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991.
The novel C2‐symmetric sulfur‐containing chiral bis(oxazoline) compound has been synthesized and characterized by X‐ray crystallography. Highly enantioselective and diastereoselective cyclopropanation reactions have been performed using the copper‐bis(oxazoline) catalyst. 相似文献
992.
K. Staff M.B. Brown R.C. Hider X.L. Kong P. Friden S.A. Jones 《Biomedical chromatography : BMC》2010,24(9):1015-1022
Ion exchange chelation chromatography is an effective means to extract metals from coordination complexes and biological samples; however there is a lack of data to verify the nature of metal complexes that can be successfully analysed using such a procedure. The aim of this study was to assess the capability of pyridine 2,6‐dicarboxylic acid (PDCA) to extract and quantify Ga(III) from a range of environments using standard liquid chromatography apparatus. The PDCA chelation method generated a single Ga(III) peak with a retention time of 2.55 ± 0.02 min, a precision of <2% and a limit of detection of 110 μM. Ga(III) hydroxide complexes (highest stability constant 15.66) were used to successfully cross‐validate the chelation method with inductively coupled plasma mass spectrometry. The PDCA assay extracted 96.9 ± 1.2% of the spiked Ga(III) from porcine mucus and 100.7 ± 2.7% from a citrate complex (stability constant 10.02), but only ca 50% from an EDTA complex (stability constant 22.01). These data suggest that PDCA chelation can be considered a suitable alternative to inductively coupled plasma mass spectrometry for Ga(III) quantification from all but the most strongly bound coordinated complexes i.e. a stability constant of <15. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
993.
Radiation-induced wood-polymer composites have been prepared using some tropical commercial woods. These included Kapur (Dryobalanop sp.), Kempas (Koompassia sp.), Red Seraya (Shorea sp.), White Seraya (Parashorea sp.), and Jelutong (Dyera sp.). The wood specimens were modified by impregnation with monomers and followed by exposure to gamma radiation. Monomer systems used were methyl methacrylate, methyl methacrylate with 5% dioxane, acrylonitrile, 60:40 styrene-acrylonitrile comonomer, vinyl acetate, and vinylidene chloride. The resulting composite specimens exhibited significant increases in hardness and compressive strength, the extent of which appeared to depend on the amount and type of polymer present. Dimensional stability increased when the woods were impregnated with polymethyl methacrylate and improved further to about 35% on addition of a swelling agent, dioxane. Wood-polyvinylidene chloride composites gave high fire resistance as opposed to wood-polymethyl methacrylate which showed increased flammability. A 4-fold decrease in weight loss was observed in the fire-tube and crib tests conducted. The impregnated polymers were not totally resistant to termites. The polymers, not being nutrients, reduced the number of survivals after a 90-d test period. Polystyrene-acrylonitrile appeared toxic to the termites. 相似文献
994.
Methodology and Computing in Applied Probability - Runs statistics have found many applications in various fields and have attracted attentions of many researchers. Traditional methods used to... 相似文献
995.
Xi Yu Kunxi Zhang Xiaobo Kong Jingbo Yin 《Journal of Polymer Science.Polymer Physics》2019,57(17):1115-1125
Soft tissues, such as fat and skin, present high flexibility and are capable of withstanding large deformation in various functions. Hydrogels that can resemble the mechanical performance of soft tissue are unique and widely demanded. In this study, micellar hydrogels based on biocompatible poly(l ‐glutamic acid) (PLGA) were designed with the enhanced capacity to bear large deformation. Amphipathic triblock copolymer poly(ethylene glycol) acrylate‐co‐poly(ε‐caprolactone)‐co‐poly (ethylene glycol) acrylate (APEG‐PCL‐APEG) with two terminal double bonds was synthesized and self‐assembled into micelles. At the same time, graft copolymers, poly(l ‐glutamic acid)‐g‐hydroxyethyl methacrylate (PLGA‐g‐HEMA) with double bonds were synthesized. APEG‐PCL‐APEG micelles and PLGA‐g‐HEMA were mixed to construct micellar hydrogel via radical polymerization. The crystalline structure and hydrophobic aggregation of copolymers (APEG‐PCL‐APEG) were found to associate with PCL molecular weight. Due to the hydrophobic stress dissipation and crystalline structure of the micelles, the softness and toughness of hydrogels were promoted, exhibiting a 25% increase in ultimate strain. Moreover, the micellar hydrogels were able to load proteins with long‐term retention. In addition, under dynamic mechanical stimulation, the release of proteins could be accelerated. Besides, the micellar hydrogels also supported rabbit adipose‐derived stem cells (rASCs) growth, thus exhibiting the potential toward soft tissue engineering. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 1115–1125 相似文献
996.
