16 results on '"G. A. Buzanov"'
Search Results
2. Synthesis and Thermal Reduction of Complexes [NiLn][B10H10] (L = DMF, H2O, n = 6; L = N2H4, n = 3): Formation of Solid Solutions Ni3C1 –xВx
- Author
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V. M. Retivov, Varvara V. Avdeeva, Lyudmila V. Goeva, N. T. Kuznetsov, Elena A. Malinina, and G. A. Buzanov
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Chemistry ,Materials Science (miscellaneous) ,Thermal decomposition ,chemistry.chemical_element ,Infrared spectroscopy ,Atmospheric temperature range ,010402 general chemistry ,010403 inorganic & nuclear chemistry ,01 natural sciences ,0104 chemical sciences ,Inorganic Chemistry ,Nickel ,Elemental analysis ,Physical and Theoretical Chemistry ,Inert gas ,Powder diffraction ,Nuclear chemistry ,Solid solution - Abstract
Nickel(II) complexes of the composition [NiLn][B10H10] (L = DMF, H2O, n = 6; L = N2H4, n = 3) have been synthesized and studied. The thermal reduction of the complexes has been studied in the temperature range 20–800°C in air and in an inert atmosphere. Precursor complexes and their reduction products have been identified by elemental analysis, X-ray powder diffraction, and IR spectroscopy. The physicochemical study of the thermolysis product of complex [Ni(DMF)6][B10H10] shows that scarcely studied solid solutions of the composition Ni3C1 –xВx are formed.
- Published
- 2020
3. Solid-State Synthesis of Lithium-Substituted Spinels Mg1 – xLixMnO3 – δ
- Author
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K. Yu. Zhizhin, G. A. Buzanov, N. T. Kuznetsov, and N. P. Simonenko
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Materials science ,Chemical substance ,Magnesium ,Materials Science (miscellaneous) ,Inorganic chemistry ,Lithium carbonate ,chemistry.chemical_element ,010402 general chemistry ,010403 inorganic & nuclear chemistry ,01 natural sciences ,0104 chemical sciences ,law.invention ,Inorganic Chemistry ,chemistry.chemical_compound ,chemistry ,Magazine ,law ,Lithium ,Physical and Theoretical Chemistry ,Science, technology and society ,Ball mill ,Solid solution - Abstract
Solid solutions based on MgMnO3 – δ in which magnesium is partially substituted for by lithium were produced by solid-phase synthesis by air annealing of mechanocomposites obtained by mechanical activation (in a vibration ball mill) of mixtures of high-purity grade precursors: oxides MgO, Mn2O3, and MnO2, and also Li2CO3 and LiOH · H2O. It was shown that using lithium hydroxide monohydrate increases the degree of substitution of lithium for magnesium with simultaneous decrease in the synthesis temperature in comparison with using lithium carbonate.
- Published
- 2019
4. Synthesis and Physicochemical Properties of Binary Cobalt(II) Borides. Thermal Reduction of Precursor Complexes [CoLn][B10H10] (L = H2O, n = 6; N2H4, n = 3)
- Author
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I. V. Kozerozhets, Lyudmila V. Goeva, N. N. Efimov, G. A. Buzanov, N. T. Kuznetsov, Elena A. Malinina, and Varvara V. Avdeeva
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Annealing (metallurgy) ,Materials Science (miscellaneous) ,Significant difference ,Infrared spectroscopy ,chemistry.chemical_element ,010402 general chemistry ,010403 inorganic & nuclear chemistry ,01 natural sciences ,0104 chemical sciences ,Inorganic Chemistry ,chemistry ,Magnetochemistry ,Elemental analysis ,Thermal ,Physical and Theoretical Chemistry ,Inert gas ,Cobalt ,Nuclear chemistry - Abstract
Complexes [CoLn][B10H10], where L = H2O, n = 6; L = N2H4, n = 3, have been synthesized and characterized. The possibility of their use as precursors for the synthesis of binary cobalt(II) borides has been shown. Cobalt(II) borides have been obtained by thermal reduction of precursor complexes in an inert atmosphere at 650 and 900°C. The purity and homogeneity of the precursors and their reduction products have been determined by elemental analysis, powder X-ray diffraction, and IR spectroscopy; magnetochemistry of precursors and their annealing products has been studied. The morphology of the final products has been studied. It has been found that the reduction products are structured oxide-boride and nitride-boride phases. The magnetochemical study of the phases showed a significant difference in their magnetic behavior.
