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AbstractAbstract
[en] Short communication. 1 ref
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S-ditiofosfaty dialkoksibora
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[en] A method for preparation of boron dithiophosphinate in the title by means of interaction between 2,4-bis (4-methoxyphenyl)-22,4-dithioxo-1,3,2λ5-dithiadiphosphetane and tris (2-bromoethyl borate at 20 deg C for 14 h has been suggested. The product yield amounts to 96%, the product being characterized by the methods of Ir-, NMR- and mass spectroscopy
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S-(O-2-bromehtil-4-metoksifenilditiofosfonat) O,O'-bis(2-bromehtoksi)bora
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6 refs.
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[en] Using the kinetic method of inhibitors the mechanism is studied of ethane influence on diethylcadmium (R2Cd) autooxidation by oxygen in toluene at 213-243 K and 0.01-0.1 mol/l R2Cd concentration. The suggestion was made that the R2Cd-R2Cd bimolecular interaction involves a reversible stage of formation of ethane and carbene complex responsible for the generation of chain-leading radicals
[ru]
С использованием кинетического метода ингибиторов изучен механизм влияния этана на автоокисление диэтилкадмия (R2Cd) кислородом в толуоле при температуре 213-243 К и концентрации R2Cd 0.01-0.1моль/л. Сделано предположение, что бимолекулярное взаимодействие R2Cd с R2Cd включает обратимую стадию образования этана и карбенового комплекса, ответственного за генерирование цепьведущих радикаловOriginal Title
Ingibirovanie avtookisleniya diehtilkadmiya ehtanom
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2 refs.
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[en] Reactions of RuCl3xnH2O with hydrochloric hydroxylamine and acetoxime have been studied. It is shown (NH4)2[RuNOCl5] is reaction product in both cases. Possible mechanisms of the reactions are considered. 3 refs
Original Title
O prevrashcheniyakh solyanokislykh gidroksilamina i atsetoksima pri vzaimodejstvii s RuCl3xnH2O
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AMINES, CHLORIDES, CHLORINE COMPOUNDS, DISPERSIONS, HALIDES, HALOGEN COMPOUNDS, HOMOGENEOUS MIXTURES, HYDROGEN COMPOUNDS, HYDROXY COMPOUNDS, INORGANIC ACIDS, INORGANIC COMPOUNDS, KINETICS, MIXTURES, ORGANIC COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, REACTION KINETICS, RUTHENIUM COMPOUNDS, SOLUTIONS, TRANSITION ELEMENT COMPOUNDS
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[en] Two methods of metallation of 1,3-diphenyl-2-benzylpropane (DBP) by diphenylytterbium (Ph2Yb) were tested aimed at developing methods of synthesis of ytterbium organic derivatives containing tribenzylidenmethane dianion. In the first case prepared in advance Ph2Yb was added to DBP solution in tetrahydrofuran. In the second case Ph2Yb was prepared in situ by means of interaction between Ph2Hg and metal ytterbium. It was ascertained that in both cases DBP was transformed into tribenzylidenemethane dianion by action of Ph2Yb and the relevant organic derivative of ytterbium(II) was formed
[ru]
C целью разработки методов синтеза иттербийорганических производных, содержащих дианион трибензилиденметана, испытаны два способа проведения металлирования 1,3-дифенил-2-бензилпропена (ДБП) дифенилиттербием (Ph2Yb). В первом случае к раствору ДБП в тетрагидрофуране добавляли заранее полученный Ph2Yb, а во втором случае Ph2Yb получали in situ путем взаимодействия Ph2Hg и металлического иттербия. Установлено, что в обоих случаях наблюдалось превращение ДБП в дианион трибензилиденметана под действием Ph2Yb, и образование соответствующего органического производного иттербия(II)Original Title
Metallirovanie 1,3-difenil-2-benzilpropena difenilitterbiem
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9 refs.
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[en] A method for preparation of phenylsilane triple labelled with tritium over the Si-H bond was suggested. Reduction of phenyltrichlorosilane with lithium aluminium hydride containing tritium (LiAlT4) was put in the basis of synthesis of labelled phenylsilane. The yield of the labelled phenylsilane made up approximately 10% (in case of gaseous tritium). The calculated specific activity of the preparation amounted to 80 Ci/mmol, which corresponds to label multiplicity 2.8-2.9
[ru]
Предложена методика получения фенилсилана, трехкратно меченого тритием по связи Si-H. В основу синтеза меченого фенилсилана положено восстановление фенилтрихлорсилана литийалюмогидридом, содержащим тритий (LiAlT4). Выход меченого фенилсилана составил примерно 10% (в расчете на газообразный тритий). Расчетная удельная активность препарата составила 80 Ки/ммоль, что соответствует кратности метки 2.8-2.9Original Title
Sintez mnogokratno mechennogo tritiem fenilsilana po svyazi kremnij-vodorod
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2 refs.
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[en] Short communication
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O zavisimosti poverkhnostnogo vklada v rabotu vykhoda ehlektrona ot khimicheskoj prirody metalla
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[en] Coordination compounds of rhenium(5) with benzimidazole (L1) and its derivatives -2-(2-pyridyl)benzimidazole (L2) and 2-mercaptobenzimidazole (L3) of the general formula (HL)2 [ReOX5] and [ReOLxXy(H2O)z]Xk(H2O)n, where HL and L - protonated and deprotonated forms of the ligands; X - chloride- and bromide-ions; x, y, z, n, k - stoichiometric coefficients, have been prepared for the first time. Individually of the compounds prepared was confirmed by the results of elementary analysis and IR spectra
[ru]
Впервые синтезированы и выделены в твердом виде координационные соединения рения(5) с бензимидазолом (L1) и его производными - 2-(2-пиридил)бензимидазолом (L2) и 2-меркаптобензимидазолом (L3) общей формулы (HL)2 [ReOX5] и [ReOLxXy(H2O)z]Xk(H2O)n, где HL и L - протонированная и депротонированная форма лиганда; Х - хлорид- и бромид-ионы; x, y, z, n, k - стехиометрические коэффициенты. Индивидуальность полученных соединений подтверждена результатами элементного анализа и ИК спектрамиOriginal Title
Sintez novykh koordinatsionnykh soedinenij reniya(5) s benzimidazolom i ego proizvodnymi
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2 refs.
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[en] Potassium-alumosilicophosphate glass activized by Eu3+ has been synthesized, its spectral properties are considered to study the practicability of its application in laser engineering. In Fu3+ electron absorption spectrum in the potassium-alumosilicophosphate glass the 5D2 level splits into three sublevels, which permits assuming the hexagonal or trigonal symmetry C3v of Eu3+ nearest surrounding in the glass
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Sintez i spektral'nye svojstva kalijalyumosilikofosfatnogo stekla, aktivirovannogo oksidom evropiya(3)
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5 refs.
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[en] A new method of preparation of bis(trifluoroacetyl)iodosoarenes and bis(difluoronitroacetyl)iodosoarenes using a system comprising XeF2 and 2 equimoles of fluorine-containing acetic acid has been suggested. the reaction was conducted in the medium of methylene chloride at -15 - -10 deg C. After evaporation of the solvent the reaction products were recrystallized from hexane. The reaction yield amounted to 65%. The products were characterized by the methods of chemical analysis. IR spectroscopy and 19F NMR. 2 refs
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Okislenie ariliodidov s pomoshch'yu sistemy XeF2+RFCOOH system
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