全文获取类型
收费全文 | 1093篇 |
免费 | 26篇 |
国内免费 | 4篇 |
专业分类
化学 | 605篇 |
晶体学 | 3篇 |
力学 | 40篇 |
数学 | 316篇 |
物理学 | 159篇 |
出版年
2023年 | 10篇 |
2022年 | 28篇 |
2021年 | 33篇 |
2020年 | 40篇 |
2019年 | 23篇 |
2018年 | 26篇 |
2017年 | 19篇 |
2016年 | 40篇 |
2015年 | 28篇 |
2014年 | 36篇 |
2013年 | 61篇 |
2012年 | 79篇 |
2011年 | 95篇 |
2010年 | 70篇 |
2009年 | 52篇 |
2008年 | 54篇 |
2007年 | 62篇 |
2006年 | 56篇 |
2005年 | 55篇 |
2004年 | 50篇 |
2003年 | 24篇 |
2002年 | 26篇 |
2001年 | 21篇 |
2000年 | 12篇 |
1999年 | 16篇 |
1998年 | 10篇 |
1997年 | 5篇 |
1996年 | 13篇 |
1995年 | 10篇 |
1994年 | 4篇 |
1993年 | 6篇 |
1992年 | 8篇 |
1991年 | 4篇 |
1990年 | 9篇 |
1989年 | 2篇 |
1988年 | 4篇 |
1987年 | 2篇 |
1986年 | 2篇 |
1985年 | 8篇 |
1984年 | 1篇 |
1983年 | 3篇 |
1982年 | 5篇 |
1981年 | 4篇 |
1980年 | 1篇 |
1979年 | 3篇 |
1978年 | 1篇 |
1968年 | 1篇 |
1932年 | 1篇 |
排序方式: 共有1123条查询结果,搜索用时 31 毫秒
161.
Transient behaviour of magnetic micro-bead chains rotating in a fluid by external fields 总被引:1,自引:0,他引:1
Magnetic micro-beads can facilitate many functions in lab-on-a-chip systems, such as bio-chemical labeling, selective transport, magnetic sensing and mixing. In order to investigate potential applications of magnetic micro-beads for mixing in micro fluidic systems, we developed a pin-jointed mechanism model that allows analysing the behaviour of rotating superparamagnetic bead chains. Our numerical model revealed the response of the chains on a rotating magnetic field over time. We could demonstrate that the governing parameters are the Mason number and number of beads in the chain. The results are in agreement with the simplified analytical model, assuming a straight chain, but also allow prediction of the transient chain shape. The modelled chains develop an anti-symmetric S-shape that is stable, if the Mason number for a given chain length does not surpass a critical value. Above that value, rupture occurs in the vicinity of the chain centre. However, variations in bead susceptibility can shift the location of rupture. Moreover, we performed experiments with superparamagnetic micro-beads in a small fluid volume exposed to a uniform rotating magnetic field. Our simulation could successfully predict the observed transient chain form and the time for chain rupture. The developed model can be used to design optimised bead based mixers in micro fluidic systems. 相似文献
162.
Litos IK Emmanouilidou E Glynou KM Laios E Ioannou PC Christopoulos TK Kampa M Castanas E Gravanis A 《Analytical and bioanalytical chemistry》2007,389(6):1849-1857
In recent years an increasing amount of interest has been directed at the study and routine testing of polymorphisms responsible
for variations in drug metabolism. Most of the current methods involve either time-consuming electrophoresis steps or specialized
and expensive equipment. In this context, we have developed a rapid, simple and robust method for genotyping of CYP2D6*3,
CYP2D6*4, CYP2C19*2, CYP2C19*3 and TPMT*2 single nucleotide polymorphisms (SNP). Genomic DNA is isolated from whole blood
and the segments that span the SNP of interest are amplified by PCR. The products are subjected directly (without purification)
to two primer extension (PEXT) reactions (three cycles each) using normal and mutant primers in the presence of biotin-dUTP.
The PEXT primers contain a (dA)30 segment at the 5′ end. The PEXT products are detected visually by a dry-reagent dipstick-type assay in which the biotinylated
extension products are captured from immobilized streptavidin on the test zone of the strip and detected by hybridization
with oligo(dT)-functionalized gold nanoparticles. Patient samples (76 variants in total) were genotyped and the results were
fully concordant with those obtained by direct DNA sequencing. 相似文献
163.
Tzeli D Petsalakis ID Theodorakopoulos G 《The journal of physical chemistry. A》2007,111(36):8892-8902
The electronic and geometric structures of gallium dinitride cation, GaN2+ and gallium tetranitride cation, GaN4+ were systematically studied by employing density functional theory (DFT-B3LYP) and perturbation theory (MP2, MP4) in conjunction with large basis sets, (aug-)cc-pVxZ, x = T, Q. A total of 7 structures for GaN2+ and 24 for GaN4+ were identified, corresponding to minima, transition states, and saddle points. We report geometries and dissociation energies for all the above structures as well as potential energy profiles, potential energy surfaces, and bonding mechanisms for some low-lying electronic states. The calculated dissociation energy (De) of the ground state of GaN2+, X1Sigma+, is 5.6 kcal/mol with respect to Ga+(1S) + N2(X1Sigmag+) and that of the excited state, ?3Pi, is 24.8 kcal/mol with respect to Ga+(3P) + N2(X1Sigmag+). The ground state and the first excited minimum of GaN4+ are of 1A1(C2v) and 3B1(C2v) symmetry with corresponding De of 11.0 and 43.7 kcal/mol with respect to Ga+(1S) + 2N2(X1Sigmag+) for X1A1 and Ga+(3P) + 2N2(X1Sigmag+) for 3B1. 相似文献
164.
