全文获取类型
收费全文 | 3791篇 |
免费 | 204篇 |
国内免费 | 34篇 |
专业分类
化学 | 1928篇 |
晶体学 | 14篇 |
力学 | 126篇 |
综合类 | 3篇 |
数学 | 627篇 |
物理学 | 868篇 |
无线电 | 463篇 |
出版年
2023年 | 44篇 |
2022年 | 52篇 |
2021年 | 87篇 |
2020年 | 77篇 |
2019年 | 81篇 |
2018年 | 93篇 |
2017年 | 78篇 |
2016年 | 157篇 |
2015年 | 110篇 |
2014年 | 124篇 |
2013年 | 247篇 |
2012年 | 200篇 |
2011年 | 191篇 |
2010年 | 144篇 |
2009年 | 122篇 |
2008年 | 163篇 |
2007年 | 162篇 |
2006年 | 151篇 |
2005年 | 125篇 |
2004年 | 96篇 |
2003年 | 86篇 |
2002年 | 104篇 |
2001年 | 65篇 |
2000年 | 74篇 |
1999年 | 67篇 |
1998年 | 56篇 |
1997年 | 53篇 |
1996年 | 49篇 |
1995年 | 46篇 |
1994年 | 36篇 |
1993年 | 27篇 |
1992年 | 34篇 |
1991年 | 31篇 |
1990年 | 32篇 |
1989年 | 23篇 |
1988年 | 21篇 |
1987年 | 25篇 |
1986年 | 26篇 |
1985年 | 33篇 |
1983年 | 18篇 |
1982年 | 21篇 |
1981年 | 26篇 |
1980年 | 29篇 |
1979年 | 25篇 |
1978年 | 21篇 |
1977年 | 31篇 |
1976年 | 25篇 |
1975年 | 17篇 |
1974年 | 19篇 |
1934年 | 17篇 |
排序方式: 共有4029条查询结果,搜索用时 15 毫秒
61.
62.
G. Münzenberg S. Hofmann H. Folger F. P. Heßberger J. Keller K. Poppensieker B. Quint W. Reisdorf K. H. Schmidt H. J. Schött P. Armbruster M. E. Leino R. Hingmann 《Zeitschrift für Physik A Hadrons and Nuclei》1985,322(2):227-235
In irradiations of207Pb and208Pb, respectively, with54Cr theα-decay of the isotopes259106,260106, and261106 could be observed for the first time. For260106 a spontaneous fission branch of (50 ?20 +30 )% was observed. The isotopes were identified by genetic relationships of α-decay after separation in-flight with the velocity filter SHIP and implantation into a position-sensitive silicon surface-barrier detector. The measured partial fission halflife of the doubly even isotope260106 of (7.2 ?2.7 +4.8 )ms exceeds the predicted values by at least a factor of 40. This result could be explained by the high shell corrections of the ground state mass, derived from the measured α-decay energies. The experimental results show evidence for an island of purely shell stabilized nuclei in the region of deformed isotopes beyond the actinides. 相似文献
63.
64.
Justicia J Rosales A Buñuel E Oller-López JL Valdivia M Haïdour A Oltra JE Barrero AF Cárdenas DJ Cuerva JM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(7):1778-1788
The titanocene-catalyzed cascade cyclization of epoxypolyenes, which are easily prepared from commercially available polyprenoids, has proven to be a useful procedure for the synthesis of C(10), C(15), C(20), and C(30) terpenoids, including monocyclic, bicyclic, and tricyclic natural products. Both theoretical and experimental evidence suggests that this cyclization takes place in a nonconcerted fashion via discrete carbon-centered radicals. Nevertheless, the termination step of the process seems to be subjected to a kind of water-dependent control, which is unusual in free-radical chemistry. The catalytic cycle is based on the use of the novel combination Me(3)SiCl/2,4,6-collidine to regenerate the titanocene catalyst. In practice this procedure has several advantages: it takes place at room temperature under mild conditions compatible with different functional groups, uses inexpensive reagents, and its end step can easily be controlled to give exocyclic double bonds by simply excluding water from the medium. 相似文献
65.
Jae Ha Kim Young Tae Jeong Seong Ihl Woo 《Journal of polymer science. Part A, Polymer chemistry》1994,32(15):2979-2987
Highly active catalysts for copolymerization have been prepared by the precipitation of MgCl2/ToCl4 complex with or without high surface area silica. Copolymerization of ethylene and 1-butene has been tested by using the prepared catalysts at various concentrations of 1-butene. The catalytic activities are 20–80 kg/g Ti h. The rate of copolymerization is strongly affected by the addition of 1-butene. The decay rate of copolymerization is first order with respect to time. Analyses of copolymers with solvent extraction, DSC, IR, XRD, and NMR were performed. Ethylene reactivity ratio (k11) for TiCl4/MgCl2/THF catalyst is calculated to be about 26 by NMR spectrum. © 1994 John Wiley & Sons, Inc. 相似文献
66.
