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The unique structure of van der Waals materials facilitates a robust mechanism for precise control of physical properties. In this study, we present a comprehensive analysis based on the intercalation of organometallics to modulate the optoelectronic behavior of two-dimensional germanium sulfide (GeS). Advanced computational exploration reveals significant and tunable features in the intercalated material. Additionally, the weak chemical interactions between organometallics and GeS support the electric-field-mediated drift and charge–discharge processes in intercalants. Controlling the concentration of organometallics in this manner enables the dynamic emergence of novel characteristics post-intercalation. These include flatbands near the Fermi level, significant enhancement of carrier mobility, and a magnetic ground state that is atypical for pristine GeS. Our findings demonstrate that organometallic intercalation offers a powerful strategy for tailoring the optoelectronic and magnetic characteristics of GeS, paving the way for harnessing emerging features for applications in next-generation devices. [ABSTRACT FROM AUTHOR]

A memristor is a two-terminal electrical component with the scope of future computing applications and analog electronics. In this report, bismuth sulfide decorated one-dimensional carbon nitride nanotube was synthesized and characterized with various analytical techniques. The electrical property of the synthesized material was measured using a two-terminal metal–insulator–metal type of device that exhibited the resistive switching characteristics with the ON to OFF ratio of 2 × 103. The electron transport mechanism of the device was followed by Schottky emission and Poole–Frenkel emission for a low conductance state and Ohmic conduction behavior at the high conductance state. A decrease in the trap depth was identified in the simulation study with increasing applied potential and that supported the proposed mechanism. Read endurance and retention behavior of the device are stable in nature, supported by the statistical analysis. Furthermore, a hybrid logic gate was designed using two identical memristors, one CMOS inverter, one resistor, one voltage divider, and a buffer gate. The designed logic gate exhibited stable nand and nor gate operation based on the control signal. [ABSTRACT FROM AUTHOR]

BackgroundBiofilms in sulfide-rich springs present intricate microbial communities that play pivotal roles in biogeochemical cycling. We studied chemoautotrophically based biofilms that host diverse CPR bacteria and grow in sulfide-rich springs to investigate microbial controls on biogeochemical cycling.ResultsSulfide springs biofilms were investigated using bulk geochemical analysis, genome-resolved metagenomics, and scanning transmission X-ray microscopy (STXM) at room temperature and 87 K. Chemolithotrophic sulfur-oxidizing bacteria, including Thiothrix and Beggiatoa, dominate the biofilms, which also contain CPR Gracilibacteria, Absconditabacteria, Saccharibacteria, Peregrinibacteria, Berkelbacteria, Microgenomates, and Parcubacteria. STXM imaging revealed ultra-small cells near the surfaces of filamentous bacteria that may be CPR bacterial episymbionts. STXM and NEXAFS spectroscopy at carbon K and sulfur L2,3 edges show that filamentous bacteria contain protein-encapsulated spherical elemental sulfur granules, indicating that they are sulfur oxidizers, likely Thiothrix. Berkelbacteria and Moranbacteria in the same biofilm sample are predicted to have a novel electron bifurcating group 3b [NiFe]-hydrogenase, putatively a sulfhydrogenase, potentially linked to sulfur metabolism via redox cofactors. This complex could potentially contribute to symbioses, for example, with sulfur-oxidizing bacteria such as Thiothrix that is based on cryptic sulfur cycling. One Doudnabacteria genome encodes adjacent sulfur dioxygenase and rhodanese genes that may convert thiosulfate to sulfite. We find similar conserved genomic architecture associated with CPR bacteria from other sulfur-rich subsurface ecosystems.ConclusionsOur combined metagenomic, geochemical, spectromicroscopic, and structural bioinformatics analyses of biofilms growing in sulfide-rich springs revealed consortia that contain CPR bacteria and sulfur-oxidizing Proteobacteria, including Thiothrix, and bacteria from a new family within Beggiatoales. We infer roles for CPR bacteria in sulfur and hydrogen cycling. Video Abstract.

Comprehensive Summary The EDA complex‐mediated reactions involving oxime esters have been few studied. Herein, an EDA complex formed by thiophenolate anion and oxime ester is reported for photoinduced divergent synthesis of thioethers, depending on different types of oxime esters. Operational simplicity, mild reaction conditions, and flexible options of leaving group demonstrate the generality and synthetic utility of this approach. Such an approach can also enable an interesting thiol‐catalysis for the synthesis of phenanthridines. [ABSTRACT FROM AUTHOR]

Comprehensive Summary The EDA complex‐mediated reactions involving oxime esters have been few studied. Herein, an EDA complex formed by thiophenolate anion and oxime ester is reported for photoinduced divergent synthesis of thioethers, depending on different types of oxime esters. Operational simplicity, mild reaction conditions, and flexible options of leaving group demonstrate the generality and synthetic utility of this approach. Such an approach can also enable an interesting thiol‐catalysis for the synthesis of phenanthridines. [ABSTRACT FROM AUTHOR]

