全文获取类型
收费全文 | 66篇 |
免费 | 5篇 |
专业分类
化学 | 41篇 |
数学 | 14篇 |
物理学 | 16篇 |
出版年
2022年 | 3篇 |
2021年 | 2篇 |
2020年 | 4篇 |
2019年 | 1篇 |
2018年 | 1篇 |
2017年 | 1篇 |
2016年 | 5篇 |
2015年 | 1篇 |
2014年 | 6篇 |
2013年 | 5篇 |
2012年 | 1篇 |
2011年 | 3篇 |
2010年 | 1篇 |
2009年 | 3篇 |
2008年 | 3篇 |
2007年 | 5篇 |
2006年 | 2篇 |
2005年 | 3篇 |
2004年 | 4篇 |
2002年 | 2篇 |
1999年 | 1篇 |
1996年 | 1篇 |
1995年 | 1篇 |
1992年 | 1篇 |
1989年 | 2篇 |
1985年 | 1篇 |
1984年 | 1篇 |
1980年 | 2篇 |
1977年 | 1篇 |
1975年 | 1篇 |
1935年 | 1篇 |
1934年 | 1篇 |
1928年 | 1篇 |
排序方式: 共有71条查询结果,搜索用时 15 毫秒
1.
LetP be a finite partially ordered set. The lengthl(x) of an elementx ofP is defined by the maximal number of elements, which lie in a chain withx at the top, reduced by one. Letw(P) (d(P)) be the maximal number of elements ofP which have the same length (which form an antichain). Further let
. The numbers
and
as well as all partially ordered sets for which these maxima are attained are determined. 相似文献
2.
Ahmad K. Haidar Niels D. Kjeldsen Nikolaj S. Troelsen Viola Previtali Kasper P. Lundquist Thomas O. Larsen Mads H. Clausen 《Molecules (Basel, Switzerland)》2022,27(2)
Recent reports of antiepileptic activity of the fungal alkaloid TMC-120B have renewed the interest in this natural product. Previous total syntheses of TMC-120B comprise many steps and have low overall yields (11–17 steps, 1.5–2.9% yield). Thus, to access this compound more efficiently, we herein present a concise and significantly improved total synthesis of the natural product. Our short synthesis relies on two key cyclization steps to assemble the central scaffold: isoquinoline formation via an ethynyl-imino cyclization and an intramolecular Friedel-Crafts reaction to form the furanone. 相似文献
3.
Langlet A Latypov NV Wellmar U Bemm U Goede P Bergman J Romero I 《The Journal of organic chemistry》2002,67(22):7833-7838
Nitration of some 2-substituted pyrimidine-4,6-diones in sulfuric acid was studied, which afforded previously unknown 5,5-gem-dinitropyrimidine-4,6-diones in high yields. The gem-dinitro products were easily attacked by nucleophiles with concomitant formation of gem-dinitroacetyl derivatives, which in turn could be further hydrolyzed to salts of dinitromethane and triureas. 相似文献
4.
Glidle A Hadyoon CS Gadegaard N Cooper JM Hillman AR Wilson RW Ryder KS Webster JR Cubitt R 《The journal of physical chemistry. B》2005,109(30):14335-14343
We describe in situ neutron reflectivity (NR) and RAIRS studies of the chemical modification of films of a polypyrrole-based conducting polymer derived from the pentafluorophenyl ester of poly(pyrrole-N-propanoic acid) (PFP) electrodeposited on electrode surfaces. We explore the role of the solvent in controlling the rate of reaction with solution-based nucleophiles (amines, which react with the ester to form amides). By varying the identity of the solvent (water vs acetonitrile) and the neutron contrast (deuteration), we find that both the identity of the solvent and its population within the film are paramount in determining chemical reactivity and electroactivity. IR signatures allow monitoring of the reaction of solution-based amine-tagged species such as amino-terminated poly(propylene glycol), ferrocene ethylamine, and lysine with film-based ester functionalities: the carbonyl bands show ester/amide interconversion and some hydrolysis to acid. Time-dependent spectral analysis shows marked variations in reaction rate with (i) (co-)polymer composition (replacement of some fluorinated ester-functionalized pyrrole with unfunctionalized pyrrole), (ii) the solvent to which the polymer film is exposed, and (iii) the rate of polymer deposition. NR data provide solvent profiles as a function of distance perpendicular to the interface, the variations of which provide an explanation for film reactivity patterns. Homopolymer films are relatively hydrophobic, thus hindering reaction with species present in water solutions. Incorporating pyrrole groups raises the solvent population-dramatically for water-thereby facilitating entry and reaction of aqueous-based lysine. Changing film deposition rate yields films with different absolute levels of solvent and reactivity patterns that are dependent on the size of the reactant molecules: more rapid deposition of polymer gives films with a more open structure leading to a higher solvent content and thence increased reactivity. These results, supported by XPS and AFM data, allow assembly of composition-structure-reactivity correlations, in which the controlling feature is film solvation. 相似文献
5.
