全文获取类型
收费全文 | 362篇 |
免费 | 0篇 |
国内免费 | 2篇 |
专业分类
化学 | 312篇 |
晶体学 | 2篇 |
力学 | 4篇 |
数学 | 30篇 |
物理学 | 16篇 |
出版年
2022年 | 6篇 |
2021年 | 6篇 |
2020年 | 6篇 |
2019年 | 5篇 |
2017年 | 4篇 |
2016年 | 2篇 |
2015年 | 2篇 |
2014年 | 5篇 |
2013年 | 25篇 |
2012年 | 13篇 |
2011年 | 15篇 |
2010年 | 6篇 |
2009年 | 7篇 |
2008年 | 26篇 |
2007年 | 23篇 |
2006年 | 19篇 |
2005年 | 20篇 |
2004年 | 21篇 |
2003年 | 21篇 |
2002年 | 12篇 |
2001年 | 2篇 |
2000年 | 2篇 |
1999年 | 2篇 |
1998年 | 9篇 |
1997年 | 5篇 |
1996年 | 8篇 |
1995年 | 5篇 |
1994年 | 3篇 |
1993年 | 8篇 |
1991年 | 7篇 |
1990年 | 5篇 |
1989年 | 3篇 |
1988年 | 2篇 |
1987年 | 2篇 |
1986年 | 4篇 |
1985年 | 4篇 |
1984年 | 3篇 |
1983年 | 2篇 |
1982年 | 5篇 |
1981年 | 3篇 |
1979年 | 4篇 |
1978年 | 11篇 |
1977年 | 2篇 |
1975年 | 4篇 |
1974年 | 1篇 |
1973年 | 1篇 |
1972年 | 3篇 |
1970年 | 1篇 |
1969年 | 4篇 |
1955年 | 1篇 |
排序方式: 共有364条查询结果,搜索用时 265 毫秒
191.
192.
193.
Hajimehdipoor H Dijoux-Franca MG Mariotte AM Amanzadeh Y Sadat-Ebrahimi SE Ghazi-Khansari M 《Natural product research》2006,20(13):1251-1257
From aerial parts of Swertia longifolia Boiss., which grows in the north of Iran, five xanthones, two of which in diglycosidic form, were isolated. The structures were confirmed by means of their spectral data as isobellidifolin, bellidin, gentisein, 1,5-dihydroxy-3-methoxy-6-O-primeverosyl xanthone, and 8-hydroxy-3,5-dimethoxy-1-O-primeverosyl xanthone, the latter two of which were new derivatives in the plant kingdom. 相似文献
194.
Boulanger AM Rennie EE Holland DM Shaw DA Mayer PM 《The journal of physical chemistry. A》2006,110(27):8563-8571
The valence shell electronic structures of methylhydrazine (CH(3)NHNH(2)), 1,1-dimethylhydrazine ((CH(3))(2)NNH(2)) and tetramethylhydrazine ((CH(3))(4)N(2)) have been studied by recording threshold and conventional (kinetic energy resolved) photoelectron spectra. Ab initio calculations have been performed on ammonia and the three methyl substituted hydrazines, with the structures being optimized at the B3-LYP/6-31+G(d) level of theory. The ionization energies of the valence molecular orbitals were calculated using the Green's function method, allowing the photoelectron bands to be assigned to specific molecular orbitals. The ground-state adiabatic and vertical ionization energies, as determined from the threshold photoelectron spectra, were IE(a) = 8.02 +/- 0.16 eV and IE(v) = 9.36 +/- 0.02 eV for methylhydrazine, IE(a) = 7.78 +/- 0.16 eV and IE(v) = 8.86 +/- 0.01 eV for 1,1-dimethylhydrazine and IE(a) = 7.26 +/- 0.16 eV and IE(v) = 8.38 +/- 0.01 eV for tetramethylhydrazine. Due to the large geometry change that occurs upon ionization, these IE(a) values are all higher than the true thresholds. New features have been observed in the inner valence region and these have been compared with similar structure in the spectrum of hydrazine. The effect of resonant autoionization on the threshold photoelectron yield is discussed. New heats of formation (Delta(f)H) are proposed for the three hydrazines on the basis of G3 calculations: 107, 94, and 95 kJ/mol for methylhydrazine, 1,1-dimethyhydrazine and tetramethylhydrazine, respectively. The previously reported Delta(f)H for tetramethylhydrazine is shown to be erroneous. 相似文献
195.
