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201.
Izgi T Parlak C Senyel M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,79(2):308-311
New Hofmann type benzene clathrates in the form of M(CyHEA)2Ni(CN)4·2benzene (where CyHEA=2-(1-cyclohexenyl)ethylamine and M=Ni or Cd) have been prepared in powder form and FT-IR and Raman spectra have been reported. The results suggest that title compounds are similar in structure to Hofmann type clathrates and their structures consist of polymeric layers of |M-Ni(CN)4|∞ with the CyHEA molecule bounded to the metal atoms (M). 相似文献
202.
Parlak C Alver O Senyel M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,78(5):1487-1491
New Hofmann-T(d) type clathrates in the form of Ni(4-Phpy)(2)M(CN)(4)·2G (where 4-Phpy=4-phenylpyridine, M=Cd or Hg and G=1,4-dioxane) have been prepared in powder form and their FT-IR and Raman spectra have been reported. The results suggest that these compounds are similar in structure to the Hofmann-T(d) type clathrates. 相似文献
203.
A new series of 1,3-thiazole and benzo[d]thiazole derivatives 10-15 has been developed, characterized, and evaluated for in vitro antimicrobial activity at concentrations of 25-200 μg/mL against Gram+ve organisms such as methicillin-resistant Staphylococcus aureus (MRSA), Gram-ve organisms such as Escherichia coli (E. coli), and the fungal strain Aspergillus niger (A. niger) by the cup plate method. Ofloxacin and ketoconazole (10 μg/mL) were used as reference standards for antibacterial and antifungal activity, respectively. Compounds 11 and 12 showed notable antibacterial and antifungal activities at higher concentrations (125-200 μg/mL), whereas benzo[d]thiazole derivatives 13 and 14 were found to display significant antibacterial or antifungal activity (50-75 μg/mL) against the Gram+ve, Gram-ve bacteria, or fungal cells used in the present study. In addition, a correlation between calculated and determined partition coefficient (log P) was established which allows future development of compounds within this series to be carried out based on calculated log P values. Moreover, compounds 13 and 14 show that the optimum logarithm of partition coefficient (log P) should be around 4. 相似文献
204.
Chowdhury MH Lakowicz JR Ray K 《The journal of physical chemistry. C, Nanomaterials and interfaces》2011,115(15):7298-7308
We present a strategy for enhancing the intrinsic emission of the enzyme cofactors flavin adenine dinucleotide (FAD), flavin mononucleotide (FMN) and nicotinamide adenine dinucleotide (NADH). Ensemble studies show that silver island films (SIFs) are the optimal metal enhanced fluorescence (MEF) substrates for flavins and gave emission enhancements of over 10-fold for both FAD and FMN. A reduction in the lifetime of FAD and FMN on SIFs was also observed. Thermally evaporated aluminum films on quartz slides were found to be the optimal MEF substrate for NADH and gave a 5-fold increase in the emission intensity of NADH. We present finite-difference time-domain (FDTD) calculations that compute the enhancement in the radiated power emitting from an excited state dipole emitting in the wavelength range of NADH in close proximity to an aluminum nanoparticle, and a dipole emitting in the emission wavelength of flavins next to a silver nanoparticle. These calculations confirm that aluminum serves as the optimal MEF substrate for NADH and silver was the optimal MEF substrate for flavins. This is because the plasmon resonance properties of aluminum lie in the UV-blue regime and that of silver lie in the visible region. We also present the results of single molecule studies on FMN which show SIFs can both significantly enhance the intrinsic emission from single FMN molecules, significantly reduce their lifetimes and also significantly reduce FMN blinking. This is the first report of the observation of MEF from cofactors both at the ensemble and single molecule level. We hope this study will serve as a platform to encourage the future use of metallic nanostructures to study cofactors using their intrinsic fluorescence to directly monitor enzyme binding reactions without the need of extrinsic labeling of the molecules. 相似文献
205.
The aerial parts and roots of Betonica officinalis were collected from three localities characterized by different ecological conditions to study the natural variability of the chemical composition of the essential oils in this plant. The leaves and inflorescences were collected during the flowering time, whereas the roots were collected at the end of the vegetative period. The plant material was dried at room temperature. The essential oils were obtained by micro-steam hydrodistillation and analyzed using gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). Overall, 69 constituents were identified in all localities and plant parts. The main compositions of the leaves in all localities were alpha-pinene, 1-octen-3-ol, beta-bourbonene, (E)-caryophyllene and germacrene D. The essential oil of the inflorescences was characterized by these main constituents: alpha-pinene, (E)-caryophyllene and trans-beta-farnesene. In all localities, the percentages of alpha-pinene and (E)-caryophyllene were higher in the inflorescences than in the leaves, whereas nonane was the main constituent in the roots. 相似文献
206.
This article studies the three-dimensional boundary layer flow of an elasticoviscous fluid over a stretching surface. Velocity
of the stretching sheet is assumed to be time-dependent. Effect of mass transfer with higher order chemical reaction is further
considered. Computations are made by the homptopy analysis method (HAM). Convergence of the obtained series solutions is explicitly
analyzed. Variations of embedding parameters on the velocity and concentration are graphically discussed. Numerical computations
of surface mass transfer are reported. Comparison of the present results with the numerical solutions is also given. 相似文献
207.
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209.
In this work, electrical measurements were performed on a polymer-dispersed LC sample so that we could demonstrate the temperature dependent molecular behavior, determined according to the electrical response of the system. Experimental results are found to be in favorable accordance with the molecular theory in several aspects. Critical temperatures, order parameters and entropy of transition are acquired for the studied system. 相似文献
210.
A. Botvina I. N. Mishustin M. Blann M. G. Mustafa G. Peilert H. Stöcker W. Greiner 《Zeitschrift für Physik A Hadrons and Nuclei》1993,345(3):297-303
Comparative analysis of three typical models of nuclear disintegration, the statistical multifragmentation model (SMM), the quantum statistical model (QSM) and a generalized evaporation model (GEM), is carried out. The thermodynamical properties of a decaying system as well as observable characteristics in heavy ion collisions predicted by the different models are discussed. It is shown that these models yield quite similar results for low charge yields at higher excitation energies (E/A>6 MeV per nucleon) and it is suggested that the coincidence measurements of the intermediate mass fragment multiplicity and the neutron and proton multiplicity (or alternatively, the total bound charge) may be very useful for deducing the decay mechanism. The GEM is shown to differ from the other models in predicting a high Z residue peak. 相似文献