The supercritical mixture ethanol-carbon dioxide (EtOH-CO2) with mole fraction of ethanol X(EtOH) congruent with 0.1 was investigated at 348 K, by employing the molecular dynamics simulation technique in the canonical ensemble. The local intermolecular structure of the fluid was studied in terms of the calculated appropriate pair radial distribution functions. The estimated average local coordination numbers and mole fractions around the species in the mixture reveal the existence of local composition enhancement of ethanol around the ethanol molecules. This finding indicates the nonideal mixing behavior of the mixture due to the existence of aggregation between the ethanol molecules. Furthermore, the local environment redistribution dynamics have been explored by analyzing the time correlation functions (TCFs) of the total local coordination number (solvent, cosolvent) around the cosolvent molecules in appropriate parts. The analysis of these total TCFs in the auto-(solvent-solvent, cosolvent-cosolvent) and cross-(solvent-cosolvent, cosolvent-solvent) TCFs has shown that the time dependent redistribution process of the first solvation shell of ethanol is mainly determined by the redistribution of the CO2 solvent molecules. These results might be explained on the basis of the CO2-CO2 and EtOH-CO2 intermolecular forces, which are sufficiently weaker in comparison to the EtOH-EtOH hydrogen bonding interactions, creating in this way a significantly faster redistribution of the CO2 molecules in comparison with EtOH. Finally, the self-diffusion coefficients and the single reorientational dynamics of both the cosolvent and solvent species in the mixture have been predicted and discussed in relationship with the local environment around the species, which in the case of the EtOH molecules seem to be strongly affected. 相似文献
165.
Ioannis K. Argyros 《Monatshefte für Mathematik》1999,127(4):265-276
Newton’s method is used to approximate a locally unique zero of a polynomial operator F of degree in Banach space. So far, convergence conditions have been found for Newton’s method based on the Newton-Kantorovich hypothesis
that uses Lipschitz-type conditions and information only on the first Fréchet-derivative of F. Here we provide a new semilocal convergence theorem for Newton’s method that uses information on all Fréchet-derivatives
of F except the first. This way, we obtain sufficient convergence conditions different from the Newton-Kantorovich hypothesis.
Our results are extended to include the case when F is a nonlinear operator whose kth Fréchet-derivative satisfies a H?lder continuity condition. An example is provided to show that our conditions hold where
all previous ones fail. Moreover, some applications of our results to the solution of polynomial systems and differential
equations are suggested. Furthermore, our results apply to solve a nonlinear integral equation appearing in radiative transfer
in connection with the problem of determination of the angular distribution of the radiant-flux emerging from a plane radiation
field.
Received 9 December 1997 in revised form 30 March 1998 相似文献
166.
Ioannis K. Argyros 《Journal of Applied Mathematics and Computing》1999,6(2):267-275
In this study we examine the applicability of Newton’s method and the modified Newton’s method for approximating a locally unique solution of a nonlinear equation in a Banach space. We assume that the Newton-Kantorovich hypothesis for Newton’s method is violated, but the corresponding condition for the modified Newton method holds. Under these conditions there is no guarantee that Newton’s method starting from the same initial guess as the modified Newton’s method converges. Hence, it seems that we must always use the modified Newton method under these conditions. However, we provide a numerical example to demonstrate that in practice this may not be a good decision. 相似文献
167.
An algebraic quantization procedure for discretized spacetime models is suggestedbased on the duality between finitary substitutes and their incidence algebras.The provided limiting procedure that yields conventional manifold characteristicsof spacetime structures is interpreted in the quantum algebraic framework as acorrespondence principle. 相似文献
168.
169.
Dodecahydro‐ closo ‐dodecaborates of the Heavy Alkaline‐Earth Metals from Aqueous Solution: Ca(H2O)7[B12H12] · H2O, Sr(H2O)8[B12H12], and Ba(H2O)6[B12H12] The crystalline hydrates of the heavy alkaline earth metal dodecahydro‐closo‐dodecaborates (M[B12H12] · n H2O, n = 6–8; M = Ca, Sr, Ba) are easily accessible by reaction of an aqueous (H3O)2[B12H12] solution with an alkaline earth metal carbonate (MCO3). By isothermic evaporation of the respective aqueous solution we obtained colourless single crystals which are characterized by X‐ray diffraction at room temperature. The three compounds Ca(H2O)7[B12H12] · H2O (orthorhombic, P212121; a = 1161.19(7), b = 1229.63(8), c = 1232.24(8) pm; Z = 4), Sr(H2O)8[B12H12] (trigonal, R3; a = 1012.71(6), c = 1462.94(9) pm; Z = 3) and Ba(H2O)6[B12H12] (orthorhombic, Cmcm; a = 1189.26(7) pm, b = 919.23(5) pm, c = 1403.54(9) pm; Z = 4) are neither formula‐equal nor isostructural. The structure of Sr(H2O)8[B12H12] is best described as a NaCl‐type arrangement, Ba(H2O)6[B12H12] rather forms a layer‐like and Ca(H2O)7[B12H12] · H2O a channel‐like structure. In first sphere the alkaline earth metal cations Ca2+ and Sr2+ are coordinated by just seven and eight oxygen atoms from the surrounding water molecules, respectively. A direct coordinative influence of the quasi‐icosahedral [B12H12]2– cluster anions becomes noticeable only for the Ba2+ cations (CN = 12) in Ba(H2O)6[B12H12]. The dehydratation of the alkaline earth metal dodecahydro‐closo‐dodecaborate hydrates has been shown to take place in several steps. Thermal treatment leads to the anhydrous compounds Ca[B12H12], Sr[B12H12] and Ba[B12H12] at 224, 164 and 116 °C, respectively. 相似文献