全文获取类型
收费全文 | 133篇 |
免费 | 0篇 |
专业分类
化学 | 103篇 |
力学 | 5篇 |
物理学 | 25篇 |
出版年
2022年 | 1篇 |
2021年 | 3篇 |
2020年 | 4篇 |
2019年 | 3篇 |
2018年 | 5篇 |
2017年 | 6篇 |
2016年 | 3篇 |
2015年 | 2篇 |
2014年 | 5篇 |
2013年 | 4篇 |
2012年 | 4篇 |
2011年 | 7篇 |
2010年 | 7篇 |
2009年 | 6篇 |
2008年 | 5篇 |
2007年 | 6篇 |
2006年 | 4篇 |
2005年 | 6篇 |
2004年 | 1篇 |
2003年 | 9篇 |
2002年 | 5篇 |
2001年 | 6篇 |
2000年 | 4篇 |
1999年 | 2篇 |
1998年 | 1篇 |
1997年 | 1篇 |
1996年 | 2篇 |
1995年 | 2篇 |
1994年 | 2篇 |
1993年 | 2篇 |
1992年 | 5篇 |
1991年 | 4篇 |
1990年 | 4篇 |
1984年 | 1篇 |
1983年 | 1篇 |
排序方式: 共有133条查询结果,搜索用时 31 毫秒
1.
Yu. M. Kargin E. I. Gritsenko V. V. Yanilkin V. V. Plemenkov L. K. Dubovik N. I. Maksimyuk B. M. Garifullin Sh. K. Letypov A. V. Il'yasov 《Russian Chemical Bulletin》1992,41(9):1572-1579
The electrochemical reduction of 1,1-dihalo-2-R-2-methylcyclopropanes was studied by polarography and preparative electrolysis. A mixture of stereoisomeric monoboro- and monochlorocyclopropanes was obtained with preparative yield of 60–70% in preparative electroreduction in methanol against a background of 0.1 M LiClO4. In the case of bromine derivatives of cyclopropanes (except when R = CN) an effect was found on the part of the current density on the ratio of cis and trans isomers, which was interpreted as a change, in dependence on current density, of the contributions of the reactions of reduction of the starting compounds (SN2 mechanism) and ionic pairs (SN1 mechanism). The effect of the solvent (CHCl3, DMF, DMSO, MeOH) and background salt (LiClO4, Et4NBr) on the ratio of stereoisomers is in agreement with this interpretation.A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center, Russian Academy of Sciences, Kazan. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 9, pp. 2023–2032, September, 1992. 相似文献
2.
Strunskaya E. I. Yanilkin V. V. Bredikhina Z. A. Nastapova N. V. Morozov V. I. Maksimyuk N. I. Sharafutdinova D. R. Bredikhin A. A. 《Russian Journal of General Chemistry》2003,73(5):806-815
The electron-acceptor nitrogen and sulfur atoms in 3,4-disubstituted 1,2,5-thiadiazoles are responsible for much decreased reduction potentials and much increased oxidation potentials of these compounds compared with the corresponding carbocyclic derivatives. The thiadiazole ring is resistant to oxidation, and the reversible electron transfer gives rise to fairly stable radical cations. Reductive stability of the heterocycle depends on the nature of its substituents and on the medium: When nucleofuge substituents are present, two-electron transfer in aprotic media results in heteroring opening with iminonitrile formation, whereas in the presence of two readily leaving groups, the electron transfer induces cleavage of the complete heteroring into inorganic anions. 相似文献
3.
V. V. Yanilkin V. P. Gubskaya N. V. Nastapova L. Sh. Berezhnaya I. E. Ismaev Yu. Ya. Efremov I. A. Nuretdinov 《Russian Chemical Bulletin》2004,53(12):2793-2797
The combined electrochemical reduction of fullerene C60 in the presence of p-bromo-benzoyldibromomethane or bis(diisopropoxyphosphoryl)dibromomethane at a brass electrode in a mixed solvent o-dichlorobenzene-MeCN (3:1 v/v)/0.05 M Bu4NBF4 at room temperature affords 61-(p-bromobenzoyl)methano[60]fullerene or 61,61-bis(diisopropoxyphosphoryl)methano[60]fullerene, respectively, in 50% yields.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2681–2685, December, 2004. 相似文献
4.
