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991.
Xiaojun Zou Yuemei Cui Xiangbing Zhu Zheng Hu Xijun Chang 《Journal of Sol-Gel Science and Technology》2009,50(1):35-43
Morin was successful as a chemical modifier to improve the reactivity of the nanometer SiO2 surface in terms of selective binding and extraction of heavy metal ions. This new functionalized nanometer SiO2 (nanometer SiO2-morin) was used as an effective sorbent for the solid-phase extraction (SPE) of Cd(II), Cu(II), Ni(II), Pb(II), Zn(II) in
solutions prior to its determination by inductively coupled plasma atomic emission spectrometry (ICP-AES). Experimental conditions
for effective adsorption of trace levels of metal ions were optimized with respect to different experimental parameters using
static and dynamic procedures in detail. The pH 4.0 was chosen as the optimum pH value for the separation of metal ions on
the newly sorbent. Complete elution of the adsorbed metal ions from the nanometer SiO2-morin was carried out using 2.0 mL of 0.5 mol L−1 of HCl. Common coexisting ions did not interfere with the separation and determination at pH 4.0. The maximum static adsorption
capacity of the sorbent at optimum conditions was found to be 22.36, 36.8, 40.37, 33.21 and 25.99 mg metal/g SiO2-morin for Cd(II), Cu(II), Ni(II), Pb(II) and Zn(II), respectively. The time for 95% sorption for Cu(II) and Ni(II) and 70%
sorption for Cd(II), Pb(II) and Zn(II) was less than 2 min. The relative standard deviation (RSD) of the method under optimum
conditions was lower than 5.0% (n = 11). The procedure was validated by analyzing the certified reference river sediment material (GBW 08301, China), the results
obtained were in good agreement with standard values. The nanometer SiO2-morin was successfully employed in the separation and preconcentration of trace Cd(II), Cu(II), Ni(II), Pb(II) and Zn(II)
from the biological and natural water samples yielding 75-folds concentration factor. 相似文献
992.
Lianghai Hu Karl-Siegfried Boos Mingliang Ye Ren’an Wu Hanfa Zou 《Journal of chromatography. A》2009,1216(28):5377-5384
As the serum peptidome gets increasing attention for biomarker discovery, one of the important issues is how to efficiently extract the peptides from highly complex human serum for peptidome analysis. Here we developed a fully automated platform for direct injection, on-line extraction, multidimensional separation and MS detection of peptides present in human serum. A capillary SPE column packed with a novel mix mode restricted access material (RAM) exhibiting strong cation exchange and size exclusion chromatography (SCX/SEC) properties were coupled with a nanoliquid chromatography–mass spectrometry (nanoLC-MS) system. The capillary SPE column excludes the high abundant serum proteins such as HSA by size exclusion chromatography and simultaneously extracts the low molecular weight peptides by binding to sulfonic acid residues. Subsequently, the trapped peptides are eluted to a capillary LC column packed with a RP-C18 stationary phase. After injection of only 2 μL human serum to the one-dimensional nanoLC-MS system around 400 peptides could be identified. When conducting a multidimensional separation, the described SCX/SEC/RP-MS platform allows the separation and identification of 1286 peptides present in human serum by the injection and on-line processing of 20 μL human serum sample. 相似文献
993.
994.
Two bis-(1-arylliminomethylenyl-2-oxy-naphthalen) nickel complexes (aryl = 2-methylphenyl, complex 1; aryl = 2,6-diisoproylphenyl, complex 2) were reacted with alkylaluminium in presence of equimolar PPh3 and tested as catalysts in methyl methacrylate (MMA) polymerization. The two nickel catalysts can initiate polymerization of MMA with good to high activity, the highest activity reaching 1.1 × 105 g PMMA/(mol Ni · h) by less bulky complex 1 at 0.8 mol/L of MMA, 400 of Al/Ni ratio and 0 °C. In addition, the structures of nickel complexes and polymerization conditions, such as monomer concentration, polymerization temperature and Al/Ni molar ratio on catalytic activity of polymerization have great influences on catalytic activity and product properties. 相似文献
995.
