全文获取类型
收费全文 | 337篇 |
免费 | 6篇 |
专业分类
化学 | 278篇 |
晶体学 | 10篇 |
力学 | 1篇 |
数学 | 32篇 |
物理学 | 22篇 |
出版年
2022年 | 2篇 |
2021年 | 7篇 |
2020年 | 10篇 |
2019年 | 22篇 |
2018年 | 15篇 |
2017年 | 5篇 |
2016年 | 10篇 |
2015年 | 4篇 |
2014年 | 10篇 |
2013年 | 12篇 |
2012年 | 21篇 |
2011年 | 13篇 |
2010年 | 19篇 |
2009年 | 19篇 |
2008年 | 11篇 |
2007年 | 17篇 |
2006年 | 7篇 |
2005年 | 18篇 |
2004年 | 8篇 |
2003年 | 6篇 |
2002年 | 8篇 |
2001年 | 8篇 |
2000年 | 9篇 |
1999年 | 1篇 |
1998年 | 7篇 |
1997年 | 17篇 |
1996年 | 8篇 |
1995年 | 5篇 |
1994年 | 4篇 |
1993年 | 1篇 |
1992年 | 3篇 |
1991年 | 3篇 |
1990年 | 1篇 |
1989年 | 2篇 |
1985年 | 6篇 |
1984年 | 2篇 |
1983年 | 2篇 |
1982年 | 3篇 |
1980年 | 1篇 |
1976年 | 1篇 |
1975年 | 1篇 |
1974年 | 1篇 |
1973年 | 1篇 |
1972年 | 3篇 |
1971年 | 6篇 |
1970年 | 3篇 |
排序方式: 共有343条查询结果,搜索用时 37 毫秒
1.
Victor N. Khrustalev Eugene A. Komissarov Oleg V. Kulikov 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(7):o374-o377
The macrocyclic title compound crystallizes as a dioxane solvate, C30H22Cl2N4O4·C4H8O2, with two independent formula units in the unit cell. The observed syn conformation is controlled by both intramolecular N—H...O hydrogen bonds and intermolecular C—H...π interactions. The relative macrocyclic inner bore is estimated to be 4.19 Å. In the crystal structure, molecules form dimers via intermolecular C—H...π interactions, and these dimers are, in turn, linked to form columns along the a axis by intermolecular C—H...O hydrogen bonds. Both X‐ray diffraction analysis and density functional theory (DFT) calculations reveal that the macrocycle possesses very high flexibility. This property, as well as the presence of six donor atoms accessible for coordination, makes the title macrocycle a very promising ligand for complexation with the majority of transition metals. 相似文献
2.
I. S. Belostotskaya V. B. Vol'eva N. L. Komissarova M. O. Dekaprilevich V. N. Khrustalev A. Yu. Karmilov V. V. Ershov 《Russian Chemical Bulletin》1997,46(7):1272-1280
Oxidative transformations of 2-dialkylaminomethyl-4,6-di-tert-butylphenols depend on the nature of the oxidant, the character of the substituents at the nitrogen atom, and the medium.
A mechanism of the oxidation of these compounds is suggested. The molecular structure of the compound obtained as a result
of oxidative trimerization of 2-dimethylaminomethyl-4,6-di-tert-butylphenol was established by X-ray structural analysis.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1328–1335, July, 1997. 相似文献
3.
Sessler JL Roznyatovskiy V Pantos GD Borisova NE Reshetova MD Lynch VM Khrustalev VN Ustynyuk YA 《Organic letters》2005,7(23):5277-5280
[reaction: see text] Two easy-to-synthesize polypyrrolic 2,5-diamidothiophene Schiff base macrocycles are reported, along with their anion binding properties as determined via UV-vis spectroscopic titrations carried out in dichloroethane. There is a striking difference between the interactions with anions of the two macrocycles, a finding ascribed to differences in their rigidity. For example, the more flexible dipyrromethane-derived macrocycle displays a 1.2:1 hydrogen sulfate versus nitrate selectivity, while its more rigid bipyrrole-derived congener shows a 7.4:1 selectivity in favor to hydrogen sulfate. 相似文献
4.
Data on the synthesis, on the basis of amidrazones, of mono-, di-, tri-, and tetrazoles, diazoles containing boron, oxygen, silicon, phosphorus, and sulfur atoms in the ring, mono-, di-, tri-, and tetrazines, triazepines, and benzotriazepines, as well as a number of condensed heterocyclic derivatives, are systematized.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 867–887, July, 1989. 相似文献
5.
