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991.
PengZHANG JiCunREN ZuoJunSHEN 《中国化学快报》2004,15(9):1091-1094
In this paper, we first presented a novel method for quantification of circulating DNA in human serum based on capillary zone electrophoresis with laser-induced fluorescence detection (CZE-LIF). The serum was digested by proteinase to release free DNA, and then CZE-LIF system was used for the quantification of total circulating DNA. This method was successfully used to quantify the circulating DNA levels in sera from healthy individuals and certain cancer patients.We found the significantly elevated circulating DNA levels in certain prostate cancer patients. Our results demonstrated that CZE-LIF system has good linearity, excellent sensitivity (0.5 ng/mL DNA),satisfactory reproducibility (RSDs in one day and between days were both less than 5%) and reliability, and is well suitable to the quantification of the circulating DNA in human serum or plasma. 相似文献
992.
采用密度泛函理论(DFT)B3LYP方法,6-311G(d,p)(C,H,O)/LANL2DZ(Ag)基组,计算了黄曲霉素B2(AFB2)分子吸附在Ag2团簇的表面增强拉曼散射(SERS)光谱和预共振拉曼光谱,并与实验结果比较. 结果显示:AFB2分子在基态Ag2团簇表面吸附时,增强因子最大达到102,对应吡喃(pyrane)环C=O伸缩振动,主要是由AFB2分子周围化学环境改变而引起的基态静极化率改变导致的化学增强. 不同激发波长下的AFB2分子预共振拉曼光谱的增强强度不同:电荷转移态激发波长为1144 和544 nm时拉曼信号增强了102倍,而选择电荷转移预共振波长432和410 nm作为入射光时,其拉曼信号增强了104倍,增强机理为银团簇和黄曲霉素分子之间的电荷转移共振增强. 因此通过改变入射光波长,选择电荷转移共振激发波长,更有利于强致癌物AFB2分子的痕量检测. 相似文献
993.
994.
995.
Wei Jun Jin 《Analytica chimica acta》2004,522(1):1-8
Luminescent surface-modified CdSe semiconductor quantum dots (QDs), with nanoparticle (NP) size distribution in the order of 2-7 nm, have been synthesized for optical determination of cyanide ions. The nanoparticles have been functionalised with tert-butyl-N-(2-mercaptoethyl)-carbamate (BMC) groups and exhibit a strong fluorescent emission at about 580 nm with rather long fluorescence lifetimes (several hundred nanoseconds) in aerated methanolic solution. The observed luminescence emitted by the synthesized nanocrystals was tremendously increased by photo-activation under sunlight exposure. The functionalised QDs turned out to exhibit excellent long-term stability when stored in the dark (no significant changes in QDs luminescence emission intensity was observed even after two months from synthesis). The functionalisation of the NPs with carbamate ligand allowed a highly sensitive determination of free cyanide via analyte-induced changes in the photoluminescence (fluorescence quenching of intensity at 580 nm and lifetime changes) of the modified quantum dots (excited at 400 nm). A detection limit of 1.1 × 10−7 M (2.9 μg l−1) of cyanide ions was obtained, while the interfering effect of other inorganic anions (including NO3−, Cl− or SCN−) was negligible even at 200-fold level concentrations in excess of cyanide. 相似文献
996.
一种基于磁性纳米粒子PCR的高通量SNP分型方法 总被引:1,自引:0,他引:1
利用磁性纳米粒子PCR扩增(MNPs-PCR)和等位基因特异性双色荧光探针(Cy3, Cy5)杂交, 建立了一种单核苷酸多态性(SNP)分型的新方法. 应用该方法对9个样本MTHFR基因的C677T多态进行检测, 野生和突变型样本正错配信号比大于9.0, 杂合型正错配信号比接近1.0, 分型结果经测序验证. 此方法无须产物纯化、浓缩, 扫描分型结果快速、直观, 是一种操作简单、快速、高通量、高灵敏度的分型方法. 相似文献
997.
Yanchen Liu Chenchen Wang Shuo Zhao Lin Zhang Kai Zhang Fujun Li Jun Chen 《Chemical science》2021,12(3):1062
Layered manganese-based oxides are promising candidates as cathode materials for sodium-ion batteries (SIBs) due to their low cost and high specific capacity. However, the Jahn–Teller distortion from high-spin Mn3+ induces detrimental lattice strain and severe structural degradation during sodiation and desodiation. Herein, lithium is introduced to partially substitute manganese ions to form distorted P′2-Na0.67Li0.05Mn0.95O2, which leads to restrained anisotropic change of Mn–O bond lengths and reinforced bond strength in the [MnO6] octahedra by mitigation of Jahn–Teller distortion and contraction of MnO2 layers. This ensures the structural stability during charge and discharge of P′2-Na0.67Li0.05Mn0.95O2 and Na+/vacancy disordering for facile Na+ diffusion in the Na layers with a low activation energy barrier of ∼0.53 eV. It exhibits a high specific capacity of 192.2 mA h g−1, good cycling stability (90.3% capacity retention after 100 cycles) and superior rate capability (118.5 mA h g−1 at 1.0 A g−1), as well as smooth charge/discharge profiles. This strategy is effective to tune the crystal structure of layered oxide cathodes for SIBs with high performance.Li-Substitution in P′2-Na0.67MnO2 mitigates the anisotropic change of Mn–O bonds and Na/vacancy ordering, and hence significantly promotes its cycling stability and rate capability as a cathode material for sodium-ion batteries. 相似文献
998.
In this paper, we used bond-length equalization, aromatic stabilization energies (ASE) and nucleus-independent chemical shifts
(NICS), calculated with (density functional theory) B3LYP levels at the 6-311+G** basis set, to evaluate the aromaticity of a set of 38 five-member planar π-electron aromatic systems: sila-, aza- and phospha-
derivatives and their parent systems. The result revealed statistically significant correlations among the above three criteria,
and the order of aromaticity of the whole set was: Aza- derivatives rings > Phospha- derivatives rings > Sila- derivatives
rings > Carbon-containing rings; NICS(0.6) and NICS(0.8) had the same results in evaluating the order of aromaticity in our
case. 相似文献
999.
Jung Kwon Oh Jun Wu Mitchell A. Winnik Gary P. Craun Jude Rademacher Rajeev Farwaha 《Journal of polymer science. Part A, Polymer chemistry》2002,40(17):3001-3011
We describe the synthesis and characterization of three new polymerizable benzophenone derivatives [2‐acryloxy‐5‐methyl benzophenone ( 8 ), 4′‐dimethylamino‐2‐acryloxy‐5‐methyl benzophenone ( 9 ), and 4′‐dimethylamino‐2‐(β‐acryloxyethyl)oxy‐5‐methyl benzophenone ( 10 )]. We show that these monomers can successfully be incorporated into vinyl acetate (VAc) copolymer latex particles. These particles were prepared by semicontinuous emulsion polymerization and mini‐emulsion polymerization of VAc with butylacrylate (BA) for VAc/BA = 4/1 by weight. The two monomers 9 and 10 bearing the 4′‐dimethylamino group satisfy the important spectroscopic criteria required of a dye to serve as an acceptor chromophore for nonradiative energy transfer from phenanthrene (Phe) as the donor. Their UV absorption spectra suggest significant overlap with the emission spectrum of Phe, which can be incorporated into P(VAc‐co‐BA) latex through copolymerization with 9‐acryloxymethyl Phe ( 2 ). In addition, these chromophores provide a window in their absorption spectra for excitation of the Phe chromophore at 300 nm. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3001–3011, 2002 相似文献
1000.