W. Franz A. Grießel F. Steglich D. Wohlleben 《Zeitschrift für Physik B Condensed Matter》1978,31(1):7-17
We report measurements of the electrical resistivity, the thermal conductivityk and the thermoelectric powerS between 1.5K and 300K on the anomalous CeCu2Si2 compound and on LaCu2Si2 as reference compound. For LaCu2Si2 the temperature dependences of andS are in accord with those found in otherd band metals. For CeCu2Si2 the observed resistivity (220 µ cm at 200K) leads to a very short electronic mean free path which is of the order of the Ce-Ce spacing. Correspondingly,k is almost identical with the phonon contributionk
p
. Below 20K, resistivity and thermoelectric power strongly suggest Fermi liquid behavior with a degeneracy temperature between 20K and 40K. Above 200K, both andS decrease proportionally to –ln(T/1 K).Work performed within the research program of the Sonderforschungsbereich 125 Aachen/Jülich/KölnPart of this work will be presented at the Int. Conf. on Rare Earths in the Metallic State, St. Pierre de Chartreuse, Sept. 1978 相似文献
67.
Katja Schulz R. Klaus Mueller Werner Engewald Adelgunde Graefe Jan Dreßler 《Chromatographia》2007,66(11-12):879-886
Some aroma compounds found in alcoholic beverages are characteristic of a certain beverage (i.e. 2,4-decadienoic acid ethyl ester is characteristic of pear spirit and 5-butyltetrahydro-4-methylfuran-2-on “whiskey lactone” is characteristic of aged spirits like whiskey). These substances were detectable in beverages but not in blood samples. The aim of this investigation was to find a sensitive sampling technique for aroma compounds in whole blood samples. This technique may be used in forensic toxicology for examination of drinking claims. The method comprises dynamic headspace sampling using a purge and trap concentrator, followed by quantitative gas chromatography–mass spectrometry (dynamic HS–GC–MS). The influence of sample preparation, trap adsorbents and sample temperature as well as desorption time and purge time on the quality of the analytical results were investigated. The following optimal parameters were determined: stirred and diluted whole blood sample without salt addition, use of Carbotrap C as trap material, sample temperature at 80 °C, desorption time 20 min and purge time 30 min. These optimal parameters were used for the determination of detection limits (LOD). The LOD of aroma compounds by means of dynamic headspace sampling were compared with the results of conventional sampling: the static headspace technique. Limits of detection for the aroma compounds with conventional static headspace GC are in the range 400–10,000 μg L?1. Dynamic headspace–GC was found to be a more sensitive sampling technique for most of the aroma compounds investigated (e.g. C4–C8 ethyl esters, benzoic acid ethyl ester, linalool oxide and 4-ethylguaiacol) with detection limits between 1 and 50 μg L?1, but there were also limits to the sampling of substances with lower volatility like decanoic acid ethyl ester, 2,4-decadienoic acid ethyl ester, eugenol and whiskey lactone with detection limits of about 1,000 μg L?1. 相似文献
68.
Ahn YH Park EJ Cho K Kim JY Ha SH Ryu SH Yoo JS 《Rapid communications in mass spectrometry : RCM》2004,18(20):2495-2501
The enrichment of phosphopeptides using immobilized metal ion affinity chromatography (IMAC) and subsequent mass spectrometric analysis is a powerful protocol for detecting phosphopeptides and analyzing their phosphorylation state. However, nonspecific binding peptides, such as acidic, nonphosphorylated peptides, often coelute and make analyses of mass spectra difficult. This study used a partial chemical tagging reaction of a phosphopeptide mixture, enriched by IMAC and contaminated with nonspecific binding peptides, following a modified beta-elimination/Michael addition method, and dynamic mass analysis of the resulting peptide pool. Mercaptoethanol was used as a chemical tag and nitrilotriacetic acid (NTA) immobilized on Sepharose beads was used for IMAC enrichment. The time-dependent dynamic mass analysis of the partially tagged reaction mixture detected intact phosphopeptides and their mercaptoethanol-tagged derivatives simultaneously by their mass difference (-20 Da for each phosphorylation site). The number of new peaks appearing with the mass shift gave the number of multiply phosphorylated sites in a phosphopeptide. Therefore, this partial chemical tagging/dynamic mass analysis method can be a powerful tool for rapid and efficient phosphopeptide identification and analysis of the phosphorylation state concurrently using only MS analysis data. 相似文献
69.
70.
Tae -Kyu Ha 《Theoretical chemistry accounts》1977,43(4):337-349
Configuration interaction (CI) studies of ground, n *, * * electronically excited states are reported for pyridine N-oxide. The transition energy to the lowest * excited 1
B
2 state is calculated at 4.35 eV, compared to the experimental spectrum range of 3.67–4.0 eV. This state lies below the lowest n * excited 1
A
2 state calculated at 4.81 eV above the ground state. The only experimentally reported triplet state at 2.92 eV above the ground state is predicted to be the 3
A
1 (*) state. The calculated energy lies at 3.27 eV. Numerous other high-lying singlet states as well as the triplet states have also been calculated. The intramolecular charge transfer character of the ground and the excited states have been studied in terms of the calculated dipole moment and other physical properties. 相似文献