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101.
A strain-optic law for a certain class of birefringent fiber-reinforced composite materials is developed. The strain-optic law requires both mechanical and optical characterization of the material. Previous investigations have hypothesized the existence of three independent optical properties for the anisotropic birefringent material. The strain-optic relation developed in this study, however, requires only a single strain-optic coefficient, coupled with four independent mechanical material properties, for prediction of the optical response of a birefringent anisotropic material. Experimental results are presented which show good agreement with the developed strain-optic relation. Finally, the isoclinic parameter is investigated and preliminary evidence is presented which indicates a correspondence between principal-strain direction and optical isoclinic angle. 相似文献
102.
Experimental techniques are developed to study and measure the shear-wave velocity in an aluminum cylindrical shell subjected to a radial impact. The radial impact is obtained by exploding an electrical detonator inserted in plastic plugs mounted on the end of the shell. Strain gages, mounted on the outside surface of the shell at various axial locations, are used to obtain oscilloscope traces from which the shear-wave velocity can be calculated. 相似文献
103.
Planar chiral arenetricarbonylchromium complexes have been intensively investigated and they have been applied as valuable building blocks for asymmetric synthesis and as ligands for asymmetric catalysis. In contrast, in the field of the isoelectronic cationic [(η(6)-arene)Mn(CO)(3)](+) complexes, until these last 10 years, very few studies were published involving nonracemic planar chiral cationic complexes and their potential applications, certainly because of the difficult access to enantiopure starting material. In 2009, however, the discovery of the first resolution of such compounds opened a new area for their application in the field of organic as well as of organometallic enantioselective syntheses. We felt it important to write a review on this subject to give an up-to-date summary of the methodologies used to prepare enantiomerically pure planar chiral neutral [(η(5)-cyclohexadienyl)Mn(CO)(3)] and cationic [(η(6)-arene)Mn(CO)(3)](+) complexes as well as their potential in enantioselective synthesis. 相似文献
104.
Here we report the syntheses and crystal structures of a series of cobalt(II) and nickel(II) complexes derived from (R)NP2 ligands (where R = OMe(Bz), H(Bz), Br(Bz), Ph) bearing ethylene linkers between a single N and two P donors. The Co(II) complexes generally adopt a tetrahedral configuration of general formula [(NP2)Co(I)(2)], wherein the two phosphorus donors are bound to the metal center but the central N-donor remains unbound. We have found one case of structural isomerism within a single crystal structure. The Co(II) complex derived from (Bz)NP2 displays dual coordination modes: one in the tetrahedral complex [((Bz)NP2)Co(I)(2)]; and the other in a square pyramidal variant, [((Bz)NP2)Co(I)(2)]. In contrast, the Ni(II) complexes adopt a square planar geometry in which the P(Et)N(Et)P donors in the ligand backbone are coordinated to the metal center, resulting in cationic species of formula [((R)NP2)Ni(I)](+) with iodide as counterion. All Ni(II) complexes exhibit sharp (1)H and (31)P spectra in the diamagnetic region. The Co(II) complexes are high-spin (S = 3/2) in the solid state as determined by SQUID measurements from 4 to 300 K. Solution electron paramagnetic resonance (EPR) experiments reveal a high-spin/low-spin Co(II) equilibrium that is dependent on solvent and ligand substituent. 相似文献
105.
Rose RA Greaves SJ Oliver TA Clark IP Greetham GM Parker AW Towrie M Orr-Ewing AJ 《The Journal of chemical physics》2011,134(24):244503
The dynamics of reactions of CN radicals with cyclohexane, d(12)-cyclohexane, and tetramethylsilane have been studied in solutions of chloroform, dichloromethane, and the deuterated variants of these solvents using ultraviolet photolysis of ICN to initiate a reaction. The H(D)-atom abstraction reactions produce HCN (DCN) that is probed in absorption with sub-picosecond time resolution using ~500 cm(-1) bandwidth infrared (IR) pulses in the spectral regions corresponding to C-H (or C-D) and C≡N stretching mode fundamental and hot bands. Equivalent IR spectra were obtained for the reactions of CN radicals with the pure solvents. In all cases, the reaction products are formed at early times with a strong propensity for vibrational excitation of the C-H (or C-D) stretching (v(3)) and H-C-N (D-C-N) bending (v(2)) modes, and for DCN products there is also evidence of vibrational excitation of the v(1) mode, which involves stretching of the C≡N bond. The vibrationally excited products relax to the ground vibrational level of HCN (DCN) with time constants of ~130-270 ps (depending on molecule and solvent), and the majority of the HCN (DCN) in this ground level is formed by vibrational relaxation, instead of directly from the chemical reaction. The time-dependence of reactive production of HCN (DCN) and vibrational relaxation is analysed using a vibrationally quantum-state specific kinetic model. The experimental outcomes are indicative of dynamics of exothermic reactions over an energy surface with an early transition state. Although the presence of the chlorinated solvent may reduce the extent of vibrational excitation of the nascent products, the early-time chemical reaction dynamics in these liquid solvents are deduced to be very similar to those for isolated collisions in the gas phase. The transient IR spectra show additional spectroscopic absorption features centered at 2037 cm(-1) and 2065 cm(-1) (in CHCl(3)) that are assigned, respectively, to CN-solvent complexes and recombination of I atoms with CN radicals to form INC molecules. These products build up rapidly, with respective time constants of 8-26 and 11-22 ps. A further, slower rise in the INC absorption signal (with time constant >500 ps) is attributed to diffusive recombination after escape from the initial solvent cage and accounts for more than 2/3 of the observed INC. 相似文献
106.
