全文获取类型
收费全文 | 15368篇 |
免费 | 587篇 |
国内免费 | 36篇 |
专业分类
化学 | 10601篇 |
晶体学 | 118篇 |
力学 | 405篇 |
综合类 | 1篇 |
数学 | 2094篇 |
物理学 | 2772篇 |
出版年
2023年 | 116篇 |
2022年 | 252篇 |
2021年 | 339篇 |
2020年 | 292篇 |
2019年 | 283篇 |
2018年 | 298篇 |
2017年 | 269篇 |
2016年 | 625篇 |
2015年 | 501篇 |
2014年 | 516篇 |
2013年 | 1008篇 |
2012年 | 1038篇 |
2011年 | 1109篇 |
2010年 | 675篇 |
2009年 | 637篇 |
2008年 | 1010篇 |
2007年 | 968篇 |
2006年 | 825篇 |
2005年 | 739篇 |
2004年 | 579篇 |
2003年 | 546篇 |
2002年 | 465篇 |
2001年 | 324篇 |
2000年 | 284篇 |
1999年 | 205篇 |
1998年 | 161篇 |
1997年 | 135篇 |
1996年 | 172篇 |
1995年 | 128篇 |
1994年 | 117篇 |
1993年 | 139篇 |
1992年 | 124篇 |
1991年 | 88篇 |
1990年 | 68篇 |
1989年 | 56篇 |
1988年 | 57篇 |
1987年 | 55篇 |
1986年 | 50篇 |
1985年 | 98篇 |
1984年 | 90篇 |
1983年 | 60篇 |
1982年 | 63篇 |
1981年 | 49篇 |
1980年 | 59篇 |
1979年 | 27篇 |
1978年 | 47篇 |
1977年 | 32篇 |
1976年 | 29篇 |
1975年 | 34篇 |
1974年 | 29篇 |
排序方式: 共有10000条查询结果,搜索用时 10 毫秒
61.
Paital AR Mitra T Ray D Wong WT Ribas-Ariño J Novoa JJ Ribas J Aromí G 《Chemical communications (Cambridge, England)》2005,(41):5172-5174
Based on a combined theoretical-experimental study, we propose that substituted m-phenylene ligands (m-N-Phi-N) can act as tuneable strong ferromagnetic couplers connecting Cu(II) ions; a new complex presenting that bridge with J close to +15 cm(-1) has been suggested and synthesized. 相似文献
62.
Alves Lourdes A. Felipe Maria G. A. Silva JoÃo B. Almeida E. Silva Silvio S. Prata Arnaldo M. R. 《Applied biochemistry and biotechnology》1998,70(1):89-98
Applied Biochemistry and Biotechnology - In order to remove or reduce the concentrations of toxic substances present in the sugarcane bagasse hemicellulose hydrolysate for xyloseto-xylitol... 相似文献
63.
Burguera JL Quintana IA Salager JL Burguera M Rondón C Carrero P Anton de Salager R Petit de Peña Y 《The Analyst》1999,124(4):593-599
An on-line time based injection system used in conjunction with cold vapor generation atomic absorption spectrometry and microwave-aided oxidation with potassium persulfate has been developed for the determination of the different mercury species in fish-eggs oil samples. A three-phase surfactant-oil-water emulsion produced an advantageous flow when a peristaltic pump was used to introduce the highly viscous sample into the system. The optimum proportion of the oil-water mixture ratio was 2:3 v/v with a Tween 20 surfactant concentration in the emulsion of 0.008% v/v. Inorganic mercury was determined after reduction with sodium borohydride while total mercury was determined after an oxidation step with persulfate prior to the reduction step to elemental mercury with the same reducing agent. The difference between total and inorganic mercury determined the organomercury content in samples. A linear calibration graph was obtained in the range 0.1-20 micrograms l-1 of Hg2+ by injecting 0.7 ml of samples. The detection limits based on 3 sigma of the blank signals were 0.11 and 0.12 microgram l-1 for total and inorganic mercury, respectively. The relative standard deviation of ten independent measurements were 2.8 and 2.2% for 10 micrograms l-1 and 8.8 and 9.0% for 0.1 microgram l-1 amounts of total and inorganic mercury, respectively. The recoveries of 0.3, 0.6 and 8 micrograms l-1 of inorganic and organic mercury added to fish-eggs oil samples ranged from 93.0 to 94.8% and from 100 to 106%, respectively. Good agreement with those values obtained for total mercury content in real samples by electrothermal atomic absorption spectrometry was also obtained, differences between mean values were < 7%. With the proposed procedure, 22 proteropterous catfish-eggs oil samples from the northwestern coast of Venezuela were measured; while the organic mercury lay in the range 2.0 and 3.3 micrograms l-1, inorganic mercury was not detected. 相似文献
64.
