Projected distribution patterns of in China under future climate scenarios: insights from optimized Maxent and Biomod2 models.

, commonly known as Galangal, is not only widely used as a medicinal plant but also holds significant ornamental value in horticulture and landscape design due to its unique plant structure and floral aesthetics in China. This study evaluates the impact of current and future climate change scenarios (ssp126, ssp245, ssp370, and ssp585) on the suitable habitats for in China. A total of 73 reliable distribution points for were collected, and 11 key environmental variables were selected.

Structure-Induced Reversing Basicity of α-Anionic Fischer Carbenes.

Group VI metal carbenes and their α-anionic complexes play an important role in organic synthesis, yet structural characterizations and thermodynamic studies for reactive α-anions remain challenging. This work investigated the molecular structures and thermodynamics of α-anionic Fischer carbenes and their conjugated acids. The results clarify the negative charge localized on the M(CO) moiety and the C═X (X = C, N, or O) double bond in all anionic structures.

Narrowband emission from fully-bridged triphenylamine derivatives: insights into effects of structure modification and pressure.

Triphenylamine derivatives with narrowband emission have attracted growing attention in purely organic thermally-activated fluorescence (TADF) materials owing to their enhanced color purity and flexible molecular design strategy. Combined time-dependent density functional theory (TD-DFT) and ONIOM (QM/MM) calculations indicate that the excellent planarity of the experimentally developed DQAO could result in gradually decreased intermolecular interactions in the aggregated state at ambient pressure and upon compression, which is unfavorable for suppressing structural relaxation and achieving narrowband emission in its non-doped practical application. Therefore, three structure-modified derivatives, DQAO-Cb, DQAO-Ph, and DQAO-PhCb, were theoretically designed by introducing the spherical -carborane and dangling phenyl units positioned to the N atom of the DQAO to provide additional geometrical distortion and steric hindrance.

Redox-Active Ligand Assisted Multielectron Catalysis: A Case of Electrocatalyzed CO-to-CO Conversion.

The selective reduction of carbon dioxide remains a significant challenge due to the complex multielectron/proton transfer process, which results in a high kinetic barrier and the production of diverse products. Inspired by the electrostatic and H-bonding interactions observed in the second sphere of the [NiFe]-CODH enzyme, researchers have extensively explored these interactions to regulate proton transfer, stabilize intermediates, and ultimately improve the performance of catalytic CO reduction. In this work, a series of cobalt(II) tetraphenylporphyrins with varying numbers of redox-active nitro groups were synthesized and evaluated as CO reduction electrocatalysts.

Selective Four-Electron Reduction of Oxygen by a Nonheme Heterobimetallic CuFe Complex.

We report herein the first nonheme CuFe oxygen reduction catalyst ([Cu (bpbp)(μ-OAc) Fe ] , CuFe-OAc), which serves as a functional model of cytochrome c oxidase and can catalyze oxygen reduction to water with a turnover frequency of 2.4×10  s and selectivity of 96.0 % in the presence of Et NH .

Heterobimetallic NiFe Cooperative Molecular Water Oxidation Catalyst.

We reported herein the development of heterobimetallic NiFe molecular platform to understand NiFe synergistic effect in water oxidation catalysis. Compared to homonuclear bimetallic compounds (NiNi and FeFe), NiFe complex possesses more remarkable catalytic water oxidation performance. Mechanistic studies suggest that this remarkable difference is attributed to the fact that NiFe synergy can effectively promote O-O bond formation.

Efficient capture and stabilization of iodine via gas-solid reaction using cyclodextrin metal-organic frameworks.

For treatment of wound infection with stabilized iodine, potassium iodide cyclodextrin metal-organic frameworks (KI-CD-MOF) was prepared to carry iodine via gas-solid reaction. Apart from highly ordered porous frameworks, KI-CD-MOF contains uniformly distributed iodide ions which stabilize iodine (I). X-ray photoelectron spectroscopy and potentiometric titration were utilized to confirm the formation of I in the highly porous KI-CD-MOF as I@KI-CD-MOF.

"Three-in-One" Structural-Building-Mode-Based Ti-Type Titanium Oxo Cluster Entirely Protected by the Ligands Benzoate and Salicylhydroxamate.

Titanium oxo clusters (TOCs) with accurate molecular structures have potential applications in photocatalysis, such as photocatalytic degradation, hydrogen production, and water oxidation. The hydrolytic stability and light absorption ability of TOCs have important impacts on photocatalysis, where the selection of peripheral organic ligands plays a significant role. In this regard, salicylhydroxamic acid (abbreviated as HL) attracts our attention, acting as a ligand for its multidentate and dye-functional features, which can increase the hydrolytic stability and broaden light absorption for TOCs.

