld heat treatment (PWHT). The formation of the interfacial martensite layer during welding was clarified and its evolution during PWHT was discussed by means of scanning electron microscopy (SEM), electron backscatter diffraction (EBSD), electron probe microanalysis (EPMA), focused ion beam (FIB), transmission electron microscopy (TEM), energy dispersive X-ray (EDX), transmission kikuchi diffraction (TKD), phase diagrams, and theoretical analysis. In as-welded DMW, the Ni/Fe interface structures consisted of the BCC quenched martensite layer and the FCC partially mixed zone (PMZ), which was the result of inhomogeneous solid phase transformation due to the chemical composition gradient. During the PWHT process, the BCC interfacial microstructure further evolved to a double-layered structure of tempered martensite and quenched martensite newly formed by local re-austenitization and austenite-martensite transformation. These types of martensitic structures induced inhomogeneous hardness distribution near the Ni/Fe interface, aggravating the mismatch of interfacial mechanical properties, which was a potential factor contributing to the degradation and failure of DMW.

A Stabilized Polyacrylonitrile-Encapsulated Matrix on a Nanolayered Vanadium-Based Cathode Material Facilitating the K-Storage Performance.

Layered vanadium-based metal oxides were regarded as promising cathode materials accounting for suitable K+ transport channels as well as high work potential in K-ion batteries. Nevertheless, because of the large radius of K+ and the rigid structure of inorganic materials, the typical K0.486V2O5 suffers from volume expansion seriously in the repeated charging and discharging processes along with poor ionic and electronic conductivity, consequently determining inevitably poor electrochemical properties. Herein, we proposed a stabilized polymer (PAN) matrix on K0.486V2O5 nanobelts by a liquid-assisted methodology and further electrospinning technology. As a result, a nanocomposite containing a 3D conductive and interconnected mesh structure was thus constructed. By avoiding the full carbonization of polyacrylonitrile (PAN) with appropriate thermal treatment, the elastic properties of the PAN precursor can be retained, effectively inhibiting the volume effect, and the stabilized PAN-encapsulated matrix can also greatly accelerate transport rates of K+ and electrons at a high rate as well as restrict the decomposition of organic electrolytes and side reactions. This work can supply significant basic scientific value of the polymer surface coating methodology for the far-reaching development of inorganic cathode materials in K-ion batteries.

[Corrigendum] Metformin reverses multidrug resistance in human hepatocellular carcinoma Bel­7402/5­fluorouracil cells.

Subsequently to the publication of the above paper, the authors have reviewed its content and the primary data, and have realized that the western blots selected to show the ß­actin experiments featured in Fig. 4A and Fig. 3C were the same blot, albeit with a different exposure time. The control blots correctly presented for Fig. 3C were inadvertently copied into Fig. 4A owing to an error made during the figure compilation process. The revised version of Fig. 4, containing the correct ß­actin blots for Fig. 4A, is shown below. Note that this error did not significantly affect the results or the conclusions reported in this paper, and all the authors agree to this Corrigendum. The authors thank the Editor of Molecular Medicine Reports for allowing them the opportunity to publish this corrigendum, and apologize to the readership for any inconvenience caused. [Molecular Medicine Reports 10: 2891­2897, 2014; DOI: 10.3892/mmr.2014.2614].

2,5-Bis[2-(4-methyl-phen-yl)ethyn-yl]benzyl methacrylate.

In the title bis-tolane derivative, C(29)H(24)O(2), the central benzene ring forms dihedral angles of 29.12 (9) and 26.46 (9)° with the other two benzene rings. The dihedral angle between two terminal benzene rings is 55.58 (8)°.

A Smart Design Strategy for Super-Elastic Hydrogel with Long-Term Moisture, Extreme Temperature Resistance, and Non-Flammability.

Elastic hydrogel is a promising material category for designing biological muscles, repairable building materials, flexible electronic devices, and vulcanized rubber substitutes, which is required to have a long life, good self-healing performance and extreme temperature tolerance. Herein, a super-elastic mineral hydrogel is developed with long-lasting moisture, based on dynamic physical crosslinking between hydrated calcium ion clusters and amide groups of polyacrylamide (PAM). The complex hydrogel exhibits a super stretchability of 13 600% at room temperature, and can maintain the super flexibility in a wide temperature range of -40-50 °C or for a long period of 28 days. Particularly, the soft material cannot be ignited under an open flame at 400-500 °C, because of coupling dual flame retardant mechanisms containing the endothermic effect of liquid water evaporation and the barrier effect of calcium mineral salt on oxygen. In conclusion, the novel complex hydrogel with excellent tensile property, stability in extreme temperature or long operating time, and flame retardancy may become a promising candidate in the fields of agriculture, food, construction, medicine, and machinery.

2',10'-Dibromo-spiro-[cylohexane-1,6-di-benzo[d,f][1,3]dioxepine].

In the title compound, C(18)H(16)Br(2)O(2), the dihedral angle between the aromatic rings is 35.55 (17)° and the cyclohexyl ring adopts a chair-like conformation. In the crystal, molecules are linked by van der Waals forces.

Ultra-fast and stable extraction of Li metal from seawater.

Ultra-dense (99.2%) and ultra-stable Li7La3Zr2O12 were synthesized via a spark plasma sintering (SPS) technique, which were applied as solid-state electrolytes in Li metal extraction from seawater. 198 µg cm-2 h-1 of extraction efficiency and 1.0%-3.7% of power comsumption showed their promising potential for Li metal extraction.

Efficient Nondoped Pure Blue Organic Light-Emitting Diodes Based on an Anthracene and 9,9-Diphenyl-9,10-dihydroacridine Derivative.

