全文获取类型
收费全文 | 160篇 |
免费 | 12篇 |
专业分类
化学 | 114篇 |
力学 | 25篇 |
数学 | 14篇 |
物理学 | 19篇 |
出版年
2023年 | 3篇 |
2021年 | 5篇 |
2020年 | 2篇 |
2019年 | 11篇 |
2018年 | 6篇 |
2017年 | 6篇 |
2016年 | 3篇 |
2015年 | 8篇 |
2014年 | 9篇 |
2013年 | 11篇 |
2012年 | 20篇 |
2011年 | 15篇 |
2010年 | 8篇 |
2009年 | 7篇 |
2008年 | 8篇 |
2007年 | 4篇 |
2006年 | 5篇 |
2005年 | 7篇 |
2004年 | 4篇 |
2003年 | 2篇 |
2002年 | 2篇 |
1999年 | 1篇 |
1991年 | 1篇 |
1989年 | 1篇 |
1987年 | 1篇 |
1986年 | 3篇 |
1985年 | 3篇 |
1984年 | 2篇 |
1983年 | 1篇 |
1982年 | 3篇 |
1978年 | 2篇 |
1977年 | 1篇 |
1976年 | 1篇 |
1974年 | 3篇 |
1973年 | 1篇 |
1972年 | 1篇 |
1971年 | 1篇 |
排序方式: 共有172条查询结果,搜索用时 15 毫秒
1.
I. G. Yudelevich B. I. Zaksas Ye. A. Petrova A. S. Cherevko 《Fresenius' Journal of Analytical Chemistry》1991,340(9):560-563
Summary A method for the atomic emission spectrometric analysis of air and water with inductively coupled and two-jet direct current plasmas has been developed. The method has been applied to the determination of impurity contents with good accuracy and sensitivity. 相似文献
2.
Meyer F Demeshko S Leibeling G Kersting B Kaifer E Pritzkow H 《Chemistry (Weinheim an der Bergstrasse, Germany)》2005,11(5):1518-1526
Pyrazolate-based dinucleating ligands with thioether-containing chelate arms have been used for the synthesis of a family of novel tetranuclear nickel(II) complexes [L2Ni4(N3)3(O2CR)](ClO4)2 that incorporate three azido bridges and one carboxylate (R = Me, Ph). Molecular structures have been elucidated by X-ray crystallography in four cases, revealing Ni4 cores with a unique topology in which two of the azido ligands adopt an unusual mu3-1,1,3 bridging mode. The compounds were further characterized by mass spectrometry, IR spectroscopy, and variable-temperature magnetic susceptibility measurements. Magnetic data analyses indicate a combination of significant intramolecular ferromagnetic and antiferromagnetic exchange interactions that give rise to an overall S(T) = 0 ground state. The sign and the magnitude of the individual couplings have been rationalized in the framework of the common magnetostructural correlations for end-to-end and end-on azido linkages, suggesting that these correlations also remain valid for the respective fragments of multiply bridging mu3-1,1,3 azido ligands. 相似文献
3.
4.
Christian Schneider Dr. Serhiy Demeshko Prof. Dr. Franc Meyer Dr. C. Gunnar Werncke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(20):6348-6353
A [Fe-S-Fe] subunit with a single sulfide bridging two low-coordinate iron ions is the supposed active site of the iron-molybdenum co-factor (FeMoco) of nitrogenase. Here we report a dinuclear monosulfido bridged diiron(II) complex with a similar complex geometry that can be oxidized stepwise to diiron(II/III) and diiron(III/III) complexes while retaining the [Fe-S-Fe] core. The series of complexes has been characterized crystallographically, and electronic structures have been studied using, inter alia, 57Fe Mössbauer spectroscopy and SQUID magnetometry. Further, cleavage of the [Fe-S-Fe] unit by CS2 is presented. 相似文献
5.
6.
