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排序方式: 共有237条查询结果,搜索用时 31 毫秒
1.
E. V. Sennikova A. S. Antsyshkina G. G. Sadikov A. V. Bicherov O. Yu. Korshunov G. S. Borodkin M. S. Korobov V. S. Sergienko N. N. Kharabaev A. D. Garnovskii 《Russian Journal of Coordination Chemistry》2008,34(5):315-321
The chelate and molecular complexes of 2-(2-benzazolyl, perimidyl)-indandiones-1,3 were synthesized for the first time. The structures of the ligands (tautomeric forms) and complex compounds were determined from the X-ray diffraction, 1H, 13C NMR, and IR data and the quantum-chemical calculations (RHF SCF in 6-31 G** basis). 相似文献
2.
Borodkin G. I. Popov S. A. Pokrovskii L. M. Shubin V. G. 《Russian Journal of Organic Chemistry》2003,39(5):747-749
Russian Journal of Organic Chemistry - 相似文献
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G. I. Borodkin I. R. Elanov R. V. Andreev M. M. Shakirov V. G. Shubin 《Russian Journal of Organic Chemistry》2006,42(3):406-411
The reaction of [2.2]paracyclophane with nitrosonium tetrachloroaluminate was studied by NMR (1H, 13C) spectroscopy using deuterium isotopic perturbation technique. The resulting cationic complexes containing one and two nitrosonium ions are involved in fast (on the NMR time scale) interconversion. Quantum-chemical calculations performed on the DFT level (using triple zeta basis set) indicate the higher stability of 2η single-charged π-complexes relative to σ complexes corresponding to the addition of NO+ ion at the ipso and ortho positions. The formation of the single-charged π-complex is energetically more favorable, compared to the double-charged π-complex. The affinity of NO+ for [2.2]paracyclophane is much greater than for p-xylene, presumably due to stacking interaction between the aromatic rings in the π-complex. 相似文献
5.
I. S. Vasil’chenko T. E. Shestakova V. N. Ikorskii T. A. Kuz’menko V. G. Vlasenko L. N. Divaeva A. S. Burlov A. I. Uraev I. V. Pirog G. S. Borodkin P. B. Chepurnoi I. G. Borodkina O. A. Beletskii O. A. Karpov I. E. Uflyand A. D. Garnovskii 《Russian Journal of Coordination Chemistry》2007,33(3):176-183
Azomethine derivatives of 1-amino-2-thiobenzimidazole (H2L) were synthesized and studied by IR and 1H NMR spectroscopy. Thiobenzimidazoline tautomeric form of these compounds was found to predominate in a solid state and DMSO solution. Novel mono-and binuclear metal chelates M(HL)2 and M2L2 (M = Ni(II), Cu(II), Co(II), Zn(II), Cd(II)) were synthesized on the basis of H2L derivatives and their composition and structures were established from IR, 1H NMR, EXAFS, and magnetochemical data. The composition of coordination sphere was shown to produce no effect on ferromagnetic exchange in binuclear Cu(II) complexes. 相似文献
6.
A Study of Competitive Coordination of Benzochalcogenazole Ligands by Heteronuclear NMR Spectroscopy
Borodkina I. G. Uraev A. I. Borodkin G. S. Sadekov I. D. Garnovskii A. D. Minkin V. I. 《Russian Journal of General Chemistry》2003,73(11):1810-1814
Complexes of 2-methyl(phenyl)benzo-1,3-tellurazole and 2-methyl(phenyl)benzo-1,3-selenazole with tungsten pentacarbonyl and boron trifluoride were studied by heteronuclear NMR spectroscopy (1H, 13C, 77Se, and 125Te). The coordination mode of the ambident ligand can be determined from the coordination shifts of the 125Te and 77Se NMR signals: upfield at coordination via Te and Se atoms and downfield at N coordination. 相似文献
7.
V. F. Borodkin V. A. Burmistrov M. K. Islyaikin 《Chemistry of Heterocyclic Compounds》1981,17(1):49-51
The PMR spectra of the macroheterocyclic compound obtained by the reaction of 5-tert-butyl-1,3-diiminoisoindoline with 1,3-phenylenediamine in refluxing butyl alcohol and purified by chromatography on aluminum oxide were recorded. It is shown that the compound does not contain a unified conjugated macroring system. The dependence of the chemical shift of the protons of the endocyclic imino groups on the nature of the solvent was investigated. It is shown that the formation of compound-solvent intermolecular hydrogen bonds is complicated by steric factors.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 62–64, January, 1981. 相似文献
8.
Synthesis, structures, and properties of spiro[6-azaperimidine-2,4′-cyclohexa-2′,5′-dien]-1′-one derivatives 总被引:1,自引:0,他引:1
V. N. Komissarov E. N. Gruzdeva L. P. Olekhnovich G. S. Borodkin V. N. Khrustalev S. V. Lindeman Yu. T. Struchkov V. A. Kogan V. I. Minkin 《Russian Chemical Bulletin》1997,46(11):1924-1930
The reaction of 5-amino-4-chloroquinolines with 4-amino-2,6-di-tert-butylphenol yielded derivatives of spiro[6-azaperimidine-2,4′-cyclohexa-2′,5′-dien]-1′-one, which exhibit photo-and thermochromic
properties in solutions. The structure of 2′,6′-di-tert-butyl-5,7,9-trimethylspiro[6-aza,-2,3-dihydroperimidine-2,4′-cyclohexa-2′,5′-dien]-1′-one was established by X-ray diffraction
study. The ring-chain isomerization of 2′,6′-di-tert-butyl-5,7-dimethyl-and 2′,6′-di-tert-butyl-5,7,8-trimethylspiro[6-aza-2,3-dihydroperimidine-2,4′-cyclohexa-2′,5′-dien]-1′-ones was studied by dynamic NMR spectroscopy.
Deceased.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2028–2034, November, 1997. 相似文献
9.
10.
Shvets A. A. Borodkin S. A. Kogan V. A. Safaryan G. P. Safoklov B. B. Tkachev V. V. Filipenko O. S. 《Russian Journal of Coordination Chemistry》2003,29(1):28-32
The structure of the Cu[(2-O–)(5-NO2)C6H3N–CH=CH–+PPh3]2 complex with the CuN2O2 coordination core of distorted square-planar geometry was established by X-ray diffraction analysis. The molecules in the crystal structure of the Cu[(2-O–)(5-NO2)C6H3N–CH=CH–+PPh3]2 · 2CHCl3 solvate are bound via hydrogen bonds of two types, namely, C(sp
2)–H···O and C(sp
3)–H···O. 相似文献