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131.
Mass spectrometry (MS) is a powerful technique for protein identification in proteomic research. Two-dimensional gel electrophoresis (2-DE) combined with MS is a significant method for protein separation and identification. For protein identification, peptide sequencing is usually carried out by an effective but expensive nano-flow liquid chromatographic system combined to tandem mass spectrometry (MS/MS). However, protein identification based on such method is time-consuming, and contamination may occur as a result of column overloading. In this study, we establish an alternative nanoscale system for protein identification using MS/MS. The system consists of several devices that can be purchased from commercial sources and can be connected to an electrospray ionization quadrupole-time of flight (ESI-Q-TOF) MS in order to analyze proteins from 2D gels. This inexpensive strategy provides an attractive alternative method for rapid identification of proteins using a nanospray source. In addition, the device is disposable so that contamination is avoided. It is shown that peptide sequencing based on this device using ESI-Q-TOF MS is accomplished within 10 min. 相似文献
132.
Two new compounds, including petasinoside A and chloridate-[N-chloromethyl-hectorine], were isolated from Senecio nemorensis. The structures of these compounds were elucidated by spectroscopic methods including 1D and 2D NMR experiments. 相似文献
133.
A novel PEGylated biodegradable hyperbranched PEG‐b‐PDMAEMA has been synthesized. The low toxicity, small molecular weight PDMAEMA chains were crosslinked using a biodegradable disulfide‐based dimethacrylate (DSDMA) agent to yield higher molecular weight hyperbranched polymers. PEG chains were linked onto the polymer surface, masking the positive charge (as shown by Zeta potential measurements) and reducing the toxicity of the polymer. The hyperbranched structures were also cleaved under reducing conditions and analyzed, confirming the expected component structures. The hyperbranched polymer was mixed with DNA and efficient binding was shown to occur through electrostatic interactions. The hyperbranched structures could be reduced easily, generating lower toxicity oligomer chains.
134.
Wei Huang Jie-Min Li Li-Mei Yang Zhong-Liang Jin Zheng-Gen Zhong Yu Liu Qin-Ying Chou Feng Li 《Optics & Laser Technology》2011,43(1):214-217
A 32 in RGB LED backlight unit is developed. A local dimming algorithm is designed for the backlight, and grid-noise artifacts in the LC driving signal are successfully removed with consideration of the backlight distribution to provide identical intensity from each LED block. The 32 in RGB LED backlight LCD display has achieved a static display contrast of over 20000:1 and an average power reduction of 30%. We have also obtained the color gamut transformation matrix for transferring a cold cathode fluorescent lamp BLU LCD display gamut system to our RGB LED BLU LCD display gamut system, and extended the color saturation by suppositional color expansion method. As a result, the color has been accurately reproduced in RGB LED BLU LCD display with more richness and more saturation. 相似文献
135.
Zhan-Shuo Hu Fei-Yi Hung Shoou-Jinn Chang Kuan-Jen Chen Yi-Wei Tseng Bohr-Ran Huang Bo-Cheng Lin Wei-Yang Chou Jay Chang 《Journal of nanoparticle research》2011,13(10):4757-4763
The photo-current of n-ZnO/p-Si heterojunction photodiodes was improved by embedding Ag nanoparticles in the interface (ZnO/nano-PAg/p-Si), and the ratio between photo- and dark-current increased by about three orders more than that of a n-ZnO/p-Si specimen. The improvement in the photo-current resulted from the light scattering of embedded Ag nanoparticles. The I–V curve of n-ZnO/p-Si degraded after thermal treatment (A-ZnO/p-Si) because the silicon robbed the oxygen from ZnO to form amorphous silicon dioxide and left an oxygen vacancy. Notably,
the properties of ZnO/nano-PAg/p-Si were better in the time-dependent photoresponse under 10 V bias. Ag nanoparticles (15–20 nm) scattered the UV light randomly
and increased the probability for the absorption of ZnO to enhance the properties of the photodiode. 相似文献
136.
研究典型干旱区的罗布泊,对揭示区域环境演变特征和全球变化具有重要意义.从遥感影像上的"耳纹"特征入手,通过光谱、土壤和地表参数等分析,认为:地表全盐含量和结构差异是形成罗布泊遥感影像"耳纹"特征的直接原因;光谱、全盐含量和土壤粒径的分析结果具有很好的一致性."耳纹"记录下了罗布泊地区的环境演变特征,这些特征表明:受全球环境影响,湖水在气候不断干旱的过程中逐渐干涸,干涸过程的气候调整,使罗布泊地区经历了两次相对湿润的气候环境,前一次较长,后一次很短. 相似文献
137.
We derive an exact analytic expression for the three-body local correlations in the Lieb-Liniger model of 1D Bose gas with contact repulsion. The local three-body correlations control the thermalization and particle loss rates in the presence of terms which break integrability, as is realized in the case of 1D ultracold bosons. Our result is valid not only at finite temperature but also for a large class of nonthermal excited states in the thermodynamic limit. We present finite temperature calculations in the presence of external harmonic confinement within local density approximation, and for a highly excited state that resembles an experimentally realized configuration. 相似文献
138.
Guangxin Wu Jieyu Zhang Yongquan Wu Qian Li Kuochih Chou Xinhua Bao 《Applied Physics A: Materials Science & Processing》2011,102(3):739-745
With density-functional theory, the dissociative chemisorptions and diffusion processes of hydrogen on both pure and La-doped
Mg(0001) surfaces are studied. Calculation results show that the energy barrier obtained for hydrogen dissociation on the
La-doped Mg(0001) surface is smaller due to back-donated bonding between molecular H2 and doped La atom. The obtained diffusion barriers (0.8–0.22 eV) imply a fast motion of atomic H on La-doped Mg(0001) surface. 相似文献
139.
140.
Apparent correlations are found between the N-H chemical shifts of congeneric series of compounds and the dipole moments of the molecules, such as lactams and thiolactams, cyclic ureas and thioureas. When there is a high degree of correlation, either the N-H chemical shift or the dipole moment of the molecule can be used as an electronic parameter in correlating the biological activity with the chemical structure. In a series of substituted salicylaldehydes the Hammett σ constant gives better correlation with the biological activity than the O-H chemical shift. This is probably due to the anisotropic effect of the substituent besides the electronic effect. Other factors affecting the N-H chemical shift, e.g. intramolecular hydrogen-bonding of nitrosoureas and the deshielding effect of a benzene ring, in o-phenyleneureas are also presented. In spite of the limitations, the chemical shifts of many compounds can be obtained very easily, therefore, their uses in structure-activity correlations deserve further investigation. 相似文献