K.V. Cherevko D.A. Gavryushenko J.V. Kulyk V.M. Sysoev 《Journal of Molecular Liquids》2005,120(1-3):71-74
The diffusion phenomena were analyzed using the phenomenological equations of the thermodynamics of irreversible processes. The diffusion coefficient was thought to be dependent on local concentrations and pressure, unlike it was done in the linear theories. The reversible chemical reactions were modeled as intermolecular interaction. The ideal and regular solutions and solutions, described by the Margules's and Sketchard–Hammer's equations, were investigated and analytical solutions were found. 相似文献
7.
A. G. Cherevko 《Colloid Journal》2009,71(6):869-876
An analysis of nucleation processes that occur during a vapor-liquid phase transition and temperature fluctuations that take
place in clusters of stable phases is employed to derive a semiempirical relation between the capillary and thermophysical
characteristics of substances. The relation enables one to calculate the surface tension of elementary substances based on
their thermophysical characteristics in a wide temperature range from melting to boiling points. The surface tension of metals
is calculated within this temperature range. In most cases, the calculated results agree with available experimental data. 相似文献
8.
9.
Marc Ostermeier Dipl.‐Chem. Marie‐Anne Berlin Dipl.‐Chem. Robert M. Meudtner Dr. Serhiy Demeshko Dr. Franc Meyer Prof. Dr. Christian Limberg Prof. Dr. Stefan Hecht Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(33):10202-10213
2,6‐Bis(1,2,3‐triazol‐4‐yl)pyridine (btp) ligands with substitution patterns ranging from strongly electron‐donating to strongly electron‐accepting groups, readily prepared by means of Cu‐catalyzed 1,3‐dipolar cycloaddition (the “click” reaction), were investigated with regard to their complexation behavior, and the properties of the resulting transition‐metal compounds were compared. Metal–btp complexes of 1:1 stoichiometry, that is, [Ru(btp)Cl2(dmso)] and [Zn(btp)Br2], could be isolated and were crystallographically characterized: they display octahedral and trigonal‐bipyramidal coordination geometries, respectively, and exhibit high aggregation tendencies due to efficient π–π stacking leading to low solubilities. Metal–btp complexes of 1:2 stoichiometry, that is, [Fe(btp)2]2+ and [Ru(btp)2]2+, could also be synthesized and their metal centers show the expected octahedral coordination spheres. The iron compounds exhibit quite a complex magnetic behavior in the solid state including spin crossover near room temperature, and hysteresis and locking into high‐spin states on tempering at 400 K, depending on the substituents on the btp ligands. Cyclic voltammetry studies of [Ru(btp)2]2+ reveal strong modulation of the oxidation potentials by more than 0.6 V and a clear linear correlation to the Hammett constant (σpara) of the substituent at the pyridine core. Isothermal titration calorimetry was used to measure the thermodynamics of the FeII–btp complexation process and enabled accurate determination of the complexation enthalpies, which display a linear relationship with the σpara values for the terminal phenyl substituents. Detailed NMR spectroscopic studies finally revealed that in the case of FeII complexation, dynamics are rapid for all investigated btp derivatives in acetonitrile, while replacing FeII by RuII or changing the solvent to dichloromethane effectively slows down ligand exchange. The results nicely demonstrate the utility of substituent parameters, originally developed for linear free‐energy relationships to explain reactivity in organic reactions, in coordination chemistry, and to illustrate the potential to custom‐design btp ligands and complexes thereof with predictable properties. The fast equilibration of the [Fe(btp)2]2+ complexes together with their tunable stability and interesting magnetic properties should enable the design of dynamic metallosupramolecular materials with advantageous properties. 相似文献
10.
A. A. Cherevko A. P. Chupakhin 《Proceedings of the Steklov Institute of Mathematics》2012,278(1):267-278
We study a multidimensional self-similar solution of the dynamic equations of an ideal compressible fluid. The solution describes swirling motions of a gas and is partially invariant with respect to the rotation group extended by dilations. The analysis of the solution reduces to the analysis of the singular points and manifolds of a system of fourth-order ordinary differential equations. We also give an example of a solution that describes the expansion of a swirling gas cloud into vacuum. 相似文献