Let G be a non-compact connected semisimple Lie group with finite center and let GK denote the centralizer of a maximal compact subgroup K of G inG, the universal enveloping algebra over of the Lie algebra of G. In [4] Lepowsky defines an injective anti-homo morphism P:G
KK
MA, where M is the centralizer in K of a Cartan subalgebraa of the symmetric pair (G,K),K andA are the universal enveloping algebras over corresponding to K anda, respectively, andK
M is the centralizer of M inK. The subalgebra P(G
K) ofK
MA has considerable significance in the infinite dimensional representation theory of G. In this paper we explicitly compute P(G
K) when G=S0o(4,1), and show how this result leads to the determination of all irreducible representations of G and its universal covering group Spin(4,1).Partially supported by CONICET (Argentina) grants. 相似文献
65.
66.
Bañares L Aoiz FJ González-Lezana T Herrero VJ Tanarro I 《The Journal of chemical physics》2005,123(22):224301
Integral cross sections and thermal rate constants have been calculated for the N((2)D)+H(2) reaction and its isotopic variants N((2)D)+D(2) and the two-channel N((2)D)+HD by means of quasiclassical trajectory and statistical quantum-mechanical model methods on the latest ab initio potential-energy surface [T.-S. Ho et al., J. Chem. Phys. 119, 3063 (2003)]. The effect of rotational excitation of the diatom on the dynamics of these reactions has been investigated and interesting discrepancies between the classical and statistical model calculations have been found. Whereas a net effect of reagent rotation on reactivity is always observed in the classical calculations, only a very slight effect is observed in the case of the asymmetric N((2)D)+HD reaction for the statistical quantum-mechanical method. The thermal rate constants calculated on this Potential-Energy Surface using quasiclassical trajectory and statistical model methods are in good agreement with the experimental determinations, although the latter are somewhat larger. A reevaluation of the collinear barrier of the potential surface used in the present study seems timely. Further theoretical and experimental studies are needed for a full understanding of the dynamics of the title reaction. 相似文献
67.
Eugenio?Garcia-Pa?eda Pilar?Guardado Alfredo?MaestreEmail author 《Journal of solution chemistry》2004,33(10):1277-1293
Partial molar volumes at infinite dilution, V02, of alkali–metal halides (LiCl, NaCl KCl RbCl CsCl, NaBr, KBr, KI), tetra-n-alkylammonium bromides, R4NBr (R=Me, Et, n-Pr, n-Bu, n-Pen), NaBPh4, and Ph4PCl have been determined in binary solvent mixtures of water with 2-methyl-2-butanol covering the water-rich region and the alcohol-rich region at 298.15 K. V02 for alkali–metal halides show relatively little dependence on the solvent composition. However, in the case of hydrophobic electrolytes the observed effects are more pronounced. A good linear dependence between V02(R4NBr) and the molecular weight of the tetra-n-alkylammonium cation is found. Limiting single-ion volumes have been obtained using the assumption that V0(Ph4P+)–V0(BPh–4)=2.0 cm3-mol–1. The trends in the single-ion volumes are discussed in both solvent regions. 相似文献
68.
The diamagnetic square planar d(8) complexes [meso-arylcorrolato]copper(III) become paramagnetic upon warming, indicative of the equilibrium between the [corrolato]copper(III) and the [corrolato](+)* copper(II) forms of the complex. [meso-Triphenylcorrolato]copper(III) was structurally characterized and found to be saddled. 相似文献
69.
S. Suarez A. R. Goñi W. Meckbach P. R. Focke 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1987,6(1):55-59
Using a coaxial cylindric electron spectrometer and an electrostatic ion energy analyzer in tandem, a direct measurement of the difference of the energy of convoy peak electron and the electron equivalent ion energy of protons emerging from the downstream surface of C, Au and Al foils is performed in the proton energy range from 60 to 250 keV. This measurement is made possible using the accepted evidence that for a gas target these energies are equal. It is found that also for the beam foil convoy peak electrons, within an experimental average uncertainty of about ±0.1 eV, there is no difference between these energies. If one accepts that the origin of convoy electrons is from inside the solid, the conclusion is that no retardation by the solid surface potential barrier, which is of the order of a few eV, is observed. This is attributed to the strong electron-ion Coulomb interaction which almost completely overshadows the force exerted on the electron by the field of the surface barrier. 相似文献
70.
We examined the variation with ionic strength (I, adjusted with KCl, KNO3, KBr, NaCl or NaClO4) of the formal potential (Econst) for glass electrodes exhibiting a Nernstian response (i.e. Ecell=Econst−s log [H+]). For this purpose, we investigated the different factors included in the formal potential, so we obtained reported values for the liquid junction potential as a function of ionic strength and determined the logarithm of the activity coefficient for the proton in various saline media, using Pitzer equations. 相似文献