- Published
- 2019
5. Hydride Intercalation of Lithium into the Spinel MgMnO3 – δ
- Author
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K. Yu. Zhizhin, G. A. Buzanov, and N. T. Kuznetsov
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Materials science ,Hydride ,Materials Science (miscellaneous) ,Spinel ,Intercalation (chemistry) ,Inorganic chemistry ,chemistry.chemical_element ,engineering.material ,010402 general chemistry ,010403 inorganic & nuclear chemistry ,01 natural sciences ,0104 chemical sciences ,Ion ,Inorganic Chemistry ,chemistry.chemical_compound ,chemistry ,Lithium hydride ,visual_art ,visual_art.visual_art_medium ,engineering ,Lithium ,Ceramic ,Physical and Theoretical Chemistry ,Solid solution - Abstract
Lithium-rich superstoichiometric solid solutions MgLixMnO3 – δ were obtained by intercalation into the spinel MgMnO3 – δ using lithium hydride LiH as an intercalating agent through the stage of the formation of mechanocomposites. The accompanying chemical transformations involving the hydride ion were studied. Conventional ceramic synthesis methods and alternative intercalating agents were analyzed. It was shown that hydride intercalation produces pure samples of single-phase spinels with high lithium content (MgLi0.75MnO3), which is three times higher than that reachable by conventional ceramic synthesis methods.
- Published
- 2019
6. Complex [Ag(PPh3)4][2-B10H9NH3 · 2DMF]: Synthesis and Structure
- Author
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I. N. Klyukin, Andrey P. Zhdanov, N. T. Kuznetsov, K. Yu. Zhizhin, G. A. Buzanov, V. V. Voinova, and M. S. Grigor’ev
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chemistry.chemical_classification ,Hydrogen bond ,General Chemical Engineering ,Salt (chemistry) ,Infrared spectroscopy ,General Chemistry ,010402 general chemistry ,010403 inorganic & nuclear chemistry ,01 natural sciences ,0104 chemical sciences ,Ion ,Crystallography ,chemistry ,Moiety - Abstract
The formation of complex salt [Ag(PPh3)4][2-B10H9NH3 ∙ 2DMF] (I) by the reaction of the salts of the [2-B10H9NH3]– anion with [Ag(PPh3)4]NO3 is studied. The anionic moiety of complex I is a stable solvate linked by hydrogen bonds of two types. Compound I is identified by IR spectroscopy and elemental, X-ray structure, and X-ray diffraction analyses (CIF file CCDC no. 1884451).
- Published
- 2019
7. A New Method for Synthesis of Binary Borides with Desired Properties
- Author
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N. N. Efimov, G. A. Buzanov, Varvara V. Avdeeva, Nikolay T. Kuznetsov, Lyudmila V. Goeva, and Elena A. Malinina
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010405 organic chemistry ,Annealing (metallurgy) ,chemistry.chemical_element ,Infrared spectroscopy ,General Chemistry ,010402 general chemistry ,01 natural sciences ,0104 chemical sciences ,Magnetization ,chemistry ,Elemental analysis ,Physical chemistry ,Diamagnetism ,Inert gas ,Cobalt ,Powder diffraction - Abstract
Complexes [Co(solv)n][B10H10], where (I: solv = H2O, n = 6; II: solv = N2H4, n = 3) have been synthesized and characterized. The possibility to use them as precursors in the synthesis of binary borides has been demonstrated. The purity and homogeneity of the precursors and the products of their thermal reduction (in an inert atmosphere at 650 and 900°С) has been established by elemental analysis, X-ray powder diffraction, and IR spectroscopy; magnetochemical studies of the precursors and their annealing products have been carried out. According to the data obtained, the reduction products are structured oxide-boride and nitride-boride phases, respectively. Magnetochemical study of the phases has revealed a significant difference in their magnetic behavior: the oxide-boride phase is characterized by a significant ferromagnetic contribution to the total magnetization of the sample, while the nitride-boride phase, by a diamagnetic contribution.
