O-Mediated Cu-Catalyzed Dehydrogenative Phenothiazination.

In contrast to what one can be led to believe upon inspecting some of the recent literature, the dehydrogenative phenothiazination reaction does not require onerous technologies, complicated setups, or advanced catalysts in order to be mild and sustainable. We demonstrate this herein with a most facile, cost-effective, and sustainable Cu(II) catalyzed method, under 1 atm of O at room temperature in methanol, providing broad scope and high yields. These new results further set the dehydrogenative phenothiazination reaction among the green and practical coupling concepts of chemistry.

The Importance and Discovery of Highly Connected Covalent Organic Framework Net Topologies.

Furthering the field of synthetic organic chemistry from the discrete molecules regime to the extended structure regime, covalent organic frameworks (COFs) represent a new genre of crystalline porous materials featuring designability with molecular-level precision, well-defined porosity, and exceptional stability imparted by the robust covalent linkages reticulating organic molecules. The topology of COFs is a principal feature that regulates their functionality and usability for emerging technologies. Profound comprehension of network topologies and maneuvering them toward targeted applications are crucial to advancing the realm of COF research and developing novel functional materials for exciting breakthroughs.

Combined application of rhizobacteria, organic and inorganic amendments reduce lead and cadmium uptake and improve growth of chickpea by modulating physiology and antioxidant status.

Due to a lack of high-quality water, farmers have been compelled to use sewage water for irrigation, contaminating agricultural soils with multiple heavy metals. For the remediation of contaminated soil, plant growth-promoting rhizobacteria (PGPR), pressmud (PM), and iron (III) oxide were used to improve the growth and phytostabilization potential of chickpea grown in contaminated soil. Contaminated soil was collected from a nearby field, receiving sewage and factory water over the last 60 years.

Unravelling the Role of Sterically Encumbered Ligands in Tuning the Magnetic Properties of Lanthanide-Based D5h Single-Ion Magnets.

Isostructural Dy(III) and Er(III) complexes [L12Ln(H2O)5][I]3·L12·(CH2Cl2) (Ln = Dy (1), Er (3)) and [L22Ln(H2O)5][I]3·L22·(CH2Cl2)2 (Ln = Dy (2), Er (4)), with distorted pentagonal bipyramidal geometry (D5h) around the central metal were synthesized by utilizing two bulky phosphonamide ligands, adamantyl phosphonamide, (Ad)P(O)(NHiPr)2 (L1) and carbazolyl phosphoramide (Cz)P(O)(NHiPr)2 (L2). The resultant complexes were investigated for their magnetic properties in order to elucidate the impact of modification of the coordinating P-O bond environment either by increasing steric bulk and/or introduction of a third P-N bond at the central phosphorus atom. Magnetic studies revealed substantial energy barriers (Ueff) of 640 K and 560 K for Dy compounds 1 and 2, respectively, rendering them as some of the best-performing air-stable SIMs amongst the class of SIMs with D5h symmetry.

Experimental and Theoretical Force Constants as Meaningful Indicator for Interatomic Bonding Characteristics and the Specific Case of Elemental Antimony.

Stable Sb exhibits a rhombohedral structure, often referred to as distorted primitive cubic, with each Sb atom having three short and three longer first neighbor bonds. However, this crystal structure can also be interpreted as being layered, putting emphasis on only three short first neighbor bonds. Therefore, temperature-dependent extended X-ray absorption fine structure (EXAFS) spectroscopy is carried out at the Sb K-edge in order to obtain more detailed information on local structural and vibrational properties.

Experimental and Computational Synthesis of TiO Sol-Gel Coatings.

During the experimental formation of sol-gel coatings, the colloid dispersions go through a drying process, and the structure of the coatings is formed as a result of complex chemical, colloidal, and capillary interactions. While computer simulations provide guidelines to tune and even design the nanomaterials synthesis, simulations of coating structure formation are hitherto unknown in the literature. Based on real experiments, we establish here a ReaxFF reactive force field-based molecular dynamics simulation protocol in order to investigate and determine the role of the experimental conditions on the pore structure formation in the coatings.

Rational Fabrication of Functionally-Graded Surfaces for Biological and Biomedical Applications.

As a ubiquitous feature of the biological world, gradation, in either composition or structure, is essential to many functions and processes. Taking protein gradation as an example, it plays a pivotal role in the development and evolution of human bodies, including stimulation and direction of the outgrowth of peripheral nerves in a developing fetus. It is also critically involved in wound healing by attracting and guiding immune cells to the site of injury or infection.

Succinate Nanomaterials Boost Tumor Immunotherapy via Activating Cell Pyroptosis and Enhancing MHC-I Expression.