This review introduces solid electrolytes based on sulfide/polymer composites which are used in all‐solid‐state lithium batteries, describing the use of polymers as plasticizer, the lithium‐ion conductive channel, the preparation methods of solid‐state electrolytes (SSEs), including dry methods and wet methods with their advantages and disadvantages. In addition, the physicochemical stability of sulfide/polymer composite based solid‐state electrolytes is analyzed. The sulfide/polymer composite based solid‐state electrolyte can be utilized in lithium metal or lithium sulfur batteries. However, there are still many problems left to be solved in practical applications of these solid‐state electrolytes. In this review, several solutions are explored. Firstly, the ultra‐long life cycle of batteries can be achieved by thinning the composite electrolyte. Secondly, when sulfur is applied as the positive electrode, the thinning electrolyte can reduce polarization and other problems. Finally, an integrated battery is employed to reduce the interface impedance. By addressing these aspects, the review aims to provide valuable insights into the future development of high‐performance solid‐state electrolytes in lithium battery technology. [ABSTRACT FROM AUTHOR]

Information about the spectra of noble metal minerals obtained by Raman spectroscopy, using the example of a new copper–gold–platinum ore occurrence in the Polar Urals, is presented. For the first time, spectra of temagamite and minerals of the intermediate merenskyite–moncheite series were obtained, and some of the previously detected minerals are refined and confirmed. The prerequisites for new mineral phases of the intermediate series are noted, difficulties in using the method and the need for further development of this area of research are indicated. It is shown that the use of Raman spectroscopy, in controversial cases, complements and often clarifies the data of microprobe studies. [ABSTRACT FROM AUTHOR]

Herein, we disclosed a protocol for the deoxygenation of allyl arylsulfones to access the corresponding thioethers under photoredox conditions by a "cut-sew" strategy. The key to the success of the deoxygenation process is using triarylphosphines not only as the terminal reductants, but also as the reaction initiators. Deeper understanding of this deoxygenation process enabled the intermolecular deoxygenative allylation. [ABSTRACT FROM AUTHOR]

Two layered compounds Cs2Ag2Sb2S5 (1) and CsAgSb4S7 (2) were successfully synthesized using a mild solvothermal method with thiourea as a mineralizer. The syntheses of these two silver-containing quaternary sulfides indicate that thiourea is a novel effective mineralizer. Both compounds are semiconductors and compound 1 exhibits excellent photocurrent response properties. [ABSTRACT FROM AUTHOR]

A very simple and atom‐economical method for the synthesis of vicinal trifluoromethyl thioethers via DBN‐catalyzed hydrothiolation of α‐(trifluoromethyl)styrenes with thiols was reported. The reaction proceeded smoothly under mild reaction conditions and provided the β‐CF3‐thioethers in moderate to good yields in an anti‐Markovnikov manner. Furthermore, this method features several remarkable advantages, such as the use of a catalytic amount of DBN, broad substrate scope, excellent functional group compatibility, and easy scalability. [ABSTRACT FROM AUTHOR]

Compounds bearing the sulfoxide moiety display an important class of molecules in pharmaceutical industry. Many efforts have been made towards the development of novel, sustainable, easy‐to‐execute and industrially friendly processes. A novel iodonium‐salt‐mediated oxidation protocol for the conversion of sulfides into the corresponding sulfoxides is reported, employing DMSO as the oxidant. Several sulfides decorated with various functional groups were tested, leading to the corresponding products in good to excellent yields with remarkable chemoselectivity. The oxidation protocol was successfully applied to the synthesis of the pharmaceutical active ingredients (APIs) Sulforaphane and Modafinil. [ABSTRACT FROM AUTHOR]

Transconductance (gm) is one important figure of merit for benchmarking organic electrochemical transistor (OECT) biosensors, which nevertheless experiences undesired fluctuation instead of keep constant during the target detection of varied concentrations. Light‐matter interplay is recently shown as a potential way to regulate the OECT characteristics, e.g. maximum gm at zero gate bias is achieved. In this work, the challenge of unstable gm is addressed by using a unique metal‐organic framework (MOF)‐derived hollow tube indium sulfide (m‐In2S3) as the photogate. Interestingly, the light irradiation on m‐In2S3 generate a straight transfer curve, leading to a stable gm that is desirable for biological application. Exemplifying by an aptasening, such a device is then tested for protein quantification with a stable sensitivity during the detection. This work features the feasibility of light‐matter interplay to achieve a stable gm in organic electronics. [ABSTRACT FROM AUTHOR]

Copper sulfides exhibit various significant physical properties and have wide potential applications. In order to synthesize copper sulfides and investigate the anion substitution possibility of Cu3P, we immersed Cu3P in sodium sulfide solution. From X‐ray diffraction spectra results, copper sulfides, namely Cu2S and Cu7.2S4, were observed, indicating that anion substitution between S2− and P3− ions did occur. Consequently, we investigated the resistive switching (RS) properties of these two phases in the presence of Cu3P. We found that the Cu2S‐Cu3P composite exhibited a high Off/On ratio (88) and a long retention time (>103 s). However, the Cu7.2S4‐Cu3P composite exhibited no RS performance. In addition, we discussed the conduction and resistive switching mechanisms. Our work enriches the preparation method of copper sulfides and provides a reference for enhancing RS performance. [ABSTRACT FROM AUTHOR]

The He isotopic composition and the He and Ne ratio of fluid inclusions in magnetite and pyrite from carbonatite breccias of the Sallanlatva alkali-ultramafic complex of the Kola alkaline province (Northwest Russia) are studied using the step-crushing method. The results indicate the highly likely involvement of fluids from several sources trapped in various proportions during the formation of the Sallanlatva explosive carbonatite breccias. The R/Ra ratio, where R is the measured 3He/4He ratio and Ra of 1.382 × 10–6 is the same ratio of atmospheric air, reaches 2.3, which is a reliable indicator of the presence of mantle gases. A low (1–44) 4He/20Ne ratio allows us to suggest the involvement of atmospheric gases dissolved in paleometeoric waters. A combination of these two facts favors a hypothesis of the phreatomagmatic nature of the studied breccias, i.e., their formation at the expense of interaction between the intruding hot orthomagmatic fluids and meteoric waters with dissolved atmospheric gases. [ABSTRACT FROM AUTHOR]

