P. A. Marmaza, N. P. Ivanov, V. O. Kaptakov, Ya. G. Zernov, V. Yu. Maiorov, A. N. Fedorets, O. O. Shichalin, E. K. Papynov
{"title":"Optimized Hydrothermal Synthesis of Pharmacosiderite-Type Titanosilicates for Extraction of 137Cs and 90Sr from High-Salinity Liquid Media","authors":"P. A. Marmaza, N. P. Ivanov, V. O. Kaptakov, Ya. G. Zernov, V. Yu. Maiorov, A. N. Fedorets, O. O. Shichalin, E. K. Papynov","doi":"10.1134/S0036023625600224","DOIUrl":"10.1134/S0036023625600224","url":null,"abstract":"<p>Pharmacosiderite-type titanosilicates were prepared hydrothermally. The influence of the duration of hydrothermal synthesis on the cesium-137 and strontium-90 sorption properties of the titanosilicates, structural phase composition, surface morphology, and textural characteristics was investigated. The composition, morphology, and structure of the samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). The textural characteristics of materials were studied by BET and EDX. The sorption properties of disubstituted pharmacosiderite-type titanosilicates toward cesium and strontium radionuclides in microconcentrations were studied in adsorption experiments from model solutions of liquid radioactive waste (LRW) with low and medium concentrations of interfering impurities.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 and Development Prospects","pages":"355 - 363"},"PeriodicalIF":1.5,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145144987","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Wen-Xiu Yu, Yu-Shu Zhu, Zhen Zhao, Shao-Dong Su, Xi Liu
{"title":"Effects of Terminal Halide Ions on Structures and Photoluminescence Properties of three Mercury Coordination Polymers","authors":"Wen-Xiu Yu, Yu-Shu Zhu, Zhen Zhao, Shao-Dong Su, Xi Liu","doi":"10.1134/S0036023625600649","DOIUrl":"10.1134/S0036023625600649","url":null,"abstract":"<p>The halide anions have shown crucial influence on the structures of the Hg(II) halide coordination polymers (CPs) and these interesting phenomena have been widely explored, while it still remains elusive to predict which halide anions give similar or different structures. The present three novel CPs [Hg(Hbpt)X<sub>2</sub>]<sub><i>n</i></sub> (X = Cl (<b>1</b>), Br (<b>2</b>), I (<b>3</b>), Hbpt is 4,4'-bis(4-pyridyl)-1,2,4-triazoles) give a special example to verify the effect of halide ions on the structures and photoluminescence properties. Single crystal X-ray diffraction analyses indicated the terminal coordinated halide ions play important roles in the structural diversity since the 1D chains in the three CPs display various configurations, symmetries and packing modes although they are all formed by Hbpt ligand connecting Hg(II) cations. The photoluminescence experiments and DFT calculations results suggest that both the halide anions and conjugated Hbpt ligands show significant roles in the emission process, while halide anions have a limited effect on tuning the photoluminescence properties.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 6","pages":"877 - 887"},"PeriodicalIF":1.5,"publicationDate":"2025-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144868669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Synthesis and Characterization of Twin Barrel-Like Tungsten Trioxide Obtained by Hydrothermal Treatment","authors":"Sonia Amokrane, Fahim Hamidouche, Amar Irekti, Souad Saadi, Zineb Meguellati, Kaouthar Bouguerra, Souad Hammadou née Mesdour","doi":"10.1134/S0036023625600583","DOIUrl":"10.1134/S0036023625600583","url":null,"abstract":"<p>Various methods have been presented lately in literature for the elaboration of tungsten oxide (WO<sub>3</sub>) materials. Herein, WO<sub>3</sub> was prepared under properly controlled conditions by hydrothermal route, using Na<sub>2</sub>WO<sub>4</sub>·2H<sub>2</sub>O as a raw material in the presence of different structure directing agents (SDAs) and by acidifying the medium with nitric acid to pH 1. The influence of the SDAs on the structure and morphology of the obtained tungsten oxide has been investigated by scanning electron microscopy (SEM), micro-Raman spectroscopy and X-ray powder diffraction. The obtained WO<sub>3</sub> materials have a barrel-like morphology independently of the SDA used. However the crystalline structure obtained is a pure hexagonal WO<sub>3</sub> with CoSO<sub>4</sub>·7H<sub>2</sub>O, CuSO<sub>4</sub>·5H<sub>2</sub>O, ZnSO<sub>4</sub>·7H<sub>2</sub>O and Zn(CH<sub>3</sub>COO)<sub>2</sub>·2H<sub>2</sub>O and a hydrated hexagonal WO<sub>3</sub>: WO<sub>3</sub>·1/3H<sub>2</sub>O with MnCl<sub>2</sub>·4H<sub>2</sub>O. The results demonstrate a noteworthy effect of the SDA anion on the crystalline structure of the synthesized tungsten oxide as compared to the minor effect from the cation of the SDA. Furthermore, a formation mechanism of the nanobarrel WO<sub>3</sub> is proposed.