Despite the promising clinical applications of immunotherapy, its effectiveness is often limited by low immune responses and tumor immune escape. In this study, we introduce a simple and drug-free inorganic nanomaterial, sodium succinate (CHNaO NPs), prepared using a rapid microemulsion method to enhance cancer immunotherapy. The synthesized CHNaO NPs can release high concentrations of Na and succinate ions into tumor cells, leading to an increase in intracellular osmolarity.

Electrooxidation of 5-Hydroxymethylfurfural via NiP-NiSe Heterostructure Nanosheet Arrays.

The electrooxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) has been deeply investigated. However, developing a durable electrocatalyst for fast production of FDCA at low potentials remains a challenge. Herein, we report NiP-NiSe heterostructure nanosheet arrays as efficient electrocatalysts for HMF electrooxidation.

Interfacial Engineering of Pillared Co(II) Metal-Organic Framework@NiMn-Layered Double Hydroxide Nanocomposite for Oxygen Evolution Reaction Electrocatalysis.

Clean energy conversion and storage require simple, economical, and effective electrode materials to achieve promising results. The development of high-performance electrocatalysts with adequate stability and cost-effectiveness is essential to ensure low overpotentials toward the oxygen evolution reaction (OER). Herein, a cobalt-based metal-organic framework with 4,4,4-6T14 topology in combination with various ratios of NiMn-layered double hydroxide (Co-MOF@%NiMn-LDH, = 5, 10, 20, and 40%) is applied as an effective electrocatalyst for the oxidation of water.

Component analysis and source identification of atmospheric aerosols at the neighborhood scale in a coastal industrial city in China.

A multiple-site filter-sampling observation study was conducted in a coastal industrial city (Rizhao, 35°10'59″N, 119°23'57″E) to understand the main components, formation mechanisms, and potential sources of particulate matter. The average (±σ) mass concentration of PM across all the sites was 42 (±27) μg/m, with high variability (6∼202 μg/m). Water-soluble inorganic ions (WSIIs) were the major contributors (54%∼60%) to PM with mean values for sulfate (13 μg/m), nitrate (6 μg/m), and ammonium (7 μg/m) (SNA).

Magnetic particles (FeO) magnify ion transfer processes at the electrified liquid-liquid interface. Case study: Levamisole detection.

This article describes the effect of non-stabilized magnetic particles FeO (nanoparticles aggregates) addition to the aqueous phase of the polarized liquid-liquid interface (LLI) on the interfacial ion transfer processes. LLI was formed between 1,2-dichloroethane and water solutions (1,2 DCE)|water. The synthesis of FeO magnetic particles (MPs) was achieved by the co-precipitation method, after which their appearance, size of aggregates, and zeta potential were assessed.

Responses of biogenic trace gases to atmospheric deposition and acid-processed atmospheric deposition in the oligotrophic western Pacific Ocean.

Dimethylsulfide (DMS) and very short-lived bromocarbons (VSL) are important biogenic trace gases emitted from oceans that can affect the global climate. Atmospheric deposition (AD) can provide nutrients and trace metals to the ocean, which can enhance primary productivity, but the complex effects of AD on DMS and VSL are still largely unexplored. A deck incubation experiment with aerosol additions was conducted to simulate the effects of acid-processed AD on the production of trace gases, including DMS and four VSL such as bromoform (CHBr), dibromomethane (CHBr), dibromochloromethane (CHBrCl), and bromodichloromethane (CHBrCl), in the oligotrophic western Pacific Ocean (WPO).

Synergistic interface regulation for achieving fast kinetics and highly reversible zinc metal anodes.

Uncontrolled zinc dendrite growth and adverse side reactions at the Zn anode interface severely limit its practical application. Based on theoretical calculations, this study in situ constructs a functional interface (ICFI Zn) on the Zn anode surface, consisting of a surface-textured structure and a zinc-philic protective layer. Benefiting from the synergistic effect of ion regulation and atomic anchoring of this functional interface, the ICFI Zn anode achieves homogenised regulation of ion fluxes, facilitates ion transport kinetics, effectively suppresses side reactions and guides the deposition of dendrite-free Zn.

Elucidation of the Off-Center Displaced Mo in Octahedral Coordination in BaMoO.

The detailed crystal structure as well as the heat capacity at low temperature and standard entropy of BaMoO are reported for the first time. High-resolution X-ray and neutron diffraction were employed to reveal the structural features of this compound. BaMoO has a six-coordinated Mo and a strongly negative excess volume with respect to the binary oxides.

Study of the Anti-MYC Potential of Lanostane-Type Triterpenes.

One of the most investigated molecular targets for anticancer therapy is the proto-oncogene , which is amplified and thus overexpressed in many types of cancer. Due to its structural characteristics, developing inhibitors for the target has proven to be challenging. In this study, the anti-MYC potential of lanostane-type triterpenes was investigated for the first time, using computational approaches that involved ensemble docking, prediction of structural properties and pharmacokinetic parameters, molecular dynamics (MD), and binding energy calculation using the molecular mechanics-generalized born surface area (MM-GBSA) method.

