全文获取类型
收费全文 | 6895篇 |
免费 | 959篇 |
国内免费 | 952篇 |
专业分类
化学 | 5249篇 |
晶体学 | 80篇 |
力学 | 383篇 |
综合类 | 91篇 |
数学 | 798篇 |
物理学 | 2205篇 |
出版年
2024年 | 10篇 |
2023年 | 103篇 |
2022年 | 186篇 |
2021年 | 220篇 |
2020年 | 259篇 |
2019年 | 283篇 |
2018年 | 199篇 |
2017年 | 190篇 |
2016年 | 336篇 |
2015年 | 344篇 |
2014年 | 402篇 |
2013年 | 540篇 |
2012年 | 572篇 |
2011年 | 550篇 |
2010年 | 468篇 |
2009年 | 400篇 |
2008年 | 525篇 |
2007年 | 457篇 |
2006年 | 435篇 |
2005年 | 410篇 |
2004年 | 314篇 |
2003年 | 252篇 |
2002年 | 213篇 |
2001年 | 198篇 |
2000年 | 154篇 |
1999年 | 122篇 |
1998年 | 96篇 |
1997年 | 81篇 |
1996年 | 83篇 |
1995年 | 61篇 |
1994年 | 48篇 |
1993年 | 56篇 |
1992年 | 45篇 |
1991年 | 41篇 |
1990年 | 25篇 |
1989年 | 18篇 |
1988年 | 14篇 |
1987年 | 15篇 |
1986年 | 15篇 |
1985年 | 14篇 |
1984年 | 8篇 |
1983年 | 4篇 |
1982年 | 5篇 |
1981年 | 3篇 |
1979年 | 5篇 |
1977年 | 2篇 |
1975年 | 2篇 |
1974年 | 4篇 |
1971年 | 2篇 |
1935年 | 2篇 |
排序方式: 共有8806条查询结果,搜索用时 15 毫秒
101.
Xiaobin Wang Xincan Fu Min Chen An Wang Jinghua Yan Yudong Mei Mengqi Wang Chunlong Yang 《中国化学快报》2019,30(7):1419-1422
A series of novel 1,3,5-thiadiazine-2-thione derivatives bearing a hydrazide moiety were designed, synthesized and evaluated for their biological activities against phytopathogenic fungi. The antifungal bioassays indicated that the title compound 5b impressively displayed the obvious selectivity and specificity aganist Rhizoctonia solani (Rs) in vitro and in vivo. The above researches provide a significant reference for the further structural optimization of 1,3,5-thiadiazine-2-thione derivatives bearing a hydrazide moiety as potential fungicides. 相似文献
102.
The threat and global concern of energy crises have significantly increased over the last two decades. Because solar light and water are abundant on earth, photocatalytic hydrogen evolution through water splitting has been considered as a promising route to produce green energy. Therefore, semiconductor photocatalysts play a key role in transforming sunlight and water to hydrogen energy. To date, various photocatalysts have been studied. Among them, TiO2 has been extensively investigated because of its non-toxicity, high chemical stability, controllable morphology, and high photocatalytic activity. In particular, 1D TiO2 nanofibers (NFs) have attracted increasing attention as effective photocatalysts because of their unique 1D electron transfer pathway, high adsorption capacity, and high photoinduced electron–hole pair transfer capability. However, TiO2 NFs are considered as an inefficient photocatalyst for the hydrogen evolution reaction (HER) because of their disadvantages such as a large band gap (~3.2 eV) and fast recombination of photoinduced electron–hole pairs. Therefore, the development of a high-performance TiO2 NF photocatalyst is required for efficient solar light conversion. In recent years, several strategies have been explored to improve the photocatalytic activity of TiO2 NFs, including coupling with narrow-bandgap semiconductors (such as ZnIn2S4). Recently, microwave (MW)-assisted synthesis has been considered as an important strategy for the preparation of photocatalyst semiconductors because of its low cost, environment-friendliness, simplicity, and high reaction rate. Herein, to overcome the above-mentioned limiting properties of TiO2 NFs, we report a 2D/1D ZnIn2S4/TiO2 S-scheme heterojunction synthesized through a microwave (MW)-assisted process. Herein, the 2D/1D ZnIn2S4/TiO2 S-scheme heterojunction was constructed rapidly by using in situ 2D ZnIn2S4nanosheets decorated on 1D TiO2 NFs. The loading of ZnIn2S4 nanoplates on the TiO2 NFs could be easily controlled by adjusting the molar ratios of ZnIn2S4 precursors to TiO2 NFs. The photocatalytic activity of the as-prepared samples for water splitting under simulated solar light irradiation was assessed. The experimental results showed that the photocatalytic performance of the ZnIn2S4/TiO2 composites was significantly improved, and the obtained ZnIn2S4/TiO2 composites showed increased optical absorption. Under optimal conditions, the highest HER rate of the ZT-0.5 (molar ratio of ZnIn2S4/TiO2= 0.5) sample was 8774 μmol·g-1·h-1, which is considerably higher than those of pure TiO2 NFs (3312 μmol·g-1·h-1) and ZnIn2S4nanoplates (3114 μmol·g-1·h-1) by factors of 2.7 and 2.8, respectively. Based on the experimental data and Mott-Schottky analysis, a possible mechanism for the formation of the S-scheme heterojunction between ZnIn2S4 and TiO2 was proposed to interpret the enhanced HER activity of the ZnIn2S4/TiO2heterojunctionphotocatalysts.
相似文献
103.
Six new 4″-benzyloxyimino-4″-deoxyavermectin Bla derivatives were synthesized from avermectin Bla by the selective protection of C-5-hydroxy group,oxidation of C-4″-hydroxy group,and deprotection followed by reaction with O-substituted hydroxylamine hydrochlorides.Their structures were confirmed by IR,~1H NMR,~(13)C NMR and MS.Insecticidal activities of the derivatives against Phopalosiphum pseudobrassicae,Spodoptera exigua and Pluteua xylosteua were evaluated. 相似文献
104.
尼龙1010/尼龙6共聚物的表观相图研究 总被引:2,自引:0,他引:2
采用显微熔点法和DSC测定了尼龙1010/尼龙6共聚物的表观相图;分析了投料比与链节结构单元含量的关系。最低熔点时尼龙1010/尼龙6的理论重量投料比为60/40,摩尔比为33.3/66.7,实验结果与此相近。 相似文献
105.
Zhichao Tao Yong fang Chenghua Zhang Tingzhen Li Mingyue Ding Hongwei Xiang Yongwang Li 《天然气化学杂志》2007,16(3):278-285
The effects of Manganese(Mn)incorporation on a precipitated iron-based Fischer-Tropsch synthesis(FTS)catalyst were investigated using N_2 physical adsorption,air differential thermal analysis (DTA),H_2 temperature-programmed reduction(TPR),and M(?)ssbauer spectroscopy.The FTS perfor- mances of the catalysts were tested in a slurry phase reactor.The characterization results indicated that Mn increased the surface area of the catalyst,and improved the dispersion ofα-Fe_2O_3 and reduced its crystallite size as a result of the high dispersion effect of Mn and the Fe-Mn interaction.The Fe-Mn inter- action also suppressed the reduction ofα-Fe_2O_3 to Fe_3O_4,stabilized the FeO phase,and(or)decreased the carburization degree of the catalysts in the H_2 and syngas reduction processes.In addition,incorporated Mn decreased the initial catalyst activity,but improved the catalyst stability because Mn restrained the reoxidation of iron carbides to Fe_3O_4,and improved further carburization of the catalysts.Manganese suppressed the formation of CH_4 and increased the selectivity to light olefins(C_(2-4)~=),but it had little effect on the selectivities to heavy(C_(5 )) hydrocarbons.All these results indicated that the strong Fe-Mn interaction suppressed the chemisorptive effect of the Mn as an electronic promoter,to some extent,in the precipitated iron-manganese catalyst system. 相似文献
106.