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 6","pages":"821 - 832"},"PeriodicalIF":1.5,"publicationDate":"2025-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144868827","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. A. Lopera, E. A. Chavarriaga, A. I. Moreno, V. D. N. Bezzon, J. A. Perez-Taborda, M. T. D. Orlando, C. A. C. Passos, A. Pelaez, C. P. Bergmann, C. Garcia
{"title":"Influence of Silver on Formation of Biphasic Calcium Phosphates by Solution Combustion for Potential Antibacterial and Photocatalytic Applications","authors":"A. A. Lopera, E. A. Chavarriaga, A. I. Moreno, V. D. N. Bezzon, J. A. Perez-Taborda, M. T. D. Orlando, C. A. C. Passos, A. Pelaez, C. P. Bergmann, C. Garcia","doi":"10.1134/S0036023625600327","DOIUrl":"10.1134/S0036023625600327","url":null,"abstract":"<p>Silver-doped calcium phosphate powders were synthesized by solution combustion synthesis. X-ray powder diffraction confirmed the phase composition, demonstrating the influence of silver on the formation of hydroxyapatite (HAP) and tricalcium phosphate (β-TCP). Specifically, increasing silver concentration led to a decrease in HAP and an increase in the β-TCP phase. Rietveld refinement analysis revealed a corresponding increase in β-TCP crystallite size (from 62 to 98 nm) with higher silver concentrations, suggesting the incorporation of silver into the β-TCP lattice. Silver phosphate was observed only at an Ag/(Ag + Ca) cationic ratio of 0.12. Scanning electron microscopy (SEM) revealed aggregates formed during combustion, while transmission electron microscopy (TEM) showed Ag nanoparticles supported on the calcium phosphate. Antimicrobial assays demonstrated activity against both Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria for the powders with Ag/(Ag + Ca) ratios of 0.12 and 0.09. Additionally, potential photocatalytic activity was assessed via methylene blue (MB) degradation under sunlight. UV-Vis spectroscopy revealed significant MB degradation after 4 h of sunlight exposure, with the blue solution becoming transparent. These results indicate that the synthesized powders are promising for use in antimicrobial and photocatalytic applications.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 6","pages":"915 - 926"},"PeriodicalIF":1.5,"publicationDate":"2025-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144868828","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Morphology Control, High-Temperature Fluorescence Properties, and Their Application in Fingerprint Detection of GdPO4·H2O:12%Eu3+ Nanophosphors","authors":"Jinxiu Wu, Shengquan Wang, Baolong Wu, Meng Zhang, Zhaogang Liu, Yanhong Hu, Xiaowei Zhang, Jianfei Li, Feng Guo, Qi Lu, Qianqian Zhang","doi":"10.1134/S003602362560008X","DOIUrl":"10.1134/S003602362560008X","url":null,"abstract":"<p>To enhance the efficiency of latent fingerprint detection, the development of nanoscale, highly stable red phosphors is essential. In this study, a series of GdPO<sub>4</sub>·H<sub>2</sub>O:12%Eu<sup>3+</sup> nanophosphors were synthesized via the hydrothermal method by adjusting the pH value. The synthesized products were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), and fluorescence spectrophotometry. The results indicate that the pH value does not affect the crystal structure of the product but effectively regulates the morphology and size of the nanophosphors. The fluorescence intensity of the product gradually decreases with increasing pH. Additionally, the product exhibits excellent thermal stability. The red phosphor can clearly reveal the multilayered features of latent fingerprints and remains successfully identifiable even after 24 h of UV exposure. This study provides new insights into the development of efficient and stable rare-earth nanomaterials for fingerprint visualization.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 6","pages":"927 - 941"},"PeriodicalIF":1.5,"publicationDate":"2025-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144868829","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sudipta Pathak, Aparup Paul, Chandan Bodhak, Mohammad Raish, Abdulla Al Masum, Yeasin Sikdar, Saugata Konar
