Monocarboxylic Acid Structural Analogues Facilitate In Situ Composite of Functional Complexes for Aqueous Batteries.

In situ composite methods have aroused research interest in materials science and acted as a novel strategy to achieve structural tailoring of materials. However, the controllable preparation of composites containing functional groups remains a challenge. Herein, we report an approach based on competitive coordination between structural analogues, by which the functionally composite metal complex (NiSH@Ni-FSA) was synthesized.

MOF-based nanomaterials for advanced aqueous-ion batteries.

Metal-organic frameworks (MOFs)-based nanomaterials have great potential in the field of electrochemical energy storage due to their abundant pore size, high specific surface area, controllable structure and porosity, and homogeneous metal center. MOFs complexes and derivatives not only inherit the original morphology characteristics of MOFs but also provide excellent electrochemical performance. Batteries operating in aqueous electrolytes are cheaper, safer, and have higher ionic conductivity than those operating in conventional organic electrolytes.

Partially sulfurized NiMn-ZIF with high stability for aqueous nickel-zinc batteries.

Partial sulfurization can effectively enhance the electrical conductivity and cycling stability of Ni-ZIF while maintaining the Ni-ZIF skeleton and porosity. Partial sulfurization was carried out by a simple hydrothermal method and metal doping was used as an aid.

Valence Engineering via Polyoxometalate-Induced on Vanadium Centers for Efficient Aqueous Zinc-Ion Batteries.

Layered vanadium-based compounds have attracted attention as cathode materials for aqueous zinc-ion batteries (AZIBs) because of their low cost, high theoretical specific capacity, and abundant vanadium valence states. However, the slow migration of Zn ions and their poor cycling stability hinder their practical application in AZIBs. Herein, using a one-pot solvothermal method, the polyoxometalates (POMs) were inserted into the aluminum vanadate interlayer spacing, and a series of novel 3D nanoflower cathode materials (HAVO-MMo-X) were successfully fabricated.

Enhanced Photocatalytic Nitrogen Fixation over Nano-UiO-66(Zr) via Natural Chlorophyll Sensitization.

Metal-organic frameworks (MOFs) are potential semiconductor materials, but they still face limitations, such as insufficient photoresponse, high recombination rates, and inadequate N adsorption/activation capabilities. Herein, a UiO-66-based system is designed via a natural chlorophyll sensitization strategy. Density functional theory calculations confirm the coordination interactions between chlorophyll and UiO-66.

Metal-Hydroxide Organic Frameworks for Aqueous Nickel-Zinc Batteries.

Hydroxides exhibit a high theoretical capacity for energy storage by ion release and are often intercalated with anions to enhance the ion migration kinetics. In this study, a series of metal-hydroxide organic frameworks (MHOFs) are synthesized by intercalating aromatic organic linkers into hydroxides using I-M/Ni(OH) (where M = Co, Cu, Mg, Fe). The coordination environment and layer spacing (1.

Charged organic ligands inserting/supporting the nanolayer spacing of vanadium oxides for high-stability/efficiency zinc-ion batteries.

Given their high safety, environmental friendliness and low cost, aqueous zinc-ion batteries (AZIBs) have the potential for high-performance energy storage. However, issues with the structural stability and electrochemical kinetics during discharge/charge limit the development of AZIBs. In this study, vanadium oxide electrodes with organic molecular intercalation were designed based on intercalating 11 kinds of charged organic carboxylic acid ligands between 2D layers to regulate the interlayer spacing.

Enhanced Capacitive Deionization of Hollow Mesoporous Carbon Spheres/MOFs Derived Nanocomposites by Interface-Coating and Space-Encapsulating Design.

Exploring new carbon-based electrode materials is quite necessary for enhancing capacitive deionization (CDI). Here, hollow mesoporous carbon spheres (HMCSs)/metal-organic frameworks (MOFs) derived carbon materials (NC(M)/HMCSs and NC(M)@HMCSs) are successfully prepared by interface-coating and space-encapsulating design, respectively. The obtained NC(M)/HMCSs and NC(M)@HMCSs possess a hierarchical hollow nanoarchitecture with abundant nitrogen doping, high specific surface area, and abundant meso-/microporous pores.

Architectural design and optimization of internal structures in 3D printed electrodes for superior supercapacitor performance.

The architecture of electrodes plays a pivotal role in the transfer and transportation of charges during electrochemical reactions. Selecting optimal electrode materials and devising well-conceived electrode structures can substantially enhance the electrochemical performance of devices. This manuscript leverages 3D printing technology to fabricate asymmetric supercapacitor devices featuring regular layered configurations.