Preparation and Study of Folate Modified Albumin Targeting Microspheres.

In this study, folate modified bovine serum albumin was successfully synthesized, while preparation of Nintedanib albumin microspheres (ND-FSA NPs) as a carrier was carried out via electrospinning technology. Folate modified albumin was used to enhance the targeting potential of the prepared microspheres. The prepared microspheres had spherical appearance and smooth outer surface.

The changes in spatial layout of steel industry in China and associated pollutant emissions: A case of SO.

The spatial layout of the steel industry has an impact on the regional atmospheric environment. In this study, the steel industry evolution model and the driving force analysis model were combined to analyze the evolution of spatial layout of the steel industry in China and the driving factors of this evolution. In addition, the WRF-SMOKE-CMAQ model was used to analyze the spatial dynamics of SO emissions from the steel industry.

Task compliance predicts suppression-induced forgetting in a large sample.

Suppression-induced forgetting (SIF) refers to a memory impairment resulting from repeated attempts to stop the retrieval of unwanted memory associates. SIF has become established in the literature through a growing number of reports built upon the Think/No-Think (TNT) paradigm. Not all individuals and not all reported experiments yield reliable forgetting, however.

A Novel Azaphilone Muyophilone A From the Endophytic Fungus 0307-2.

Two known azaphilone derivatives, 4,6-dimethylcurvulinic acid () and austdiol (), and their novel heterotrimer, muyophilone A (), were isolated and identified from an endophytic fungus, 0307-2. Their structures and stereochemistry were established by extensive spectroscopic analyses including HRMS, NMR spectroscopy, electronic circular dichroism (ECD) and vibrational circular dichroism (VCD) spectroscopic methods, as well as single crystal X-ray diffraction. In the structure of , two compound -derived azaphilone units were connected through an unprecedented five-membered carbon bridge which was proposed to be originated from compound .

Memory Suppression Ability can be Robustly Predicted by the Internetwork Communication of Frontoparietal Control Network.

Memory suppression (MS) is essential for mental well-being. However, no studies have explored how intrinsic resting-state functional connectivity (rs-FC) predicts this ability. Here, we adopted the connectome-based predictive modeling (CPM) based on the resting-state fMRI data to investigate whether and how rs-FC profiles in predefined brain networks (the frontoparietal control networks or FPCN) can predict MS in healthy individuals with 497 participants.

Tetrahedral μ-chloride and in situ generated octahedral μ-sulfide templating Co complexes with different distortions of the cube.

Herein two unprecedented octanuclear Co8 clusters are presented, [Cl@Co8 (TEOA)4(CH3CN)Cl3] (1) and [S@Co8(DEOA)6(NCS)2] (2) (H3TEOA = triethanolamine, H2DEOA = diethanolamine), in which tetrahedral μ4-chloride and in situ generated octahedral μ6-sulfide are used as templates. In spite of them being derivatives of cubes, eight Co atoms in 1 consist of two co-centered tetrahedra of different sizes, whereas in 2 they appear as a rhombohedron formed via elongating a cube along the C3-axis direction. Strong intra-cluster antiferromagnetic interactions were found.

Redox-Active Ligand Assisted Catalytic Water Oxidation by a Ru =O Intermediate.

Water splitting is one of the most promising solutions for storing solar energy in a chemical bond. Water oxidation is still the bottleneck step because of its inherent difficulty and the limited understanding of the O-O bond formation mechanism. Molecular catalysts provide a platform for understanding this process in depth and have received wide attention since the first Ru-based catalyst was reported in 1982.

[Secondary metabolites from Epicoccum nigrum 14one,an endophytic fungus isolated from plant Leptogium masiaticum].

Phytochemical investigation of the culture of Epicoccum nigrum,an endolichenic fungus inhabiting Leptogium masiaticum,led to the isolation of 11 compounds. Based on NMR spectroscopy and HRESIMS data,their structures were determined as one alkaloid fusaricide( 1),and seven benzofuran derivatives including epicoccone( 2),4,6-dihydroxy-5-methoxy-7-methyl-1,3-dihydro isobenzofuran( 3),5-methyl-epicoccone B( 4),3,6,7-trihydroxy-5-methoxy-4-methylisobenzo furan-1( 3 H)-one( 5),3-methoxyepicoccone B( 6),2,3,4-trihydroxy-6-( hydroxymethyl)-5-methylbenzyl-alcohol( 7),and isoochracinic acid( 8),together with three epicoccolide analogs epicocconigrones A( 9),epicoccolide B( 10),and epicocconigrones B( 11). Compounds 1,9 and 10 showed potent microorganism inhibitory effects.

