全文获取类型
收费全文 | 222篇 |
免费 | 5篇 |
国内免费 | 3篇 |
专业分类
化学 | 159篇 |
力学 | 6篇 |
数学 | 22篇 |
物理学 | 43篇 |
出版年
2023年 | 2篇 |
2021年 | 5篇 |
2020年 | 8篇 |
2019年 | 4篇 |
2017年 | 1篇 |
2016年 | 5篇 |
2015年 | 3篇 |
2014年 | 3篇 |
2013年 | 10篇 |
2012年 | 13篇 |
2011年 | 16篇 |
2010年 | 6篇 |
2009年 | 5篇 |
2008年 | 9篇 |
2007年 | 10篇 |
2006年 | 2篇 |
2005年 | 6篇 |
2004年 | 10篇 |
2003年 | 11篇 |
2002年 | 11篇 |
2001年 | 3篇 |
2000年 | 3篇 |
1999年 | 2篇 |
1997年 | 3篇 |
1996年 | 8篇 |
1995年 | 6篇 |
1994年 | 6篇 |
1993年 | 1篇 |
1992年 | 3篇 |
1991年 | 4篇 |
1990年 | 4篇 |
1989年 | 3篇 |
1988年 | 2篇 |
1987年 | 4篇 |
1986年 | 4篇 |
1984年 | 3篇 |
1983年 | 1篇 |
1982年 | 4篇 |
1981年 | 3篇 |
1980年 | 1篇 |
1979年 | 1篇 |
1978年 | 4篇 |
1977年 | 2篇 |
1976年 | 1篇 |
1975年 | 4篇 |
1974年 | 2篇 |
1968年 | 3篇 |
1965年 | 1篇 |
1948年 | 1篇 |
1936年 | 2篇 |
排序方式: 共有230条查询结果,搜索用时 31 毫秒
1.
Azuelos G. Benslama K. Costanzo D. Couture G. Garcia J.E. Hinchliffe I. Kanaya N. Lechowski M. Mehdiyev R. Polesello G. Ros E. Rousseau D. 《The European Physical Journal C - Particles and Fields》2004,39(2):13-24
The European Physical Journal C - We discuss possible searches for the new particles predicted by Little Higgs Models at the LHC. By using a simulation of the ATLAS detector, we demonstrate how the... 相似文献
2.
Lorraine R. Gardiner Ralph E. Steuer 《The Journal of the Operational Research Society》1994,45(12):1456-1466
It has previously been shown that nine of the most prominent procedures of interactive multiple objective programming can be considered as special cases of a common procedure called the unified algorithm. In this paper, we show how four additional procedures can be similarly included in the unified approach. Also, the paper presents a procedure-switching matrix that depicts the possibilities for switching from one procedure to another, one iteration to the next, in the unified algorithm if so directed by a user. 相似文献
3.
4.
We study quantitatively the reactions \(e^ + e^ - \to W^ + e\bar \nu _e \) ,e R ? e + and the rare decay \(Z^0 \to W^ \pm l^ \mp \mathop {\nu _e }\limits^{( - )} \) forl=e, μ and τ, as a test for anomalous γW + W ? andZ 0 W + W ? structure. If κ denotes the anomalous magnetic moment of theW-boson and ω its anomalous coupling to theZ 0, values of |ω|>2.5 and |κ|>1.5 can be ruled out at LEP and SLC rather easily. This will put constraints on composite model building. 相似文献
5.
Total synthesis of amaryllidaceae alkaloid buflavine 总被引:1,自引:0,他引:1
A concise synthesis of the amaryllidaceae alkaloid buflavine (1) and its regioisomer (2) involving sequential Meyers' biaryl coupling, enecarbamate formation, and hydrogenation followed by ultimate intramolecular reductive amination is presented. 相似文献
6.
Abstract— Comparison of spectroradiometric and meter measurements of a series of ultraviolet radiation sources indicates that a wide divergence between readings can occur. We found that with a xenon are filtered as a solar simulator producing UV-A (320–400 nm) and UV-B (290–320 nm) radiation, the meter can either over-or underestimate the emission of the source when different cutoff filters are used. The most severe discrepancy appears with the UV-B meter reading, although the UV-A reading can also be problematic. Meters should be calibrated against the specific sources they will be used to measure. 相似文献
7.