An efficient route for the chemoselective deoxygenation of benzylphenyl sulfones to the corresponding sulfides has been developed using a mixture of 1,2-bis(diphenylphosphino)ethane(dppe) and NBS as an effective promoter. This is the first development on the deoxygenation of diverse benzylphenyl sulfones under metal-free conditions. The mild reaction conditions, formation of the water soluble by-product and tolerance of a wide range of functional groups promote its broad applications in organic synthesis. [ABSTRACT FROM AUTHOR]

Tandem aromatic rearrangements represent a potent strategy for modulating the regioselectivity of a rearrangement process. In this article, we disclose two novel tandem aromatic rearrangements triggered by sulfonium [5,5]-rearrangement recently developed in our laboratory. Specifically, the [5,5]-rearrangement of aryl sulfoxides with allyl nitriles, followed by [3,3]-Cope rearrangement, forges a seamless tandem [5,5]-/[3,3]-rearrangement cascade, affording ortho -functionalized aryl sulfides. The other tandem process involves [5,5]-rearrangement of aryl sulfoxides with allyl nitriles, followed by nucleophilic addition/DDQ-oxidation-induced [3,3]-Cope rearrangement, eventually yielding meta -functionalized aryl sulfides. Both consecutive rearrangements enrich the repertoire of tandem aromatic rearrangement methodologies. [ABSTRACT FROM AUTHOR]

Difluoroalkyl sulfide (‐CF2S‐) moieties are an important class of skeletons in medicinal chemistry. Herein, a photoredox radical‐polar crossover reaction is reported for the three‐component thiofluorination, thiohydroxylation, thioalkoxylation, thioaminolation, and thiochlorination of gem‐difluoroalkenes towards diverse α‐functionalized difluoroalkyl sulfides. Such an approach features mild conditions, operational simplicity, and good substrate scope. [ABSTRACT FROM AUTHOR]

A practical and efficient trifluoromethylation of readily available and bench stable N‐Thiophthalimides and N‐Thioimides with Ruppert‐Prakash reagent (TMS‐CF3) is described. The reaction proceeds at room temperature and only requires NaOAc as the mild promoter to prepare a series of trifluoromethyl thioethers in good to excellent yields. Both aryl and alkyl derivates are well trifluoromethylated under transition‐metal‐free reaction conditions. Moreover, the reaction features with scale‐up synthesis and late‐stage modification of bioactive molecule. [ABSTRACT FROM AUTHOR]

Two heats of steel are melted using a vacuum induction furnace in the laboratory, with one heat undergoing magnesium treatment and the other being subjected to a combined magnesium–calcium treatment. The precipitation and agglomeration behaviors of inclusions of these two steel samples are observed using a high‐temperature confocal laser scanning microscopy. MnS precipitates form around oxide cores and undergo rapid growth during the solidification process of molten steel, and these MnS precipitates with oxide cores react with the cores, resulting in the transformation of the MnS into complex sulfides. In comparison with Al2O3 inclusions, MgO·Al2O3 inclusions have a lower critical velocity (V c), making them more susceptible to being engulfed by the solid–liquid interface. As the size of colliding inclusions increases, the coalescence–collision frequency (E 0) initially decreases until it reaches a minimum value. After that, with further size increments, the frequency starts to increase. During the inclusions growth process through collision, there is a distinct zone where coalescence–collision frequency is low. Inclusions that reach this zone struggle to grow further due to reduced collision coalescence, consequently leading to a predominance of inclusions with diameters in this zone. [ABSTRACT FROM AUTHOR]

A palladium-catalyzed cycloisomerization of carbamimidothioates with the formation of a quaternary carbon and a sulfide is described. The use of (IPr)Pd(allyl)Cl (CX21), K3 PO4 , and Me-C(OTBS)=NTBS in refluxing xylenes was optimal, and the methoxycarbonyl group was the most suitable substituent for the nitrogen atom of the carbamimidothioate. Phenyl and alkyl groups can be used as tethers for carbamimidothioates, and alkyl and aryl carbamimidothioates can undergo Pd-catalyzed cycloisomerization in high yields. [ABSTRACT FROM AUTHOR]

A Pd-catalyzed carbothiolation using thioesters, with the formation of a quaternary carbon, is described. Carbothiolation using thioesters was problematic due to a direct-coupling side reaction that produced a sulfide, but this side reaction was successfully suppressed by an appropriate selection of the thioester and the reaction conditions. In the preparation of chroman or coumaran derivatives by this method, the reaction using S -phenyl 4-methoxybenzenecarbothioate Pd(PPh3)4 , and Cs2 CO3 at 100 °C in toluene afforded the desired products in good yields (77–92%). The carbothiolation reaction also proceeded with esters of alkanethiols in higher yields (56–93%) than those obtained from the previously reported carbothiolation using triisopropylsilyl (TIPS) thioethers (12–63%). The developed Pd-catalyzed carbothiolation is applicable in the preparation of a wide range of products, including a tetralin derivative and an indoline derivative. The Pd-catalyzed carbothiolation using thioesters was found to be comparable with a previously reported carbothiolation using TIPS thioethers in terms of the yield and substrate scope, and to be a superior alternative owing to the stability and lower cost of thioesters. [ABSTRACT FROM AUTHOR]