V. V. Yanilkin V. I. Morozov F. F. Nigmadzyanov T. V. Gryaznova A. M. Kibardin 《Russian Chemical Bulletin》1998,47(8):1478-1480
Electrooxidation of 2-R-1,3-dibutyl-4,5-dimethyl-2,3-dihydro-1H-1,3,2-diazaphospholes with tri- and tetracoordinated phosphorus atoms were studied. Reversible one-electron oxidation gives
radical cations at potentials of −0.37 to +0.36 V. Magnetic parameters of the radical cations were measured.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1522–1524, August, 1998. 相似文献
5.
V. A. Mamedov A. A. Kalinin V. V. Yanilkin N. V. Nastapova V. I. Morozov A. A. Balandina A. T. Gubaidullin O. G. Isaikina A. V. Chernova Sh. K. Latypov I. A. Litvinov 《Russian Chemical Bulletin》2007,56(10):2060-2073
The oxidative dehydrocyclization of the 3-(indolizin-2′-yl)-2-oxoquinoxaline monopodand performed either electrochemically
or under the action of molecular iodine affords new redox-active heterocyclophane consisting of the redox-switchable biindolizine
fragment combined with the polyether-bridged π-deficient quinoxaline systems. The single-crystal X-ray diffraction study showed
that the trioxaundecane chain of heterocyclophane adopts an extended conformation, and one of the phenyl substituents of the
molecule closes the pseudocavity formed by the spacer from one of the sides. The cyclic voltammetric study of heterocyclophane
in MeCN and DMF showed the three-step oxidation of the indolizine fragments accompanied by the single-electron transfer in
each step. The first and third steps are reversible, and the second step is irreversible. The oxidation at potentials of the
first peak gives rise to stable radical cations detected by the ESR method (g = 2.0024, a
2N = 0.26 mT).
Dedicated to Professor E. A. Berdnikov on the occasion of his 70th birthday.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1991–2003, October, 2007. 相似文献
6.
V. V. Yanilkin N. I. Maksimyuk E. I. Strunskaya B. M. Garifullin Yu. M. Kargin 《Russian Chemical Bulletin》1993,42(8):1340-1343
The effect of the nature of organic electron transfer agents and of PtII, PdII, RhII, CoII, NiII, CuII, CrIII, MnII, TiIII, VIII, ZnII, and AgI metal ions on the kinetics of the homogeneous reduction ofgem-dichlorocyclopropanes has been studied. PtII, PdII, RhIII, CoII, and NiII ions accelerate this process, VIII and AgI ions exert practically no effect on the reduction rate, and the rest of the metal ions exhibit inhibitor properties.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1407–1410, August, 1993. 相似文献
7.
D. E. Vervikishko E. I. Shkol’nikov I. V. Yanilkin Yu. G. Chirkov V. I. Rostokin 《Russian Journal of Electrochemistry》2017,53(5):500-508
For supercapacitors with sulfuric acid electrolyte, a promising carbon material was suggested, namely, activated carbon from waste wood. It was shown how the synthesis conditions of activated carbon affect its porous structure and electrochemical characteristics of supercapacitors on its basis. The changes in the porous material under different synthesis conditions were controlled using the highly informative limited evaporation method, which allows us to obtain complete information about the porous structure of the micro- and mesopores of the material within a relatively short period of time. The negative effect of the excess volume of macropores in the electrode on the capacity and energy based on the dry mass of electrodes was shown experimentally and analyzed. The properties of the synthesized material were compared with those of other carbon materials. The best samples of the developed material possess a specific electric capacity of over 390 F/g. 相似文献
8.
9.
V. V. Yanilkin M. K. Kadirov Yu. M. Kargin A. V. Il'yasov S. V. Larionov 《Russian Chemical Bulletin》1991,40(12):2395-2398
Electrochemical reactions of Co(II), Cu(II), and Zn(II) complexes with 4-(2-oxopropylidene)-2,2,5,5-tetramethyl-3-imidazolidine-1-oxyl are studied by voltammetry and electrolysis-EPR. The radical centers of the ligands in these complexes undergo one-electron irreversible oxidation and reduction. In the Co(II) and Cu(II) complexes, the metals also undergo one-electron oxidation and reduction, respectively.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2750–2754, December, 1991. 相似文献
10.
V. V. Yanilkin A. R. Mustafina A. S. Stepanov N. V. Nastapova G. R. Nasybullina A. Yu. Ziganshina S. E. Solovieva A. I. Konovalov 《Russian Journal of Electrochemistry》2011,47(10):1082-1090
The results of authors on designing electroswitchable supramolecular systems based on calix[4]arenes, calix[4]resorcinols,
and transition metal ions and complexes are summarized. We consider systems in which the switching is performed owing to electrochemical
reactions both of groups grafted to the macrocycle and bound substrates. Examples of electrochemically switchable luminescence
are given. 相似文献