{"title":"Unveiling Iron(III) Complex: Structural Elucidation, DFT Insights, Hirshfeld Surface Analysis, and Cytotoxic Activity","authors":"Sudipta Pathak, Aparup Paul, Chandan Bodhak, Mohammad Raish, Abdulla Al Masum, Yeasin Sikdar, Saugata Konar","doi":"10.1134/S0036023625600650","DOIUrl":"10.1134/S0036023625600650","url":null,"abstract":"<p>In this present research, coordination compound [Fe(pydc)<sub>2</sub>](Hapym)(H<sub>2</sub>O)<sub>2</sub> (<b>1</b>), where pydcH<sub>2</sub> is pyridine-2,6-dicarboxylic acid, Hapym is protonated 2-aminopyrimidine, has been synthesized and characterized by single crystal X-ray diffraction. Crystallographic analysis reveals that complex <b>1</b> has distorted octahedral geometry with pydc coordinated as a tridentate ligand to a metal ion. The B3LYP/LanL2MB method is employed for DFT and TD-DFT calculations to examine the spectral properties and stability of the complex. The experimental findings align with the computational results. Hirshfeld surface analysis and two-dimensional fingerprint plots of the synthesized complex provide a comparative overview of the non-covalent interaction modes. Complex <b>1</b> shows high in vitro cytotoxic properties against A549 lung cells.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 6","pages":"868 - 876"},"PeriodicalIF":1.5,"publicationDate":"2025-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144868668","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. V. Makarova, I. A. Borodulina, N. V. Eremina, I. Yu. Prosanov, N. V. Bulina
{"title":"Effect of the Nature of Initial Reagent on the Mechanochemical Synthesis of Silver-Substituted Hydroxyapatite","authors":"S. V. Makarova, I. A. Borodulina, N. V. Eremina, I. Yu. Prosanov, N. V. Bulina","doi":"10.1134/S0036023624602721","DOIUrl":"10.1134/S0036023624602721","url":null,"abstract":"<p>Hydroxyapatite samples where calcium cations are substituted by silver cations have been obtained by mechanochemical method using silver nitrate and phosphate as the sources of substituting ions. Prepared samples have been studied by X-ray diffraction and infrared spectroscopy. On the use of AgNO<sub>3</sub>, synthesis products contain residual nitrate, while employment of Ag<sub>3</sub>PO<sub>4</sub> allows preparation of monophase silver-substituted carbonate–hydroxyapatite. The introduction of silver cations instead of calcium cations increases parameters of crystal lattice of hydroxyapatite.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 2","pages":"130 - 138"},"PeriodicalIF":1.5,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145165220","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Effect of Boron Oxide on the Ionic Conductivity of the Li1.2Al0.2Zr0.1Ti1.7(PO4)3 Ceramics with a NASICON Structure","authors":"A. B. Pyrkova, I. A. Stenina, A. B. Yaroslavtsev","doi":"10.1134/S0036023624603271","DOIUrl":"10.1134/S0036023624603271","url":null,"abstract":"<p>The effect of 1–4 wt % boron oxide, which is considered to be a good sintering additive, on the morphology and ionic conductivity of Li<sub>1.2</sub>Al<sub>0.2</sub>Zr<sub>0.1</sub>Ti<sub>1.7</sub>(PO<sub>4</sub>)<sub>3</sub> with a NASICON structure has been studied. The resulting materials have been investigated by X-ray powder diffraction, scanning electron microscopy; Raman, IR, and impedance spectroscopy; solid state <sup>27</sup>Al, <sup>7</sup>Li, <sup>31</sup>P, and <sup>11</sup>B MAS NMR. It has been shown that the introduction of B<sub>2</sub>O<sub>3</sub> at the stage of synthesis of Li<sub>1.2</sub>Al<sub>0.2</sub>Zr<sub>0.1</sub>Ti<sub>1.7</sub>(PO<sub>4</sub>)<sub>3</sub> leads to materials doped with boron ions. The sample containing 2% boron oxide exhibits the highest conductivity (2.9 × 10<sup>–4</sup> S/cm) at 25°C. At the same time, adding B<sub>2</sub>O<sub>3</sub> to Li<sub>1.2</sub>Al<sub>0.2</sub>Zr<sub>0.1</sub>Ti<sub>1.7</sub>(PO<sub>4</sub>)<sub>3</sub>, where boron oxide is localized mainly at the interfaces, leads to the release of LiTiPO<sub>5</sub> impurity and does not have a significant effect on the conductivity of the resulting samples.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 2","pages":"274 - 282"},"PeriodicalIF":1.5,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145164565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E. A. Bondar’, O. A. Shilova, I. A. Lebedev, E. A. Dmitrieva, A. I. Fedosimova, A. S. Kovalenko, A. M. Nikolaev, S. A. Ibraimova, A. K. Shongalova, U. B. Isaeva
