A. S. Mokrushin, S. A. Dmitrieva, Y. M. Gorban, A. R. Stroikova, N. P. Simonenko, A. A. Averin, E. P. Simonenko
{"title":"AACVD Synthesis of Bilayer Thin-Film ZnO/Cr2O3 Nanocomposites for Chemoresistive Gas Sensors","authors":"A. S. Mokrushin, S. A. Dmitrieva, Y. M. Gorban, A. R. Stroikova, N. P. Simonenko, A. A. Averin, E. P. Simonenko","doi":"10.1134/S0036023624603763","DOIUrl":"10.1134/S0036023624603763","url":null,"abstract":"<p>Using aerosol-assisted vapor deposition (AACVD), bilayer ZnO/Cr<sub>2</sub>O<sub>3</sub> thin-film nanocomposites were prepared and validated using various physicochemical analyses. The thermal behavior of precursors—zinc and chromium acetylacetonates—was studied using TGA/DSC. The chemical composition of the obtained coatings was confirmed by EDX method, and the physical composition was confirmed by X-ray diffraction and Raman spectroscopy. The microstructural features were studied by SEM method. It was found that by varying the precursor concentration it is possible to change the morphology of the obtained coatings from an island structure to a continuous film. It is shown that ZnO/Cr<sub>2</sub>O<sub>3</sub> bilayer films demonstrate a noticeable chemoresistive response in acetone detection.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 4","pages":"624 - 632"},"PeriodicalIF":1.5,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145171799","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. V. Novikova, I. A. Lutsenko, O. B. Bekker, Yu. V. Nelyubina, A. V. Ivanov
{"title":"Binding of Gold(III) from Solutions Using Bismuth Hexamethylenedithiocarbamate: Double Complexes of Composition [Au(S2CNHm)2][Bi(S2CNHm)2Cl2] and [Au(S2CNHm)2]2[Bi2(S2CNHm)2Cl6] (Preparation, Crystal Structure, Thermal Behavior, and Anti-Mycobacterial Activity)","authors":"E. V. Novikova, I. A. Lutsenko, O. B. Bekker, Yu. V. Nelyubina, A. V. Ivanov","doi":"10.1134/S0036023625600595","DOIUrl":"10.1134/S0036023625600595","url":null,"abstract":"<p>It has been found that the reaction of bismuth hexamethylenedithiocarbamate (HmDtc) with an H[AuCl<sub>4</sub>]/2 M HCl solution leads to formation of double complexes of composition [Au(S<sub>2</sub>CNHm)<sub>2</sub>][Bi(S<sub>2</sub>CNHm)<sub>2</sub>Cl<sub>2</sub>] (<b>I</b>) and [Au(S<sub>2</sub>CNHm)<sub>2</sub>]<sub>2</sub>[Bi<sub>2</sub>(S<sub>2</sub>CNHm)<sub>2</sub>Cl<sub>6</sub>] (<b>II</b>) as individual forms of gold(III) binding in the solid phase. The structures of the prepared compounds contain centrosymmetric/noncentrosymmetric (in <b>I</b>/<b>II</b>) Au(III) complex cations and heteroleptic bismuth anions: mononuclear and binuclear with ratio Bi : Dtc : Cl = 1 : 2 : 2/2 : 2 : 6 (<b>I</b>/<b>II</b>). Secondary S<span>( cdots )</span>S and S<span>( cdots )</span>Cl interactions between these ionic structural units result in formation of 3D supramolecular architectures. In the IR spectra of the compounds, the absorption bands of N–C(S)S bonds have been assigned to HmDtc ligands in the inner sphere of Au(III) complex cations and Bi(III) anions. Thermal behavior of compounds <b>I</b> and <b>II</b> has been studied by simultaneous thermal analysis. Residual substance obtained after thermolysis of samples consists of metallic particles of bismuth solid solution in gold coated with Bi<sub>2</sub>O<sub>3</sub> layer. Complex <b>I</b> exhibits a high level of antimycobacterial activity <i>in vitro</i> toward non-pathogenic strain of <i>Mycolicibacterium smegmatis</i>.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 4","pages":"472 - 488"},"PeriodicalIF":1.5,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145171810","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. V. Ishchenko, N. S. Akhmadullina, I. I. Leonidov, V. P. Sirotinkin, I. A. Weinstein, Yu. F. Kargin
