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201.
Sunandan Gangopadhyay Anirban Saha S. Mukherjee 《International Journal of Theoretical Physics》2016,55(10):4445-4452
The possibility of an emergent universe solution to Einstein’s field equations allowing for an irreversible creation of matter at the expense of the gravitational field is shown. With the universe being chosen as spatially flat FRW spacetime together with equation of state proposed in Mukherjee et al. (Class. Quant. Grav. 23, 6927, 2006), the solution exists when the ratio of the phenomenological matter creation rate to the number density times the Hubble parameter is a number β of the order of unity and independent of time. The thermodynamic behaviour is also determined for this solution. Interestingly, we also find that an emergent universe scenario is present with usual equation of state in cosmology when the matter creation rate is chosen to be a constant. More general class of emergent universe solutions are also discussed. 相似文献
202.
A combined solid and solution phase methodology for the synthesis of a series of mononuclear and polynuclear zinc benzoate complexes is described. The substituent on the aromatic ring and the effect of solvent on deciding the composition of the complexes is presented. From the 4-substituted benzoic acids 4-methylbenzoic acid (ptolH), 4-nitrobenzoic acid (pnitrobenH) and 4-chlorobenzoic acid (pchlorbenH), the mononuclear complexes [Zn(ptol)2(H2O)2], [Zn(pnitroben)2(H2O)(DMSO)2] and [Zn(pchlorben)2py)2] (where DMSO = dimethylsulfoxide, py = pyridine) have been synthesized and structurally characterised. Zinc complexes from the reaction of zinc sulfate heptahydrate with 3-methylbenzoic acid (mtolH) and 2-methylbenzoic acid (otolH), the dinuclear complexes [Zn2(μ2-mtol)4(py)2], [Zn2(μ2-otol)4(py)2], pentanuclear complex [Zn5(μ2-mtol)6(mtol)2(μ3-OH)2 (py)2] and tetranuclear complex [Zn4(μ2-otol)6(μ4-O) (DMSO)2], have been prepared by varying the reaction conditions and the complexes have been structurally characterized. 相似文献
203.
204.
Anirban Karmakar Ana E. Platero‐Prats Lars
hrstrm 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(3):251-254
The structure of 2,3,6,7,10,11‐hexahydroxytriphenylene (hhtp) methanol monosolvate, C18H12O6·CH3OH, has triclinic symmetry (space group P). The compound has a three‐dimensional layered network structure formed by intermolecular hydrogen bonding. Structure analysis with Hirshfeld surfaces is shown to be a sensitive method for comparing π‐stacking effects in the five known solvates of hhtp. The title structure shows slightly weaker π‐stacking than the dihydrate, but stronger π‐stacking than the other three solvates. 相似文献
205.
Here we demonstrate the aqueous synthesis of colloidal nanocrystal heterostructures consisting of the CdTe core encapsulated by CdS/ZnS or CdSe/ZnS shells using glutathione (GSH), a tripeptide, as the capping ligand. The inner CdTe/CdS and CdTe/CdSe heterostructures have type-I, quasi-type-II, or type-II band offsets depending on the core size and shell thickness, and the outer CdS/ZnS and CdSe/ZnS structures have type-I band offsets. The emission maxima of the assembled heterostructures were found to be dependent on the CdTe core size, with a wider range of spectral tunability observed for the smaller cores. Because of encapsulation effects, the formation of successive shells resulted in a considerable increase in the photoluminescence quantum yield; however, identifying optimal shell thicknesses was required to achieve the maximum quantum yield. Photoluminescence lifetime measurements revealed that the decrease in the quantum yield of thick-shell nanocrystals was caused by a substantial decrease in the radiative rate constant. By tuning the diameter of the core and the thickness of each shell, a broad range of high quantum yield (up to 45%) nanocrystal heterostructures with emission ranging from visible to NIR wavelengths (500-730 nm) were obtained. This versatile route to engineering the optical properties of nanocrystal heterostructures will provide new opportunities for applications in bioimaging and biolabeling. 相似文献
206.
