全文获取类型
收费全文 | 125篇 |
免费 | 6篇 |
专业分类
化学 | 48篇 |
力学 | 2篇 |
数学 | 45篇 |
物理学 | 36篇 |
出版年
2023年 | 1篇 |
2022年 | 2篇 |
2021年 | 4篇 |
2020年 | 1篇 |
2019年 | 3篇 |
2018年 | 3篇 |
2017年 | 3篇 |
2016年 | 6篇 |
2015年 | 2篇 |
2014年 | 4篇 |
2013年 | 2篇 |
2012年 | 4篇 |
2011年 | 6篇 |
2010年 | 6篇 |
2009年 | 6篇 |
2008年 | 4篇 |
2007年 | 4篇 |
2006年 | 4篇 |
2005年 | 5篇 |
2004年 | 4篇 |
2003年 | 1篇 |
2002年 | 2篇 |
2001年 | 3篇 |
2000年 | 5篇 |
1999年 | 2篇 |
1998年 | 2篇 |
1997年 | 1篇 |
1996年 | 3篇 |
1995年 | 2篇 |
1994年 | 7篇 |
1993年 | 4篇 |
1992年 | 3篇 |
1991年 | 4篇 |
1990年 | 3篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1987年 | 2篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 3篇 |
1983年 | 1篇 |
1981年 | 1篇 |
1979年 | 1篇 |
1976年 | 1篇 |
排序方式: 共有131条查询结果,搜索用时 296 毫秒
1.
We present a new verified optimization method to find regions for Hénon systems where the conditions of chaotic behaviour
hold. The present paper provides a methodology to verify chaos for certain mappings and regions. We discuss first how to check
the set theoretical conditions of a respective theorem in a reliable way by computer programs. Then we introduce optimization
problems that provide a model to locate chaotic regions. We prove the correctness of the underlying checking algorithms and
the optimization model. We have verified an earlier published chaotic region, and we also give new chaotic places located
by the new technique. 相似文献
2.
Models, describing relativistic particles, where Lagrangian densities depend linearly on both the curvature and the torsion of the trajectories, are revisited in D=3 space forms. The moduli spaces of trajectories are completely and explicitly determined using the Lancret program. The moduli subspaces of closed solitons in the three sphere are also determined. 相似文献
3.
Mauricio D Garay 《Topology》2004,43(5):1081-1088
We introduce a cohomological approach to isochore deformation problems. We use this formulation in order to prove an isochore versal deformation theorem for holomorphic function germs. 相似文献
4.
1,4-Phenylenebis(methylene) sulfonium salts were polymerized under different conditions to yield p-xylylene sulfonium salt polyelectrolytes in a broad range of molecular weights. The aqueous reaction mixture formed a reversible gel at initial monomer concentrations higher than 1.0M, but at lower concentrations it remained as an emulsion until reaction completion. The effect of reaction time on intrinsic viscosities and polymer yields for both the emulsion and the gel state is discussed. The higher yields obtained when the reaction was carried out in the presence of a water-immiscible organic solvent were apparently due to the effect of this solvent on increasing the concentration of the reactive intermediate that led to the polyelectrolyte. Both the addition of an organic solvent and the variation of the initial monomer concentrations allowed some control over the molecular weight of the polyelectrolyte formed. 相似文献
5.
6.
In this paper,we study the surface instability of a cylindrical pore in the absence of stress. This instability is called the Rayleigh-Plateau instabilty. We consider the model developed by Spencer et ... 相似文献
7.
8.
Ebraheem Abdu Musad Saleh Abdullah Mohammed AL Dawsari Kakul Husain Ismail Hassan Kutty K.M.Lokanatha Rai 《Molecules (Basel, Switzerland)》2021,26(2)
A novel synthesis of thiazolo[2,3-b]quinazolines 4(a–e), pyrido[2′,3′:4,5]thiazolo[2,3-b]quinazolines {5(a–e), 6(a–e), and 7(a–e)}, pyrano[2′,3′:4,5]thiazolo[2,3-b]quinazolines 8(a–e), and benzo[4,5]thiazolo[2,3-b]quinazoloine9(a–e) derivatives starting from 2-(Bis-methylsulfanyl-methylene)-5,5-dimethyl-cyclohexane-1,3-dione 2 as efficient α,α dioxoketen dithioacetal is reported and the synthetic approaches of these types of compounds will provide an innovative molecular framework to the designing of new active heterocyclic compounds. In our study, we also present optimization of the synthetic method along with a biological evaluation of these newly synthesized compounds as antioxidants and antibacterial agents against the bacterial strains, like S. aureus, E. coli, and P. aeruginosa. Among all the evaluated compounds, it was found that some showed significant antioxidant activity at 10 μg/mL while the others exhibited better antibacterial activity at 100 μg/mL. The results of this study showed that compound 6(c) possessed remarkable antibacterial activity, whereas compound 9(c) exhibited the highest efficacy as an antioxidant. The structures of the new synthetic compounds were elucidated by elemental analysis, IR, 1H-NMR, and 13C-NMR. 相似文献
9.
Gomez L Slutzky C Ferron J de La Figuera J Camarero J Vazquez De Parga AL de Miguel JJ Miranda R 《Physical review letters》2000,84(19):4397-4400
Generic computer simulations using empiric interatomic potentials suggest a new, collective mechanism that could be responsible for mixing at heteroepitaxial interfaces. Even if single adsorbate atoms diffuse by hopping on the substrate surface and do not mix at the terraces, two-dimensional islands formed by nucleation may become unstable above a certain critical size and explode upwards forming clusters of several atomic layers. This process is accompanied by strong distortions of the underlying atomic layers, and on soft materials it can result in surface etching and incorporation of substrate atoms into the islands. 相似文献
10.
M. Teresa Garay Leire Ruiz J. Ramón Marín J. Manuel Laza Matilde Rodriguez Luis M. León 《Colloid and polymer science》2010,288(16-17):1593-1599
Poly(N-tert-butylacrylamide) (PNtBAm) and poly(acrylic acid) (PAA) form interpolymer complexes in 1- and 2-propanol, blend in ethanol, whereas a segregative phase separation is observed when using methanol as solvent as shown by Fourier transform infrared (FTIR) spectrometry and elemental analysis studies. The composition of PNtBAm/PAA complexes has been determined. Thermal studies demonstrated that all complexes show unique glass transition temperatures, higher than those of the polymer components. Complexation of PAA with PNtBAm results in an improvement of its thermal stability. Solvent effects and specific interactions in the system PNtBAm/PAA have been studied by FTIR, revealing that differences in the polymer–solvent interactions are a decisive factor governing complex formation in solution. 相似文献