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排序方式: 共有68条查询结果,搜索用时 31 毫秒
1.
Water-soluble polymers of acrylamide and acrylic acid that contain fullerene (more than 90% C60) have been prepared by the low-temperature radiation-induced living polymerization. In the absorption spectra of these polymers, a monotonically decaying absorption typical of the covalently bound fullerene or its associates is observed in the range 240–700 nm. The radiation initiation of the process allows preparation of high-purity polymers useful for designing medicinal preparations. 相似文献
2.
Addition of excess R(2)NCN to an aqueous solution of K(2)[PtCl(4)] led to the precipitation of [PtCl(2)(NCNR(2))(2)] (R(2) = Me(2) 1; Et(2) 2; C(5)H(10) 3; C(4)H(8)O, 4) in a cis/trans isomeric ratio which depends on temperature. Pure isomers cis-1-3 and trans-1-3 were separated by column chromatography on SiO(2), while trans-4 was obtained by recrystallization. Complexes cis-1-3 isomerize to trans-1-3 on heating in the solid phase at 110 degrees C; trans-1 has been characterized by X-ray crystallography. Chlorination of the platinum(II) complexes cis-1-3 and trans-1-4 gives the appropriate platinum(IV) complexes [PtCl(4)(NCNR(2))(2)] (cis-5-7 and trans-5-8). The compound cis-6 was also obtained by treatment of [PtCl(4)(NCMe)(2)] with neat Et(2)NCN. The platinum(IV) complex trans-[PtCl(4)(NCNMe(2))(2)] (trans-5) in a mixture of undried Et(2)O and CH(2)Cl(2) undergoes facile hydrolysis to give trans-[PtCl(4)[(H)=C(NMe(2))OH](2)] (9; X-ray structure has been determined). The hydrolysis went to another direction with the cis-[PtCl(4)(NCNR(2))(2)] (cis-5-7) which were converted to the metallacycles [PtCl(4)[NH=C(NR(2))OC(NR(2))=NH]] (11-13) due to the unprecedented hydrolytic coupling of the two adjacent dialkylcyanamide ligands giving a novel (for both coordination and organic chemistry) diimino linkage. Compounds 11-13 and also 14 (R(2) = C(4)H(8)O) were alternatively obtained by the reaction between cis-[PtCl(4)(MeCN)(2)] and neat undried NCNR(2). The structures of complexes 11, 13, and 14 were determined by X-ray single-crystal diffraction. All the platinum compounds were additionally characterized by elemental analyses, FAB mass-spectrometry, and IR and (1)H and (13)C[(1)H] NMR spectroscopies. 相似文献
3.
Wagner G Pakhomova TB Bokach NA Fraústo Da Silva JJ Vicente J Pombeiro AJ Kukushkin VY 《Inorganic chemistry》2001,40(7):1683-1689
A novel method is reported for generation of the difficult-to-obtain (imine)Pt(II) compounds that involves reduction of the corresponding readily available Pt(IV)-based imines by carbonyl-stabilized phosphorus ylides, Ph3P=CHCO2R, in nonaqueous media. The reaction between neutral (imino)Pt(IV) compounds [PtCl4[NH=C(Me)ON=CR1R2]2] [R1R2 = Me2, (CH2)4, (CH2)5, (Me)C(Me)=NOH], [PtCl4[NH=C(Me)ONR2]2] (R = Me, Et, CH2Ph), (R1 = H; R2 = Ph or C6H4Me; R3 = Me) as well as anionic-type platinum(IV) complexes (Ph3PCH2Ph)[PtCl5[NH=C(Me)ON=CR2]] [R2 = Me2, (CH2)4, (CH2)5] and 1 equiv of Ph3P=CHCO2R (R = Me, Et) proceeds under mild conditions (ca. 4 h, room temperature) to give selectively the platinum(II) products (in good to excellent isolated yields) without further reduction of the platinum center. All thus prepared compounds (excluding previously described Delta4-1,2,4-oxadiazoline complexes) were characterized by elemental analyses, FAB mass spectrometry, IR and 1H, 13C[1H], 31P[1H] and 195Pt NMR spectroscopies, and X-ray single-crystal diffractometry, the latter for [PtCl2[NH=C(Me)ON=CMe2]2] [crystal system tetragonal, space group P4(2)/n (No. 86), a = b = 10.5050(10) A, c = 15.916(3) A] and (Ph3PCH2CO2Me)[PtCl3(NCMe)] [crystal system orthorhombic, space group Pna2(1) (No. 33), a = 19.661(7) A, b = 12.486(4) A, c = 10.149(3) A]. The reaction is also extended to a variety of other Pt(II)/Pt(IV) couples, and the ylides Ph3P=CHCO2R are introduced as mild and selective reducing agents of wide applicability for the conversion of Pt(IV) to Pt(II) species in nonaqueous media, a route that is especially useful in the case of compounds that cannot be prepared directly from Pt(II) precursors, and for the generation of systematic series of Pt(II)/Pt(IV) complexes for biological studies. 相似文献
4.
Saulius Kaciulis Alessio Mezzi Roberto Montanari Maria Richetta Ekaterina Pakhomova Alessandra Varone 《Surface and interface analysis : SIA》2020,52(12):1093-1097
The W-1%La2O3 alloy has been irradiated by a single laser pulse (λ = 1064 nm) to simulate transient thermal loads of high energy occurring in a tokamak under operative conditions. A zone with a diameter of ~2 mm, namely, much larger than the focal spot, results to be affected by the pulse, and a crater of about 300 μm is observed in its center. La2O3 particles are not present inside the crater. The change of surface morphology is accompanied by elemental redistribution. Multipoint XPS analysis evidenced that the concentration of La is very low in the crater and increases moving toward the border of the affected zone while that of W shows an opposite trend. The composition changes involve only the outmost 5 nm of the sample: through depth profiling, no differences of chemical composition were detected deeper in the alloy between the center and external border of the affected area. 相似文献
5.
