Doklady ChemistryPub Date : 2022-11-03DOI: 10.1134/S0012500822700033
A. I. Rudskoi, S. G. Parshin
{"title":"Electrochemical Removal of Hydroxyl and Diffusible Hydrogen in Aluminum Fluoride Slags of Welding Flux-Cored Wires","authors":"A. I. Rudskoi, S. G. Parshin","doi":"10.1134/S0012500822700033","DOIUrl":"10.1134/S0012500822700033","url":null,"abstract":"<p>This paper presents the scientific and technological principles of electrochemical removal of diffusible hydrogen by reactions of hydroxyl and hydrogen in molten aluminum fluoride slag and in the gas phase. A model was proposed for the electrochemical processes in the weld pool with the formation of aluminum fluoride polymer clusters in TiO<sub>2</sub>–CaF<sub>2</sub>–Na<sub>3</sub>AlF<sub>6</sub> slag to reduce the content of diffusible hydrogen, decrease the volume of slag inclusions, and improve the mechanical properties of bainitic steel welded joints.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"504 2","pages":"118 - 121"},"PeriodicalIF":0.8,"publicationDate":"2022-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4137964","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}
Doklady ChemistryPub Date : 2022-11-03DOI: 10.1134/S0012500822700045
A. S. Lebedev, V. N. Anfilogov, V. G. Kuz’min, V. M. Ryzhkov
{"title":"Spectral Characteristics of Quartz Glass Smelted by Vacuum Compression Technology from Various Types of Raw Materials","authors":"A. S. Lebedev, V. N. Anfilogov, V. G. Kuz’min, V. M. Ryzhkov","doi":"10.1134/S0012500822700045","DOIUrl":"10.1134/S0012500822700045","url":null,"abstract":"<p>A study was made of glass samples obtained from highly purified natural quartz, synthetic silica, and glass grit made of synthetic quartz crystals smelted according to a technology that included elements of the KS-4V technology. It was determined that the transmission spectra of the glasses smelted from various materials have differences in the UV and IR regions.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"504 2","pages":"122 - 125"},"PeriodicalIF":0.8,"publicationDate":"2022-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4140163","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}
Doklady ChemistryPub Date : 2022-11-02DOI: 10.1134/S0012500822600092
E. R. Lopat’eva, I. B. Krylov, I. V. Kuzmin, S. V. Suchkov, A. O. Terent’ev
{"title":"Oxidative C–O Coupling: Radical and Ionic Pathways of Reaction in Bu4NI/t-BuOOH System","authors":"E. R. Lopat’eva, I. B. Krylov, I. V. Kuzmin, S. V. Suchkov, A. O. Terent’ev","doi":"10.1134/S0012500822600092","DOIUrl":"10.1134/S0012500822600092","url":null,"abstract":"<p>The Bu<sub>4</sub>NI/<i>t-</i>BuOOH oxidative system is widely used in organic synthesis, but mechanistic principles underlying its reactivity are only partially explored. In this work, drawing on the example of the oxidative C–O coupling reaction between compounds with a carbonyl group and (or) a benzyl moiety with <i>N</i>-hydroxyphthalimide, it has been discovered that the coupling with the CH-acidic fragment of the carbonyl group proceeds <i>via</i> ionic mechanism, and the coupling with the benzyl fragment proceeds <i>via</i> radical mechanism. When dimethylacetamide is used as a solvent, the ionic process with the participation of the carbonyl group prevails, while in MeCN the radical process involving the benzyl moiety is realized along with the ionic process. For the oxidative C–O coupling with participation of the benzyl moiety without affecting the α-CH fragment of the carbonyl group, it is advisable to use PhI(OAc)<sub>2</sub>, Ce(NH<sub>4</sub>)<sub>2</sub>(NO<sub>2</sub>)<sub>6</sub>, or <i>t‑</i>BuOO<i>t-</i>Bu as oxidants for which only radical pathway is characteristic.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"504 1","pages":"67 - 73"},"PeriodicalIF":0.8,"publicationDate":"2022-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4099532","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}
Doklady ChemistryPub Date : 2022-11-02DOI: 10.1134/S0012500822600146
A. P. Krinochkin, Ya. K. Shtaitz, E. A. Kudryashova, E. D. Ladin, D. S. Kopchuk, G. V. Zyryanov, Yu. M. Shafran, E. V. Nosova, O. N. Chupakhin