A highly sensitive and selective catalytic adsorptive cathodic striping procedure for the determination of trace germanium is presented. The method is based on adsorptive accumulation of the Ge(IV)‐gallic acid (GA) complex onto a hanging mercury drop electrode, followed by reduction of the adsorbed species. The reduction current is enhanced catalytically by addition of vanadium(IV)‐EDTA. The optimal experimental conditions include the use of 0.03 mol/L HClO4 (pH1.6), 6.0×10?3 mol/L GA, 3.0×10?3 mol/L V(IV), 4.0×10?3 mol/L EDTA, an accumulation potential of ?0.10 V(vs. Ag/AgCl), an accumulation time of 120 s and a differential pulse potential scan mode. The peak current is proportional to the concentration of Ge(IV) over the range of 3.0×10?11 to 1.0×10?8 mol/L and the detection limit is 2×10?11 mol/L for a 120 s adsorption time. The relative standard deviation at 5.0×10?10 mol/L level is 3.1%. No serious interferences were found. The method was applied to the determination of germanium in ore, mineral water and vegetable samples with satisfactory results. 相似文献
107.
Yao Zu Liao Mei Hua Xin Ming Chun Li Sheng Su College of Materials Science Engineering Huaqiao University Quanzhou China 《中国化学快报》2007,18(2):213-216
O-Lauroyl chitosan/poly(L-lactide) (OCS/PLLA) blend membranes with different compositions were prepared by solution-casting approach using chloroform as common solvent. The experimental results of FT-IR, DSC and WAXD indicated that inter-association hydrogen-bond interactions existed between OCS and PLLA in the blend membranes. And SEM observation confirmed that the blend membranes with suitable compositions were compatible. 相似文献
108.
Lee JS Zhang MH Yun EK Geum D Kim K Kim TH Lim YS Seo JS 《Experimental & molecular medicine》2005,37(5):427-435
Vimentin is an intermediate filament that regulates cell attachment and subcellular organization. In this study, vimentin filaments were morphologically altered, and its soluble subunits were rapidly reduced via cadmium chloride treatment. Cadmium chloride stimulated three major mitogen-activated protein kinases (MAPKs): extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), and p38, and led apoptotic pathway via caspase-9 and caspase-3 activations. In order to determine whether MAPKs were involved in this cadmium-induced soluble vimentin disappearance, we applied MAPK-specific inhibitors (PD98059, SP600125, SB203580). These inhibitors did not abolish the cadmium-induced soluble vimentin disappearance. Caspase and proteosome degradation pathway were also not involved in soluble vimentin disappearance. When we observed vimentin levels in soluble and insoluble fractions, soluble vimentin subunits shifted to an insoluble fraction. As we discovered that heat-shock protein 27 (HSP27) was colocalized and physically associated with vimentin in unstressed cells, the roles of HSP27 with regard to vimentin were assessed. HSP27-overexpressing cells prevented morphological alterations of the vimentin filaments, as well as reductions of soluble vimentin, in the cadmium-treated cells. Moreover, HSP27 antisense oligonucleotide augmented these cadmium-induced changes in vimentin. These findings indicate that HSP27 prevents disruption of the vimentin intermediate filament networks and soluble vimentin disappearance, by virtue of its physical interaction with vimentin in cadmium-treated SK-N-SH cells. 相似文献
109.
110.
Capillary electrophoresis with end-column amperometric detection of urinary 8-hydroxy-2'-deoxyguanosine 总被引:1,自引:0,他引:1
Urinary 8-hydroxy-2'-deoxyguanosine (8OHdG) is an excellent marker of oxidative DNA damage. Until now, urinary 8OHdG has been measured by high-performance liquid chromatography with electrochemical detection. A simple and sensitive method for the analysis of urinary 8OHdG by capillary electrophoresis with end-column amperometric detection has been developed in our laboratory. A single-step solid-phase extraction procedure was optimized and used for extracting 8OHdG from human urine. To improve the sensitivity of this method, a new focusing technique based on a dynamic pH junction was used. The limit of detection was 20 nM (signal-to-noise ratio S/N = 3), the linear range was 50 nM-10 microM, and the correlation coefficient was better than 0.999. The relative standard deviation (RSD) was found to be 0.57% for migration time, and 4.79% for peak current. To show the usefulness of the method, the urinary concentration of 8OHdG in nine healthy persons and ten cancer patients was determined. The urinary concentration of 8OHdG in cancer patients was significantly higher than that in healthy persons. 相似文献