The solid electrolyte (SE) membrane plays a crucial role in sulfide‐based all‐solid‐state batteries (ASSBs). However, the challenge of finding appropriate polymer binders with excellent (electro‐)chemical compatibility and adhesive properties, remains a significant obstacle for wet slurry processing of sulfide SE membranes. Herein, a novel “polar‐nonpolar synergistic” finely‐tuned strategy is employed to design an ethylene‐methyl acrylate (EMA) copolymer binder to facilitate wet‐slurry‐based fabrication of sulfide SE membranes. Significantly, by adjusting the ratio of polar and nonpolar groups, this methodology enables the binder to dissolve effectively in a toluene‐based slurry and also ensures good adhesion between the EMA binder and SE particles. The SE membrane prepared with EMA binder exhibits an ultra‐thin thickness (36 µm), flexibility, and excellent ionic conductivity (1.43 mS cm−1). The ASSB assembled with the SE membrane shows an excellent capacity retention rate of 92.9% after 120 cycles at 0.5 C. This work on the “polar‐nonpolar synergistic” finely‐tuned effect of binder provides insight for manufacturing high‐quality sulfide SE membranes. [ABSTRACT FROM AUTHOR]

Multi-component synergy and the rational design of structures are effective methods for preparing electrode materials for high-performance energy storage devices. Transition metal-based hydroxides offer advantages such as a large specific surface area, large interlayer spacing, multiple redox states, and high theoretical capacity, making them commonly used as positive materials for supercapacitors. However, challenges like low conductivity and severe agglomeration limit their practical application. This study focuses on the preparation of Ni, Co, and Mo ternary transition metal hydroxides by incorporating the Mo element to optimize their structure. Furthermore, sulfide ions were utilized in an ion exchange process to replace hydroxides, resulting in the formation of NiCoMo ternary sulfide electrode materials. By adjusting the amount of Mo added, a spherical nanoneedle-shaped N2C1MS0.2-2 electrode material was successfully synthesized. This electrode exhibited a specific capacity of 2094 F g-1 at a current density of 1 A g-1. In addition, an asymmetric supercapacitor was assembled with activated carbon as the negative electrode and N2C1MS0.2-2 as the positive electrode, which had an energy density of 46.2 W h kg-1 at a power density of 800 W kg-1, a capacity retention of 89.7% and a coulombic efficiency of 97.8% after 10 000 cycles. This study provides a reference for the design and preparation of ternary sulphide electrode materials. [ABSTRACT FROM AUTHOR]

The commercialization of all‐solid‐state Li batteries (ASSLBs) demands solid electrolytes with strong cost‐competitiveness, low density (for enabling satisfactory energy densities), and decent anode compatibility (the need for cathode compatibility can be circumvented by the cathode coating techniques that are widely applied in sulfide‐based ASSLBs). However, none of the reported oxide, sulfide, or chloride solid electrolytes meets these requirements simultaneously. Here, we design a Li7P3S7.5O3.5 (LPSO) solid electrolyte, which shows a combination of all the aforementioned characteristics. The synthesis of this material does not need the expensive Li2S, so the raw materials cost is only $14.42/kg, which, unlike most solid electrolytes, lies below the $50/kg threshold for commercialization. The density of LPSO is 1.70 g cm−3, considerably lower than those of the oxide (typically above 5 g cm−3) and chloride (around 2.5 g cm−3) solid electrolytes. Besides, LPSO also shows excellent anode compatibility. The Li|LPSO|Li cell cycles stably with a potential of ~50 mV under 0.1 mA cm−2 for over 4200 h at 25 °C, and the all‐solid‐state pouch cell with the Si anode shows a capacity retention of 89.29 % after 200 cycles under 88.6 mA g−1 at 60 °C. [ABSTRACT FROM AUTHOR]

Developing cost‐effective and high‐active electrocatalysts is vital to enhance the electrocatalytic performance for oxygen evolution reaction (OER). However, traditional pyrolysis methods require complicated procedures, exact temperatures, and long reaction times, leading to high costs and low yields of electrocatalysts in potential industrial applications. Herein, a rapid and economic laser‐induced preparation strategy is proposed to synthesize three bimetallic sulfide/oxide composites (MMoOS, M=Fe, Co, and Ni) on a nickel foam (NF) substrate. A focused CO2 laser with high energy is applied to decompose Anderson‐type polyoxometalate (POM)‐based precursors, enabling the creation of abundant heteropore and defective structures in the MMoOS composites that have multi‐components of MS/Mo4O11/MoS2. Remarkably, owing to the structural interactions between the active species, FeMoOS shows superior electrocatalytic performance for OER in an alkaline medium, exhibiting a low overpotential of 240 mV at 50 mA cm−2, a small Tafel slope of 79 mV dec−1, and good durability for 80 h. Physical characterizations after OER imply that partially dissolved Mo‐based species and new‐formed NiO/NiOOH can effectively uncover abundant active sites, fasten charge transfer, and modify defective structures. This work provides a rapid laser‐induced irradiation method for the synthesis of POM‐derived nanocomposites as promoted electrocatalysts. [ABSTRACT FROM AUTHOR]