Chun Huang Chang-Gua Zhen Siew Ping Su Zhi-Kuan Chen Xiao Liu De-Chun Zou Yan-Rong Shi Kian Ping Loh 《Journal of organometallic chemistry》2009,694(9-10):1317-1324
We report the synthesis and electrophosphorescent behavior of a series of novel iridium complex materials (Complexes A–F), which are composed of ligands bearing polyphenylphenyl dendron groups and acetylacetonate. Yellow to saturated red organic light-emitting diodes (OLEDs) based on these newly developed Ir complexes were fabricated through solution process by doping the complex materials into polyvinyl carbazole (PVK)/2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (PBD) matrices. The emission wavelengths of the materials could be effectively tuned from 549 nm to 640 nm by changing the conjugation of the ligands either through incorporating additional aromatic segment (e.g. phenyl or fluorenyl group) onto the basic dendron ligand or fusing two of the phenyl rings on the polyphenylphenyl dendron group. High performance devices with the configuration of ITO/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS) (50 nm)/PVK:PBD (40%):Ir complex (6%) (70 nm)/2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) (12 nm)/Alq3 (20 nm)/Mg:Ag (150 nm) have been demonstrated. For example, when Complex B was used as the emissive layer, maximum current efficiency of 34.0 cd/A and external quantum efficiency of 10.3% have been achieved. When 1,3,5-tris(N-phenylbenzimidazol-2-yl) benzene (TPBI) was used as the block layer, the efficiencies can be further improved to 46.3 cd/A and 13.9%, respectively. These solution processed OLED devices demonstrated quite stable EL efficiencies over a large range of current density, which indicated that triplet–triplet annihilation in electrophosphorescence could be effectively suppressed by incorporation of the polyphenylphenyl dendron structure into iridium complexes. 相似文献
996.
Jianjun Zou Dingwei Wu Dawei Xiao Dan Qi Li Liu Li Ding Guangji Wang 《Chromatographia》2009,69(5-6):453-458
A sensitive and specific liquid chromatography–electrospray ionization–tandem mass spectrometry method has been developed and validated for the quantification of huperzine A in human plasma. After the addition of trimetazidine, the internal standard (IS) and sodium hydroxide, plasma samples were extracted using 5 mL ethyl acetate. The compounds were separated on an Agilent Zorbax SB C18 column (100 mm × 2.1 mm ID, dp 3.5 μm) using an elution system of 10 mM ammonium acetate solution–methanol–formic acid (18:82:0.1, v/v) as the mobile phase. The quantification of target compounds was obtained by using multiple reaction monitoring (MRM) transitions: m/z 243.1, 210.1 and 267.2, 166.0 were measured in positive mode for huperzine A and IS. Linearity was established for the range of concentrations 0.01–4.0 ng mL?1 with a coefficient of correlation (r) of 0.9991. The lower limit of quantification (LLOQ) was identifiable and reproducible at 0.01 ng mL?1. The method has been successfully applied to study the pharmacokinetics of huperzine A in healthy male Chinese volunteers. 相似文献
997.
High-performance liquid chromatography with tandem mass spectrometry has been used for rapid, specific, and sensitive analysis of busulfan in human plasma. Busulfan-d8 was used as internal standard. Analysis was performed on a C18 column (50 mm × 2.1 mm, 3.5-µm particles) with water–methanol 80:20 (v/v) as mobile phase at a flow-rate of 0.30 mL min?1. Detection was by tandem triple–quadrupole mass spectrometry with turbo ion-spray ionization. Linear calibration plots were obtained over the concentration range 1.096–1,096 ng mL?1. The assay is ideally suited to monitoring of busulfan and determination of its pharmacokinetic data. 相似文献
998.
分析了火花直读光谱法测定铝合金中Si、Fe、Cu、Mg、Mn、Zn、Cr、Ti元素含量测量结果的不确定度来源,对不确定度分量进行了评定与计算,Si、Fe、Cu、Mg、Mn、Zn、Cr、Ti测量结果的相对扩展不确定度分别为2. 9%、2. 5%、2. 6%、2. 7%、2. 6%、2. 6%、2. 5%、2. 7%(包含因子k均为2). 相似文献
999.
Jian-Ping Zou Sheng-Ping Guo Xiao-Ming Jiang Guang-Ning Liu Guo-Cong Guo Jin-Shun Huang 《Solid State Sciences》2009,11(9):1717-1721
A new supramolecular complex [Hg6Sb4](InBr6)Br (1) has been prepared by the solid-state reaction of HgBr2 with elemental In and Sb at 450 °C. The crystal structure of 1 features a three-dimensional [Hg6Sb4]4+ framework with cavities of two different sizes occupied by different kinds of guest anions. The bigger cavities are filled with the octahedral InBr63− ions, while the smaller cavities trap Br− ions. The optical properties were investigated in terms of the diffuse reflectance and infrared spectra. The electronic band structure along with density of states (DOS) calculated by DFT method indicates that the present compound is semiconductor, and the optical absorption is mainly originated from the charge transitions from Sb-5p and Br-4p to In-5s and Hg-6s states. 相似文献
1000.
Qingqing Liang Chengyin Wu Zhifeng Wu Min Liu Yongkai Deng Qihuang Gong 《International journal of mass spectrometry》2009,286(1):28-31
We experimentally study the ionization, fragmentation and Coulomb explosion of CO using 6 fs laser pulses. Different from previous observations in tens or hundreds of femtoseconds laser pulses, strong charge asymmetric dissociation and CO2+ are observed in the current intense few-cycle laser field. 相似文献