Bykov M. V. Abramov Z. D. Pakhomova M. V. Borodina T. N. Smirnov V. I. Suslov D. S. 《Journal of Structural Chemistry》2022,63(1):125-139
Journal of Structural Chemistry - The structure of complex [Pd(acac){P(NEt2)3}2]BF4 (I) is determined by XRD. In the crystal structure of I, the coordination sphere of palladium is characterized by... 相似文献
6.
Dr. Anna Pakhomova Birgit Fuchs Prof. Dr. Leonid S. Dubrovinsky Prof. Dr. Natalia Dubrovinskaia Prof. Dr. Hubert Huppertz 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(19):6007-6014
Based on the results from previous high-pressure experiments on the gadolinite-type mineral datolite, CaBSiO4(OH), the behavior of the isostructural borates β-HfB2O5 and β-ZrB2O5 have been studied by synchrotron-based in situ high-pressure single-crystal X-ray diffraction experiments. On compression to 120 GPa, both borate layer-structures are preserved. Additionally, at ≈114 GPa, the formation of a second phase can be observed in both compounds. The new high-pressure modification γ-ZrB2O5 features a rearrangement of the corner-sharing BO4 tetrahedra, while still maintaining the four- and eight-membered rings. The new phase γ-HfB2O5 contains ten-membered rings including the rare structural motif of edge-sharing BO4 tetrahedra with exceptionally short B−O and B⋅⋅⋅B distances. For both structures, unusually high coordination numbers are found for the transition metal cations, with ninefold coordinated Hf4+, and tenfold coordinated Zr4+, respectively. These findings remarkably show the potential of cold compression as a low-energy pathway to discover metastable structures that exhibit new coordinations and structural motifs. 相似文献
7.
Sebastian Vogel Maxim Bykov Elena Bykova Sebastian Wendl Simon D. Kloß Anna Pakhomova Natalia Dubrovinskaia Leonid Dubrovinsky Wolfgang Schnick 《Angewandte Chemie (International ed. in English)》2020,59(7):2730-2734
Owing to its outstanding elastic properties, the nitride spinel γ‐Si3N4 is of considered interest for materials scientists and chemists. DFT calculations suggest that Si3N4‐analog beryllium phosphorus nitride BeP2N4 adopts the spinel structure at elevated pressures as well and shows outstanding elastic properties. Herein, we investigate phenakite‐type BeP2N4 by single‐crystal synchrotron X‐ray diffraction and report the phase transition into the spinel‐type phase at 47 GPa and 1800 K in a laser‐heated diamond anvil cell. The structure of spinel‐type BeP2N4 was refined from pressure‐dependent in situ synchrotron powder X‐ray diffraction measurements down to ambient pressure, which proves spinel‐type BeP2N4 a quenchable and metastable phase at ambient conditions. Its isothermal bulk modulus was determined to 325(8) GPa from equation of state, which indicates that spinel‐type BeP2N4 is an ultraincompressible material. 相似文献
8.
Different gas carburization methods intended for processing quality assurance are compared by analyzing the indices of the applied processing atmosphere, i.e., the carbon potential level and the possibility of its regulation, as well as the weight transfer ratio. The efficiency of vacuum carburization is shown, wherein a sound processing atmosphere accompanies the advantages of automated processing equipment that combines carburization and dry high-pressure nitrogen hardening. The advisability of setting up a specialized vacuum unit manufacturing plant for thermal production upgrade is substantiated. 相似文献
9.
Spin effects in the weak two-body hadronic decays of the B c and B c * mesons into J/ψ and ρ(π) mesons are considered within the model of hard one-gluon exchange between quarks at high momentum transfers. It is shown that the polarization of the J/ψ meson in the decays of the B c * meson differs substantially from that in the decays of the B c * meson. The decay widths of the B c * meson differ significantly from the widths of the B c * meson. 相似文献
10.
V. N. Demidov S. A. Simanova A. I. Savinova A. V. Zinchenko T. B. Pakhomova E. A. Aleksandrova 《Journal of Structural Chemistry》2010,51(2):296-302
A neutral complex of palladium(II) with 2,9-dimethyl-1,10-phenanthroline [Pd(2,9-Me2-phen)Cl2] (goldish orange colored) is examined by single crystal X-ray diffraction. The crystals of [Pd(2,9-Me2-phen)Cl2] are monoclinic and belong to the space group P21/n (a = 11.8670(7) Å, b = 7.8195(5) Å, c = 14.2418(9) Å, β = 92.5450(10)°, Z = 4, V = 1320.25 Å3, R = 0.0289). The complex [Pd(2,9-Me2-phen)Cl2] exhibits a strong distortion of the usual square-planar geometry with a deviation of the central Pd2+ ion and two chloride acido-ligands from the plane of coordinated 2,9-dimethyl-1,10-phenanthroline. The lengths of two Pd-N bonds are slightly different and are 2.058 Å and 2.067 Å, the lengths of the Pd-Cl bonds are equal and are 2.285 Å. 2,9-Me2-phen itself also suffers some distortion of the planar geometry resulting in the boat conformation of the molecule. The crystal structure of the [Pd(2,9-Me2-phen)Cl2] complex is characterized by the presence of π-π stacked dimers arranged in infinite tilted stacks. 相似文献