Polysaccharide-Containing Carboxymethyl Cellulose Bilayer Structure Membrane for Prevention of Postoperative Adhesion and Achilles Tendon Repair.

Postoperative tissue adhesion and poor tendon healing are major clinical problems associated with tendon surgery. To avoid postoperative adhesion and promote tendon healing, we developed and synthesized a membrane to wrap the surgical site after tendon suturing. The bilayer-structured porous membrane comprised an outer layer [1,4-butanediol diglycidyl ether cross-linked with carboxymethyl cellulose (CX)] and an inner layer [1,4-butanediol diglycidyl ether cross-linked with polysaccharides and carboxymethyl cellulose (CXB)].

Thiosalicylic-Acid-Mediated Coordination Structure of Nickel Center via Thermodynamic Modulation for Aqueous Ni-Zn Batteries.

Uniquely functional nanocomplexes with rich coordination environments are critical in energy storage. However, the construction of structurally versatile nanocomplexes remains challenging. In this study, a nickel-based complex with structural variations is designed via thermodynamic modulation using a dual-ligand synthesis strategy.

Understanding the link between different types of maternal diabetes and the onset of autism spectrum disorders.

Autism spectrum disorders (ASD) encompass a collection of neurodevelopmental disorders that exhibit impaired social interactions and repetitive stereotypic behaviors. Although the exact cause of these disorders remains unknown, it is widely accepted that both genetic and environmental factors contribute to their onset and progression. Recent studies have highlighted the potential negative impact of maternal diabetes on embryonic neurodevelopment, suggesting that intrauterine hyperglycemia could pose an additional risk to early brain development and contribute to the development of ASD.

Streamlined synthesis of superstructure Ni-benzimidazole MOFs: Glucose electrochemical analysis.

The design and synthesis of efficient electrochemical sensors are crucial transformation technologies in electrochemistry. We successfully synthesize a three-dimensional Ni-metal-organic framework (MOF) nanostructured material with a superior architecture using benzimidazole and nickel nitrate as precursors at room temperature which is being applied in glucose electrochemical sensors. The reaction mechanism of M-6 during glucose detection is thoroughly studied using various characterization techniques, such as in situ Raman spectroscopy, in situ ultraviolet-visible spectrophotometry, synchrotron radiography, X-ray diffraction, X-ray photoelectron spectroscopy, and scanning electron microscopy.

Association between a maternal vegetarian diet during pregnancy and the occurrence of atopic dermatitis in children.

Background: Atopic dermatitis (AD) is rising globally, with genetics and environmental factors both playing crucial roles. Dietary habits during pregnancy are linked to children's allergic disease risk. However, limited studies have explored the association between maternal vegetarian diets during pregnancy and child AD.

Enhancing Zn Storage Performance by Constructing the Interfaces Between VO and Co-N-C Layers.

Vanadium oxides have aroused attention as cathode materials in aqueous zinc-ion batteries (AZIBs) due to their low cost and high safety. However, low ion diffusion and vanadium dissolution often lead to capacity decay and deteriorating stability during cycling. Herein, vanadium dioxides (VO) nanobelts are coated with a single-atom cobalt dispersed N-doped carbon (Co-N-C) layer via a facile calcination strategy to form Co-N-C layer coated VO nanobelts (VO@Co-N-C NBs) for cathodes in AZIBs.

Nanoscaled biphasic calcium phosphate modulates osteogenesis and attenuates LPS-induced inflammation.

Micron-scale structure biphasic calcium phosphate (BCP) materials have demonstrated promising clinical outcomes in the field of bone tissue repair. However, research on biphasic calcium phosphate materials at the nanoscale level remains limited. In this study, we synthesize granular-shaped biphasic calcium phosphate nanomaterials with multiple desirable characteristics, including negatively charged surfaces, non-cytotoxicity, and the capability to penetrate cells, using a nanogrinding dispersion process with a polymeric carboxylic acid as the dispersant.

Regulating Intramolecular Electron Transfer of Nickel-Based Coordinations through Ligand Engineering for Aqueous Batteries.

The integration of electronic effects into complexes for the construction of novel materials has not yet attracted significant attention in the field of energy storage. In the current study, eight one-dimensional (1D) nickel-based salicylic acid  complexes (Ni-XSAs, X = pH, pMe, pMeO, mMe, pBr, pCl, pF, and pCF ), are prepared by ligand engineering. The coordination environments in the Ni-XSAs are explored using X-ray absorption fine structure spectroscopy.