L. V. Baikalova V. I. Sokol I. A. Zyryanova I. V. Fedyanin V. N. Khrustalev E. A. Zel’bst O. A. Tarasova V. S. Sergienko B. A. Trofimov 《Russian Journal of General Chemistry》2006,76(5):791-797
The crystal and molecular structures of bis(1-isopropenylimidazole)dichlorocobalt (C12H16Cl2·N4Co) [R 0.036 (R W 0.089) for 3229 unique reflections with I > 2σ(I)] and tetra(1-vinylimidazole)dichlorocobalt (C20H24Cl2N8Co) [R 0.031 (R W 0.072) for 1863 unique reflections with I > 2σ(I)] were determined. In these molecular complexes, the monodentate terminal 1-alkenylimidazole ligands coordinate to the metal via a “pyridine” nitrogen atom. In C12H16Cl2N4Co, the Co atom has a distorted tetrahedral 2N,2Cl coordination. The coordination polyhedron of cobalt in C20H24Cl2N8Co is a strongly elongated 4N,2Cl octahedron. The Co-N and Co-Cl bonds [Co-N 2.015(2) and 2.032(4) Å; Co-Cl 2.229(2) Å] in the tetrahedral complex C12H16Cl2N4Co are shorter than those in the octahedral complex C20H24Cl2N8Co [Co-N 2.134(2) and 2.157(2) Å; Co-Cl 2.518(1) Å]. In the structures of both complexes there are short contacts involving the Cl atoms. 相似文献
6.
T. S. Ulbaev Yu. S. Mardashev M. P. Koroteev V. N. Khrustalev M. Yu. Antipin 《Journal of Structural Chemistry》2005,46(5):891-894
Metallocomplexes with optically active ligands are of considerable interest as catalysts of stereoselective processes. A complex of 1,2-isopropylidene-α-D-glucofuranose 3,5,6-bis-cyclophosphite with tungsten(0) pentacarbonyl has been synthesized for the first time and studied by X-ray crystallography. 相似文献
7.
Ya. S. Kayukov O. E. Nasakin Ya. G. Urman V. N. Khrustalev V. N. Nesterov M. Yu. Antipin A. N. Lyushchikov P. M. Lukin 《Chemistry of Heterocyclic Compounds》1996,32(10):1200-1212
2-Aryl-1,2,3,4-tetrahydropyridine-3,3,4,4,-tetracarbonitriles and 1,3,5-triaryl-9-oxo-1,2,3,4b,5,6,8a,9-octahydropyrido[3,4:3,4]pyrrolo[1,2-a][1,3,5]triazine-4b,8a-dicarbonitriles are formed by the reaction of 4-oxoalkane-1,1,2,2-tetracarnonitriles with 1,3,5-triaryl-2,4-diaza-1,4-pentadienes depending on the solvent used.Chuvash State University, Cheboksary 428015. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1395–1409, October, 1996. Original article submitted October 2, 1996. 相似文献
8.
L. I. Kryvenko A. T. Soldatenkov O. V. Zvolinskii L. N. Kuleshova V. N. Khrustalev V. N. Gryshev S. A. Soldatova 《Chemistry of Heterocyclic Compounds》1997,33(6):691-697
Reaction of 2-acetylpyridine with 4-[2.2]paracyclophanyllithium or 4-acetyl[2.2]paracyclophane with 2-pyridllithium gives 1-([2.2]paracyclophan-4-yl)-1-(2-pyridyl)ethanol. Its molecular and crystalline structures have been studied by x-ray analysis. It was found that heating this alcohol in acid medium causes dehydration and heterocyclization to give 1-paracyclophanyl-1-pyridylethylene and 10-methyl[2.2]paracyclophano[4,5-bindolizine.For communication 9 see [1]. This report is also communication [5] in the series Synthesis, Structure, and Biological Activity of [2.2]Paracyclophanes (for communication 4 see [2]).Russian University of National Friendship, Moscow 117198. A. N. Nesmeyanov Institute of Organoelemental Compounds, Russian Academy of Sciences, Moscow 117813. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 793–800, June, 1997. 相似文献
9.
The reaction of imidazole with benzoyl chloride in pyridine affordedcis-1,2-bis(benzoyl-amino)ethylene (1) rather than 2-benzoylimidazole, as has been suggested previously. The structure of1 was confirmed by1H NMR spectroscopy and X-ray diffraction study.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1593–1595, August, 1998. 相似文献
10.
Ya. S. Kayukov P. M. Lukin O. E. Nasakin V. N. Khrustalev V. N. Nesterov M. Yu. Antipin V. V. Sheverdov 《Chemistry of Heterocyclic Compounds》1997,33(4):423-425
It has been established by x-ray structural analysis that on reacting 4-oxoalkane-1,1,2,2-tetracarbonitriles with aldehydes
6-imino-2,7-dioxabicyclo[3.2.1]octane-4,4,5-tricarbonitriles are formed and not 3-imino-2,6-dioxabicyclo[2,2,2] octane-4,8,8-tricarbonitriles
as has been proposed.
Chuvash State University, Cheboksary 428015. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 497–499,
April, 1997. 相似文献