A convenient and practical multicomponent strategy for the sulfenoamination of alkenes was realized, which using free‐thiols as the sulfur‐reagent, NIS both as radical initiator and an N‐nucleophile. This protocol excellent in terms of transition‐metal‐free, good functional group tolerance, easily available substrates and facile scale‐up. And provided a direct‐ and general way to synthesize various β‐succinimide sulfides with high regioselectivity. [ABSTRACT FROM AUTHOR]

In the following research, meso‐tetrakis(4‐carboxyphenyl)porphyrinatomanganese (III) acetate (MnTCPP(OAc)) was immobilized onto the surface of two functionalized magnetic nanoparticles (MNPs) with different linker length via amide bond (Fe3O4@SiO2‐NH2‐MnTCPP(OAc) (A1) and Fe3O4@SiO2‐NHCO‐NH2‐MnTCPP(OAc) (A2)). The prepared catalysts were characterized by standard methods such as: atomic absorption spectroscopy (AAS), Ultra violet‐visible (UV‐Vis), Fourier‐transform infrared (FT‐IR), vibrating sample magnetometry (VSM), field emission scanning electron microscopy (FE‐SEM) and transmission electron microscopy (TEM) techniques and also the effect of the length of the linker on the catalytic activity of supported magnetic nanohybrids was investigated. The prepared magnetic nano‐catalysts with different linker lengths were participated in a comparative study of the clean oxidation of sulfides with urea hydrogen peroxide (UHP) in ethanol. The higher catalytic activity, selectivity and also reusability were achieved in the presence of the catalyst with longer linker length (A2) at ambient temperature. Moreover, the turnover number (TON) of catalytic reactions using A2 as catalyst was highly enough to consider the catalyst as an efficient material to oxidize various sulfides. Both A1 and A2 catalysts simply have accomplished 5 runs of recycling without significant decrease in the catalytic activity. [ABSTRACT FROM AUTHOR]

A novel and concise synthetic method for arenastatin A, a cytotoxic cyclic depsipeptide of marine origin, was developed in this study. The convergent assembly of the four segments, including the cross-metathesis reaction, gave a cyclization precursor, and Fmoc deprotection caused simultaneous macrocyclization. The Corey–Chaykovsky reaction using a chiral sulfur ylide afforded arenastatin A with complete stereoselectivity in the longest linear sequence of seven reaction steps from the known compound. Using this synthetic method, some analogs of segment B were prepared through a late-stage diversification strategy. The simple SN2 reaction of the thiolate toward the tosylate precursor, prepared using almost the same synthetic method as described above, provided the desired sulfide analogs. [ABSTRACT FROM AUTHOR]

Germanium (Ge) is a critical raw material for emerging high-tech and green industries, resulting in considerable recent interest in understanding its distribution and geochemical behavior in ore deposits. In this contribution, the distribution of Ge and related trace elements in the Fule Pb-Zn(-Ge) deposit, South China, is investigated to reveal the distribution of Ge in the hydrothermal ores and during sulfide weathering, using multiple microanalytical techniques, including scanning electron microscopy, electron probe microanalysis and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). In the Fule MVT deposit, sphalerite (ZnS) is the most significant Ge-carrier relative to other sulfides, though the five recognized textural types of sphalerite display progressive depletion in Ge from the first sphalerite generation to the late one. In the early stage, sphalerite with fine-grained chalcopyrite inclusions has the highest Ge concentrations, probably accounting for a significant proportion of the total Ge. We interpret that high Ge concentrations in the early sphalerite may be attributable to high Cu activity in the mineralizing fluids. During oxidative weathering, Ge was redistributed from its original host, sphalerite, to the weathering product willemite (Zn2SiO4) rather than smithsonite (ZnCO3), with high levels of Ge (up to 448 μg/g) present in the willemite. The formation of abundant willemite largely prevents the dispersion of Ge during weathering. In principle, willemite-hosted Ge should be fully recoverable, and the Zn-silicate ores may, therefore, be a potential target to meet future demand. This study provides new information on how Ge behaves from sulfide- to weathering-stage in MVT systems, which directly impacts Ge mobility and deportment changes and the development of metallurgical strategies for Ge recovery. [ABSTRACT FROM AUTHOR]

Molybdenum (IV) sulfide is widely employed in electronic device applications. Recognized as one of the most efficacious methods for fabricating high-quality molybdenum (IV) sulfide, the chemical vapor deposition (CVD) method's application necessitates the development of a straightforward, swift and nondestructive characterization tool. Thus, this paper presents a rapid and reliable differential reflectance spectroscopy (DRS) instrumentation, grounded on the optical microscope, capable of characterizing two-dimensional materials prepared by CVD. This universal nondestructive identification tool facilitates the investigation of two-dimensional materials on both opaque and transparent substrates. MoS2 samples prepared by CVD were characterized on SiO2/Si and sapphire substrate. The results indicate that the exciton absorption peak can be accurately identified, validating the instrumentation's utility for material detection and monolayer identification. The characterization results, corroborated by the Raman spectra with a wavenumber difference of approximately 20 cm−1 and the triangular appearance of the optical image, affirm the application of this instrumentation. Ultimately, the DRS instrumentation provides a swift and nondestructive route to characterize physical properties such as bandgap and optical properties for two-dimensional materials. [ABSTRACT FROM AUTHOR]

This review presents an updated data on various technologies for the processing of refractory gold-bearing sulfide concentrates. It primarily focuses on the hydrometallurgical treatment for sulfide mineral oxidation and gold extraction, including the use of bacteria, pressure oxidation, ultrafine grinding, and the Albion ProcessTM. The main operating plants that use hydrometallurgical technologies and their key characteristics are listed, along with schematics of primary processing routes. Besides, advantages and disadvantages of each technology are discussed, along with their cost comparisons. [ABSTRACT FROM AUTHOR]

