全文获取类型
收费全文 | 318篇 |
免费 | 12篇 |
专业分类
化学 | 203篇 |
晶体学 | 2篇 |
力学 | 14篇 |
数学 | 18篇 |
物理学 | 93篇 |
出版年
2023年 | 2篇 |
2022年 | 15篇 |
2021年 | 14篇 |
2020年 | 10篇 |
2019年 | 13篇 |
2018年 | 13篇 |
2017年 | 4篇 |
2016年 | 14篇 |
2015年 | 6篇 |
2014年 | 14篇 |
2013年 | 23篇 |
2012年 | 24篇 |
2011年 | 26篇 |
2010年 | 12篇 |
2009年 | 15篇 |
2008年 | 7篇 |
2007年 | 15篇 |
2006年 | 10篇 |
2005年 | 12篇 |
2004年 | 6篇 |
2003年 | 7篇 |
2002年 | 6篇 |
2001年 | 1篇 |
2000年 | 2篇 |
1999年 | 3篇 |
1998年 | 1篇 |
1997年 | 2篇 |
1995年 | 3篇 |
1994年 | 4篇 |
1993年 | 4篇 |
1991年 | 1篇 |
1990年 | 5篇 |
1989年 | 2篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 4篇 |
1984年 | 5篇 |
1983年 | 4篇 |
1982年 | 2篇 |
1981年 | 2篇 |
1979年 | 3篇 |
1978年 | 1篇 |
1976年 | 1篇 |
1975年 | 2篇 |
1974年 | 1篇 |
1973年 | 2篇 |
1972年 | 1篇 |
1962年 | 1篇 |
1961年 | 1篇 |
排序方式: 共有330条查询结果,搜索用时 15 毫秒
311.
The properties of low frequency (coupled acoustic and drift wave) nonlinear structures including solitary waves and double layers in an inhomogeneous magnetized electron–positron–ion (EPI) nonthermal plasma with density and temperature inhomogeneities are studied in a simplified way. The nonlinear differential equation derived here for the study of double layers in the inhomogeneous EPI plasma resembles with the modified KdV equation in the stationary frame. But the method used for the derivation of nonlinear differential equation is simple and consistent to give both the stationary solitary waves and double layers. Further, the illustrations show that superthermality κ, drift velocity and temperature inhomogeneity have significant effects on the amplitude, width, and existence range of the structures. 相似文献
312.
The synthesis and characterisation of a homologous series of monodentate benzimidazolium salts, 1–4 and their mononuclear silver(I)–NHC (where NHC = N-heterocyclic carbene) complexes, 5–8, are reported. The benzimidazolium salts were prepared from the N-alkylation of 1-methyl-benzimidazole with alkyl halides of varying carbon chain lengths. The mono silver(I)-NHC complexes, 5–8, were prepared by the reaction of the benzimidazolium salts with Ag2O. All the synthesised compounds were fully characterised by 1H-nuclear magnetic resonance (1H-NMR), 13C-NMR and fourier-transform infrared (FTIR) spectroscopy. The molecular structures of compounds 3·PF6, 4·PF6, 7 and 8 were elucidated through single-crystal X-ray diffraction analyses. We postulate that the attachment of long alkyl chains to the heterocyclic core of 1-methyl benzimidazole could induce mesophase formation. The liquid crystalline behaviour of the benzimidazolium salts was investigated by polarised optical microscope and differential scanning calorimetry. Salts 3 and 4 were found to be thermotropic liquid crystals which exhibited a smectic A phase. However, upon complexation with silver(I) ions, all the Ag(I)–NHC complexes are found to be non-mesogenic. 相似文献
313.
