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21.
Fry B Silva SR Kendall C Anderson RK 《Rapid communications in mass spectrometry : RCM》2002,16(9):854-858
Elemental analyzers have been successfully coupled to stable-isotope-ratio mass spectrometers for online measurements of the delta(34)S isotopic composition of plants, animals and soils. We found that the online technology for automated delta(34)S isotopic determinations did not yield reproducible oxygen isotopic compositions in the SO(2) produced, and as a result calculated delta(34)S values were often 1-3 per thousand too high versus their correct values, particularly for plant and animal samples with high C/S ratio. Here we provide empirical and analytical methods for correcting the S isotope values for oxygen isotope variations, and further detail a new SO(2)-SiO(2) buffering method that minimizes detrimental oxygen isotope variations in SO(2). 相似文献
22.
Huygens A Huyghe D Bormans G Verbruggen A Kamuhabwa AR Roskams T de Witte PA 《Photochemistry and photobiology》2003,78(6):607-614
The aim of this study was to investigate the in vitro cellular accumulation, distribution and photocytotoxic effect of hypericin in two-dimensional (2-D) and three-dimensional (3-D) cultured RT-112 transitional cell carcinoma cells of the bladder. In addition, two iodinated derivatives of hypericin were incorporated to investigate whether these analogs, with their increased lipophilicity and heavy-atom effect, display a different biological behavior and optimized photodynamic effect. The results indicate that hypericin and mono-iodohypericin behave similarly in terms of cellular accumulation, spheroidal distribution and photocytotoxic effect. In contrast, di-iodohypericin concentrated to a higher extent in monolayers and spheroids, but the accumulation was restricted to the outermost part of the spheroid. An inverse correlation therefore seems to exist between the extent of cellular uptake under 2-D conditions and the penetration of the compounds in multicellular systems. Moreover, a less pronounced photocytotoxic effect was observed for di-iodohypericin in both 2-D and 3-D cell culture systems. It can be concluded that iodinated derivatives of hypericin do not show an increased cytotoxic effect upon irradiation in either monolayers or spheroids. Moreover, this study shows that when new photosensitizers are preclinically developed, the use of 3-D cell aggregates is critical for a correct evaluation of their efficacy. 相似文献
23.
在理学3064X荧光仪上采用十八烷基马来酸(OHM)晶体作为色散单元,通过改造电路,调整晶体倾角,获得对碳分析的良好线性,在流气正比计数器(FPC)窗膜分别为5μm和0.6μm条件下,碳元素的峰背比分别达到38.91和54.04。作者分析了白口铸铁和碳化硅中的碳,结果表明在理学3064X荧光仪上定量分析碳是可行了,具有快速、简便、准确、多元素同时分析的特点,可用于日常分析 相似文献
24.
根据复合材料单层的实际构造,提出了串并联组合模型,采用微观力学与宏观力学相结合的方法,推导出一组计算单向复合材料弹性模量的新公式。其优点是:E1和v(12)、E2和G(12)的计算式形式对称,结构简单,计算容易,物理意义明确。我们把由世界上许多著名学者提出的多组预测公式和本文导出式计算所得的结果与国内外已发表的硼/环氧、碳/环氧、玻璃/环氧复合材料的实验数据相比较,结果表明:导出式比其他公式精确、更有价值,可供二程设计使用。 相似文献
25.
Discontinuous molecular dynamics simulations are performed on homopolymer/solvent and surfactant/solvent systems. The homopolymer and surfactant molecules are modeled as freely jointed square-well chains. Solvent molecules are modeled as both hard spheres and square-well spheres. We explore how the various interaction parameters affect the types of phase behavior and micellization observed in the homopolymer/solvent and surfactant/solvent systems. Increasing the packing fraction of homopolymers in both hard-sphere solvents and square-well solvents increases the solvent's ability to dissolve homopolymers only when the segment-solvent interaction strength exceeds a critical value. Although only upper critical solution temperature (UCST) behavior is observed for homopolymers in hard-sphere solvents, both UCST and lower critical solution temperature (LCST) behavior are observed for homopolymers in square-well solvents, depending upon the interaction strengths and chain length. This indicates that it is necessary to account for the solvent-solvent attraction to model LCST behavior in supercritical CO2. Our simulation results on surfactants in hard-sphere solvents show that it is necessary to account for the interactions experienced by both the head and tail blocks in order to capture the essential features of surfactant/supercritical CO2 systems. 相似文献
26.