- Published
- 2019
8. Zinc(II) and cadmium(II) halide complexes with caffeine: Synthesis, X-ray crystal structure, cytotoxicity and genotoxicity studies
- Author
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N. S. Rukk, G. A. Davydova, Alena Yu. Skryabina, Svetlana K. Belus, Elena A. Mironova, Andrej N. Streletskii, Lyudmila G. Kuzmina, Ravshan S. Shamsiev, Vasilii M. Retivov, Valeriya N. Krasnoperova, Galina A. Vorob'eva, Evgeniya I. Kozhukhova, G. A. Buzanov, Artem M. Ermakov, and Pavel A. Volkov
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010405 organic chemistry ,Chemistry ,Hydrogen bond ,Tetrahedral molecular geometry ,chemistry.chemical_element ,Infrared spectroscopy ,Zinc ,Crystal structure ,010402 general chemistry ,01 natural sciences ,0104 chemical sciences ,Inorganic Chemistry ,chemistry.chemical_compound ,Crystallography ,Cadmium iodide ,Materials Chemistry ,Proton NMR ,Molecule ,Physical and Theoretical Chemistry - Abstract
Molecular complexes [Zn(caf)(H2O)I2] (I), [Zn(caf)(H2O)Cl2] (IV), and the polymeric ones {[Cd(H2O)2I2](caf).2H2O}n (II) and {[Cd(H2O)2Br2](caf).2H2O}n (III) consisting of infinite Cd-containing chains with bridging halide ions and water molecules in trans-position and connected with each other due to hydrogen bonding with participation of caffeine (caf) and water molecules, were prepared and characterized by the powder and single crystal X-ray diffraction, IR vibrational spectroscopy, 1H NMR, ESI-MS spectroscopy, thermal analysis and DFT calculations. It was found that the complexes (I) and (IV) are characterized by tetrahedral geometry, the caffeine molecule being coordinated by the central atom via its N9 atom. The preferability of complex formation was evaluated by quantum-chemical calculations. Cyto- and genotoxicity of the compounds have been investigated and discussed in comparison with that of [Zn(AP)2I2] (1) and [Cd(AP)6][Cd(AP)I3]2 (2). It was demonstrated that the prepared complexes, primarily that of cadmium iodide with caffeine (II), are the promising ones for further studies both in vitro and in vivo.
- Published
- 2019
9. Formation of Nanoscale Sodium Dodecahydro-closo-Dodecaborate Na2[B12H12] on the Surface of a Silicate Matrix
- Author
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A. A. Berlin, I. V. Kozerozhets, V. K. Skachkova, Elena A. Malinina, G. A. Buzanov, Nikolay T. Kuznetsov, Varvara V. Avdeeva, Lyudmila V. Goeva, and A. Yu. Shaulov
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chemistry.chemical_classification ,Morphology (linguistics) ,010405 organic chemistry ,Chemistry ,Sodium ,Composite number ,Dodecaborate ,Salt (chemistry) ,chemistry.chemical_element ,General Chemistry ,010402 general chemistry ,01 natural sciences ,Silicate ,0104 chemical sciences ,Amorphous solid ,Matrix (chemical analysis) ,chemistry.chemical_compound ,Physical chemistry - Abstract
The method of synthesis of nanoscaled sodium dodecahydro-closo-dodecaborate Na2[B12H12] is presented. The desired product has been prepared by heating to 200°C the composite formed by the introduction of the triethylammonium salt [Et3NH]2[B12H12] into the silicate matrix of sodium liquid glass. The morphology and phase composition of the synthesized sample have been studied by SEM and X-ray diffraction methods in comparison with regular Na2[B12H12] salt. According to the obtained data, the sample under study is an amorphous composite, on the surface of which nanoscale crystals of Na2[B12H12] are formed.
- Published
- 2019
10. Preparation and Characterization of MgH2 Mechanocomposites with Mg2NiH0.3 + Mg2NiH4 – δ Two-Phase Mixture
- Author
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N. P. Simonenko, N. T. Kuznetsov, N. N. Mal’tseva, K. Yu. Zhizhin, and G. A. Buzanov
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Content area ,Magnesium ,Materials Science (miscellaneous) ,Intercalation (chemistry) ,chemistry.chemical_element ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Inorganic Chemistry ,chemistry ,Phase (matter) ,High magnesium ,Physical and Theoretical Chemistry ,0210 nano-technology ,Solid solution ,Nuclear chemistry - Abstract
The thermal behavior of MgH2 mechanocomposites with Mg2NiH4 – δ + Mg2NiH0.3 two-phase mixture and phase equilibria in the system Mg–Ni–H involving MgH2 were studied by powder X-ray diffraction and TG–DSC. The graphic representation of phase equilibria involving MgH2 and Mg2NiH4 – δ and Mg2NiHx (0 < x < 0.3) solid solutions in the practically important field with high magnesium content area was revised. The possibility of MgH2 mechanocomposites with Mg2NiH4 – δ and Mg2NiHx for use as magnesium intercalating agents and alternative intercalating agents—organomagnesium compounds were considered.