Yun JH Ng YH Huang S Conibeer G Amal R 《Chemical communications (Cambridge, England)》2011,47(40):11288-11290
The CuInS(2) (CIS) nanoparticles were wrapped uniformly throughout the inner and outer walls of TNTs (TNT) by using square wave pulsed-electrodeposition. This structure enables the CuInS(2)-TiO(2) (CIS-TNT) to exhibit p-n junction diode behavior and enhanced photoelectrochemical properties. 相似文献
107.
Carneiro VA Santos HS Arruda FV Bandeira PN Albuquerque MR Pereira MO Henriques M Cavada BS Teixeira EH 《Molecules (Basel, Switzerland)》2011,16(1):190-201
Croton nepetaefolius is a native plant from northeastern Brazil that belongs to the Euphorbiaceae family. The biological action of this plant has been extensively explored, being the secondary metabolites responsible for its properties alkaloids, diterpenes, and triterpenes. This study aimed to evaluate the ability of casbane diterpene (CD), isolated from the ethanolic extract of C. nepetaefolius, to inhibit microbial growth and biofilm formation of several clinical relevant species (bacteria and yeasts). It was found that CD possessed biocidal and biostatic activity against the majority of the species screened, with minimal active concentrations ranging between 125 and 500 μg/mL. In addition, it was observed that biofilm formation was inhibited even when the planktonic growth was not significantly affected. In conclusion, CD showed potential to be a natural tool for the treatment of diseases caused by different infectious microorganisms. 相似文献
108.
Levard C Masion A Rose J Doelsch E Borschneck D Olivi L Chaurand P Dominici C Ziarelli F Thill A Maillet P Bottero JY 《Physical chemistry chemical physics : PCCP》2011,13(32):14516-14522
The synthesis protocol for Ge-imogolite (aluminogermanate nanotubes) consists of 3 main steps: base hydrolysis of a solution of aluminum and germanium monomers, stabilization of the suspension and heating at 95 °C. The successful synthesis of these nanotubes was found to be sensitive to the hydrolysis step. The impact of the hydrolysis ratio (from n(OH)/n(Al) = 0.5 to 3) on the final product structure was examined using a combination of characterization tools. Thus, key hydrolysis ratios were identified: n(OH)/n(Al) = 1.5 for the formation of nanotubes with structural defects, n(OH)/n(Al) = 2 for the synthesis of a well crystallized Ge imogolite and n(OH)/n(Al) > 2.5 where nanotube formation is hindered. The capability of controlling the degree of the nanotube's crystallinity opens up interesting opportunities in regard to new potential applications. 相似文献
109.
Unresolved transition arrays (UTAs) are a method of approximating complex atomic physics in plasma opacity calculations, and as such are very important in modern plasma dynamic simulations. In this paper we use full atomic physics calculations to test various UTA models, paying particular attention to the lineshape and its effect on the mean opacity. We find that a Gaussian lineshape is sufficient provided that the line width is correctly determined. This width can be calculated using existing formulae, or approximated by neglecting correlations between term line energies and strengths or the selection rules on term - term transitions. We have quantified transition array narrowing due to correlations for a set of iron transitions and shown that a simple model for these incurs fairly large random errors. The neglect of the selection rules is also seen to result in random errors of up to an order of magnitude. These results may prove very useful in the future development of opacity codes, in particular those intended to run in line with hydrodynamic simulations. 相似文献
110.
Let An(ω) be the nxn matrix An(ω)=(aij with aij=ωij, 0?i,j?n?1, ωn=1. For n=rs we show =(Ar?Is)Tsr(Ir?As). When r and s are relatively prime this identity implies a wide class of identities of the form PAn(ω)QT=Ar(ωαs)?As(ωβr). The matrices Psr, Prs, P, and Q are permutation matrices corresponding to the “data shuffling” required in a computer implementation of the FFT, and Tsr is a diagonal matrix whose nonzeros are called “twiddle factors.” We establish these identities and discuss their algorithmic significance. 相似文献