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951.
B.J. Chen Y.D. Li C.D. Feng H.M. Zhang C. Yan W.B. Xiao 《Magnetic resonance in chemistry : MRC》2020,58(10):921-928
The local structures and the g factors gi (i = x, y, z) for Ni3+ centers in Na2Zn(SO4)2·4H2O (DPPH) and K2Zn(SO4)2·6H2O (PHZS) crystals are theoretically studied by using the perturbation formulas of the g factors for a 3d7 ion with low spin (S = 1/2) in orthorhombically compressed octahedra. In these formulas, the contributions to g factors from both the spin-orbit coupling interactions of the central ion and ligands are taken into account, and the required crystal-field parameters are estimated from the superposition model and the local geometry of the systems. Based on the calculations, the Ni-O bonds are found to suffer the axial compression δz (or Δz) of about 0.111 Å (or 0.036 Å) along the z-axis for Ni3+ centers in DPPH (or PHZS) crystals. Meanwhile, the Ni-O bonds may experience additional planar bond length variation δx (≈0.015 Å) along x- and y-axes for the orthorhombic Ni3+ center in DPPH. The theoretical g factors agree well with the experimental data. The obtained local structural parameters for both Ni3+ centers are discussed. 相似文献
952.
An ns Nd:YAG pulsed laser was used to deposit thin films in a vacuum and to generate nanoparticles in the water of Ni, Ti, and NiTi alloys. Laser ablation was measured in terms of removing mass per laser pulse. The laser-generated plasma in vacuum was characterized in terms of temperature and energy of emitted particles. The ablation in water produces nanoparticles with dimensions of the order of 25 nm and solutions with concentrations of the order of some mg/ml. The NiTi alloy stoichiometry is well reported in the deposited thin film and in the composition of the produced nanoparticles. 相似文献
953.
A stable nickel‐decorated SBA‐15 nanocomposite (Ni/TCH@SBA‐15) was synthesized through surface modification of silica nanoparticles with 3‐chloropropyltriethoxysilane (CPTES) and thiocarbohydrazide (TCH) followed by metal–ligand coordination with Ni (II). The structure of this organometallic nanocomposite was characterized by Fourier transform‐infrared, field emission‐scanning electron microscopy, EDAX, transmission electron microscopy, atomic absorption spectroscopy and N2 adsorption–desorption (Brunauer–Emmett–Teller) techniques. The catalytic performance of Ni/TCH@SBA‐15 (NNTS‐15) was determined for the synthesis of 2‐aryl‐substituted benzimidazoles and 2,3‐dihydroperimidines. The excellent yields within shorter reaction times, simplicity of catalytic methods, non‐toxicity and clean reactions, mild reaction conditions and easy work‐up procedure are the important merits of these synthetic protocols. Moreover, the Ni (II) bonded to the SBA‐15 surface was stable under the catalytic reaction conditions resulting in its efficient recycling and reuse. 相似文献
954.
A series of Ni supported on activated carbon are prepared by excessive impregnation and the desulfurization activity is investigated. It has been shown that the activated carbon-supported Ni is an efficient solid catalyst for flue gas desulfurization. The activated carbon treated by HNO3 exhibits high desulfurization activity, and different amounts of loaded-Ni on activated carbon significantly influence the desulfurization activity. The catalysts are studied by X-ray diffraction (XRD) and X-ray photoelectr... 相似文献
955.
Electrocarboxylation of Carbon Dioxide with Polycyclic Aromatic Hydrocarbons Using Ni as the Cathode
Using Ni cathode and Al sacrificial anode, the electrocarboxylation of polycyclic aromatic hydrocarbons (naphthalene, 5‐methylnaphthalene, anthracene, phenanthrene and 1H‐indene) with carbon dioxide (4 MPa) could be successfully performed in an undivided cell containing n‐Bu4NBr‐DMF supporting electrolyte with a constant current at room temperature, affording the corresponding trans‐dicarboxylic acids in good to excellent yields (62% –90%). Among the examined cathode materials (Ni, Pt, Ag, Cu and Zn), Ni and Pt cathodes exhibited a good catalytic activity for the electrocarboxylations. In addition, the experimental results indicated that electrolytic conditions (conducting salts, electricity, CO2 pressure and temperature) could also affect the result of the electrocarboxylation. According to the results of the electrocarboxylations and CV (cyclic voltammetry), a possible electrochemical reaction mechanism was also proposed. 相似文献
956.