In situ HO production from self-sufficient heterogeneous Fenton reaction over Fe/MoS for potential environmental remediation applications.

Fenton reaction technology has worked well in water and wastewater treatment; however it is often limited by such problems as continuous external supply of HO, slow Fe/Fe cycle rate, high energy requirements, and maintenance of low pH during operation. Herein, a novel self-sufficient heterogeneous Fenton system based on Fe/MoS was designed, fabricated, and optimized to effectively address these problems. The combined presence of Fe and sulfur vacancies sites in MoS played a pivotal role in the generation of HOvia two-step single-electron reduction process without any energy consumption.

Two Alkaline Metal Borates: from Layer to Layer-Pillared Framework.

Two borates, NaK[BO(OH)]·HO () and NaK[{BO}{BO}{BO(OH)}]·2HO () have been designed and made under solvothermal conditions. Compound exhibits a 2D fluctuant layer based on the [BO(OH)] clusters, containing two types of 9-membered ring (MR) channels and showing a four-connected sql topology net. By modifying the reactants and reaction temperature, compound was obtained from compound .

Nitrogen use efficiency underlies cross-ecosystem variation in marine primary production.

The supply of nitrogen (N) and the efficiency with which it is used by phytoplankton serve as two fundamental controls on the productivity of many marine ecosystems. Shifts in nitrogen use efficiency (NUE) can decouple primary production from N-supply but how NUE varies across systems is poorly known. Through a global synthesis of how total N (TN) is apportioned among phytoplankton, particulate, dissolved inorganic, and dissolved organic pools, we demonstrate that NUE underlies broad variations in primary production.

Synergistic effect of mulch and nitrogen management on growth and essential oil yield of Salvia sclarea L.

Balanced plant nutrition and optimal micro-climate are critical for achieving higher production sustainably. Substituting mineral fertilizers with organic amendments under water-conserving strategies like mulch can enhance the quality and yield and improve soil health. Therefore, a two-year study was conducted to examine the synergistic effects of mulch and reducing inorganic fertilizers and partially substituting organic amendments on essential oil (EO) yield and its composition, and soil properties in Salvia sclarea, an industrially important crop.

Root exudates in mangrove forests accelerate bicarbonate production in the soil environment.

Mangrove forests are increasingly recognized as vital blue carbon ecosystems due to their high carbon sequestration capacity, primarily through the accumulation of soil organic carbon (SOC). Recent research highlights that, in addition to SOC, dissolved inorganic carbon (DIC), particularly in the form of bicarbonate (HCO₃⁻), plays a crucial role in carbon sequestration by being exported from these ecosystems to adjacent coastal waters. This study aims to investigate the previously unexamined mechanisms behind bicarbonate production in mangrove soils.

Spin-polarized lasing in manganese doped perovskite microcrystals.

Spin-polarized lasers have demonstrated many superiorities over conventional lasers in both performance and functionalities. Hybrid organic-inorganic perovskites are emerging spintronic materials with great potential for advancing spin-polarized laser technology. However, the rapid carrier spin relaxation process in hybrid perovskites presents a major bottleneck for spin-polarized lasing.

Facile and Regioselective Deuteration of C2-Alkylated Imidazolium Salts in the Presence of Cesium Carbonate.

Thirteen imidazolium iodides bearing benzyl, mesityl, or 2,6-diiso-propyl-phenyl substituents on their nitrogen atoms, and C1 to C4 alkyl chains on their C2 carbon atom were readily deuterated with D2O as a cheap and non-toxic deuterium source in the presence of Cs2CO3, a weak, innocuous, inorganic base. The isotopic exchange proceeded quickly and efficiently under mild, aerobic conditions to afford a range of aNHC and NHO precursors regioselectively labeled on their C2α exocyclic position and/or C4=C5 heterocyclic backbone. A "carbene-free" mechanism was postulated, in which the carbonate anion acts as a catalyst to activate an exocyclic, acidic C-H bond and ease a deuterium transfer from D2O to the imidazolium salt in a concerted fashion.

Stabilizing the Fe Species of Nickel-Iron Double Hydroxide via Chelating Asymmetric Aldehyde-Containing THB Ligand for Long-Lasting Water Oxidation.

Nickel-iron layered double hydroxides (NiFe LDHs) are considered as promising substitutes for precious metals in oxygen evolution reaction (OER). However, most of the reported NiFe LDHs suffer from poor long-term stability because of the Fe loss during OER resulting in severe inactivation. Herein, a dynamically stable chelating interface through in situ transformation of asymmetric aldehyde-ligand (THB, 1,3,5-Tris(3'-hydroxy-4'-formylphenyl)-benzene) modified NiFe LDHs to anchor Fe and significantly enhance the OER stability is reported.