New α-pyrones from an endophytic fungus, J2.

Four new α-pyrones, hypotiens A-D (1-4), were isolated from a fungal endophyte, J2, harbored in the medicinal plant . Their structures were determined through detailed HRMS and NMR spectroscopic data. Compounds 1-4 are new α-pyrone derivatives containing an unusual dimethyl substitution in the highly unsaturated side chain.

ZnO Porous Nanosheets with Partial Surface Modification for Enhanced Charges Separation and High Photocatalytic Activity Under Solar Irradiation.

ZnO porous nanosheets (PNSs) with partial surface modification were fabricated by means of depositing amorphous BiVO on basic zinc carbonate nanosheets followed by calcining at 500 °C. At low levels of anchored amorphous BiVO, the surface of ZnO PNSs was partially evolved into BiZnVO (BZVO). The measurements for photocurrent and photoluminescence demonstrate that partial-surface BZVO-modified ZnO PNSs (ZB_0.

Proton-coupled electron transfer oxidation of O-H bond by the N-radical cation of Wurster's blue salt (TMPDA˙).

Here, we report the proton-coupled electron transfer reaction between TEMPO-H and Wurster's blue salt (TMPDA˙+). TMPDA˙+ could abstract a hydrogen atom from 2,2,6,6-tetramethyl-1-hydroxy-piperidine (TEMPO-H) via concerted electron-proton transfer and displayed a large KIE (7.05 ± 0.

High-Efficiency and Wide-Angle Versatile Polarization Controller Based on Metagratings.

Metamaterials with their customized properties enable us to efficiently manipulate the polarization states of electromagnetic waves with flexible approaches, which is of great significance in various realms. However, most current metamaterial-based polarization controllers can only realize single function, which has extremely hindered the expansion of their applications. Here, we experimentally demonstrate highly efficient and multifunctional polarization conversion effects using metagrating by integrating single-structure metallic meta-atoms into the dielectric gratings.

Physicochemical properties of polysaccharides separated from Camellia oleifera Abel seed cake and its hypoglycemic activity on streptozotocin-induced diabetic mice.

Two homogeneous polysaccharide fractions named SCP-1 (7.16 × 10 Da) and SCP-2 (2.00 × 10 Da) were purified by DEAE-52 cellulose and Sephadex G-200 column chromatography successively from Camellia oleifera Abel seed cake.

Syntheses, crystal-solution structures and magnetic properties of a series of decanuclear heterometallic [LnCoCo] (Ln = Eu, Gd, Tb, Dy) clusters.

Four unprecedented decanuclear heterometallic [Ln2CoII4CoIII4] clusters based on a diethanolamine ligand (H2dea), namely [Eu2CoII4CoIII4(dea)8(HCOO)4(OH)2(Cl)2(CH3OH)2]Cl2·4CH3OH·2H2O (1), [Gd2CoII4CoIII4(dea)8(HCOO)4(OH)2(Cl)2(CH3OH)2]Cl2·4CH3OH·2H2O (2), [Tb2CoII4CoIII4(dea)8(HCOO)4(OH)2(Cl)2(CH3OH)2]Cl2·2CH3OH·4H2O (3) and [Dy2CoII4CoIII4(dea)8(HCOO)4(OH)2(Cl)2(CH3OH)2]Cl2·2CH3OH·4H2O (4) were synthesized through a facile solution method. Single-crystal X-ray diffraction analyses reveal that complexes 1-4 consist of a [Ln2CoII4CoIII4] core, which is constructed by bridging a quasi-double cuboidal [Ln2CoII2CoIII2] core with two [CoIICoIII] units. Electrospray ionization mass spectrometry (ESI-MS) using methanol solution reveals that complexes 1-4 are stable in the solution, and the clusters undergo three different substitution reactions (Cl- replaced by OH-, OH- replaced by CH3O- and HCOO- replaced by OH-/CH3O-) at the same time in the ionization state.

MiR-139-5p suppresses osteosarcoma cell growth and invasion through regulating DNMT1.

Background: Accumulating evidence has suggested the crucial roles of differentially expressed miRNAs in osteosarcoma progression. MiR-139-5p was decreased in various cancers. However, the role of miR-139-5p in the development of osteosarcoma and the underlying mechanism remain to be addressed.

A supramodal role of the basal ganglia in memory and motor inhibition: Meta-analytic evidence.

The ability to stop actions and thoughts is essential for goal-directed behaviour. Neuroimaging research has revealed that stopping actions and thoughts engage similar cortical mechanisms, including the ventro- and dorso-lateral prefrontal cortex. However, whether and how these abilities require similar subcortical mechanisms remains unexplored.