{"title":"Interaction of 2-Amino-1,3,4-thiadiazoles with 1,2,4-Triazine-5-carbonitriles","authors":"A. P. Krinochkin, Ya. K. Shtaitz, E. A. Kudryashova, E. D. Ladin, D. S. Kopchuk, G. V. Zyryanov, Yu. M. Shafran, E. V. Nosova, O. N. Chupakhin","doi":"10.1134/S0012500822600146","DOIUrl":"10.1134/S0012500822600146","url":null,"abstract":"<p>A possibility of preparation of 1,2,4-triazines with a residue of 2-amino-1,3,4-thiadiazoles at the C5 position by the solvent-free reaction of <i>ipso</i>-amination of 3,6-di(het)aryl-1,2,4-triazine-5-carbonitriles has been studied. It has been found that the reaction also leads to the corresponding 5-amino-1,2,4-triazines as minor products.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"504 1","pages":"79 - 82"},"PeriodicalIF":0.8,"publicationDate":"2022-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4099539","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}
Doklady ChemistryPub Date : 2022-11-02DOI: 10.1134/S0012500822600122
N. V. Klimova, A. G. Ivanov, A. V. Lebedev, P. A. Storozhenko
{"title":"Processes in H2PtCl6 ⋅ 6H2O–Solvent Systems. Part I: Alcohol Solutions","authors":"N. V. Klimova, A. G. Ivanov, A. V. Lebedev, P. A. Storozhenko","doi":"10.1134/S0012500822600122","DOIUrl":"10.1134/S0012500822600122","url":null,"abstract":"<p>Transformation of H<sub>2</sub>PtCl<sub>6</sub> over time under the action of 2-octanol has been studied by NMR, IR spectroscopy, GLC, and GC/MS. It has been found for the first time that the alcohol in a H<sub>2</sub>PtCl<sub>6</sub> ⋅ 6H<sub>2</sub>O–2-octanol solution is hydrochlorinated to give 2-chlorooctane. Dehydrated platinum chlorides catalyze the elimination of methyl groups in trimethylchlorosilane and hexamethyldisiloxane, which leads to the formation of polydimethylsiloxanes. It has been assumed that the resulting π-complex of H<sub>2</sub>PtCl<sub>4</sub> with octene-1 is not stable in a hydrochloric medium and rapidly decomposes to release chloroalkyl.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"504 1","pages":"88 - 91"},"PeriodicalIF":0.8,"publicationDate":"2022-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4100582","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}
Doklady ChemistryPub Date : 2022-11-02DOI: 10.1134/S0012500822600079
S. A. Sokov, S. S. Zlotsky, A. V. Vologzhanina, A. A. Golovanov
{"title":"Original Synthesis of Enyne Dicarboxylic Acids","authors":"S. A. Sokov, S. S. Zlotsky, A. V. Vologzhanina, A. A. Golovanov","doi":"10.1134/S0012500822600079","DOIUrl":"10.1134/S0012500822600079","url":null,"abstract":"<p>The condensation of arylpropargyl aldehydes with malonic acid in AcOH has led to the formation of 2-(3-arylprop-2-yn-1-ylidene)malonic acids in 68–85% yields. A similar reaction with 4-fluorophenylpropargyl aldehyde in ethanol in the presence of 2-aminopyridine has resulted in intramolecular cyclization to give previously unknown 5-(4-fluorobenzylidene)-2-oxo-2,5-dihydrofuran-3-carboxylate. The structure of this compound has been studied in detail by X-ray diffraction.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"504 1","pages":"83 - 87"},"PeriodicalIF":0.8,"publicationDate":"2022-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4099533","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}
Doklady ChemistryPub Date : 2022-11-02DOI: 10.1134/S0012500822600109
Yu. V. Myasoedova, G. N. Sakhabutdinova, E. R. Belyaeva, G. Z. Raskil’dina, G. Yu. Ishmuratov, S. S. Zlotsky
{"title":"New Method for the Synthesis of Phenylglyoxal Derivatives","authors":"Yu. V. Myasoedova, G. N. Sakhabutdinova, E. R. Belyaeva, G. Z. Raskil’dina, G. Yu. Ishmuratov, S. S. Zlotsky","doi":"10.1134/S0012500822600109","DOIUrl":"10.1134/S0012500822600109","url":null,"abstract":"<p>The paper proposes a new one-pot ozonolytic synthesis of acylhydrazones from phenylacrolein acetals, which includes ozonolytic cleavage of the substrate in methanol and treatment of the intermediate peroxides with hydrazides of capric, nicotinic, isonicotinic, benzoic, and <i>para</i>-hydroxybenzoic acids taken in excess.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"504 1","pages":"74 - 78"},"PeriodicalIF":0.8,"publicationDate":"2022-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4099828","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}
