V. A. Shkrumeliak, R. M. Mironenko, O. B. Belskaya, A. B. Arbuzov, O. V. Gorbunova, T. I. Gulyaeva, I. V. Muromtsev, V. A. Likholobov
{"title":"Regulation of the activity and selectivity of the Pd/C catalyst in the aqueous-phase hydrogenation of furfural by preliminary modification of the functional properties of the carbon support surface during its oxidative treatment","authors":"V. A. Shkrumeliak, R. M. Mironenko, O. B. Belskaya, A. B. Arbuzov, O. V. Gorbunova, T. I. Gulyaeva, I. V. Muromtsev, V. A. Likholobov","doi":"10.1007/s11172-026-5054-7","DOIUrl":"10.1007/s11172-026-5054-7","url":null,"abstract":"<div><p>The effect of oxidative treatment of thermal grade T900 nanoglobular carbon with a HNO<sub>3</sub> solution (20 wt.%) with a duration of 0.5 to 4 h on the structure and functional properties of the carbon surface of the supported palladium catalyst was investigated. As a result of this treatment the pore structure of the carbon material remains virtually unchanged, but its surface becomes significantly enriched with acidic oxygen-containing groups; their concentration depends on the intensity of the formation and destruction of amorphous carbon and other disordered carbon structures. Changes in the functional properties of the T900 surface caused by oxidative treatment lead to an increase in the dispersion of palladium nanoparticles in the Pd/T900 system. Varying the duration of oxidative treatment of T900 affects the catalytic properties of the Pd/T900 system in the aqueous-phase hydrogenation of furfural (423 K, 3.0 MPa). An increase in the concentration of oxygen-containing groups on the surface of T900 during oxidative treatment results in an increase in catalytic activity and selectivity in the formation of 4-oxopentanal and 5-hydroxypentan-2-one.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 7","pages":"2058 - 2070"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189966","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. D. Korobitsyna, O. V. Melchakova, A. V. Pestov, E. O. Zemlyakova, N. V. Pechishcheva
{"title":"Imidazolylmethyl derivatives of amino-containing polymers for rhenium recovery from aqueous solutions","authors":"A. D. Korobitsyna, O. V. Melchakova, A. V. Pestov, E. O. Zemlyakova, N. V. Pechishcheva","doi":"10.1007/s11172-026-5085-0","DOIUrl":"10.1007/s11172-026-5085-0","url":null,"abstract":"<div><p>The sorption of Re<sup>VII</sup> on materials based on polyallylamine (PAA), polyethyleneimine (PEI), and polyaminostyrene (PAST) was studied. The derivatives containing imidazolylmethyl groups (IMPAA, IMPEI, and IMPAST), some of which (IMPAA and IMPEI) were additionally treated with epichlorohydrin, were used as sorbents. In the presence of these sorbents, sorption equilibrium is readily (10 min) achieved, adsorption capacity reaches high values (from 391 to 800 mg g<sup>−1</sup>), and rhenium is efficiently consumed in acidic media. The introduction of the imidazolylmethyl group into the initial polymer chain increases the affinity of the materials to Re<sup>VII</sup>, enhances the adsorption capacity and, in some cases, improves the selectivity to Re<sup>VII</sup> in the presence of Mo<sup>VI</sup> ions. The competitive effect of concomitant ions on the adsorption of Re<sup>VII</sup> decreases in the order SO<sub>4</sub><sup>2−</sup> > Cl<sup>−</sup> > NO<sub>3</sub><sup>−</sup> > Mo<sup>VI</sup> > Cu<sup>II</sup>. For the sorbent modified with epichlorohydrin, the selectivity to Re<sup>VII</sup> increases even in the presence of excessive amounts of Mo<sup>VI</sup>. In this case, a high adsorption ability is retained, although a slight decrease in the sorption capacity compared to that of the non-crosslinked sorbents is observed.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 8","pages":"2382 - 2393"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189973","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
V. V. Zamalyutin, E. A. Katsman, E. V. Okuneva, V. R. Flid
{"title":"Stereochemical features and kinetic model of the heterogeneous catalytic hydrogenation of 5-ethylidene-2-norbornene","authors":"V. V. Zamalyutin, E. A. Katsman, E. V. Okuneva, V. R. Flid","doi":"10.1007/s11172-026-5086-z","DOIUrl":"10.1007/s11172-026-5086-z","url":null,"abstract":"<div><p>Specific features of the stereochemistry and kinetics of the liquid-phase hydrogenation of <i>E/Z</i>-5-ethylidene-2-norbornene (<b>1</b>) in the presence of the palladium catalyst Pd(0.25%)/<i>γ</i>-Al<sub>2</sub>O<sub>3</sub> are considered. The process proceeds under mild conditions (25–75 °C, hydrogen pressure 1 atm) sequentially and stereoselectively without destruction of the carbocyclic framework. The molar ratio of <i>E/Z</i>- and <i>endo/exo</i>-isomers of the compounds at all reaction steps is unchanged and coincides with the stereoisomer ratio in the initial diene. The kinetic data indicate a distinct separation of the steps in time: the partial hydrogenation of the norbornene bond is first observed, and then the ethylidene bond is hydrogenated. The activation energies for each step are determined. The results of the detailed kinetic studies made it possible to propose a consistent mathematical model for the hydrogenation of compound <b>1</b>.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 8","pages":"2394 - 2401"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189986","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E. D. Kazakova, V. O. Cheblokova, A. I. Nemytov, N. P. Belskaya, T. O. Fomin, M. A. Kiskin, I. A. Utepova, O. N. Chupakhin