Dan-Dan Zhao Zhi Yang Eric Siu-Wai Kong Cai-Ling Xu Ya-Fei Zhang 《Journal of Solid State Electrochemistry》2011,15(6):1235-1242
Manganese oxide (MnOx) has been coated on carbon nanotubes (CNTs) and fabricated as the electrodes for electrochemical capacitors (ECs) by cathodic
electrodeposition. In the process, randomly oriented CNT arrays are grown directly onto the Ti/Si substrates by chemical vapor
deposition method. Potentiostatic method has been utilized for cathodic electrodeposition of MnOx onto the surface of CNTs while immersed in KMnO4 solution. The highly porosity and fibrous microstructure of the as-prepared MnOx/CNT electrode is beneficial for the electrolyte access to the active material, whereas CNTs provide improved electronic conductivity.
Electrochemical investigations show that the increase in the loading mass of MnOx results in a significant reduction in the specific capacitances (SCs) of the MnOx/CNT electrodes. The MnOx/CNT electrode with MnOx loading mass of 50 μg shows a high SC of 400 F g−1 with good long cycle stability at a current density of 10 A g−1, suggesting its potential application in ECs. 相似文献
997.
Xin Huang Yage Zhang Chaoshen Zhang Lei Zhang Ying Xu Lichun Kong Zhi‐Xiang Wang Bo Peng 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(18):6017-6022
Presented herein is an intriguing effect of fluorine, and it allows difluoroenol silyl ethers to couple with aryliodanes in a redox‐neutral manner to afford ortho‐iodo difluoroalkylated arenes. The remaining iodide group provides a versatile platform for converting the products into various valuable difluoroalkylated arenes. The reaction shows excellent functional‐group compatibility and broad substrate scope. A DFT mechanistic study suggests that the fluorine effect facilitates a subtle nucleophilic attack of the oxygen atom of enol silyl ethers onto aryliodanes, therefore leading to a rearrangement. 相似文献
998.
999.
In this paper, the effect of temporal separation of two Geiger mode avalanche photodiodes and the variation of time bin widths on detection probabilities in LADAR system using two Geiger mode avalanche photodiodes (GmAPDs) was investigated. The system is implemented by using two GmAPDs with a beam splitter and applying comparative process to their ends. Then, the timing circuitry receives the electrical signals only if each GmAPD generates the electrical signals simultaneously. Although this system decreases the energy of a laser-return pulse scattered from the target, it is highly effective in reducing the false alarm probability because of the randomly distributed noise on the time domain. The temporal separation of two GmAPDs and the variation of the time bin widths result in the variation of detection probabilities. The experiments were performed to verify the effect of temporal separation of two GmAPDs and the variation of time bin widths on the detection probability in the LADAR system. As a result, the optimal temporal difference and the optimal time bin width were. Using these optimal values, a clear 3D image could be obtained by the simple acquisition of the raw time-of-flight data with high SNR. 相似文献
1000.
X‐ray structures,spectroscopic, electrochemical,thermal, antibacterial,and DFT studies of two nickel(II) and cobalt(III) complexes constructed from a new quinazoline‐type ligand
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Two two‐dimensional supramolecular Nickel(II) and Cobalt(III) complexes, [Ni( L 2 )2]·2CH3OH ( 1 ) and [2Co( L 2 )2] ( 2 ) ( HL 2 = 1‐(2‐{[(E)‐3‐bromo‐5‐chloro‐2‐hydroxybenzylidene]amino}phenyl)ethanone oxime), were synthesized via complexation of salts acetate with HL 1 (2‐(3‐bromo‐5‐chloro‐2‐hydroxyphenyl)‐4‐methyl‐1,2‐dihydroquinazoline 3‐oxide, H is the deprotonatable hydrogen). During the reaction, the C–N bond in HL 1 is converted into the C=N–OH group in HL 2 . The spectroscopic data of both complexes were compared with the ligand HL 1 . HL 1 and both complexes were determined by single‐crystal X‐ray crystallography. The differently geometric features of the obtained complexes 1 and 2 are observed. In the crystal structure, 1 and 2 form an infinite 1‐D chain‐like and 2‐D supramolecular frameworks. EPR spectroscopy of 2 was investigated. Moreover, electrochemical properties and antimicrobial activities of both complexes were also studied. In addition, the calculated HOMO and LUMO energies show the character of HL 1 , complexes 1 and 2 . The electronic transitions and spectral features of HL 1 and both complexes were discussed by TD‐DFT calculations. 相似文献