Three decavanadate (V10O28)6- containing compounds were used to test their catalytic activity in the sulfoxidation reaction of diphenyl sulfide using environmentally friendly conditions (low temperature, non-toxic solvent). The compounds of interest for our study, (NH4)2(H2en)2{V10O28}·4H2O, (H2en)3{V10O28}·6H2O and {Li2(H2O)10}(V10O28)(NH4)4, were evaluated, showing good activity in sulfoxidation reaction and leading to complete conversion of the sulfide even after three runs. The tetraammonium decaaqualithium decavanadate, with the formula {Li2(H2O)10}(V10O28)(NH4)4 was obtained through a modified literature method and its structure re-determined and investigated, giving similar results as previously described and confirming the structure of the used material. [ABSTRACT FROM AUTHOR]

Abstract This article is devoted to the synthesis of a new magnetic palladium catalyst that has been immobilized on A-TT-Pd coated-magnetic Fe3O4 nanoparticles. Such surface functionalization of magnetic particles is a promising method to bridge the gap between heterogeneous and homogeneous catalysis approaches. The structure, morphology, and physicochemical properties of the particles were characterized through different analytical techniques, including TEM, FT-IR, XRD, SEM, EDS, TGA-DTG, ICP, and VSM techniques. The obtained Fe3O4@SiO2@A-TT-Pd performance can show excellent catalytic activity for the synthesis of diaryl ethers and oxidation of sulfides, and the corresponding products were obtained with high yields. The advantages of this catalyst include a simple test method, green reaction conditions, no use of dangerous solvents, short reaction time, low catalyst loading, and reusability. Also, the nanocatalyst was easily separated from the reaction mixture with the help of a bar magnet and recovered and reused several times without loss of stability and activity.

Abstract Defects-rich heterointerfaces integrated with adjustable crystalline phases and atom vacancies, as well as veiled dielectric-responsive character, are instrumental in electromagnetic dissipation. Conventional methods, however, constrain their delicate constructions. Herein, an innovative alternative is proposed: carrageenan-assistant cations-regulated (CACR) strategy, which induces a series of sulfides nanoparticles rooted in situ on the surface of carbon matrix. This unique configuration originates from strategic vacancy formation energy of sulfides and strong sulfides-carbon support interaction, benefiting the delicate construction of defects-rich heterostructures in MxSy/carbon composites (M-CAs). Impressively, these generated sulfur vacancies are firstly found to strengthen electron accumulation/consumption ability at heterointerfaces and, simultaneously, induct local asymmetry of electronic structure to evoke large dipole moment, ultimately leading to polarization coupling, i.e., defect-type interfacial polarization. Such “Janus effect” (Janus effect means versatility, as in the Greek two-headed Janus) of interfacial sulfur vacancies is intuitively confirmed by both theoretical and experimental investigations for the first time. Consequently, the sulfur vacancies-rich heterostructured Co/Ni-CAs displays broad absorption bandwidth of 6.76 GHz at only 1.8 mm, compared to sulfur vacancies-free CAs without any dielectric response. Harnessing defects-rich heterostructures, this one-pot CACR strategy may steer the design and development of advanced nanomaterials, boosting functionality across diverse application domains beyond electromagnetic response.

The rock composition and ore mineralization of the Malenkiy site located within the Khengur gabbro-dolerite complex of the Pay-Khoy were examined. Petrogeochemical analysis revealed two varieties of the studied rocks: fine-crystalline quartz and medium- and coarse-crystalline quartz containing metagabbro-dolerite. The Y, Zr, and Nb contents suggest that metagabbro-dolerites formed in an intraplate setting from enriched mantle sources during the melting of garnet peridotite, with a small contribution from the melt source of ancient continental crust. Two types of ore mineralization were distinguished: nest- and veinlet-disseminated sphalerite-chalcopyrite-pyrrhotite (type I) and veinlet-disseminated cobaltite-pentlandite-chalcopyrite-pyrrhotite (type II). The most efficient ore mineralization was type II, which is characterized by the presence of both high-temperature cobalt- and nickel-bearing sulfide minerals, as well as low-temperature tellurides of palladium (kotulskite) and silver (hessite).

The paper presents the results of studies of dust residues of snow cover within various climatic zones and copper deposits of the Ural region. Snow cover research is one of the methods for environmental assessment of territories. This concerns the study of dust residues from snow cover samples, as shown by the example of the territories of the Northern and Southern Urals at different stages of work on copper deposits. The initial stage of study and development is considered using the example of porphyry copper deposits in the Chelyabinsk region, where snow samples reveal organic matter in dust residues, typical birch seeds, a small amount of minerals at a low dust load (P ˂ 100 kg/day per km2). For the deposits of the Ivdel region (Northern Urals), the dust residues largely contain organic dust, fragments of ore minerals (pyrite, chalcopyrite) and minerals of volcanic rocks and metasomatic rocks. The maximum value of the dust load is set for the Novo-Shemurskoye deposit currently being developed. A study of dust residues in the zone of influence of the Karabash copper smelter (before its reconstruction) has shown that in some parts of the sanitary protection zone the level of snow cover pollution is very high with dust load values up to 12,633 kg/day per km2, which is determined primarily by the widespread use of crushed copper smelting slag. In general, the study of dust residues of snow cover provides information about both the ecological state of the territories and the mineral composition of the residues, which must be used for practical purposes.