{"title":"Synthesis and photophysical properties of 2-alkylamino-4-(2-hydroxynaphthalen-1-yl)quinazolinium tetrafluoroborates","authors":"E. D. Kazakova, V. O. Cheblokova, A. I. Nemytov, N. P. Belskaya, T. O. Fomin, M. A. Kiskin, I. A. Utepova, O. N. Chupakhin","doi":"10.1007/s11172-026-5069-0","DOIUrl":"10.1007/s11172-026-5069-0","url":null,"abstract":"<div><p>An approach to the functionalization of 2-chloroquinazoline was developed, which includes the S<sub>N</sub><sup>H</sup> arylation with 2-naphthol and the subsequent alkylamination of C—Cl bond. The corresponding quinazolinium tetrafluoroborates were obtained from the functionalized quinazolines, and their photophysical properties were evaluated. Structure of the resulting compounds was confirmed by the single crystal X-ray diffraction data.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 7","pages":"2207 - 2218"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189612","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Photocatalytic addition of acceptor alkyl halides to ethyl vinyl ether: synthesis of acetals on a multigram-scale","authors":"V. V. Levin, S. A. Imaev, A. D. Dilman","doi":"10.1007/s11172-026-5061-8","DOIUrl":"10.1007/s11172-026-5061-8","url":null,"abstract":"<div><p>Addition of alkyl halides containing acceptor fragments to ethyl vinyl ether under photocatalytic conditions and subsequent treatment of the intermediate α-halo ethers with ethanol afforded the corresponding diethyl acetals. The photocatalytic reaction occurred under blue light irradiation in the presence of 0.05 mol.% (5•10<sup>−4</sup> equiv.) of the organic photocatalyst 3DPA2FBN and involved radical addition to the double bond, followed by the halogen atom transfer. The reaction is rapid, does not require solvent, and can be used for obtaining multigram quantities of the products.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 7","pages":"2130 - 2137"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Modeling of the mechanism of endo—exo-isomerization of dicyclopentadiene hydrogenation products in the presence of AlCl3","authors":"N. A. Dontsenko, R. S. Shamsiev, V. R. Flid","doi":"10.1007/s11172-026-5056-5","DOIUrl":"10.1007/s11172-026-5056-5","url":null,"abstract":"<div><p>The quantum chemical modeling (PBEO/cc-pVTZ) of the catalytic <i>endo</i>—<i>exo</i>-iso-merization of products of dicyclopentadiene hydrogenation, tetrahydrocyclopentadiene, tetrahydrodicyclopentadiene (THDCPD) and dihydrodicyclopentadiene (DHDCPD), showed that the reactions include three steps: hydride ion transfer from <i>endo</i>-THDCPD (<i>endo</i>-DHDCPD) molecule to AlCl<sub>3</sub>, [1,2]-sigmatropic rearrangement of the carbocation, and backward hydride ion transfer from [AlHCl<sub>3</sub>]<sup>−</sup> to the carbocation. The energy profiles and mechanisms of THDCPD and DHDCPD isomerization do not differ substantially. The maximum Gibbs activation energy (Δ<i>G</i><sup>≠</sup><sub>298</sub>) is achieved in the H<sup>−</sup> transfer step. The solvation effects (CH<sub>2</sub>Cl<sub>2</sub>, CCl<sub>4</sub>) result in an appreciable decrease in the energy barrier, and the influence of CH<sub>2</sub>Cl<sub>2</sub> turns out to be more significant. The introduction of three solvent molecules into the system leads to an additional decrease in Δ<i>G</i><sup>≠</sup><sub>298</sub> of the hydride ion transfer step (38.2 kcal mol<sup>−1</sup>). It has been shown for the first time that the first reaction step can involve the H atom in both <i>exo</i>- and <i>endo</i>-position. The energy barrier of the <i>exo</i>-H<sup>−</sup> transfer step is lower (by 1.5 kcal mol<sup>−1</sup>). The results obtained indicate a principal possibility of <i>endo</i>—<i>exo</i>-isomerization in the product of incomplete dicyclopentadiene hydrogenation, which can be of practical significance. However, it should be taken into account that the isomerization of DHDCPD on AlCl<sub>3</sub> can be impeded by the formation of η<sup>2</sup>-complexes.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 7","pages":"2079 - 2086"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189704","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Oxidation of aminofurazans to azofurazans with electrically generated alkali metal hypohalites","authors":"B. V. Lyalin, D. F. Fadeev, A. B. Sheremetev","doi":"10.1007/s11172-026-5098-8","DOIUrl":"10.1007/s11172-026-5098-8","url":null,"abstract":"<div><p>Transformation of aminofurazans into azofurazans <i>via</i> anodic oxidation of amino group at the furazan ring was investigated. Azofurazans were obtained in high yields (to 99%) by electrolysis in an undivided cell in aqueous solutions of alkali metal halides with participation of electrochemically generated alkali metal hypohalites acting as redox mediators. The electrochemical method is environmentally friendly and the electrolyte can be recycled with no appreciable decrease in the efficiency of aminofurazan oxidation.