Schreiner E Nicolini C Ludolph B Ravindra R Otte N Kohlmeyer A Rousseau R Winter R Marx D 《Physical review letters》2004,92(14):148101
The temperature-dependent behavior of a solvated oligopeptide, GVG(VPGVG), is investigated. Spectroscopic measurements, thermodynamic measurements, and molecular dynamics simulations find that this elastinlike octapeptide behaves as a two-state system that undergoes an "inverse temperature" folding transition and reentrant unfolding close to the boiling point of water. A molecular picture of these processes is presented, emphasizing changes in the dynamics of hydrogen bonding at the protein/water interface and peptide backbone librational entropy. 相似文献
6.
Pekker D Babadi M Sensarma R Zinner N Pollet L Zwierlein MW Demler E 《Physical review letters》2011,106(5):050402
We study the quench dynamics of a two-component ultracold Fermi gas from the weak into the strong interaction regime, where the short time dynamics are governed by the exponential growth rate of unstable collective modes. We obtain an effective interaction that takes into account both Pauli blocking and the energy dependence of the scattering amplitude near a Feshbach resonance. Using this interaction we analyze the competing instabilities towards Stoner ferromagnetism and pairing. 相似文献
7.
In this study, multilayers from polyethylene imine, heparin and chitosan are prepared at three different pH values of 5, 7 and 9. Water contact angle and quartz microbalance measurements show that resulting multilayers differ in terms of wetting behaviour, layer mass and mechanical properties. The multilayer is then formed within a gradient generation microfluidic (μFL) device. Polyethylene imine or heparin solutions of pH 5 are introduced into one inlet and the same solutions but at pH 9 into another inlet of the μFL device. The pH gradient established during the multilayer formation can be visualized inside the microchamber by pH sensitive fluorophores and confocal laser scanning microscopy. From this setup it is expected that properties of multilayers displayed at distinct pH values can be realised in a gradient manner inside the μFL device. Behaviour of the osteoblast cell line MG-63 seeded and cultured on top of multilayers created inside the μFL device support this hypothesis. It is observed that more cells adhere and spread on multilayers build-up at the basic side of the μFL channel, while those cells on top of multilayers built at pH 5 are fewer and smaller. These results are consistent with the behaviour of MG-63 cells seeded on multilayers formed at discrete pH values. It is particularly interesting to see that cells start to migrate from multilayers built at pH 5 to those built at pH 9 during 6 h of culture. Overall, the presented multilayer formation setup applying pH gradients leads to surfaces that promote migration of cells. 相似文献
8.
9.
The method of random sampling was introduced for the first time in the nutation nuclear quadrupole resonance (NQR) spectroscopy
where the nutation spectra show characteristic singularities in the form of shoulders. The analytic formulae for complex two-dimensional
(2-D) nutation NQR spectra (I = 3/2) were obtained and the condition for resolving the spectral singularities for small values of an asymmetry parameter
η was determined. Our results show that the method of random sampling of a nutation interferogram allows significant reduction
of time required to perform a 2-D nutation experiment and does not worsen the spectral resolution. 相似文献
10.