- Published
- 2018
11. Synthesis and Structure of [М(DMF)6][B10H10] (M = Zn(II), Cd(II)) as Precursors for Solid-Phase Synthesis of Trischelate Complexes [М(L)3][B10H10]
- Author
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Elena A. Malinina, Lyudmila V. Goeva, Varvara V. Avdeeva, Svetlana E. Korolenko, G. A. Buzanov, and N. T. Kuznetsov
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Chemistry ,Materials Science (miscellaneous) ,010402 general chemistry ,010403 inorganic & nuclear chemistry ,01 natural sciences ,Medicinal chemistry ,Metal nitrate ,0104 chemical sciences ,Inorganic Chemistry ,Solid-phase synthesis ,Ultraviolet visible spectroscopy ,Molecule ,Reactivity (chemistry) ,Acid–base reaction ,Physical and Theoretical Chemistry ,Isostructural ,Powder diffraction - Abstract
The reactivity of the decahydro-closo-decaborate anion in the complexation of metals being among intermediates acids in the concept of the Pearson’s theory of hard and soft acids and bases is studied systematically in the presence of competitive ligands L. In continuing these studies, we have synthesized Zn(II) and Cd(II) complexes of the composition [М(DMF)6][B10H10] (M = Zn(II), Cd(II)) and studied them by physicochemical analyses (IR and UV spectroscopy, X-ray powder diffraction). The possibility of their use in solid-phase synthesis of the corresponding trischelate complexes [M(Bipy)3][B10H10] has been found. Complexes [М(DMF)6][B10H10] are formed by the reaction between triethylammonium closo-decaborate with metal nitrates in DMF. The compounds are isostructural with the corresponding Co(II) and Ni(II) complexes [М(DMF)6][B10H10]. Specific interactions have been found between the BH groups of the boron clusters and CH groups of the DMF molecules. According to the data of IR and UV spectroscopy, the complexes contain specific B–H···C–H interactions. The corresponding tris-chelate complexes of the metals [M(Bipy)3][B10H10] are also isostructural.
- Published
- 2018
12. Decachloro-closo-decaborate anion in copper(II) complexation reactions with N-donor ligands: 35Cl NQR and X-ray studies
- Author
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Elena A. Malinina, E. A. Kravchenko, Nikolay T. Kuznetsov, G. A. Buzanov, A. A. Gippius, Anna V. Vologzhanina, S. V. Zhurenko, and Varvara V. Avdeeva
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Diffraction ,Hydrogen ,Chemistry ,Analytical chemistry ,X-ray ,chemistry.chemical_element ,010402 general chemistry ,010403 inorganic & nuclear chemistry ,01 natural sciences ,Copper ,Redox ,0104 chemical sciences ,Ion ,Inorganic Chemistry ,Crystallography ,X-ray crystallography ,Materials Chemistry ,Physical and Theoretical Chemistry ,Spectroscopy - Abstract
Copper(II) complexation reactions with neutral N-donor ligands (Bipy, Phen, NH3) in the presence of the bulky decachloro-closo-decaborate dianion were studied. Copper(II) complexes can be prepared from copper(II) salts or copper(I) salts by redox reactions proceeding in air. The complexes [Cu(Bipy)3][B10Cl10]·2CH3CN (1·2CH3CN), [Cu(Bipy)3][B10Cl10]·2Bipy (1·2Bipy), [Cu(Bipy)2Cl]2[B10Cl10]·2DMF (2·2DMF), [Cu(Phen)2Cl]2[B10Cl10]·DMSO·1.25H2O (3·DMSO·1.25H2O) and [Cu(NH3)4(CH3CN)2][B10Cl10] (4) were prepared and characterized by X-ray diffraction as well as IR and 11B NMR spectroscopies. Complexes 1·2CH3CN, 2·2DMF, and 4 were also studied using 35Cl NQR spectroscopy. Secondary interactions were selected from all the interatomic contacts found in these crystals by X-ray diffraction. Hydrogen N–H⋯Cl–B, C–H⋯Cl–B and p⋯π (B–Cl⋯C) secondary bonds were identified in all the compounds, the spectroscopic data being generally in accordance with the results of the X-ray diffraction.