Tumor suppressor p53 mediates interleukin-6 expression to enable cancer cell evasion of genotoxic stress.

The tumor suppressor p53 primarily functions as a mediator of DNA damage-induced cell death, thereby contributing to the efficacy of genotoxic anticancer therapeutics. Here, we show, on the contrary, that cancer cells can employ genotoxic stress-induced p53 to acquire treatment resistance through the production of the pleiotropic cytokine interleukin (IL)-6. Mechanistically, DNA damage, either repairable or irreparable, activates p53 and stimulates Caspase-2-mediated cleavage of its negative regulator mouse double minute 2 (MDM2) creating a positive feedback loop that leads to elevated p53 protein accumulation.

SbCl initiated conjunctive C-H bond functionalization and carbochlorination between glycine esters and methylenecyclopropanes (MCPs).

In the presence of dioxygen, an antimony trichloride enabled conjunctive sp C-H bond functionalization and carbochlorination of glycines was realized, providing a series of chlorinated quinolines in high yields. The mechanistic study shows that the antimony(V) species might be involved in the oxidation of the sp C-H bond and is followed by carbochlorination through a radical intermediate.

Oxidation of the inert sp C-H bonds of tetrahydroisoquinolines through C-H activation relay (CHAR): construction of functionalized isoquinolin-1-ones.

A TBN/O-initiated oxidation of the relatively inert 3,4-C-H bonds of THIQs was accomplished, in which the existence of an α-phosphoric ester group is crucial to enable dioxygen trapping and intramolecular HAT (C-H activation relay, CHAR), realizing the synthesis of a series of isoquinolin-1-ones in high yields. The mechanistic study confirmed that the formation of the 3,4-double bond is mediated by the CHAR process. This work provides a new strategy to achieve remote C-H bond activation.

Tris(4-bromophenyl)aminium Hexachloroantimonate-Initiated Oxidative Povarov-Type Reaction between Glycine Esters and (Cyclopropylidenemethyl)benzenes Using the Counterion as a Chlorine Donor.

A tris(4-bromophenyl)aminium hexachloroantimonate-initiated oxidative Povarov-type reaction between glycines and methylenecyclopropanes was realized in the presence of dioxygen, in which the counterion, SbCl, served as a chlorine atom donor, enabling the synthesis of a series of chlorinated quinolines in high yields. The mechanistic study showed that the chlorination step might be related to antimony chloride via a radical chlorine atom transfer.

Emergency percutaneous nephrostomy versus emergency percutaneous nephrolithotomy in patients with sepsis associated with large uretero-pelvic junction stone impaction: a randomized controlled trial.

Introduction: A randomized trial was conducted prospectively to evaluate the efficacy, related complications, and convalescence of emergency percutaneous nephrolithotomy compared to percutaneous nephrostomy for decompression of the collecting system in cases of sepsis associated with large uretero-pelvic junction stone impaction.

Materials And Methods: The inclusion criteria included a WBC count of 10.000/mm3 or more and/or a temperature of 38°C or higher.

The association between skull bone fractures and outcomes in patients with severe traumatic brain injury.

Background: In traumatic brain injury (TBI), computed tomography (CT) provides a good assessment of anatomic pathologic findings and the prognostic value of CT characteristics has been well discussed. However, few studies have focused on skull bone fracture and its clinical prognostic importance. Hence, this study aims to evaluate the effects of skull bone fracture on patients with severe TBI admitted to the emergency unit.

A delta-doped quantum well system with additional modulation doping.

A delta-doped quantum well with additional modulation doping may have potential applications. Utilizing such a hybrid system, it is possible to experimentally realize an extremely high two-dimensional electron gas (2DEG) density without suffering inter-electronic-subband scattering. In this article, the authors report on transport measurements on a delta-doped quantum well system with extra modulation doping.

Laboratory risk indicator for necrotizing fasciitis score and the outcomes.

Background: Laboratory risk indicator for necrotizing fasciitis (LRINEC score) is a simple laboratory tool used to distinguish between necrotizing soft-tissue infections (NSTI) and other soft-tissue infections. A LRINEC score of > or =6 is considered as denoting a high risk of necrotizing fasciitis. A certain LRINEC score might also be associated with mortality and other outcomes of patients with NSTI.