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1.
V. A. Lopyrev L. I. Larina L. Kh. Baumane E. F. Shibanova R. A. Gavar S. M. Ponomareva T. I. Vakul'skaya Ya. P. Stradyn' 《Chemistry of Heterocyclic Compounds》1984,20(9):1021-1026
The electrochemical reduction of 2-substituted 5(6)-benzimidazoles has been studied with the aid of classical polarography and cyclic voltammetry in acetonitrile. The influence of the substituents in position 2 on the magnitudes of the half-wave potentials of the first stage is exerted by induction and resonance mechanisms with approximately the same contributions, and that on the magnitudes of the half-wave potentials of the second stage predominantly by the resonance mechanism. The possibilities of taking the radical-stabilizing factor into account in the correlations are discussed. In order to study the 2-substituted 5(6)-nitrobenzimidazole series, their pK
a
values in acetonitrile have been determined by potentiometric titration.For communication 3, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1246–1251, September, 1984. 相似文献
2.
Using dyes of known redox potentials the specific mechanisms of dark and light potential generation is analyzed in pigmented lipid membranes. The role of the ionic and electronic conductance, as well as the redox potential gradient is specifically related to the observed open circuit voltage developed across the membrane. The results can be most easily explained by the redox electrode model. 相似文献
3.
T. I. Vakul'skaya L. I. Larina O. B. Nefedova V. A. Lopyrev 《Chemistry of Heterocyclic Compounds》1982,18(4):400-404
The results of an EPR investigation are presented with polarographs of electrochemical excitation of nitropyrazoles in acetonitrile. It is shown that 3- and 4-nitropyrazoles are excited in two single-electron stages with formation of dianion radicals. Upon excitation, N-alkylnitropyrazoles form stable anion radicals. 1-Nitro- and 1,4-dinitropyrazoles are excited upon splitting off of the NO2 anion. Excitation potentials of the nitropyrazoles and hyperfine interaction constants for the corresponding ion radicals are given.See [1] for Communication 2.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 523–527, April, 1982. 相似文献
4.
Amosova S. V. Gavrilova G. M. Vakul'skaya T. I. Biryukova E. I. Cherkashina V. G. 《Russian Journal of Organic Chemistry》2003,39(4):532-535
Reaction of 3,6-bis(vinylsulfonyl)-1,2,4,5-tetrafluorobenzene with dialkyl phosphites at thermal initiation (70°C) gives rise to 3,6-bis(dialkoxyphosphonoethylsulfonyl)-1,2,4,5-tetrafluorobenzenes in up to 45% yield. The formation of diethoxyphosphonyl radicals in the course of the reaction was observed with the use of ESR method applying spin trapping by 2-methyl-2-nitrosopropane. The use as initiator of the azo-bis-isobutyronitrile increased the yield of diadducts to 60%. 相似文献
5.
B. A. Trofimov G. F. Myachina S. A. Korzhova A. G. Mal'kina L. V. Sokolyanskaya T. I. Vakul'skaya Yu. V. Mikhailik T. A. Skotheim 《Russian Journal of Electrochemistry》2002,38(2):188-192
The electrochemical activity of new highly sulfurized polyconjugated polymers is studied. The polymers, polythienothiophene, poly(4,5,6,7-tetrathieno-4,5,6,7-tetrahydro-2,3-dehydrobenzothiophene), poly(6-methylthieno[2,3-b]pyridine-4-thione-5-thiol), and poly(6H-thieno[2,3-b]-azepine-6,7(8H)-dithione) are obtained in a deep sulfurization of polyethylene, polystyrene, and poly(5-vinyl-2-methylpyridine) by elemental sulfur. Employed as active cathodic material in lithium batteries, these polymers ensure their prolonged cycling with specific discharge capacity of up to 339 mA h/g. The effect of the conducting additive and electrolyte on the energy capacity and cycling of polymer cathodes in lithium batteries is discussed. 相似文献
6.
Nataliya F. Lazareva Tamara I. Vakul'skaya Alexander I. Albanov Vadim A. Pestunovich 《应用有机金属化学》2006,20(10):696-705
The introduction of the organosilicon substituent into the α‐position of an amino group results in cardinal change of the amine reactivity irrespective of the coordination state of silicon. Amines R2NCH2SiX3 [R = Me, Et, PhCH2, CH2SiX3; SiX3 = SiMe3, Si(OEt)3, Si(OCH2CH2)3N] easily react with AgNO3, to give the corresponding ammonium salts (R2NH+ CH2SiX3)·NO3?. At the same time, Ag(I) is reduced to Ag(0). The interaction of N‐methyl‐N,N‐bis(silatranylmethyl)amine with AgNO3 has been investigated by EPR spectroscopy. It was proven that the reaction involved a single electron transfer stage with the formation of cation radical of this amine. A mechanism of the reaction is proposed. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
7.
D. A. Bravo-Zhivotovskii T. I. Vakul'skaya I. S. Biltueva N. S. Vyazankin M. G. Voronkov 《Russian Chemical Bulletin》1989,38(6):1334-1334
Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, p. 1453, June, 1989. 相似文献
8.
9.
Visible light of the solar spectrum is directly converted to stored chemical energy of hydrogen from artificial sea water in a novel electrochemical photovoltaic cell. The principal element of the cell, modeled after the photosynthetic thylakoid membrane, is a semiconductor septum made of polycrystalline n-CdSe thin film deposited on nickel foil, which separates two aqueous solutions. Under short-circuit conditions, vigorous hydrogen evolution was seen at the Ni surface and continued as long as the cell was operated. The novel cell, the concept of which was derived from pigmented bilayer lipid membrane studies, is easy to construct, simple to operate, and appears to be a practical approach to the photochemical conversion and storage of solar energy. 相似文献
10.
B. A. Trofimov T. A. Skotheim L. V. Andriyankova A. G. Malkina G. F. Myachina S. A. Korzhova T. I. Vakul'skaya I. P. Kovalev Yu. V. Mikhailik 《Russian Chemical Bulletin》1999,48(3):459-462
Polydiethylsiloxane reacts with elemental sulfur at 300–320 °C (ZnCl2 slightly accelerates the process) with evolution of hydrogen sulfide and formation of black lustrous paramagnetic powders (sulfur content up to 38.50%), which possess a noticeable electric conductivity (3.20·10−7 S cm−1 when doped with I2) and redox properties. Polydimethylsiloxanes are stable under the same conditions. In rechargeable lithium batteries, the sulfurized polydiethylsiloxane behaves as an active cathode material allowing charging and discharging of the battery. The specific capacities of the cathodic and anodic processes (80–100 (mA h) g−1) change insignificantly. The hydrolytic stability, elemental analysis, IR and ESR spectra, DSC-TGA and derivatographic analyses data, the electric conductivity, and the character of the electrochemical activity of the polymers synthesized indicate that the polymers contain the polyvinylene disulfide blocks cross-linked by the polysiloxane chain. 相似文献