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1.
K. B. Aleinikova E. N. Zinchenko A. V. Arakcheeva V. V. Grinevich 《Crystallography Reports》2002,47(4):555-558
An amorphous sediment was prepared by the decomposition of potassium oxofluoroniobate K2 ? x Nb4O3(O, F)3F in water. For this sediment, the atomic radial distribution function was analyzed with the use of a fragment model, which allows one to interpret expanded coordination spheres as being formed by first several strongest diffusion maxima. These spheres carry the most reliable information on the structure. It is shown that the amorphous sediment consists of the randomly packed Nb(O,F)6-octahedra with interatomic distances close to those observed in the ordered region in the N-Nb2O5 structure. During decomposition in water, the initial K2 ? x Nb4O3(O, F)3F phase loses KF-layers, whereas Nb6 clusters with metal bonds are destroyed. 相似文献
2.
V. P. Antonovich I. V. Stoyanova N. A. Chivireva E. V. Timukhin V. F. Zinchenko N. P. Efryushina 《Journal of Analytical Chemistry》2007,62(3):238-244
Diffuse reflectance spectroscopy in the UV, visible, and near-IR regions is found to allow the detection and identification of lanthanide oxides, fluorides, sulfides, and sulfofluorides without decomposing and dissolving samples. A nondestructive method for the detection and quantitative determination of more than 1 wt % of Eu(II) in the corresponding fluorides is proposed. 相似文献
3.
4.
5-Methoxy-3-carbethoxyindoles are nitrated primarily in the 4 position. Replacement of the methoxy group by an acetoxy group leads to a change in orientation — only the 6 isomer is obtained. In the case of the similarly constructed 5-hydroxyindoles, monosubstitution cannot be accomplished under various conditions, and only the 4,6-dinitro derivative is formed. The synthesis of the corresponding amines by reduction of the nitro compounds is described.See [1] for communication XXXVIII.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1646–1653, December, 1973. 相似文献
5.
E. V. Zhernosek S. V. Kvach L. A. Eroshevskaya E. N. Kalinichenko A. I. Zinchenko 《Chemistry of Natural Compounds》2006,42(2):208-211
Previously undescribed conjugates of 2′,3′-dideoxyuridine-5′-monophosphate-(L)-methoxytryptophylphosphoramidate (5) and 2′,3′-dideoxycytidine-5′-monophosphate-(L)-methoxytryptophylphosphoramidate (7) were isolated by a chemical enzymatic method in order to study their pharmacological properties and to prepare new medicinal
preparations based on them.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 173–175, March–April, 2006. 相似文献
6.
O. V. Bryanskii V. V. Tolstikhina S. V. Zinchenko A. A. Semenov 《Chemistry of Natural Compounds》1993,28(6):556-560
A sesquiterpene glucoside has been isolated from a tissue culture ofScorzonera hispanica, and its structure has been established by mass spectrometry and two-dimensional NMR as 6,9-dihydroxy-4,10,14,15-tetradehydroguaian-6,12-olide 9-O--D-glucopyranoside.Irkursk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 640–645, November–December, 1992. 相似文献
7.
V. A. Tkach V. A. Gruznykh N. A. Murasheva S. V. Zinchenko F. K. Shmidt 《Reaction Kinetics and Catalysis Letters》1991,43(2):431-437
1H NMR, EPR and IR spectroscopic studies of the products of the interaction between components of the Ni[PPh3]4+EtOH+BF3.OEt2 and Ni(PPh3)4+BF3OEt2 systems suggest the formation of two types of complexes [HNi(PP3)3L]+[BF3OEt]– and [Ni(PPh3)3L]+BF
4
–
, which are catalytically active in propene dimerization.
1H, , - Ni(PPh3)4+ EtOH+BF3OEt2 Ni(PPh3)4+BF3·OEt2 [HNi (PPh3)3L]+ [BF3OEt]– [Ni (PPh3)L2]+BF 4 – .相似文献
8.
9.
Integral equations for the shape functions in the adiabatic, quasi-static, and improved quasi-static approximations are presented. The approach to solving these equations by the Monte Carlo method is described. 相似文献
10.
Maxim V. Musalov Vladimir A. Potapov Vladimir A. Yakimov Maria V. Musalova Arkady A. Maylyan Sergey V. Zinchenko Svetlana V. Amosova 《Molecules (Basel, Switzerland)》2021,26(12)
The regioselective synthesis of novel functionalized condensed organochalcogen compounds by chalcogenocyclofunctionalization reactions based on chalcogen halides and the natural products thymol and carvacrol has been developed. The reactions of selenium dibromide with allyl thymol and allyl carvacrol proceeded in methylene chloride at room temperature in the presence of NaHCO3 affording bis[(7-isopropyl-4-methyl-2,3-dihydro-1-benzofuran-2-yl)methyl] and bis[(4-isopropyl-7-methyl-2,3-dihydro-1-benzofuran-2-yl)methyl] selenides in 90–92% yield. Similar sulfides were obtained in 70–72% yields by the reaction of sulfur dichloride in chloroform under reflux. Trihalotellanes containing the same organic moieties were synthesized from allyl thymol, allyl carvacrol and tellurium tetrachloride or tetrabromide in quantitative yields. Corresponding functionalized ditellurides were prepared in 91–92% yields by the reduction of the trichlorotellanes with sodium metabisulfite in two-phase solvent system. The comparison of reactivity of sulfur, selenium and tellurium halides in chalcogenocyclofunctionalization and distinguishing features of each reaction were discussed. 相似文献