{"title":"Composition and Morphology of Transparent Thin Films Prepared from Water–Ethanol Sols Based on Tin(IV) Compounds","authors":"E. A. Bondar’, O. A. Shilova, I. A. Lebedev, E. A. Dmitrieva, A. I. Fedosimova, A. S. Kovalenko, A. M. Nikolaev, S. A. Ibraimova, A. K. Shongalova, U. B. Isaeva","doi":"10.1134/S0036023624602769","DOIUrl":"10.1134/S0036023624602769","url":null,"abstract":"<p>The results of a comparative study of the compositions and structured of thin films deposited from film-forming sol–gel compositions based on SnCl<sub>4</sub>/EtOH/H<sub>2</sub>O and SnCl<sub>4</sub>/EtOH/H<sub>2</sub>O/NH<sub>4</sub>ОН precursors are presented. The surface morphology features and Sn, N, and Cl distributions in the film structure are analyzed, as well as the transparency of the films depending on the amount of ammonium hydroxide added to the sol–gel composition. Possible chemical processes and reaction products involved in film formation and crystallization are considered. The sizes and shapes of the resulting skeletal crystals are shown to depend on the amount of ammonium hydroxide added to the sol–gel system. Optical microscopy, electron microscopy, and X-ray powder diffraction show that nano- and microscale SnO<sub>2</sub> crystals and NH<sub>4</sub>Cl-containing crystals are formed in the films studied. The newly gained data make it possible to control the morphology and composition of the synthesized thin films via the changing precursor ratio in sol–gel synthesis.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 2","pages":"121 - 129"},"PeriodicalIF":1.5,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145164584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. D. Nafikov, M. I. Rakhmanova, N. V. Pervukhina, D. Yu. Naumov, M. M. Syrokvashin, K. A. Vinogradova
{"title":"Synthesis, Structures, and Photoluminescent Properties of Manganese(II) Complexes with 3-Chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridazine","authors":"M. D. Nafikov, M. I. Rakhmanova, N. V. Pervukhina, D. Yu. Naumov, M. M. Syrokvashin, K. A. Vinogradova","doi":"10.1134/S0036023624603805","DOIUrl":"10.1134/S0036023624603805","url":null,"abstract":"<p>Manganese(II) complexes based on 3-chloro-6-(3,5-dimethyl-1<i>H</i>-pyrazol-1-yl)pyridazine (L) with different anions (bromide, perchlorate and salicylate) have been synthesized and structurally characterized. Complex compounds [MnL<sub>2</sub>Br<sub>2</sub>] (<b>I</b>), [MnL<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>](ClO<sub>4</sub>)<sub>2</sub> (<b>II</b>), and [Mn<sub>3</sub>L<sub>2</sub>(Sal)<sub>6</sub>]·2CH<sub>3</sub>CN (<b>III</b>) have been obtained by a reaction of appropriate manganese(II) salts and L in organic media at a molar ratio of 1 : 1. According to the single-crystal X-ray diffraction, complexes <b>I</b> and <b>II</b> have a mononuclear molecular structure and an ionic structure, respectively, and complex <b>III</b> has a trinuclear molecular structure. The Mn centers in these solids exhibit a distorted octahedral coordination geometry, the coordination polyhedron in <b>I</b>, <b>II</b>, and <b>III</b> is MnN<sub>4</sub>Br<sub>2</sub>, MnN<sub>4</sub>O<sub>2</sub>, and Mn(1)N<sub>2</sub>O<sub>4</sub> or Mn(2)O<sub>6</sub>, respectively. The photoluminescent properties for complexes <b>I</b>–<b>III</b> have been studied in the solid state and in solution. The absorption spectrum of <b>III</b> as compared to the spectrum of ligand L shows new bands at 310 and 340 nm; upon excitation in this region a dual-band emission with maxima at 390 and 445 nm with nanosecond lifetimes is observed. Solid complex <b>III</b> shows weak phosphorescence (λ<sub>max</sub> = 420 nm). Upon cooling at 77 K, in the PL spectrum of <b>III</b> two additional bands (520 and 585 nm) appear, and bands at 520 and 460 nm are observed in the excitation spectrum, due to transitions in the Mn<sup>2+</sup> ion. For complexes <b>I</b> and <b>III</b>, the values of the effective magnetic moment at 300 K were determined to be 5.82 and 5.70 µ<sub>B</sub>, respectively.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 2","pages":"238 - 253"},"PeriodicalIF":1.5,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145165215","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}