Sunusi Y. Hussaini Rosenani A. Haque Tabinda Fatima Taleb M. Agha A. M. S. Abdul Majid Hassan H. Abdallah Mohd. R. Razali 《Transition Metal Chemistry》2018,43(4):301-312
A series of aliphatic nitrile functionalized benzimidazolium salts and their respective mononuclear N-heterocyclic carbene Ag(I)-NHC complexes are reported. The benzimidazolium salts were synthesized by N-alkylation of 1H-benzimidazole with an appropriate alkyl bromide, followed by reaction with either 5-bromovaleronitrile or 6-bromohexanenitrile. The respective mononuclear Ag(I)-NHC complexes were prepared by the reaction of the benzimidazolium salts with Ag2O. All the synthesized compounds were characterized by physico-chemical and spectroscopic techniques. The molecular structures of the two complexes were elucidated through single-crystal X-ray diffraction analyses. Density functional theory was used to model the structures of the other complexes. The benzimidazolium salts and their complexes were screened for cytotoxicity against a breast cancer cell line (MCF-7), using the MTT assay. All the Ag(I)-NHC complexes gave IC50 values ranging from 7.0 ± 1.06 to 12.9 ± 1.55 µM which are comparable to the standard drug, tamoxifen (IC50 = 11.2 ± 1.84 µM), while all of the benzimidazolium salts proved to be inactive. 相似文献
314.
Afaque Ahmed Ismail Mohd Saaid Rashidah M Pilus Abdelazim Abbas Ahmed Abdul Haque Tunio Mirza Khurram Baig 《Journal of Dispersion Science and Technology》2018,39(10):1469-1475
The present study examines and compares the effect of surface treatments of nano-silica using internal olefins sulphonates (IOS20–24 and IOS19–23), anionic surfactants. The effect of surface modification on colloidal stability, wettability alteration and oil-water interfacial tension reduction were analyzed. Silica nanoparticles were characterized using Field Emission Scanning Electron Microscope (FESEM) and integrated energy-dispersive X-ray spectroscopy (EDX) before and after surface treatment. Using Turbiscan classic, the optimal nanosilica concentration and inspection of the coated particles dispersion stability with the help of light transmission behavior through the nanofluid was carried out. The stability was found to be enhanced as the mean light transmission declined only after surfactant treatment in both IOS coated nano-silicas but IOS19–23 O-342 coated dispersions proved to be more stable among all three. RAME-HART Goniometer was used to perform interfacial tension (IFT) and contact angle measurements. IFT was found to be reduced by 48% after the surfactant treatment in case of IOS19–23 O-342 coated nanosilica. Both surface treatments of nanosilica and increasing silica concentration caused significant reduction and altering wettability towards more water wet. The results revealed that IOS coatings improved the efficiency of NPs dispersion in terms of altered wettability and reduced IFT that mimics their potential for EOR applications. 相似文献
315.
Md. Aminul Haque Md. Mahedi Hasan Tamanna Islam Md. Abdur Razzak Nabeel H. Alharthi Abdullah Sindan Mohammad R. Karim Shaik Inayath Basha Md. Abdul Aziz A. J. Saleh Ahammad 《Electroanalysis》2020,32(9):1957-1970
We have prepared activated porous carbon material through simple pyrolysis method from rice husks (rhAC) for sensitive detection of dopamine (DA) and uric acid (UA). The prepared rhAC material was thoroughly characterized using various spectroscopic, microscopic, and electroanalytical techniques. Analysis of the voltammetric data showed that the analytes followed a first order reaction kinetics while following a 2e?/2H+ transfer process. We have discussed the possible oxidation mechanism for the analytes based on the results from our experimental analysis. The rhAC_GCE sensor was tested for interference, reproducibility, and stability. The sensor was also tested to evaluate its applicability in real life. 相似文献
316.
Absorption spectra of a number of shellfish extracts have been obtained and reveal prominent absorptions in all samples at 210 and 260 nm and at 325 nm in some of them. These absorptions preclude the use of chromophores with similar absorptions in testing of shellfish samples for paralytic shellfish toxins. Two crown ether chemosensors featuring a boron azadipyrrin chromophore have been synthesized; both have absorption maxima at 650 nm, where all the shellfish extracts are transparent. The synthetic sensors feature either 18- or 27-membered crown ether rings and have been evaluated as visible sensors for the paralytic shellfish toxin saxitoxin. The binding constant for one of them is in the range of 3-9x10(5) M-1 and exhibits a fluorescence enhancement of over 100% at 680 nm in the presence of 40 microM saxitoxin. 相似文献
317.