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 8","pages":"2506 - 2512"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Sandmeyer isatin synthesis. Preparation and cyclization of isonitrosoacetanilides","authors":"A. N. Izmest’ev","doi":"10.1007/s11172-026-5079-y","DOIUrl":"10.1007/s11172-026-5079-y","url":null,"abstract":"<div><p>The review summarizes the data on methods for the synthesis of various substituted isatins and their benzo- and heteroannulated analogs, as well as on the cyclization conditions of isonitrosoacetanilides used in the isatin synthesis, published since Sandmeyer discovered a novel synthetic method in 1919 up to the present.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 8","pages":"2323 - 2340"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149190001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Fucosylated chondroitin sulfates of Holothuria: ten years of research (2016–2025) at the N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences","authors":"A. I. Usov, M. I. Bilan, N. E. Nifantiev","doi":"10.1007/s11172-026-5050-y","DOIUrl":"10.1007/s11172-026-5050-y","url":null,"abstract":"<div><p>Holothurians (sea cucumbers) contain unique sulfated polysaccharides, known as fucosylated chondroitin sulfates (FCSs). These biopolymers have a regular backbone composed of alternating 4-linked β-<span>d</span>-glucuronic acid (GlcA) and 3-linked <i>N</i>-acetyl-β-<span>d</span>-galactosamine (GalNAc) residues with branches, most commonly in the form of single α-<span>l</span>-fucopyranose residues attached to the O(3) atom of GlcA. Fucobiose residues and several other disaccharides may also serve as side chains, and their attachment site can be the O(6) atom of the GalNAc residue. Molecules of FCSs are abundantly sulfated, and sulfate groups can be located at any hydroxy group of the polymer. Fucosylated chondroitin sulfates isolated from various sea cucumber species possess distinct structures, whose specificity is determined by the number and location of substituents in the backbone. These structural features also dictate the biological properties of FCSs. The anticoagulant and antithrombotic activities of FCSs have been well studied; recently, their immunomodulatory, anti-inflammatory, antiviral, antitumor, and antiangiogenic properties have also been reported. Most promising from a practical standpoint is their ability to stimulate hematopoiesis.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 7","pages":"2011 - 2024"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
T. V. Bermeshev, S. N. Vereshchagin, M. P. Bundin, O. V. Belousov, A. S. Samoilo, A. N. Zaloga, D. V. Khlystov
{"title":"Study of the feasibility of obtaining the compound Bi2Si3O9 via annealing from the amorphous state and investigation of the catalytic properties of bismuth germanate and silicate Bi2O3—GeO2 and Bi2O3—SiO2 (25: 75, mol.%) in the oxidative dimerization of methane","authors":"T. V. Bermeshev, S. N. Vereshchagin, M. P. Bundin, O. V. Belousov, A. S. Samoilo, A. N. Zaloga, D. V. Khlystov","doi":"10.1007/s11172-026-5089-9","DOIUrl":"10.1007/s11172-026-5089-9","url":null,"abstract":"<div><p>Partially crystallized amorphous samples with the compositions Bi<sub>2</sub>O<sub>3</sub>—GeO<sub>2</sub> and Bi<sub>2</sub>O<sub>3</sub>—SiO<sub>2</sub> (25: 75, mol.%) were obtained in this study; their catalytic properties in the reaction of oxidative dimerization of methane (ODM) were investigated. The annealing of bismuth silicate at various temperatures and holding times did not result in the formation of a compound with the benitoite structure (Bi<sub>2</sub>Si<sub>3</sub>O<sub>9</sub>). The analysis of the phase composition and microstructure of the obtained samples revealed the presence of compounds such as Bi<sub>2</sub>SiO<sub>5</sub>, Bi<sub>4</sub>Si<sub>3</sub>O<sub>12</sub>, Bi<sub>12</sub>SiO<sub>20</sub>, and SiO<sub>2</sub> in three different modifications (cristobalite, tridymite, and quartz), depending on the annealing conditions. The annealing of bismuth germanate leads to the rapid and reliable formation of a compound with the benitoite structure (Bi<sub>2</sub>Ge<sub>3</sub>O<sub>9</sub>). Monolithic samples of bismuth germanate and silicate exhibit low activity in the ODM reaction. The bismuth germanate sample exhibits exclusively deep oxidation of CH<sub>4</sub>. In contrast, in the presence of the bismuth silicate sample the ODM reaction proceeds with a selectivity of up to 71% for the total C<sub>2</sub> hydrocarbons at 820 °C.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"75 8","pages":"2416 - 2425"},"PeriodicalIF":1.6,"publicationDate":"2026-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149189971","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}