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991.
Swift heavy ions interact predominantly through inelastic scattering while traversing any polymer medium and produce excited/ionized atoms. Here samples of the polycarbonate Makrofol of approximate thickness 20 μm, spin coated on GaAs substrate were irradiated with 50 MeV Li ion (+3 charge state). Build-in modifications due to irradiation were studied using FTIR and XRD characterizations. Considerable changes have been observed in the polymer while varying the fluence from 1E11 ion/cm2 to 1E13 ion/cm2 Li ions. AFM images of the surface modifications caused by ion irradiation on the polymer are also presented.   相似文献   
992.
Artificial Neural Networks are developed as an important technique for equalization and have been widely used to mitigate the nonlinear effects in coherent optical systems. For the compensation of nonlinearities in coherent optical orthogonal frequency division multiplexing technique, the most popular artificial neural network model is a multilayer perceptron (MLP), as it is able to perform complex mapping between input and output spaces with significant success. However due to the complexity of multilayer perceptron nonlinear equalizer (MLP-NLE) model training of neural network is difficult. To overcome computational complexity issues of MLP-NLE, a single neuron based functional link artificial neural network nonlinear equalizer (FLANN-NLE) has been developed in this paper. Better performance of an equalizer is attributed to the usage of aPSO-BP algorithm for training the FLANN-NLE. The proposed FLANN-NLE surpasses the existing works both in terms of Q-Factor and computational complexity. For a fiber length of 1000 km and at launch power of ?6 dBm, the improvement in Q-Factor is approximately equal to 3.3 and 1 dB in contrast to the previously reported values of approximately 3 and 0.7 dB at bit rate of 40 and 80 Gbps respectively.  相似文献   
993.
The paper presents an accurate charge control model for a fully strained (FS), and partially relaxed (PR) lattice mismatched AlGaN/GaN HEMT, taking into consideration the effect of spontaneous and piezoelectric polarization. The model also accounts for the mobility degradation with increase in temperature, which is one of the major causes in deterioration of the driving current. By using the variation of band gap with temperature, the temperature dependence on threshold voltage, sheet carrier concentration and drain current is studied. Further, the temperature variation shows the applicability of the device in a variable thermal environment. A close agreement of calculated data with simulated/experimental data proves the validity of the model.  相似文献   
994.
The synthesis of 4′-(2-methylphenyl)-2,2′:6′,2″-terpyridine (L) has been improved. The coordination chemistry of the ligand was explored using Ni(II), Cu(II), Zn(II), and Ag(I) ions. X-ray crystallography, elemental analysis, NMR, and mass spectrometry were used to characterize the 13 new compounds that have been synthesized. Under different reaction conditions, Ni(II), Cu(II), and Zn(II) produced discrete complexes, sometimes containing more than one metal ion, while Ag(I) furnished a polymeric spiral complex in which the central pyridine nitrogen of each terpyridine ligand bridges two Ag(I) ions. Crystallographically characterized complexes are [Ni(L)2]Cl2, [Ni2Cl4(L)2], [Ni(L)(OH2)3]Cl2, [Ni(L)2]Br2, [Cu(L)(OH2)(OSO3)], [Cu3Cl6(L)2], [Cu(L)(OH)(OH2)2]PF6, [Cu(L)2](OTf)2, [Cu(L)(OAc)2], [Zn(L)(OAc)2], [Zn(L)Cl2], [Zn(L)2](NO3)2, [{Ag2(μ-L)2(μ-NO3)}n](NO3)n.  相似文献   
995.
The photophysics of green fluorescent protein (GFP) is remarkable because of its exceptional property of excited state proton transfer (ESPT) and the presence of a functional proton wire. Another interesting property of wild‐type GFP is that its absorption and fluorescence excitation spectra are sensitive to the presence of polar organic solvents even at very low concentrations. Here, we use a combination of methodologies including site‐specific mutagenesis, absorption spectroscopy, steady‐state and time‐resolved fluorescence measurements and all‐atom molecular dynamics simulations in explicit solvent, to uncover the mechanism behind the unique spectral sensitivity of GFP toward organic solvents. Based on the evidences provided herein, we suggest that organic solvent‐induced changes in the proton wire prevent ground state movement of a proton through the wire and thus bring about the spectral changes observed. The present study can not only help to understand the mechanism of proton transfer by further dissecting the intricate steps in GFP photophysics but also encourages to develop GFP‐based organic solvent biosensors.  相似文献   
996.
Navjeet Kaur 《合成通讯》2019,49(7):879-916
Nitrogen, oxygen, and sulfur-containing heterocycles have a wide range of biological activities. Metal catalysts are used in organic reactions with high activity. New methods have been explored for the synthesis of heterocyclic compounds in the past few years. The preparation of heterocycles with the assistance of metal catalyst is becoming a highly rewarding strategy in organic synthesis. In this review article, the synthesis of seven and higher-membered heterocycles is presented using copper as a catalyst.  相似文献   
997.
The metal catalyzed synthesis of heterocycles is becoming an important and highly rewarding protocol in organic synthesis. Traditional approaches require expensive or highly specialized equipment or would be of limited use to the synthetic organic chemist due to their highly inconvenient approaches. Titanium-mediated cyclization reactions have been recognized as some of the simplest and useful tools for regio- as well as stereoselective syntheses of five-membered N-heterocycles. This review summarizes the applications of titanium catalysts with emphasis of their synthetic applications for different heterocylces. This review covered interesting discoveries in the past few years.  相似文献   
998.
The welcome and adaptation of optical wireless technology by the modern era has brought forward the concept of an inter-satellite free-space optical communication system. In the present work, I study the combined effect of selection of different operating wavelengths and detector types along with the pointing errors at the transmitter and receiver side on the performance of an inter-satellite free-space optical link. The link performance has been optimized by measuring and analyzing the bit error rate and quality-factor of received signal under different scenarios. Performance of the inter-satellite link has also been investigated considering different modulation formats and data rates for LEO and MEO distances.  相似文献   
999.
Optical and Quantum Electronics - We have investigated the potential of using the E-field induced birefringence for improving the sensitivity of uniaxial anisotropic slab waveguide sensor based on...  相似文献   
1000.
A highly sensitive and selective potentiometric and voltammteric assay for the detection of Fe3+ using (E)‐3‐((2‐(2‐(2‐aminoethylamino) ethylamino) ethylimino)methyl)‐4H‐chromen‐4‐one (IFE(III)) ionophore was developed. To demonstrate the ion‐to‐electron transfer ability of MWCNT, these were incorporated in the ion‐selective membrane and response characteristics of Fe3+ electrode was compared with those of the traditional ion selective electrode. The electrode showed an improved Nernstian slope, lower detection limit, response time of less than 5 s and working in a pH range of 3.0 to 8.0. Differential pulse voltammetric studies were performed for IFE(III)‐Fe3+ complex in DMSO solvent medium at glassy carbon (GC) electrode. A linear relationship between the cathodic peak current and concentration of Fe3+ was observed in the range of 1.6×10?5 to 4.4×10?5 mol/L with a detection limit of 5.2×10?8 mol/L. The electrode shows remarkable selectivity for Fe3+ ions over alkali, alkaline earth, transition and heavy metal ions. The optimized electrode was successfully applied for the determination of Fe3+ ion in different real‐life samples using potentiometric technique. Theoretical calculations were used to support the complexation behavior of Fe3+ with IFE(III).  相似文献   
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