In this paper, the high-order perturbation formulas of spin-Hamiltonian (SH) parameters (g factors g, g and zero-field splitting D), including both the crystal-field (CF) and for the first time charge-transfer (CT) mechanisms, are established for 3d8 ions in trigonal octahedral clusters. By using these formulas, the SH parameters of Ni2+ ions in CsMgX3 (X=Cl, Br, I) crystals are calculated. The results are consistent with the experimental values. The calculations suggest that the sign of QCT (Q=Δg, Δg or D, where the g-shift Δgi=gi−ge, ge≈2.0023 is the value of free-electron) due to CT mechanism is the same as that of the corresponding QCF due to CF mechanism, and the relative importance of CT mechanism (characterized by QCT/QCF) increases with the increasing atomic number of ligand X. So, for the 3dn MLm clusters with ligand having large atomic number, the reasonable theoretical explanations of all SH parameters should take both CF and CT mechanisms into account. The defect structure of (NiX6)4− impurity centers in CsMgX3:Ni2+ crystals is also considered in our model. 相似文献
957.
Nona Ghasemi Hamedani Hassan Arabi Gholam Hossein Zohuri Francis S. Mair Andrew Jolleys 《Journal of polymer science. Part A, Polymer chemistry》2013,51(7):1520-1532
The reaction of N‐(4‐(mesitylamino)pent‐3‐en‐2‐ylidene)‐2,4,6‐trimethylbenzenamine ( 1 ) with n‐butyl lithium and then with N‐(2,4,6‐trimethyl‐phenyl)‐acetimidoyl chloride yields a new β‐triketimine ligand, N‐(4‐(mesitylamino)‐3‐(1‐(mesitylimino)ethyl)pent‐3‐en‐2‐ylidene)‐2,4,6‐trimethylbenzenamine, 2 . The addition of 2 to nickel (II) dibromide 1,2‐dimethoxyethane (NiBr2(DME)) in the presence of [Na]+[3,5‐(CF3)4C6H3]4B]? (NaBAr'4) gives a five‐coordinate dimeric complex [( 2 .NiBr)2].2 [(BAr'4)], 3 . The structure of 3 has been determined by single crystal X‐ray diffraction. This complex generates catalytically active species for the homopolymerization of ethylene in combination with methylaluminoxane to produce elastomeric, branched polyethylene. The effect of factors (temperature, pressure, and cocatalyst to catalyst molar ratio (CC)) on the polymerization process has been investigated using regression models of responses (catalyst activity, crystallinity, and weight‐average molecular weight of polymer (Mw)) and visualized via the response surface method (RSM). Activity and Mw responses show a second‐order variation with temperature and vary linearly with pressure. Conversely, crystallinity follows a second‐order model while varying temperature, pressure, and CC. Furthermore, a set of polymerization conditions for reaching desirable responses was predicted and then experimentally verified. The activities achieved challenge the best reported activities for Ni(II) catalysts with β‐connected imine ligand supports, but fall short of those for α‐diimines. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
958.
The title compounds are prepared by arc‐melting of the elements followed by heating in Ta ampules (950—1150 °C, 1—12 h). 相似文献
959.
《Analytical letters》2012,45(7):1224-1241
The combined use of a competing ligand exchange (CLE) method and a diffusive gradient in thin films (DGT) technique in a quasi-labile system provides a better understanding of dynamic metal (Cu and Ni) complexes in the presence of humic substances of different origins. The CLE and DGT techniques provide total labile (dynamic) metal complexes (Cu and Ni) and their dissociation rate constants in environmental systems. DGT was found to estimate lower concentrations of labile metal complexes than CLE. These discrepancies were caused by diffusion controlled metal flux (towards the binding resin gel) in the diffusive gel of DGT. The interactions of Cu and Ni with humic acids are stronger than their interactions with fulvic acid and natural organic matter. Changes in the lability of Ni and Cu complexes (complexed with humic substances of different origins) with the changing analytical detection window indicate that the complexes of these metals were formed with different binding sites with diverse binding energies in the humic substances. The combination of these two techniques was found to be very useful in determining diffusion coefficients of labile metal-humate complexes in quasi-labile systems. The values of diffusion coefficients of labile Ni and Cu complexes determined in this study are in good agreement with limited results from the literature. This finding is novel and can be very useful in further improving our understanding of the metal-humate interactions in natural environments. 相似文献
960.