{"title":"Phase Formation and Optical Properties of Vanadium-Doped Aluminum Oxynitride","authors":"A. V. Ishchenko, N. S. Akhmadullina, I. I. Leonidov, V. P. Sirotinkin, I. A. Weinstein, Yu. F. Kargin","doi":"10.1134/S0036023625600443","DOIUrl":"10.1134/S0036023625600443","url":null,"abstract":"<p>The phase formation, morphology, and optical properties of aluminum oxynitride (Al<sub>5</sub>O<sub>6</sub>N) doped with 0.01–5.0 at % of vanadium ions (relative to aluminum) have been studied. All samples fabricated by calcining mixtures of Al<sub>2</sub>O<sub>3</sub>, AlN, and V<sub>2</sub>O<sub>5</sub> at 1750°C in a nitrogen flow are practically single-phase γ-AlON with minor impurities of aluminum nitride, as well as VC, VN, VO, or their solid solutions at a vanadium content of ≥0.1 at %. In AlON:V, the band gap <i>E</i><sub>g</sub> = 5.82–5.94 eV varies depending on the vanadium concentration. The luminescence of AlON:V is due to intrinsic defects and impurity luminescence centers. The presence of vanadium in AlON leads to an increase in the optical absorption and a decrease in the intensity of intrinsic luminescence because of the formation of vanadium-containing impurity phases.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 4","pages":"463 - 471"},"PeriodicalIF":1.5,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145171811","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}
I. V. Egorova, I. N. Nesina, V. V. Zhidkov, N. A. Rodionova, N. V. Kuratieva, N. V. Pervukhina
{"title":"Synthesis and Structures of Stibonium Complexes {[2,6-(MeO)2C6H3]3SbCH2C(O)OEt}I3 and {[(2,6-(MeO)2C6H3)3SbEt][Hg3I7]}n","authors":"I. V. Egorova, I. N. Nesina, V. V. Zhidkov, N. A. Rodionova, N. V. Kuratieva, N. V. Pervukhina","doi":"10.1134/S003602362560011X","DOIUrl":"10.1134/S003602362560011X","url":null,"abstract":"<p>New stybonium complexes containing polyanions have been obtained. Alkylation of tris(2,6-dimethoxyphenyl)stibine with ethyl iodoacetic acid synthesized [Ar<sub>3</sub>SbCH<sub>2</sub>C(O)OEt]I<sub>3</sub>, Ar = 2,6-(MeO)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>, which is also the product of the reaction of [Ar<sub>3</sub>SbCH<sub>2</sub>C(O)OEt]I and I<sub>2</sub>. The reaction of [Ar<sub>3</sub>SbEt]I with mercury diiodide leads to {[Ar<sub>3</sub>SbEt][Hg<sub>3</sub>I<sub>7</sub>]}<sub><i>n</i></sub>, where Ar = 2,6-(MeO)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>. Compounds [Ar<sub>3</sub>SbCH<sub>2</sub>C(O)OEt]I<sub>3</sub> and {[Ar<sub>3</sub>SbEt][Hg<sub>3</sub>I<sub>7</sub>]}<sub><i>n</i></sub> were characterized by X-ray diffraction. Antimony and mercury atoms were found to have a distorted tetrahedral coordination. Bond angles are in the ranges: ∠CSbC 104.2(2)°‒113.9(1)° and ∠CSbC 102.4(4)°‒116.0(5)°, ∠IHgI 97.06(2)°–121.28(2)°.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 and Development Prospects","pages":"390 - 397"},"PeriodicalIF":1.5,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145144988","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}
N. P. Shapkin, I. G. Khal’chenko, E. A. Tokar, A. I. Matskevich, V. S. Pechnikov, K. A. Pervakov, V. B. Zubchenko
{"title":"Magnetic Materials Based on Iron−Silicon-Containing Frameworks","authors":"N. P. Shapkin, I. G. Khal’chenko, E. A. Tokar, A. I. Matskevich, V. S. Pechnikov, K. A. Pervakov, V. B. Zubchenko","doi":"10.1134/S0036023625600297","DOIUrl":"10.1134/S0036023625600297","url":null,"abstract":"<p>Polyferrophenylsiloxanes based on iron(III) chelate and polyphenylsiloxane with different siloxane-to-sodium hydroxide ratios have been synthesized under mechanochemical activation conditions. It has been shown that the polymer yield after precipitation with petroleum ether is 37–52%. The polyferrophenylsiloxane composition closest to the specified one has been obtained at the ratio Si : Na = 1. The resulting composites have been studied using IR spectroscopy, X-ray diffraction, gel chromatography, and thermogravimetry. An XRD study has shown the introduction of iron atoms into the siloxane structure. The presence of sodium ions during the reaction in subsequent syntheses has made it possible to bind the released acetylacetone and fabricate polyferrophenylsiloxane with a specified Si : Fe ratio. However, with a further increase in the hydroxide content, the Si : Fe ratio is violated. A study of the magnetic properties of polyferrophenylsiloxanes has shown that they are superparamagnets. After heating them to 600°C, magnetization increases sharply (magnetic saturation) and hysteresis is observed.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 and Development Prospects","pages":"374 - 381"},"PeriodicalIF":1.5,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145144993","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}