Organic light-emitting diodes (OLEDs) have been greatly developed in recent years owing to their abundant advantages for full-color displays and general-purpose lightings. Blue emitters not only provide one of the primary colors of the RGB (red, green and blue) display system to reduce the power consumption of OLEDs, but are able able to generate light of all colors, including blue, green, red, and white by energy transfer processes in devices. However, it remains a challenge to achieve high-performance blue electroluminescence, especially for nondoped devices. In this paper, we report a blue light emitting molecule, DPAC-AnPCN, which consists of 9,9-diphenyl-9,10-dihydroacridine and p-benzonitrile substituted anthracene moieties. The asymmetrically decoration on anthracene with different groups on its 9 and 10 positions combines the merits of the respective constructing units and endows DPAC-AnPCN with pure blue emission, high solid-state efficiency, good thermal stability and appropriate HOMO and LUMO energy levels. Furthermore, DPAC-AnPCN can be applied in a nondoped device to effectively reduce the fabrication complexity and cost. The nondoped device exhibits pure blue electroluminescence (EL) locating at 464 nm with CIE coordinates of (0.15, 0.15). Moreover, it maintains high efficiency at relatively high luminescence. The maximum external quantum efficiency (EQE) reaches 6.04 % and still remains 5.31 % at the luminance of 1000 cd m-2 showing a very small efficiency roll-off.

Geochemical and Geological Characteristics of the Upper Ordovician-Lower Silurian Shales in the Upper Yangtze Basin, South China: Implication for the Shale Gas Exploration.

Shale gas exploration in the Upper Yangtze Basin has been conducted for over ten years. The successful drillings in the region suggest that well-planned geological survey and reservoir evaluation are indispensable for the success of these drillings. In this study, the shale gas potential of Late Ordovician to Early Silurian mudstones/shales of the Wufeng-Longmaxi formations in the Upper Yangtze Basin was evaluated. First, all of the available geochemical and petrological data from Late Ordovician to Early Silurian mudstones/shales in the region were compiled. Distributional patterns of total organic carbon (TOC) values, thickness, thermal maturity, and burial depth of organic-rich mudstones/shales from the targeted formations were then analyzed. Our results show that TOC values range from 1.20 to 5.12%; R o values range from 1.92 to 2.86%; porosity varies from 0.77 to 9.2%; permeability varies from 0.015 to 1.99 md; the composition of quartz group of mineral component ranges from 18 to 85%, 59% in average; and clay mineral component ranges from 7 to 56%, 31% in average. Finally, based on these comprehensive analysis, three areas with great potential, that is, Luzhou-Xishui, western Chongqing, and Wulong-Shizhu, were selected as targets for further shale gas exploration and exploitation.

Manual aspiration versus chest tube drainage in primary spontaneous pneumothorax without underlying lung diseases: a meta-analysis of randomized controlled trials.

OBJECTIVES: Although primary spontaneous pneumothorax (PSP) is an extremely frequent pathology, there is still no clear consensus on the treatment for these patients. We performed a strict meta-analysis on the effectiveness of manual aspiration (MA) compared to chest tube drainage (CTD) for the treatment of PSP. METHODS: A literature search was performed on PubMed, EMBASE and the Cochrane Library to identify randomized controlled trials comparing MA with CTD for the treatment of PSP. Independent reviewers evaluated the methodological quality of the included randomized controlled trials. Statistical heterogeneity among studies was quantitatively evaluated using the I-squared index. RESULTS: Five randomized controlled trials were included, and a total of 358 subjects were reported on. We found that MA was related to significantly shorter hospital stays [in days; mean difference -1.70, 95% confidence interval (CI) -2.36 to -1.04; P < 0.00001, fixed effect model] compared with CTD. However, no significant differences were found between the 2 treatments for immediate success rate (risk ratio 1.15, 95% CI 0.73-1.81; P = 0.54), 1-year recurrence rate, 1-week success rate, time of recurrence, chest surgery rate or complication rate. Subgroup analysis showed that MA can provide a significantly lower hospitalization rate than CTD with a tube size of >12 Fr or a water seal drainage system. CONCLUSIONS: On the basis of the currently available literature, MA is advantageous in the treatment of PSP because of shorter hospital stays. The subgroup analysis also indicates that MA can provide a lower hospitalization rate than CTD with a tube size of >12 Fr or a water seal drainage system. However, there are no significant differences between the 2 interventions with respect to immediate success rate, 1-year recurrence rate, 1-week success rate, time of recurrence, chest surgery rate or complication rate.

2,2'-Bi[6,6'-dimethyl-dibenzo[d,f][1,3]dioxepine].

The title compound, C(30)H(26)O(4), is a dimer of 6,6'-dimethyl-dibenzo[d,f][1,3]dioxepine linked by formation of a C-C bond in the para position with respect to one O atom. The dimer is arranged around an inversion centre. As is usually observed in related compounds, the dibenzo group is twisted, the two benzene rings making a dihedral angle of 41.56 (9)°. The seven-membered ring exhibits a twisted conformation.

2,10-Dibromo-6-isobutyl-6-methyl-dibenzo[d,f][1,3]dioxepine.

In the crystal structure of the title compound, C(18)H(18)Br(2)O(2), the two benzene rings of the bridged biphenyl unit are twisted by 38.0 (1)°.

3,9-Dibromo-6,7-dihydro-5H-dibenzo[c,e]thiepine.

In the title mol-ecule, C(14)H(10)Br(2)S, the two benzene rings form a dihedral angle of 48.35 (14)°. The seven-membered ring adopts a boat conformation. In the crystal structure, mol-ecules are related by translation along the b axis and exhibit C-H⋯π inter-actions.