Magnetic anisotropy of a set of octahedral Cr(III) complexes is studied theoretically. The magnetic anisotropy is quantified in terms of zero-field splitting (ZFS) parameter D, which appeared sensitive toward ligand substitution. The increased π-donation capacity of the ligand enhances the magnetic anisotropy of the complexes. The axial π-donor ligand of a complex is found to produce an easy-plane type (D > 0) magnetic anisotropy, while the replacement of the axial ligands with π-acceptors entails the inversion of magnetic anisotropy into the easy-axis type (D < 0). This observation enables one to fabricate a single molecule magnet for which easy-axis type magnetic anisotropy is an indispensable criterion. The equatorial ligands are also found to play a role in tuning the magnetic anisotropy. The magnetic anisotropy property is also correlated with the nonlinear optical (NLO) response. The value of the first hyperpolarizability varies proportionately with the magnitude of the ZFS parameter. Finally, it has also been shown that a rational design of simple octahedral complexes with desired anisotropy characteristics is possible through the proper ligand selection. 相似文献
207.
To understand the modifications of the hydrogen bond network of water by ionic solutes, power spectra as well as static distributions of the potential energies of tagged solvent molecules and solute ions have been computed from molecular dynamics simulations of aqueous NaCl solutions. The key power spectral features of interest are the presence of high-frequency peaks due to localized vibrational modes, the existence of a multiple time scale or 1/falpha frequency regime characteristic of networked liquids, and the frequency of crossover from 1/falpha type behavior to white noise. Hydrophilic solutes, such as the sodium cation and the chloride anion, are shown to mirror the multiple time scale behavior of the hydrogen bond network fluctuations, unlike hydrophobic solutes which display essentially white noise spectra. While the power spectra associated with tagged H2O molecules are not very sensitive to concentration in the intermediate frequency 1/falpha regime, the crossover to white noise is shifted to lower frequencies on going from pure solvent to aqueous alkali halide solutions. This suggests that new and relatively slow time scales enter the picture, possibly associated with processes such as migration of water molecules from the hydration shell to the bulk or conversion of contact ion pairs into solvent-separated ion pairs which translate into variations in equilibrium transport properties of salt solutions with concentration. For anions, cations, and solvent molecules, the trends in the alpha exponents of the multiple time scale region and the self-diffusivities are found to be strongly correlated. 相似文献
208.
The retarded interaction between an electron and a spin-0 nucleus is derived from electrodynamical perturbation theory. The contribution of retardation at order v(2)c(2) mimics the Breit interaction [Phys. Rev. 34, 553 (1929); 36, 388 (1930); 39, 616 (1932)] with the Dirac matrix alpha(2) being replaced by p(2)m(2)c where p(2) is the linear momentum operator for the nucleus. An effective one-electron retardation operator is obtained in relative coordinates, and this can be used through all orders in perturbation theory without any problem of infinite degeneracy. A few steps of unitary transformation lead to the nonrelativistic limit. The leading terms in retardation corrections to energy are of order (m(e)m(n))alpha(2)Z(4)(alpha(2)m(e)c(2)). The implications for atomic systems are discussed. 相似文献
209.
Anirban Pal 《Journal of luminescence》2010,130(11):1975-1982
The enhancement of the excited state intramolecular proton transfer (ESIPT) emission of 3-hydroxy-2-naphthoic acid (3HNA) in presence of poly N-vinyl-2-pyrrolidone (PVP) has been investigated by time resolved fluorescence and anisotropy measurement. In other water soluble polymers and monomers there is no enhancement of the ESIPT emission of 3HNA. The microenvironment of the probe in PVP-water mixture is investigated by comparing the ESIPT emission of 3HNA in mixed solvents of acetonitrile-toluene. The anisotropy, rotational correlation time and the blue shift observed in the ESIPT emission in PVP-water mixture have been ascribed to both the polarity and the motional restriction of the probe imposed by the bound water region of PVP. 相似文献
210.
Our recent observations ort higher order nonclassicality are described. Recently we have shown that a generalized notion of
higher order nonclassicality (in terms of higher order moments) can be introduced. Under this generalized framework of higher
order nonclassicality, conditions of higher order squeezing and higher order subpoissonian photon statistics are derived.
Further, with the help of simple density matrices, it is shown that the higher order antibunching (HOA) and higher order subpoissonian
photon statistics (HOSPS) are not the manifestation of the same phenomenon and consequently it is incorrect to use the condition
of HOA as a test of HOSPS. It is established that the HOA and HOSPS may exist even in absence of the corresponding lower order
phenomenon. It is also shown that the potential sources of Single photon must satisfy the condition of HOA. Most of the intermediate
states are shown to satisfy the criteria of HOA. A protocol for comparison of potential Single photon sources (SPS) is reported
here and the protocol is used to compare some of the existing proposals of SPS. Further, it is shown that it is possible to
derive an arbitrarily large number of criterion for higher order nonclassicality but all of them does not yield new and interesting
information. 相似文献