We have studied silica gel by sol–gel technique for the preparation of new dye-laser materials. Silica gel rods with dimension 50 × 10 mm2 have been prepared successfully without breaking. It shows high transparency and good mechanical strength. Tetraethylorthosilicate (TEOS), formamide in molar ratio (0.25:0.70), 80 ml ethanol, 20 ml dimethylformamide (DMF), 10 ml water, hydrochloric acid as a catalyst (at pH 6), and 0.5 ml silicone defoaming agent/surfactant have been used. The synthesis has been carried out in a beaker and the reaction mixture is caste in to the flat bottom glass tubes at 40 °C after thoroughly mixing of all the ingredients. These complex reactions, that carried out by hydrolysis and condensation in the silica gel formation show less gel time ∼8–10 h at 40 °C. Coumarin. 440 dye was doped during the preparation of all the ingredients solution mixture. It has been observed that that the compatibility of Nile blue dyes with silica-gel promise good homogeneity with transparency. 相似文献
318.
Beauchamp KA Bowman GR Lane TJ Maibaum L Haque IS Pande VS 《Journal of chemical theory and computation》2011,7(10):3412-3419
Markov State Models provide a framework for understanding the fundamental states and rates in the conformational dynamics of biomolecules. We describe an improved protocol for constructing Markov State Models from molecular dynamics simulations. The new protocol includes advances in clustering, data preparation, and model estimation; these improvements lead to significant increases in model accuracy, as assessed by the ability to recapitulate equilibrium and kinetic properties of reference systems. A high-performance implementation of this protocol, provided in MSMBuilder2, is validated on dynamics ranging from picoseconds to milliseconds. 相似文献
319.
Zang Q Keire DA Buhse LF Wood RD Mital DP Haque S Srinivasan S Moore CM Nasr M Al-Hakim A Trehy ML Welsh WJ 《Analytical and bioanalytical chemistry》2011,401(3):939-955
Chemometric analysis of a set of one-dimensional (1D) (1)H nuclear magnetic resonance (NMR) spectral data for heparin sodium active pharmaceutical ingredient (API) samples was employed to distinguish USP-grade heparin samples from those containing oversulfated chondroitin sulfate (OSCS) contaminant and/or unacceptable levels of dermatan sulfate (DS) impurity. Three chemometric pattern recognition approaches were implemented: classification and regression tree (CART), artificial neural network (ANN), and support vector machine (SVM). Heparin sodium samples from various manufacturers were analyzed in 2008 and 2009 by 1D (1)H NMR, strong anion-exchange high-performance liquid chromatography, and percent galactosamine in total hexosamine tests. Based on these data, the samples were divided into three groups: Heparin, DS ≤ 1.0% and OSCS = 0%; DS, DS > 1.0% and OSCS = 0%; and OSCS, OSCS > 0% with any content of DS. Three data sets corresponding to different chemical shift regions (1.95-2.20, 3.10-5.70, and 1.95-5.70 ppm) were evaluated. While all three chemometric approaches were able to effectively model the data in the 1.95-2.20 ppm region, SVM was found to substantially outperform CART and ANN for data in the 3.10-5.70 ppm region in terms of classification success rate. A 100% prediction rate was frequently achieved for discrimination between heparin and OSCS samples. The majority of classification errors between heparin and DS involved cases where the DS content was close to the 1.0% DS borderline between the two classes. When these borderline samples were removed, nearly perfect classification results were attained. Satisfactory results were achieved when the resulting models were challenged by test samples containing blends of heparin APIs spiked with non-, partially, or fully oversulfated chondroitin sulfate A, heparan sulfate, or DS at the 1.0%, 5.0%, and 10.0% (w/w) levels. This study demonstrated that the combination of 1D (1)H NMR spectroscopy with multivariate chemometric methods is a nonsubjective, statistics-based approach for heparin quality control and purity assessment that, once standardized, minimizes the need for expert analysts. 相似文献