H Wunderli E Couture D A Vince E Kellenberger 《Journal of supramolecular structure》1977,7(2):163-190
We describe the aberrant phage multiplication of the triple conditional lethal mutant 43-(polymerase).30-(ligase).46-(exonuclease) of bacteriophage T4D in which phage DNA replication is arrested but some late protein synthesis occurs (33). The nuclear disruption is indistinguishable from wild type. Forty-five empty small and empty large particles are assembled per cell when the multiplicity of infection (m.o.i.) is 100. This number corresponds closely to the 38 phage equivalents of cleaved major head protein determined biochemically. By reducing the m.o.i. the number of observable particles decreases, reaching 1-5 per cell at an m.o.i. of 5(+5). The total synthesis of phage related proteins is not significantly dependant on the m.o.i. The synthesis of late proteins is about 10% of that of wild type at high m.o.i. and decreases with the m.o.i. The different early and late proteins do not show the same relative proportions as in wild type and respond differently to an increased m.o.i. These and other results are discussed with respect to the role of phage DNA in prehead assembly and head maturation. 相似文献
8.
Mechanisms explaining the formation of pyrroles obtained by UV irradiation of thiophen, the two methylthiophens, the four dimethylthiophens, 2-phenylthiophen, furan, the two methylfurans, and 2,4- and 2,5-dimethylfuran in the presence of n-propylamine are discussed. A comparison of the structure of thiocarbonyl and carbonyl intermediates most likely to be formed by UV irradiation of the substrates with the structure of the experimentally obtained pyrroles indicates that the formation of pyrroles from thiophenes and furans seems to follow mechanisms described in Schemes 1 and 4. 相似文献
9.
Kevin J. Sheehy Lorraine M. Bateman Niko T. Flosbach Martin Breugst Peter A. Byrne 《Chemical science》2020,11(35):9630
The preferred site of alkylation of diazine N-oxides by representative hard and soft alkylating agents was established conclusively using the 1H–15N HMBC NMR technique in combination with other NMR spectroscopic methods. Alkylation of pyrazine N-oxides (1 and 2) occurs preferentially on nitrogen regardless of the alkylating agent employed, while O-methylation of pyrimidine N-oxide (3) is favoured in its reaction with MeOTf. As these outcomes cannot be explained in the context of the hard/soft acid/base (HSAB) principle, we have instead turned to Marcus theory to rationalise these results. Marcus intrinsic barriers (ΔG‡0) and ΔrG° values were calculated at the DLPNO-CCSD(T)/def2-TZVPPD/SMD//M06-2X-D3/6-311+G(d,p)/SMD level of theory for methylation reactions of 1 and 3 by MeI and MeOTf, and used to derive Gibbs energies of activation (ΔG‡) for the processes of N- and O-methylation, respectively. These values, as well as those derived directly from the DFT calculations, closely reproduce the observed experimental N- vs. O-alkylation selectivities for methylation reactions of 1 and 3, indicating that Marcus theory can be used in a semi-quantitative manner to understand how the activation barriers for these reactions are constructed. It was found that N-alkylation of 1 is favoured due to the dominant contribution of ΔrG° to the activation barrier in this case, while O-alkylation of 3 is favoured due to the dominant contribution of the intrinsic barrier (ΔG‡0) for this process. These results are of profound significance in understanding the outcomes of reactions of ambident reactants in general.Marcus theory enables rationalisation and quantification of selectivities in reactions of ambident nucleophiles for which the HSAB principle cannot operate. 相似文献
10.
Lorraine P. McDonnell Bushnell Eric R. Evitt Robert G. Bergman 《Journal of organometallic chemistry》1978,157(4):445-456
Reactions of η5-cyclopentadienylbis(triphenylphosphine)cobalt(I) (5) with several 2,n-alkadiynes (2) were investigated. Each of these reactions leads initially to a material in which one of the acetylene functional groups is π-coordinated to cobalt; this complex then undergoes conversion to a metallocycle. In cases where the two acetylene functions are connected by three- and four-carbon bridges (2b, 2c), metallocycles formed by intramolecular reaction of two acetylene functions in the same molecule may be isolated. In cases where the acetylene functions are joined by larger or smaller bridges, the reactions are more complex, and both inter- and intramolecular metallocycles are formed. Reactions of 5 with 1,8-bis(trimethylsilyl)-1,7-octadiyne (16) gives an isolable crystalline mono-acetylene complex (17), this material is stable in the solid state but undergoes conversion to metallocycle (18) in benzene solution. The relationship of these results to the mechanism of the CpCo(CO)2-catalyzed benzocycloalkene synthesis is discussed; it is suggested that intramolecular metallocycles are intermediates in reactions leading to benzocyclopentanes and -cyclohexenes, but intermolecular metallocycles are probably involved in reactions leading to benzocyclobutenes. 相似文献