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151.
An efficient biological route to production of gold nanoparticles which allows the nanoparticles to be easily recovered remains elusive. Live cells of the green microalga Chlorella vulgaris were incubated with a solution of gold chloride and harvested by centrifugation. Nanoparticles inside intact cells were identified by transmission electron microscopy and confirmed to be metallic gold by synchrotron based X-ray powder diffraction and X-ray absorption spectroscopy. These intracellular gold nanoparticles were 40–60 nm in diameter. At a concentration of 1.4% Au in the alga, a better than 97% recovery of the gold from solution was achieved. A maximum of 4.2% Au in the alga was obtained. Exposure of C. vulgaris to solutions containing dissolved salts of palladium, ruthenium, and rhodium also resulted in the production of the corresponding nanoparticles within the cells. These were surmised to be also metallic, but were produced at a much lower intracellular concentration than achieved with gold. Iridium was apparently toxic to the alga. No nanoparticles were observed using platinum solutions. C. vulgaris provides a possible route to large scale production of gold nanoparticles.  相似文献   
152.
We discuss the dynamical generation of some low-lying 1/2+ Σ 's and Λ 's in two-meson one-baryon systems. These systems have been constructed by adding a pion in the S -wave to the ˉN pair and its coupled channels, where the 1/2- Λ(1405) -resonance gets dynamically generated. We solve Faddeev equations in the coupled-channel approach to calculate the T -matrix for these systems as a function of the total energy and the invariant mass of one of the meson-baryon pairs. This squared T -matrix shows peaks at the energies very close to the masses of the strangeness -1 , 1/2+ resonances listed in the particle data book.  相似文献   
153.
We study the single production of fourth-family quarks through the process ppQjX at the Large Hadron Collider (LHC). We have calculated the decay widths and branching ratios of the fourth-family quarks (b′ and t′) in the mass range 300–800 GeV. The cross sections for the signal and background processes have been calculated in a Monte Carlo framework. It is shown that the LHC can discover single t′ and b′ quarks if the CKM matrix elements |V tq |,|V qb|≳0.01.  相似文献   
154.
155.
Threonine Schiff base derived 2-hydroxy-1-naphthaldehyde and threonine has been isolated and investigated. The stoichiometry of this compound was derived from the results of elemental analyses, IR, 1H-NMR and UV spectroscopic techniques. X-ray diffraction method was also used to obtain the single-crystal structure. The compound crystallizes in the space group P21 with cell dimensions a=5.109(2), b=11.334(2), and β=91(3)° with Z=2. The molecule has phenol-imine tautomeric form in the crystal structure. Some of bond lengths and angles found in the molecular structure are distorted due to π-electron delocalization and steric effect of naphthylidene and threonine groups.  相似文献   
156.
Starting from a consistent SU(6) extension of the Weinberg-Tomozawa (WT) meson-baryon chiral Lagrangian ( Phys. Rev. D 74, 034025 (2006)), we study the s-wave meson-baryon resonances in the strangeness S = - 3 and negative-parity sectors. Those resonances are generated by solving the Bethe-Salpeter equation with the WT interaction used as kernel. The considered mesons are those of the 35-SU(6)-plet, which includes the pseudoscalar (PS) octet of pions and the vector (V) nonet of the rho-meson. For baryons we consider the 56-SU(6)-plet, made of the 1/2+ octet of the nucleon and the 3/2+ decuplet of the Delta. Quantum numbers I(J P) = 0(3/2-) are suggested for the experimental resonances Ω *(2250)- and Ω *(2380)-. Among other, resonances with I = 1 are found, which minimal quark content is sssˉl', being s the strange quark and l, l' any of the the light up or down quarks. A clear signal for such a pentaquark would be a baryonic resonance with strangeness -3 and electric charge -2 or 0, in proton charge units. We suggest looking for K - Ξ - resonances with masses around 2100 and 2240MeV in the sector 1(1/2-), and for π ± Ω - and K - Ξ *- resonances with masses around 2260MeV in the sector 1(3/2-).  相似文献   
157.
Differential cross-section and single polarization observables in the process γpK + Λ are investigated within a constituent-quark model and a dynamical coupled-channel formalism. The effects of two new nucleon resonances and of the K *(892)- and K1(1270)-exchanges are briefly presented.  相似文献   
158.
The hyperspherical adiabatic expansion is combined with complex scaling and used to calculate low-lying nuclear resonances of 12C in the 3α model. We use Ali-Bodmer potentials and compare results for other potentials α-α with similar 8Be properties. A three-body potential is used to adjust the 12C resonance positions to desired values extending the applicability of the method to many-body systems decaying into three α-particles. For natural choices of three-body potentials we find 14 resonances below the proton separation threshold, i.e. two 0+, three 2+, two 4+, one of each of 1±, 2-, 3±, 4-, and 6+. The partial-wave decomposition of each resonance is calculated as a function of the hyperradius. Strong variation is found from small to large distance. The connection to previous experimental and theoretical results is discussed and agreements as well as disagreements are emphasized.  相似文献   
159.
Double-lepton polarization asymmetries in Λb→Λℓ+- decay are calculated in the universal extra dimension (UED) model. It is found that numerous double-lepton polarization asymmetries are very sensitive to the UED model and therefore can be a very useful tool for establishing new physics predicted by the UED model. PACS 12.60.-i; 13.30.-a; 14.20.Mr  相似文献   
160.
N,N′‐diethoxy‐4,4′‐azobis(pyridinium) hexafluorophosphate (DEAP) has been synthesized by alkylation of the corresponding N‐oxide and characterized. DEAP exhibits UV induced cis–trans isomerization with absorptions at around λ = 459 and 360 nm, respectively. The ability of the DEAP ion to act as a photoinitiator for the cationic polymerization of cyclohexene oxide and N‐vinylcarbazole is demonstrated. The initiation step involves the decay of the excited state of the trans form of the salt with homolytic bond rupture of the nitrogen–oxygen bond. Its potential use as a photoinitiator for free radical polymerization is also demonstrated using methyl methacrylate monomer as the example.

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