O. D. Arefieva, S. V. Dovgan, A. V. Kovekhova, A. E. Panasenko, M. A. Tsvetnov, A. G. Kozlov, K. A. Pervakov
{"title":"Preparation of Micro- and Mesoporous Aluminosilicates in the Presence of Polyethylene Glycol","authors":"O. D. Arefieva, S. V. Dovgan, A. V. Kovekhova, A. E. Panasenko, M. A. Tsvetnov, A. G. Kozlov, K. A. Pervakov","doi":"10.1134/S003602362560025X","DOIUrl":"10.1134/S003602362560025X","url":null,"abstract":"<p>Natural and synthetic aluminosilicates currently have a wide application range. Silicon-containing wastes of rice production are of great interest as a source of raw materials for aluminosilicate production. The purpose of this work was the template synthesis of micro- and mesoporous materials from rice husk using PEG-6000. The prepared samples were characterized by differential thermal analysis (DTA) and IR spectroscopy, which showed the incorporation of PEG into the potassium aluminosilicate structure during the sol–gel process. The specific surface areas <i>S</i><sub>sp</sub> of the prepared samples and their pore-size distributions were determined by low-temperature nitrogen adsorption, which showed that the pore radius increased from 100 to 200 Å when the PEG concentration in sol–gel synthesis changed from 5 to 20 mmol/L. Scanning electron microscopy (SEM) showed that the template changed the surface morphology of the samples and promoted their structuring.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 and Development Prospects","pages":"328 - 336"},"PeriodicalIF":1.5,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145144947","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. N. Danilova, P. N. Tarasova, S. B. Yarusova, Iu. V. Kapitonova, A. M. Spiridonov, P. S. Gordienko, A. A. Okhlopkova, E. K. Papynov, O. O. Shichalin, A. O. Lembikov
{"title":"Synthetic Aluminosilicates as Polytetrafluoroethylene Modifiers","authors":"S. N. Danilova, P. N. Tarasova, S. B. Yarusova, Iu. V. Kapitonova, A. M. Spiridonov, P. S. Gordienko, A. A. Okhlopkova, E. K. Papynov, O. O. Shichalin, A. O. Lembikov","doi":"10.1134/S0036023625600145","DOIUrl":"10.1134/S0036023625600145","url":null,"abstract":"<p>At present time, there is fast growth in the use of polymer composite materials in all areas of industry due to their unique properties: high strength, low density, and corrosion resistance. Because of development of new technologies, there is necessity to design a new class of environmentally benign materials that provide efficient and economic employment of raw materials. In this work, synthetic nanostructured aluminosilicates with prescribed Si/Al ratio equal to 1, 3, and 5 have been considered as polytetrafluoroethylene modifiers. Phase elemental composition and thermal behavior of the prepared compounds has been studied. The use of aluminosilicates has been found to favor to increase in tensile strength by 40% and relative elongation at rupture by 70% relative to the initial polymer matrix. The introduction of aluminosilicate is accompanied by increase in wear resistance by 521 times. Thus, we have prepared a new class of modifiers for polymer composite materials.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 and Development Prospects","pages":"432 - 439"},"PeriodicalIF":1.5,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145144972","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":"Features of Reactions of α-Substituted Acetylacetonate Complexes","authors":"I. V. Svistunova, G. O. Tretyakova","doi":"10.1134/S0036023625600194","DOIUrl":"10.1134/S0036023625600194","url":null,"abstract":"<p>Chromato-mass spectrometry has been used to study the reactions of coordinated ligands in chromium and boron difluoride acetylacetonate complexes. It has been established that bromine- and thiophenyl-substituted acetylacetonates of boron difluoride, unlike chromium complexes, do not react with thiophenol. The reaction of thio-substituted chelates with SO<sub>2</sub>Cl<sub>2</sub> also