Dr. Carol Cristescu 《Monatshefte für Chemie / Chemical Monthly》1977,108(6):1455-1459
5-Substituted 4-thio-6-azauracils [I, 6-alkylthio-3,4-dihydro-5-thioxo-1,2,4-triazin-3(2H)-ones] have been converted with hexamethyldisilazane in 3-trimethylsilyloxy-5-trimethylsilylthio-derivatives(II). These were condensed with 1-O-acetyl-2,3,5-tri-O-benzoyl-d-ribofuranose in the presence of anhydrous stannic chloride to afford the corresponding 1-(2,3,5-tri-O-benzoyl--d-ribofuranosyl)-4-thioxo-5-substituted-6-azauracil (III). 相似文献
27.
Cytotoxicity and Antiproliferative Effect of Hypericin and Derivatives after Photosensitization 总被引:3,自引:1,他引:3
Ann L. Vandenbogaerde Els M. Delaey Annelies M. Vantieghem Bernard E. Himpens Wilfried J. Merlevede Peter A. de Witte 《Photochemistry and photobiology》1998,67(1):119-125
The toxicity on three human tumor cell lines (A431, HeLa and MCF7) of five phenanthroperylenequinones (hypericin and derivatives) and two perylenequinones (cercosporin and calphostin C) was investigated after photosensitization (4 J/cm2 ). Furthermore, the antiproliferative effect on HeLa cells was studied for the phenanthroperylenequinones. Hypericin, 2,5-dibromohypericin, 2,5,9,12-tetrabromohypericin and perylenequinones displayed a potent cytotoxic and antiproliferative effect in the nanomolar range. Hypericin dicarboxylic acid exhibited no photoactivity. In general, the antiproliferative activity correlated well with the photocytotoxicity. However, the nonphotocytotoxic compound hexamethylhypericin showed potent antiproliferative activity in the nanomolar range, probably exerting its action by protein kinase C inhibition. Without light irradiation, no cytotoxic and antiproliferative effect was observed for any photocytotoxic phenanthroperylenequinone compound. Furthermore, confocal laser microscopy revealed that the subcellular localization in A431 cells was similar for the photoactive compounds; the photosensitizers were mainly concentrated in the perinuclear region, probably corresponding with the Golgi apparatus and the endoplasmic reticulum. In addition, the accumulation of the photosensitizers in HeLa cells was investigated. All compounds except hypericin dicarboxylic acid were found to concentrate to a large extent in the cells. The compound 2,5,9,12-tetrabromohypericin seemed intrinsically more effective than hypericin since the intracellular concentration of the bromoderivative was a magnitude of order lower than that of hypericin although both compounds showed similar photobiological activity. 相似文献
28.
Form indexes for DTA or TG curves (S T orS x) must be treated separately. Only forS x can clear relations to be developed for the order of reactionn. In the rational range ofn between 0.5 and 3.0 we found for linear, exponential and hyperbolic programmes these functions were found to be of the type $$S_x = an^{0,5} + b$$ Since a low dependence on frequency factork 0 has been established, for a linear programme the simultaneous determination ofn andk 0 may be performed. 相似文献
29.
Lloyd C.L. Hollenberg David C. Bardos N.S. Witte 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1996,38(3):249-252
A cluster expansion of the Lanczos recursion for non-extensive systems is developed based on the plaquette expansion for extensive systems, in which an auxiliary scaling parameter, Ω, plays the role of volume and introduces extensivity into the problem. Connected Hamiltonian moments of the non-extensive system are computed and introduced into the plaquette expansion in the usual way with Ω. The extensive energy is calculated for increasing orders of the expansion in 1/Ω and the ground state and mass gap of the finite few body problem recovered in the limit Ω → ∞. This new non-perturbative method is applied to the case of N bosons interacting harmonically in one dimension and the ground state energy and mass gap in the vacuum sector are calculated exactly. 相似文献
30.
R. Witte E. E. B. Campbell C. Richter H. Schmidt I. V. Hertel 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1987,5(2):101-111
A collisional alignment and orientation study with planar symmetry is described, determining the complete density matrix for resonant charge transfer from laser excited atoms. Results are reported for the Na++Na*(3p) system over the collision energy rangeE c.m.=50?100 eV. We communicate the optimal alignment angle γ and linear polarisationP l + of the charge cloud as well as its relative height ρ00 and the angular momentumL ⊥ + transferred in the collision as a function of the scattering angle. For preparation of the sodium 3p orbital in the scattering plane (positive reflection symmetry) we observe that at small reduced scattering angles (<20 eV°) the preparation of apσ at large internuclear distances contributes most to the scattering intensity whereas at larger reduced scattering angles (>60 eV°) apπ+ preparation is more important. In contrast, preparation of thepπ? orbital (perpendicular to the scattering plane) is large at small and vanishes at larger scattering angles. We conclude that orbital following cannot be assumed in this resonant charge transfer process. The angular momentum transfer is observed to be small, indicating only little coherence in the process, but shows nevertheless an interesting behaviour as a function of scattering angle. 相似文献