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J. H. Moon M. Ebihara B. F. Ni B. Arporn P. Setyo R. M. Theresia B. S. Wee N. A. Abd. Salim P. C. B. Pabroa 《Journal of Radioanalytical and Nuclear Chemistry》2012,291(1):217-221
Since 2000, collaborative studies for applying NAA have been performed through the Forum for Nuclear Cooperation in Asia (FNCA)
sponsored by the Japanese Government. White rice is a main food for Asians and thus was selected as a common target sample
for a collaborative study in 2008. Seven Asian countries including China, Indonesia, Japan, Korea, Malaysia, Philippines and
Thailand, are greatly concerned about the composition of arsenic, heavy metals, and essential trace elements and took part
in this study. Rice samples were purchased and prepared by following a protocol that had been proposed for this study. Samples
were analyzed by their own NAA systems. In each country, more than 10 elements were examined and the results were compared.
These data will be very useful in the monitoring of the levels of food contamination and to evaluate the nutritional status
for people living in Asia. 相似文献
885.
Yao Meng Yizhou Liu Tao Li Tianli Feng Jiacheng Huang Zheng Ni Wenchao Qiao 《Molecules (Basel, Switzerland)》2022,27(3)
We report the surface morphology and the nonlinear absorption characteristics of MXene VCrC nanosheets prepared by the liquid-phase exfoliation method. The self-made MXene VCrC was applied as a saturable absorber in the Tm:YAP laser experiments, performing excellent Q-switching optical modulation characteristics in infrared range. With this absorber, a stable passively Q-switched 2 μm laser was achieved. Under an incident pump power of 3.52 W, a maximum output power of 280 mW was obtained with a T = 3% output coupler at a repetition frequency of 49 kHz. The corresponding pulse energy and peak power were 5.7 μJ and 6.6 W, respectively. The shortest pulse duration was 658 ns at the repetition rate of 63 kHz with a T = 1% output coupler. 相似文献
886.
Xin‐Ping Hui Heng‐Shan Dong Peng‐Fei Xu Zi‐Yi Zhang Qin Wang Yan‐Ni Gong 《中国化学会会志》2000,47(5):1115-1119
The condensation of 4‐amino‐5‐mercapto‐3‐(2‐phenylquinolin‐4‐yl)/3‐(1‐p‐chlorophenyl‐5‐methyl‐1,2,3‐triazol‐4‐yl)‐1,2,4‐triazoles 1a‐b with chloroacetaldehyde 2a‐b , ω‐bromo‐ω‐(1H‐1,2,4‐triazol‐1‐yl)acetophenone 3a‐b , chloranil 4a‐b , 2‐bromocyclohexanone 5a‐b , 2,4′‐dibromoacetophenone 6a‐b and 2‐bromo‐6′‐methoxy‐2′‐acetonaphthone 7a‐b are described. The structures of the compounds synthesized were confirmed by elemental analyses, IR, 1H NMR and mass spectra. The antibacterial activities were also evaluated. 相似文献
887.
The 1,2-bridged tricyclic cyclopropene, tricyclo[3.2.2.02,4]nona-2(4),6-diene (1), has been synthesized by the elimination of 2-bromo-4-chlorotricyclo[3.2.2.02,4]-non-6-ene (5). Cyclopropene 1 will undergo different isomerizations in ether solution and in neat conditions. Compound 1 rearranged to an anti-Bredt compound 4 via diradical mechanism in ether and tricyclic compound 6 via vinyl carbene mechanism in neat conditions. Compound 1 can be trapped with DPIBF at different temperatures yielding different results: the exo-endo adduct 2 (exo-addition from the view of the cyclopropene and endo-addition from the view of bicyclo[2.2.2]octene) is a sole product at 0°C by slowly addition of methyllithium, and the exo-endo adduct 2, endo-endo adduct 9, anti-Bredt adduct 3, and styrene 8 are isolated at ether refluxing temperature. Styrene 8 is proposed to be formed from endo-endo adduct 9 by diradical mechanism. The chemistry of exo-endo adduct 2 and endo-endo adduct 9 is as well studied. The exo-endo adduct 2 undergoes hydration in trifluoroacetic acid to generate 1,3-cis-diol 11 followed by eliminations of water and formaldehyde to give naphthalene 12. The endo-endo adduct 9 reacts with water in tetrahydrofuran-containing silica gel to yield 1,4-cis-diol 10. Both 9 and 10 react with trifluoroacetic acid to form trans-3-hydroxy trifluoroacetate 13. Compound 13 will undergo hydrolysis and isomerization to generate 1,3-cis-diol 11 in trifluoroacetic acid. 相似文献
888.
This work aimed to classify the categories (produced by different processes) and brands (obtained from different geographical origins) of Chinese soy sauces. Nine variables of physico-chemical properties (density, pH, dry matter, ashes, electric conductivity, amino nitrogen, salt, viscosity and total acidity) of 53 soy sauce samples were measured. The measured data was submitted to such pattern recognition as cluster analysis (CA), principal component analysis (PCA), discrimination partial least squares (DPLS), linear discrimination analysis (LDA) and K-nearest neighbor (KNN) to evaluate the data patterns and the possibility of differentiating Chinese soy sauces between different categories and brands. Two clusters corresponding to the two categories were obtained, and each cluster was divided into three subsets corresponding to three brands by the CA method. The variables for LDA and KNN were selected by the Fisher F-ratio approach. The prediction ability of all classifiers was evaluated by cross-validation. For the three supervised discrimination analyses, LDA and KNN gave 100% predications according to the sample category and brand. 相似文献
889.
Yanjiang Han Duanzhi Yin Mingqiang Zheng Wei Zhou ZhenHong Lee Lan Zhan Yufei Ma Mingxing Wu Lingli Shi Ni Wang Jianbo Lee Cheng Wang Zheng Lee Yongxian Wang 《Journal of Radioanalytical and Nuclear Chemistry》2010,284(2):279-286
The aim of this study was to develop a radiopharmaceutical for the imaging of CXCR4-expressing tumors in vivo. For 125I-labeling, 125I-SIB was synthesized and conjugated with the ε-NH2 group of Ac-TZ14011, a specific CXCR4 antagonist. The specific radioactivity of the product was 5 GBq/μmol and the radiochemical purity (RCP) was 96% (n = 3). After 6 h, the RCP of the product in PBS was 93%. The MCF-7 cell uptake of Ac-TZ14011 was rapid and high. Primary biodistribution studies indicated that 125I-IB-Ac-TZ14011 was mainly excreted via the kidney, and further evaluation in mice with induced tumors was necessary. 相似文献
890.
Herein a water-soluble ‘click’ modified coumarin-based fluorescent probe for hydrogen peroxide is reported. This probe shows significant intensity increases (up to fivefold) in near-green fluorescence upon reaction with hydrogen peroxide, and good selectivity over other reactive oxygen species. 相似文献