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101.
Three single electron charge transfer redox reactions have been studied using the faradaic rectification method. The kinetic parameters obtained for the ferricyanide-ferrocyanide redox couple are α=0.49, ka0=12×10?2 cm s?1; for the chromic-chromous system α=0.47, ka0=2×10?3 cm s?1 and for the titanic-titanous reaction α=0.49 and kao=6×10?4 cm s?1 at 27°C. 相似文献
102.
The role of anion-exchange resin beads in the initiation of reactions of tertiary amines with 2,4-dinitrophenylhydrazine has been explored. This reagent has been used for the selective detection and determination of aliphatic amines. Radiochemical studies have been performed to show that the coloured species is adsorbed but not exchanged on ion-exchange beads. A model for the interaction is proposed. 相似文献
103.
Summary Amorphous and anatase-type hydrous titanium dioxides showed typical amphoteric ion-exchange properties. The ion-exchange selectivity for bivalent transition metal ions was studied as a function of both pH and metal ion concentration in ammonium nitrate media. The selectivity series was Co<Ni<Mn<Zn<Cd<Cu for the amorphous and Ni<Co<Mn<Zn<Cd<Cu for the anatase-type material. The separation factor on the anatase-type material is larger than on the amorphous material. Effective group separation of Co–Ni and Zn–Cd–Cu could be achieved on an ion-exchange column containing the anatase-type hydrous titanium dioxide.Part XXIV in a series on synthetic inorganic ion-exchange materials. 相似文献
104.
105.
Natalija van Well Sitaram Ramakrishnan Ketty Beauvois Navid Qureshi Eric Ressouche Markos Skoulatos Robert Georgii Oksana Zaharko Sander van Smaalen 《Annalen der Physik》2020,532(7):2000147
The triangular antiferromagnetic Cs2CuCl4-xBrx mixed system is studied by neutron single-crystal diffraction in magnetic field. It shows a rich magnetic phase diagram consisting of four regimes depending on the Br concentration and is characterized by different exchange coupling mechanisms. For the investigated compositions from regime I (0 < x ≤ 1.5), a critical magnetic field Bc is found for a Br concentration x = 0.8 at Bc = 8.10(1) T and for x = 1.1 at Bc = 7.73(1) T and from regime IV (3.2 < x < 4) for x = 3.3 at Bc = 0.99(3) T. For magnetic fields larger than the respective Bc, magnetic superlattice reflections of these compounds are not found. The incommensurate magnetic wave vector q = (0, 0.470, 0) appears below the ordering temperature TN = 0.51(1) K for Cs2CuCl3.2Br0.8, and q = (0, 0.418, 0) below TN = 1.00(6) K for Cs2CuCl0.3Br3.7. Neutron diffraction experiments at around 60 mK for x = 3.7 in a magnetic field show the critical magnetic field at Bc = 7.94(16) T and the formation of the second magnetic phase at around 8.5 T depending on the temperature. Inelastic neutron scattering experiments for the compound from regime III (2 < x ≤ 3.2) with x = 2.2 show dynamical correlations at a temperature around 50 mK giving evidence for a spin liquid phase. 相似文献
106.
Mirza Nadeem Ahmad Sohail Nadeem Mohsin Javed Shahid Iqbal Sadaf ul Hassan Samar O. Aljazzar Eslam B. Elkaeed Rami Adel Pashameah Eman Alzahrani Abd-ElAziem Farouk Mohammed T. Alotaibi Hisham S. M. Abd-Rabboh 《Molecules (Basel, Switzerland)》2022,27(17)
The synthesis of MMT and poly(o-anisidine) (MMT/POA) clay nanocomposites was carried out by using the chemical oxidative polymerization of POA and MMT clay with POA, respectively. By maintaining the constant concentration of POA, different percentage loads of MMT clay were used to determine the effect of MMT clay on the properties of POA. The interaction between POA and MMT clay was investigated by FTIR spectroscopy, and, to reveal the complete compactness and homogeneous distribution of MMT clay in POA, were assessed by using scanning-electron-microscope (SEM) analysis. The UV–visible spectrum was studied for the optical and absorbance properties of MMT/POA ceramic nanocomposites. Furthermore, the horizontal burning test (HBT) demonstrated that clay nanofillers inhibit POA combustion. 相似文献
107.
108.
Emergence of classicality from quantum mechanics, a hotly debated topic, has had no satisfactory resolution so far. Various approaches including decoherence and gravitational interactions have been suggested. In the present work, the Schrödinger–Newton model is used to study the role of semi-classical self-gravity in the evolution of massive spin-1/2 particles in a Stern-Gerlach experiment. For small mass, evolution of the initial wavepacket in a spin superposition shows a splitting in the magnetic field gradient into two trajectories as in the standard Stern–Gerlach experiment. For larger mass, the deviations from the central path are less than in the standard Stern–Gerlach case, while for high enough mass, the wavepacket does not split, and instead follows the classical trajectory for a magnetic moment in inhomogeneous magnetic field. This indicates the emergence of classicality due to self-gravitational interaction when the mass is increased. In contrast, decoherence which is a strong contender for emergence of classicality, leads to a mixed state of two trajectories corresponding to the spin-up and spin-down states, and not the classically expected path. The classically expected path of the particle probably cannot be explained even in the many-worlds interpretation of quantum mechanics. Stern–Gerlach experiments in the macroscopic domain are needed to settle this question. 相似文献
109.
We introduce balanced polyominoes and show that their ideal of inner minors is a prime ideal and has a squarefree Gröbner basis with respect to any monomial order, and we show that any row or column convex and any tree‐like polyomino is simple and balanced. 相似文献
110.
Afzal Shah Muhammad Zaheer Rumana Qureshi Zareen Akhter Muhammad Faizan Nazar 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2010,75(3):1082-1087
Cyclic voltammetry (CV) coupled with UV–vis and fluorescence spectroscopy were used to probe the interaction of potential anticancer drug, 4-nitrophenylferrocene (NFC) with DNA. The electrostatic interaction of the positively charged NFC with the anionic phosphate of DNA was evidenced by the findings like negative formal potential shift in CV, ionic strength effect, smaller bathochromic shift in UV–vis spectroscopy, incomplete quenching in the emission spectra and decrease in viscosity. The diffusion coefficients of the free and DNA bound forms of the drug were evaluated from Randles–Sevcik equation. The binding parameters like binding constant, ratio of binding constants (Kred/Kox), binding site size and binding free energy were determined from voltammetric data. The binding constant was also determined from UV–vis and fluorescence spectroscopy with a value quite close to that obtained from CV. 相似文献