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1.
I. A. Nuretdinov I. P. Karaseva V. P. Gubskaya A. V. Il'yasov 《Russian Chemical Bulletin》1995,44(8):1486-1488
Cycloaddition of substituted 6,6-dimethyl-2-vinylnorpinenes with maleic anhydride occursvia the attack of a dienophile on diene from the less hindered side of the bicyclic fragment. IR, UV, CD, and1H NMR spectra of adducts have been studied.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1546–1548, August, 1995.The authors are grateful to I. E. Ismaev for recording several1H NMR spectra. 相似文献
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Kolosnitsyn D. V. Karaseva E. V. Kuz’mina E. V. Kolosnitsyn V. S. 《Russian Journal of Electrochemistry》2021,57(3):306-309
Russian Journal of Electrochemistry - In this work we considered the possibility of simulation of changes in the characteristics of lithium-sulfur batteries during cycling using an Adaptive... 相似文献
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I. A. Karaseva Yu. M. Nechepurenko A. S. Potyagalova 《Computational Mathematics and Mathematical Physics》2008,48(5):707-723
Linear control systems modeling passive integrated circuits are examined. A new algebraic method of spectral reduction equipped with efficient tools for preserving passivity is proposed and justified. For RC networks (circuits), this method is similar to and can be regarded as an extension of the well-known PACT method, which is based on congruence transforms. Up to now, such an extension seemed to be impossible, and different techniques were used for the reduction of RCL and RCLM networks. Some numerical results are presented. 相似文献
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Kuz’mina E. V. Karaseva E. V. Chudova N. V. Ivanov A. L. Kolosnitsyn V. S. 《Russian Journal of Electrochemistry》2021,57(3):255-263
Russian Journal of Electrochemistry - The possibility of using carbon materials based on petroleum coke as the cheap and available active material for negative electrodes of lithium–sulfur... 相似文献
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Anna Polishchuk Tatyna Emelina Emilya Karaseva Oana Cramariuc Vladimir Chukharev Vladimir Karasev 《Photochemistry and photobiology》2014,90(1):79-84
The effect of intermolecular proton transfer on the spectral properties of levofloxacin in the ground and excited electronic states was studied. The preferred direction of possible protolytic reactions induced by UV irradiation in this compound was studied. It was found that the proton transfer processes have a considerable effect on the capability of the compound to emit light and occur on the nanosecond timescale. The photochemical reactions of the tree forms of levofloxacin (pH: 4.0, 7.0, 10.0) were studied by laser flash photolysis and product studies. Irradiation at pH 4 yielded a pulse and transient (λmax = 395, 515, 575 nm) assigned to the protonated triplet. Irradiation at pH 7 yielded a transient species (λmax = 525, 610 nm) assigned to the neutral form. Protonation of the anionic singlet excited state was also observed (λmax = 440, 570, 680 nm). 相似文献
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A. V. Polishchuk E. T. Karaseva A. I. Cherednichenko A. V. Gerasimenko V. E. Karasev 《Russian Journal of Coordination Chemistry》2011,37(3):215-222
The complex (CfqH2AuCl4 · H2O ((CfqH2)+ is the ciprofloxacinium cation) was isolated and analyzed by spectral luminescence, X-ray photoelectron spectroscopy, and X-ray diffraction analysis. The central Au(III) atom has no direct interatomic contacts with the 1-cyclopropyl-6-fluoro-4-oxo-(1-piperazinyl)-1,4-dihydro-3-quinolinecarboxylic acid (CfqH) molecule. The structure is formed by the [AuCl4]? anions having a square structure, (CfqH2)+ cations, and water molecules combined by hydrogen bonds. The protonation of CfqH occurs at the terminal nitrogen atom of the piperazinyl group. Core-level X-ray photo-electron spectra of carbon, oxygen, nitrogen, and fluorine were measured. Cleavage of the Su-Cl bond was shown to be the primary step of the photoinduced decomposition of the compound. 相似文献