The isolation and catalytic enantioselective synthesis of configurationally stable S‐stereogenic sulfonium ylides have been significant challenges in the field of asymmetric synthesis. These reactive intermediates are crucial for a variety of synthetic transformations, yet their inherent tendency towards rapid inversion at the sulfur stereocenter has hindered their practical utilization. Conventional approaches have focused on strategies that incorporate a C=S bond‐containing cyclic framework to help mitigate this stereochemical lability. In this work, we present an alternative tactic that leverages the stabilizing influence of an adjacent N‐atom and cyclic sulfide moiety. Exploiting a copper catalyzed enantioselective intermolecular carbene transfer reaction, structurally diverse S‐stereogenic aminosulfonium ylides have been achieved in excellent yields and enantioselectivities. Experimental results indicate that the careful selection of 2‐diazo‐1,3‐diketone precursors is crucial for achieving optimal stereoinduction in this transformation. The resulting highly enantioenriched aminosulfonium ylides allow for further stereospecific elaborations to furnish aminosulfonium ylide oxides and sulfinamide. This work expands the boundaries of chiral sulfonium ylide chemistry, providing access to a broad range of previously elusive S‐stereogenic aminosulfonium ylide scaffolds. [ABSTRACT FROM AUTHOR]

The effect of sulfur content on sulfide inclusion and dendrite MnS in continuous casted 20CrMnTi gear steel is investigated. There are two main types of sulfides in 20CrMnTi steel: pure MnS and TiN–MnS composite inclusions. The number of TiN–MnS is higher than MnS, especially in the edge of the billet. TiN–MnS is smaller both in area and size than pure MnS. The statistical results of dendrite MnS show that the increase of S content decreases the average size of sulfides, whereas raises the number and the maximum size of sulfides. With the S content increasing, the proportion of large‐sized dendrite MnS in steel decreases, but the amount of large‐sized dendrite MnS increases, which results in the increase of number of large‐sized dendrite MnS. The average area of dendrite MnS inclusions first increased and then decreased from the edge to the center of billet, and the maximum area appeared at about 1/2 radius of the billet. Comparison with the microstructure of the two billets, the proportion of ferrite increased with the increase of S content. [ABSTRACT FROM AUTHOR]

A metal-free system for Doyle–Kirmse reaction of biologically important diallyl sulfide with donor–acceptor diazo compounds in an aqueous medium using blue-LED irradiation was demonstrated. The resulting sulfanyl dienes were converted into thiopyrans using ring-closing metathesis in water. Additionally, the utility of dihydro-thiopyrans was also investigated. [ABSTRACT FROM AUTHOR]

Nitrogenases are the only enzymes that activate the strong triple bond in N2. The mechanism for the activation has been very difficult to determine in spite of decades of work. In previous modeling studies it has been suggested that the mechanism for nitrogen activation starts out by four pre‐activation steps (A0–A4) before catalysis. That suggestion led to excellent agreement with experimental Elecrtron Paramagnetic Resonance (EPR) observations in the step where N2 becomes protonated (E4). An important part of the pre‐activation is that a sulfide is released. In the present paper, the details of the pre‐activation are modeled, including the release of the sulfide. Several possible transition states for the release have been obtained. An A4(E0) state is reached which is very similar to the E4 state. For completeness, the steps going back from A4(E0) to A0 after catalysis are also modeled, including the insertion of a sulfide. [ABSTRACT FROM AUTHOR]

Sulfilimines and their derivatives have garnered considerable interest in both synthetic and medicinal chemistry. Photochemical nitrene transfer to sulfides is known as a conventional synthetic approach to sulfilimines. However, the existing methods have a limited substrate scope stemming from the incompatibility of singlet nitrene intermediates with nucleophilic functional groups. Herein, we report the synthesis of N‐sulfonyl sulfilimines via visible‐light‐mediated energy transfer to sulfonyl azides, uncovering the previously overlooked reactivity of triplet nitrenes with sulfides. This reaction features broad functional group tolerance, water compatibility, and amenability to the late‐stage functionalization of drugs. Thus, this work represents an important example of energy transfer chemistry that overcomes challenges in traditional synthetic methods. [ABSTRACT FROM AUTHOR]

A method for the radical functionalization of 1,2,4‐oxadiazoles using alkyl halides as precursors of radicals is described. The reaction efficiency is determined by potassium tetrafluoropyridinyl thiolate additive, which plays dual role. First, the thiolate converts alkyl halides into more reactive fluorinated aryl sulfides, which undergo photoredox activation of the C−S bond. Second, the thiolate decreases the unproductive loss of alkyl radicals by converting them back to the sulfides. [ABSTRACT FROM AUTHOR]

Exfoliation of 2D non‐Van der Waals (non‐vdW) semiconductor nanoplates (NPs) from inorganic analogs presents many challenges ahead for further exploring of their advanced applications on account of the strong bonding energies. In this study, the exfoliation of ultrathin 2D non‐vdW chromium sulfide (2D Cr2S3) by means of a combined facile liquid‐phase exfoliation (LPE) method is successfully demonstrated. The morphology and structure of the 2D Cr2S3 material are systematically examined. Magnetic studies show an obvious temperature‐dependent uncompensated antiferromagnetic behavior of 2D Cr2S3. The material is further loaded on TiO2 nanorod arrays to form an S‐scheme heterojunction. Experimental measurements and density functional theory (DFT) calculations confirm that the formed TiO2@Cr2S3 S‐scheme heterojunction facilitates the separation and transmission of photo‐induced electron/hole pairs, resulting in a significantly enhanced photocatalytic activity in the visible region. [ABSTRACT FROM AUTHOR]