Doklady ChemistryPub Date : 2022-06-20DOI: 10.1134/S0012500822040012
K. E. Chekurov, A. I. Barabanova, I. V. Blagodatskikh, O. V. Vyshivannaya, A. V. Muranov, A. S. Peregudov, A. R. Khokhlov
{"title":"Polymerization of 2-(Perfluorohexyl)ethyl Methacrylate in the Presence of 2-Cyano-2-propyl Dithiobenzoate in Supercritical CO2","authors":"K. E. Chekurov, A. I. Barabanova, I. V. Blagodatskikh, O. V. Vyshivannaya, A. V. Muranov, A. S. Peregudov, A. R. Khokhlov","doi":"10.1134/S0012500822040012","DOIUrl":"10.1134/S0012500822040012","url":null,"abstract":"<p>The radical polymerization of 2-(perfluorohexyl)ethyl methacrylate (FHEMA) initiated by azobis(isobutyronitrile) in the presence of a commercially available chain transfer agent, 2-cyano-2-propyl dithiobenzoate, carried out in trifluorotoluene (TFT) or in supercritical carbon dioxide (scCO<sub>2</sub>) was studied for the first time. The conditions were found under which the FHEMA polymerization in TFT or in scCO<sub>2</sub> proceeds under homogeneous conditions with reversible chain transfer <i>via</i> the addition–fragmentation mechanism.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"503 2","pages":"57 - 62"},"PeriodicalIF":0.8,"publicationDate":"2022-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4793221","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}
Doklady ChemistryPub Date : 2022-06-20DOI: 10.1134/S0012500822030028
A. G. Starikov, M. G. Chegerev, A. A. Starikova, V. I. Minkin
{"title":"Organic Polyradicals Based on Acenes. Computational Modeling","authors":"A. G. Starikov, M. G. Chegerev, A. A. Starikova, V. I. Minkin","doi":"10.1134/S0012500822030028","DOIUrl":"10.1134/S0012500822030028","url":null,"abstract":"<div><div><h3>\u0000 <b>Abstract</b>\u0000 </h3><p>New organic polyspin molecules constructed on the basis of acenes and stable radicals (1,2,3,5-di-thiadiazolyl, 1,5-dimethyl-6-oxoverdazyl, and (2,2,6,6-tetramethylpiperidin-1-yl)oxyl) have been predicted by means of quantum-chemical calculations. Among the studied tetraradical systems, the structures characterized by antiferromagnetic exchange interactions between the unpaired electrons of the radical substituents and ferromagnetic coupling of paramagnetic centers of the acenes and radical groups have been revealed.</p></div></div>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"503 1","pages":"51 - 55"},"PeriodicalIF":0.8,"publicationDate":"2022-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"4799007","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}
Doklady ChemistryPub Date : 2022-06-20DOI: 10.1134/S0012500822040024
T. N. Nekrasova, N. A. Nesterova, A. I. Fischer, I. I. Gavrilova, A. P. Katasonova, E. F. Panarin
{"title":"Luminescence of Terbium Ions in Aqueous Solutions of Sodium Styrene Sulfonate Copolymers with 4-Methacrylamidosalicylic Acid","authors":"T. N. Nekrasova, N. A. Nesterova, A. I. Fischer, I. I. Gavrilova, A. P. Katasonova, E. F. Panarin","doi":"10.1134/S0012500822040024","DOIUrl":"10.1134/S0012500822040024","url":null,"abstract":"<p>Water-soluble copolymers of sodium styrene sulfonate and 4-methacrylamidosalicylic acid of 93.7 mol % composition have been synthesized, and their interaction with terbium and gadolinium ions has been investigated to fabricate luminescent probes promising for their visualization in biomedical research. It has been shown that, in aqueous solutions in the copolymer concentration range 0.15–1.7 mg mL<sup>–1</sup> and at the ratio [Tb<sup>3+</sup>]/[COO<sup>–</sup>] = 1, water-soluble luminescent metal polymer complexes with a luminescence lifetime of 823 µs are formed. When Tb<sup>3+</sup> ions are partially replaced in the complex by Gd<sup>3+</sup> ions, bimetallic complexes with intense luminescence are formed.</p>","PeriodicalId":530,"journal":{"name":"Doklady Chemistry","volume":"503 2","pages":"63 - 66"},"PeriodicalIF":0.8,"publicationDate":"2022-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5093175","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}