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The preparation, properties, and short-range order (SRO) structures of glasses in the series (1-)[2/3NaS + 1/3PS] + [1/3NaS + 2/3NaPON] = NaPSON, where 0 ≤ ≤ 0.5 (NaPSON), are reported on. In this study, these mixed oxy-sulfide-nitride (MOSN) glasses were prepared by adding the nitrided material NaPON; = 0.46 = NaPON (NaPON) to the base sulfide glass NaPS. For comparison purposes, additions of the unitrided material, = 0, NaPO, were also studied (NaPSO). Accordingly, large batches of bubble-free glass could be prepared making this route of nitrogen doping amendable toward scaling-up the glass melting process; though, only small amounts of nitrogen could be incorporated in this manner. Nitrogen and sulfur compositional analysis were combined with XPS, Raman, FT-IR, and P MAS NMR spectroscopies to determine the amount of retained nitrogen in the glass after melting and quenching and to determine the effect of the added nitrogen and oxygen on the structure of the base pure sulfide glass NaPS, = 0.0. The nitrogen content increased linearly with the addition of NaPON, but was found, through quantitative P MAS NMR analysis, to be approximately half that expected at each value of . Despite the small amount of nitrogen retained in these glasses, profound increases in the glass transition () and crystallization temperatures () were found with increasing . For the intermediate values of , 0.2 and 0.3, no crystallization of the supercooled melt was observed even 250 °C above the . It was found that the addition of NaPON to the series caused a disproportionation reaction, where the oxide and oxy-nitride SRO species preferentially formed covalent, networking phosphate chains, forcing the sodium modifier to ionic sulfide units with large fractions of nonbridging sulfurs (NBSs). This disproportionation reaction was also observed in the NaPO doped series of glasses, but to a smaller extent. Oxygen was found in both bridging oxygen (BO) and nonbridging oxygen (NBOs) structures while the sulfur was predominantly found in nonbridging sulfur (NBS) structures. N 1s XPS and P NMR studies provided insight into the nitrogen bearing phosphorus units and the wt % of nitrogen that was retained in the quenched glasses. It was found that trigonally coordinated nitrogen (N) was preferentially retained in the melt, whereas it is proposed that the linearly coordinated (doubly bonded) nitrogen (N) accounts for the lost nitrogen in the glasses.
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http://dx.doi.org/10.1021/acs.inorgchem.2c02300 | DOI Listing |
J Phys Chem C Nanomater Interfaces
September 2025
Leiden Insitute of Chemistry, Leiden University, Einsteinweg 55, Leiden 2333 CC, Netherlands.
In this study, we report the synthesis of single-crystalline h-BN on Ni(111) under ultrahigh vacuum (UHV) conditions using hexamethylborazine (HMB) as a nonclassical precursor. The novel use of HMB facilitates the diffusion of methyl groups into the bulk of Ni(111), playing a critical role in the achievement of high-quality crystalline h-BN layers. The synthesis is performed on a 2 mm-thick Ni(111) single crystal and on a 2-μm-thick Ni(111) thin film on sapphire to evaluate the feasibility of synthesizing h-BN on industrially relevant substrates.
View Article and Find Full Text PDFRSC Adv
September 2025
Department of Medicinal Chemistry, Faculty of Pharmacy, Galala University P. O. 43713 New Galala Egypt
Isatin (1-indole-2,3-dione) is a privileged nitrogen-containing heterocyclic framework that has received considerable attention in anticancer drug discovery owing to its general biological behavior and structural diversity. This review focuses on isatin-heterocyclic hybrids as a valuable model in the development of new anti-cancer drugs that may reduce side effects and help overcome drug resistance, discussing their synthetic approaches and mechanism of action as apoptosis induction through kinase inhibition. With various chemical modifications, isatin had an excellent ability to build powerful isatin hybrids and conjugates targeting multiple oncogenic pathways.
View Article and Find Full Text PDFFront Microbiol
August 2025
State Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou, China.
While soil microorganisms underpin terrestrial ecosystem functioning, how their functional potential adapts across environmental gradients remains poorly understood, particularly for ubiquitous taxa. Employing a comprehensive metagenomic approach across China's six major terrestrial ecosystems (41 topsoil samples, 0-20 cm depth), we reveal a counterintuitive pattern: oligotrophic environments (deserts, karst) harbor microbiomes with significantly greater metabolic pathway diversity (KEGG) compared to resource-rich ecosystems. We provide a systematic catalog of key functional genes governing biogeochemical cycles in these soils, identifying: 6 core CAZyme genes essential for soil organic carbon (SOC) decomposition and biosynthesis; 62 nitrogen (N)-cycling genes (KOs) across seven critical enzymatic clusters; 15 sulfur (S)-cycling genes (KOs) within three key enzymatic clusters.
View Article and Find Full Text PDFBeilstein J Org Chem
September 2025
Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya 16/10, 117997, Moscow, Russia.
Thioformylium methylide, which is readily generated from chloromethyl(trimethylsilyl)methyl sulfide by the action of fluoride, is used for the synthesis of spirocyclic derivatives from arylidene-azolones. Four types of the corresponding heterocycles have been studied. A series of 7-thia-3-azaspiro[4.
View Article and Find Full Text PDFBioinform Adv
August 2025
Department of CSE, BUET, Dhaka 1000, Bangladesh.
Motivation: Heavy usage of synthetic nitrogen fertilizers to satisfy the increasing demands for food has led to severe environmental impacts like decreasing crop yields and eutrophication. One promising alternative is using nitrogen-fixing microorganisms as biofertilizers, which use the nitrogenase enzyme. This could also be achieved by expressing a functional nitrogenase enzyme in the cells of the cereal crops.
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