proceeds differently. In chromium complexes, the reaction involves the substitution of the thioalkyl or thioaryl group with a chlorine atom. Thioethyl-substituted boron difluoride acetylacetonate reacts with SO<sub>2</sub>Cl<sub>2</sub> similarly to aromatic analogs, leading to chlorination of the ethyl group. However, thioaryl-substituted boron difluoride acetylacetonate does not react with SO<sub>2</sub>Cl<sub>2</sub>. Additionally, it was found that bromine- and thio-substituted chromium acetylacetonates react with sulfenyl chlorides, replacing the α-substituent with a chlorine atom. It is suggested that the difference in the reactivity of chromium and boron difluoride acetylacetonates is due to the different charge distribution in the chelate cycle. The strong electron-accepting nature of the BF<sub>2</sub> group leads to a positive charge on the substituent attached to the chelate ring in boron complexes.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 and Development Prospects","pages":"398 - 404"},"PeriodicalIF":1.5,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145144995","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}
O. V. Boytsova, A. Yu. Tatarenko, V. Yu. Chendev, A. M. Makarevich, I. V. Roslyakov, O. N. Makarevich
{"title":"Hydrothermal Synthesis of Vanadium Dioxide Films from Alcoholic Solutions","authors":"O. V. Boytsova, A. Yu. Tatarenko, V. Yu. Chendev, A. M. Makarevich, I. V. Roslyakov, O. N. Makarevich","doi":"10.1134/S0036023625600285","DOIUrl":"10.1134/S0036023625600285","url":null,"abstract":"<p>A new procedure for deposition of VO<sub>2</sub> films on single-crystal sapphire supports from alcoholic solutions under hydrothermal conditions has been proposed. The obtained materials show sharp dielectric–metal transition with change in electrical resistance value up to four orders of magnitude in proximity to critical temperature (68°C). Conditions for the synthesis of films comparable in electrophysical characteristics with analogs prepared in aqueous media have been found. The suggested procedure opens new possibilities for the hydrothermal synthesis of film oxide materials.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 and Development Prospects","pages":"324 - 327"},"PeriodicalIF":1.5,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145144945","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}
V. A. Boyarnikova, I. G. Khalchenko, N. P. Shapkin, V. Yu. Mayorov, A. N. Fedorets, K. A. Pervakov, N. P. Ivanov
{"title":"Vermiculite-based Sorbents Modified with Compounds of Various Natures","authors":"V. A. Boyarnikova, I. G. Khalchenko, N. P. Shapkin, V. Yu. Mayorov, A. N. Fedorets, K. A. Pervakov, N. P. Ivanov","doi":"10.1134/S0036023625600315","DOIUrl":"10.1134/S0036023625600315","url":null,"abstract":"<p>The aim of this work was to investigate the effect of organic and inorganic modifying agents on the internal structure and surface properties of vermiculite from the Kovdor deposit in an alkaline medium. Vermiculite from the Kovdor deposit was treated with various compounds in an alkaline medium (sodium hydroxide, sodium stearate) with successive addition of copper chloride and potassium hexacyanoferrate(II) solutions. According to powder X-ray diffraction data, the introduction of stearate ion leads to an increase in the interplanar spacing compared to pristine vermiculite. The increase in the coherent scattering region attests to an increase in the degree of crystallinity and considerable interaction of the modifying agent with the surface. The subsequent addition of potassium hexacyanoferrate(II) leads to further increase in the interplanar spacing because of the bulky hexacyanoferrate ion; however sharp decrease in the coherent scattering region indicates exfoliation of the layered silicate, which leads to a decrease in the surface area due to increasing content of amorphous structure.</p>","PeriodicalId":762,"journal":{"name":"Russian Journal of Inorganic Chemistry","volume":"70 and Development Prospects","pages":"448 - 454"},"PeriodicalIF":1.5,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145144979","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}