- Published
- 2017
13. Phase equilibria involving solid solutions in the Li–Mn–O system
- Author
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K. Yu. Zhizhin, G. A. Buzanov, G. D. Nipan, and N. T. Kuznetsov
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Chromatography ,Hydride ,Chemistry ,Materials Science (miscellaneous) ,Analytical chemistry ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Partial oxygen ,Inorganic Chemistry ,Homogeneous ,Phase (matter) ,Physical and Theoretical Chemistry ,0210 nano-technology ,Solid solution ,Phase diagram - Abstract
Phase equilibria involving LiMn2O4-, Li2MnO3-, LiMnO2-, Mn3O4-, and MnO-base solid solutions were studied with varied temperature and partial oxygen pressure. The $${P_{{o_2}}}$$ –T and x–y projections of the P–T–x–y phase diagram of the Li–Mn−O system were constructed, as well as the key x–y isotherms of the Li2O–MnO–MnO2 quasi-ternary system. In some experiments, the authors’ hydride lithiation method was employed to prepare lithium-rich homogeneous three-component nonstoichiometric phases.
- Published
- 2017
14. Phase states of Li(Na,K,Rb,Cs)/W/Mn/SiO2 composite catalysts for oxidative coupling of methane
- Author
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N. T. Kuznetsov, G. D. Nipan, K. Yu. Zhizhin, and G. A. Buzanov
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Materials Science (miscellaneous) ,Composite number ,Analytical chemistry ,Mineralogy ,chemistry.chemical_element ,02 engineering and technology ,Manganese ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Catalysis ,Inorganic Chemistry ,Matrix (chemical analysis) ,chemistry.chemical_compound ,Tungstate ,chemistry ,Phase (matter) ,Oxidative coupling of methane ,Crystallite ,Physical and Theoretical Chemistry ,0210 nano-technology - Abstract
This survey analyzes the results of studies into Li(Na,K,Rb,Cs)/W/Mn/SiO2 composites, which are used as catalysts for oxidative coupling of methane (OCM). The focus is on phase states. Our analysis shows that the SiO2 matrix is an active constituent of the composites and not an inert carrier of additives and the OCM heterogeneous process involves alkali-metal tungstate melts, along with polycrystalline manganese oxides. The effects of the cation ratio and synthetic routes on the phase composition of Li(Na,K,Rb,Cs)/W/Mn/SiO2 are assessed.
- Published
- 2016
15. Hydride lithiation of spinels LiMn2O4
- Author
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N. T. Kuznetsov, K. Yu. Zhizhin, G. A. Buzanov, and G. D. Nipan
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010405 organic chemistry ,Annealing (metallurgy) ,Hydride ,Inorganic chemistry ,Spinel ,chemistry.chemical_element ,General Chemistry ,engineering.material ,010402 general chemistry ,01 natural sciences ,Oxygen ,0104 chemical sciences ,chemistry.chemical_compound ,chemistry ,Lithium hydride ,engineering ,Argon atmosphere ,Stoichiometry - Abstract
Undoped lithiation of stoichiometric spinel using lithium hydride LiH up to the composition Li2.25Mn2O4 was performed. A homogeneous material with a given Li: Mn ratio was obtained by mechanochemical activation with sequential annealing of a LiMn2O4–LiH mixture in a high-purity argon atmosphere and then in air or oxygen at 373–553 K.
- Published
- 2016
16. [Co(solv)6][B10H10] (solv = DMF and DMSO) for low-temperature synthesis of borides
- Author
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I. N. Polyakova, Anna V. Vologzhanina, N. B. Generalova, Lyudmila V. Goeva, Elena A. Malinina, Varvara V. Avdeeva, K. Yu. Zhizhin, G. A. Buzanov, and Nikolay T. Kuznetsov
- Subjects
Materials Science (miscellaneous) ,Thermal decomposition ,Inorganic chemistry ,chemistry.chemical_element ,Infrared spectroscopy ,Atmospheric temperature range ,010402 general chemistry ,010403 inorganic & nuclear chemistry ,01 natural sciences ,0104 chemical sciences ,Inorganic Chemistry ,Solvent ,Ultraviolet visible spectroscopy ,chemistry ,Physical chemistry ,Physical and Theoretical Chemistry ,Thermal analysis ,Cobalt ,Powder diffraction - Abstract
The synthesis and structure of complexes [Co(solv)6][B10H10] (solv = DMF and DMSO) have been reported. Both complexes have been prepared in a high yield by the reaction between cobalt(II) salts and closo-decaborates Cat2[B10H10] in the corresponding solvent. The complexes have been characterized by elemental analysis, IR and UV spectroscopy, X-ray powder diffraction, and X-ray crystallography. The thermal properties of the compounds have been studied in the temperature range 20–600°C under argon. The conditions to form cobalt borides have been determined based on the results of thermal analysis, subsequent annealing of the complexes in various conditions, and analysis of IR spectra of the resulting thermolysis products.
- Published
- 2016
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