Musca domestica L., a common housefly, and Culex quinquefasciatus mosquito are quite well-known pests that can transfer a wide range of diseases to humans as well as animals. In this study, various isoborneol derivatives including esters, ethers, and thioethers were synthesized from isoborneol under mild conditions. These derivatives were evaluated for inhibition of house-fly M. domestica adults and Cx. quinquefasciatus larvae. Two of the synthesized isoborneol ester derivatives (2 and 3) showed good activity against both insect species. Additional two derivatives (6 and 9) were active against M. domestica L., and the derivatives (1–3, 8) were active against Cx. quinquefasciatus larvae. [ABSTRACT FROM AUTHOR]

The first examples of RE/Si FLPs (RE: rare-earth metal, FLPs: frustrated Lewis pairs), namely Yb/Si FLPs were synthesized, where Yb⋯Si distances are in the range of 3.55 to 3.72 Å. These FLPs react with triphenylphosphine sulfide and aryl isocyanide to produce novel silylyne group transfer products through dissociation of naphthalene. [ABSTRACT FROM AUTHOR]

The characterization and evolution of corrosion products deposited on/around MnSs, a typical kind of inclusive particle embedded in AISI 304 stainless steel, was analyzed using a quasi-in-situ method in a 3.5 wt.% NaCl solution. On/around the MnS inclusion, a corrosion product layer with spinel Fe3−xCrxO4 as the main component was formed, with a thickness of several hundred nanometers. Below the layer, there was a cavity layer in which part of the MnS remained, forming secondary pitting along the MnS/matrix boundary. The mechanism of corrosion product deposition and evolution accompanied by MnS dissolution, as well as the characteristics of the corrosion products, are discussed. [ABSTRACT FROM AUTHOR]

The room‐temperature sodium‐sulfur (RT Na‐S) batteries have been seriously hindered in their practical application due to the sluggish redox kinetics and incomplete conversion of polysulfides. In this study, a structure‐determined Keggin‐type heteropolyvanadotungstate of H5PW10V2O40·30H2O (PW10V2) is engineered and reveal its catalytic mechanism in RT Na‐S system. With the assistance of precise V sites and highly reversible multi‐electron redox properties, PW10V2 as a bidirectional molecular catalyst expedites the complete conversions between polysulfides and the insoluble sodium sulfide, while undergoing the reversible transformation between its reduced and oxidized states. Furthermore, PW10V2 with multicenter active sites can capture polysulfides efficiently. Consequently, the cell with the constructed PW10V2‐based modified separator achieves the perdurable cyclability up to 4000 loops even at 10 C toward an exceptionally low capacity decay rate of 0.012% per cycle, far surpassing those of current state‐of‐the‐art RT Na‐S batteries that employ the functional materials based on separator. This work first demonstrates the underlying electrochemical reaction processes of polyoxometalate‐based functional materials, which guides solving the challenging issues related to sodium polysulfides in RT Na‐S batteries. [ABSTRACT FROM AUTHOR]

Sulfur forms an immiscible liquid upon saturation in magma, and sulfide droplets are commonly found in fresh mid-ocean ridge basalt (MORB). Scanning electron microscopy (SEM) analysis revealed that the fine-grained and weakly phyric MORB samples exhibited hypocrystalline to vitreous textures. Transmission electron microscopy (TEM) of MORB glasses exhibits nanoscale sulfide droplets (10-15 nm) with rounded shapes and smooth edges, showing crystalline and homogeneous composition. Elemental distribution included S, Fe, Cu, and Ni, while Si, Al, and O were lacking. Prior research clarified the immiscibility between sulfide and silicate melts, impacting the size distribution of sulfide droplets. This is the first report on nanoscale sulfide droplets within MORB glasses, and these results suggest that nanoscale sulfide droplets represent the initial phase of sulfide saturation. Such an insight may prove useful in understanding how siderophile and chalcophile elements behaved during sulfide crystallization. In addition, this study determines the immiscibility of sulfides and silicate melts that occur in the early nanometer stage. Therefore, it is speculated that immiscibility phenomena may occur in the nanometer stage during magma evolution. [ABSTRACT FROM AUTHOR]

Robust Cu2S‐Cu3P@C Nanomatrix electrode material has been synthesized via a two‐step process involving carbonization of Cu‐MOF, HKUST‐1, followed by simultaneous phosphorization and sulphurization of the carbonized product. This seamless approach leads to the efficient incorporation of highly active Cu2S‐Cu3P hybrid nanostructures within a conductive carbon matrix, exhibiting exceptional electrochemical glucose sensing performance. Synergistic interactions between Cu2S‐Cu3P and the carbon matrix boost glucose electro‐oxidation kinetics. The resulting Cu2S‐Cu3P@C displays a broad linear response (0.005–5 mM), low detection limit (2.3 μM), and high sensitivity (10,790 μA mM−1 cm−2), with excellent selectivity towards glucose even in the presence of interferents. This biomimetic Cu2S‐Cu3P@C nanomatrix catalyst holds promise for biosensor development in bioanalysis and clinical diagnosis. [ABSTRACT FROM AUTHOR]