Rennie EE Boulanger AM Mayer PM Holland DM Shaw DA Cooper L Shpinkova LG 《The journal of physical chemistry. A》2006,110(28):8663-8675
The valence shell photoelectron spectrum, threshold photoelectron spectrum, and threshold photoelectron photoion coincidence (TPEPICO) mass spectra of acetone have been measured using synchrotron radiation. New vibrational progressions have been observed and assigned in the X 2B2 state photoelectron bands of acetone-h6 and acetone-d6, and the influence of resonant autoionization on the threshold electron yield has been investigated. The dissociation thresholds for fragment ions up to 31 eV have been measured and compared to previous values. In addition, kinetic modeling of the threshold region for CH3* and CH4 loss leads to new values of 78 +/- 2 kJ mol(-1) and 75 +/- 2 kJ mol(-1), respectively, for the 0 K activation energies for these two processes. The result for the methyl loss channel is in reasonable agreement with, but slightly lower than, that of 83 +/- 1 kJ mol(-1) derived in a recent TPEPICO study by Fogleman et al. The modeling accounts for both low-energy dissociation channels at two different ion residence times in the mass spectrometer. Moreover, the effects of the ro-vibrational population distribution, the electron transmission efficiency, and the monochromator band-pass are included. The present activation energies yield a Delta(f)H298 for CH3CO+ of 655 +/- 3 kJ mol(-1), which is 4 kJ mol(-1) lower than that reported by Fogleman et al. The present Delta(f)H298 for CH3CO+ can be combined with the Delta(f)H298 for CH2CO (-47.5 +/- 1.6 kJ mol(-1)) and H+ (1530 kJ mol(-1)) to yield a 298 K proton affinity for ketene of 828 +/- 4 kJ mol(-1), in good agreement with the value (825 kJ mol(-1)) calculated at the G2 level of theory. The measured activation energy for CH4 loss leads to a Delta(f)H298 (CH2CO+*) of 873 +/- 3 kJ mol(-1). 相似文献
196.
Anne-Marie Simon 《Algebras and Representation Theory》2009,12(2-5):385-400
The Auslander–Buchweitz theory for finitely generated modules over a Cohen–Macaulay local ring is extended to complete modules, finitely generated or not. This also allows us to extend to complete modules some other known facts concerning finitely generated ones. 相似文献
197.
Let F be a nonarchimedean local field and let GL(N) = GL(N,F). We prove the existence of parahoric types for GL(N). We construct representative cycles in all the homology classes of the chamber homology of GL(3). 相似文献
198.
199.
Daria L. Melnikova Zilya F. Badrieva Mikhail A. Kostin Corina Maller Monika Stas Aneta Buczek Malgorzata A. Broda Teobald Kupka Anne-Marie Kelterer Peter M. Tolstoy Vladimir D. Skirda 《Molecules (Basel, Switzerland)》2020,25(23)
In this work, the nuclear magnetic resonance (NMR) and IR spectroscopic markers of the complexation between 5-fluorouracil (5-FU) and β-cyclodextrin (β-CD) in solid state and in aqueous solution are investigated. In the attenuated total reflectance(ATR) spectra of 5-FU/β-CD products obtained by physical mixing, kneading and co-precipitation, we have identified the two most promising marker bands that could be used to detect complex formations: the C=O and C-F stretching bands of 5-FU that experience a blue shift by ca. 8 and 2 cm−1 upon complexation. The aqueous solutions were studied by NMR spectroscopy. As routine NMR spectra did not show any signs of complexation, we have analyzed the diffusion attenuation of spin–echo signals and the dependence of the population factor of slowly diffusing components on the diffusion time (diffusion NMR of pulsed-field gradient (PFG) NMR). The analysis has revealed that, at each moment, ~60% of 5-FU molecules form a complex with β-CD and its lifetime is ca. 13.5 ms. It is likely to be an inclusion complex, judging from the independence of the diffusion coefficient of β-CD on complexation. The obtained results could be important for future attempts of finding better methods of targeted anticancer drug delivery. 相似文献
200.
Fabio D. Cukiernik Pascale Maldivi Anne-Marie Giroud-godquin Jean-Claude Marchon Mohammed Ibn-elhaj Daniel Guillon 《Liquid crystals》2013,40(6):903-906
Abstract The syntheses and structural properties of new binuclear ruthenium (II, III) complexes with long chain carboxylates, of general formula Ru2(RCO2)4X (R = C8H17, C11H23 and X = C1, RCOO), are reported. The thermodynamic behaviour of these compounds is strongly influenced by the nature of the counterion X. The chloro complexes (X = CI) are not mesomorphic whereas the carboxylato species (X = RCOO) are shown to exhibit a thermotropic columnar mesophase, thus providing the first example of a mixed-valent liquid-crystalline material. 相似文献