全文获取类型
收费全文 | 194836篇 |
免费 | 31024篇 |
国内免费 | 21871篇 |
专业分类
化学 | 131720篇 |
晶体学 | 2359篇 |
力学 | 12860篇 |
综合类 | 1366篇 |
数学 | 23870篇 |
物理学 | 75556篇 |
出版年
2024年 | 608篇 |
2023年 | 3547篇 |
2022年 | 6528篇 |
2021年 | 7218篇 |
2020年 | 7380篇 |
2019年 | 7297篇 |
2018年 | 6417篇 |
2017年 | 6228篇 |
2016年 | 9114篇 |
2015年 | 9117篇 |
2014年 | 11188篇 |
2013年 | 14439篇 |
2012年 | 17306篇 |
2011年 | 17706篇 |
2010年 | 12217篇 |
2009年 | 11829篇 |
2008年 | 12700篇 |
2007年 | 11377篇 |
2006年 | 10589篇 |
2005年 | 8874篇 |
2004年 | 6706篇 |
2003年 | 5318篇 |
2002年 | 5078篇 |
2001年 | 4149篇 |
2000年 | 3591篇 |
1999年 | 3955篇 |
1998年 | 3325篇 |
1997年 | 3107篇 |
1996年 | 3241篇 |
1995年 | 2721篇 |
1994年 | 2515篇 |
1993年 | 2027篇 |
1992年 | 1845篇 |
1991年 | 1586篇 |
1990年 | 1340篇 |
1989年 | 961篇 |
1988年 | 777篇 |
1987年 | 637篇 |
1986年 | 663篇 |
1985年 | 540篇 |
1984年 | 375篇 |
1983年 | 297篇 |
1982年 | 223篇 |
1981年 | 175篇 |
1980年 | 118篇 |
1979年 | 83篇 |
1977年 | 57篇 |
1976年 | 62篇 |
1975年 | 61篇 |
1974年 | 57篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
41.
42.
In theory, both polarity and steric hindrance are basic factors which affect molecular interactions. To investigate the optical properties and steric structures of chiral compounds having different chiral moieties which affect the wavelength of light reflection in liquid crystal (LC) cells, a series of novel chiral compounds and azobenzene derivatives were synthesized. The liquid crystalline phases of the compounds were identified using small angle X-ray diffraction, differential scanning calorimetry and polarizing optical microscopy. Cholesteric LC cells with various synthesized chiral dopants which selectively reflect visible light were first prepared, the photochemical switching behaviour of colours was then investigated, with special reference to the change in transmittance in cholesteric LC cells containing an azobenzene derivative as a photoisomerizable guest molecule. Reversible isomerization of azobenzene molecules occurred in the cholesteric systems, resulting in a depression of TChI and a shift of the selectively reflected wavelength. We discuss the photochemically driven change in the helical pitch of the cholesteric LCs with respect to structural effects involving the chiral moieties. Molecular interactions caused by the added dopants, reliability and stability of the photoisomerization, and UV irradiation effects on the cholesteric LC cells were also investigated. A real image was recorded through a mask on a cholesteric LC cell fabricated in this investigation. 相似文献
43.
Yang Zuosheng 《国际流体数值方法杂志》2005,47(12):1423-1430
A complete boundary integral formulation for compressible Navier–Stokes equations with time discretization by operator splitting is developed using the fundamental solutions of the Helmholtz operator equation with different order. The numerical results for wall pressure and wall skin friction of two‐dimensional compressible laminar viscous flow around airfoils are in good agreement with field numerical methods. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
44.
Perovskite-type lithium fast ion conductors of Li3xLa0.67−xScyTi1−2yNbyO3 system were prepared by solid state reaction. X-Ray powder diffraction shows that perovskite solid solution form in the ranges
of x=0.10, y≤0.10. AC impedance measurements indicate that the bulk conductivities and the total conductivities are of the
order of 10−4 S·cm−1 and 10−5 S·cm−1 at 25 °C respectively. The compositions have low bulk activation energies of about 17 kJ/mol in the temperature ranges of
298 – 523 K and total activation energies of about 37 kJ/mol in the temperature ranges of 298 – 523 K. 相似文献
45.
Jie Xue Liang Chen Li Zhou Zhifeng Jia Yanping Wang Xinyuan Zhu Deyue Yan 《Journal of Polymer Science.Polymer Physics》2006,44(15):2050-2057
α‐Cyclodextrin (α‐CD) has been complexed with various poly(ethylene glycol) (PEG) derivatives in aqueous solution. It has been found that the end groups of PEG derivatives affect the complexation kinetics greatly, but have only a little influence on the thermodynamic behavior. By increasing the hydrophobicity of end groups, the complexation speeds up rapidly. On the other hand, the bulky end groups slow down the threading of polymeric guests into the cavity of CD. By changing the hydrophobicity and the size of end groups, the complexation rate can be adjusted in the range of several orders of magnitudes, which should be quite useful in the design of new supramolecular systems. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 2050–2057, 2006 相似文献
46.
Recently, molecular imaging has been rapidly developed to studyphysiological and pathological processes in vivo at the cellularand molecular levels. Among molecular imaging modalities, opticalimaging has attracted a major attention for its unique advantages.In this paper, we establish a mathematical framework for multispectralbioluminescence tomography (BLT) that allows simultaneous studiesof multiple optical reporters. We show solution existence, uniquenessand continuous dependence on data as well as the limiting behaviourswhen the regularization parameter approaches zero or when thepenalty parameter approaches infinity. Then, we propose twonumerical schemes for multispectral BLT and derive error estimatesfor the corresponding solutions. 相似文献
47.
The crystal and molecular structure of the complex containing cobalt-carbon and iron-sulfur cluster cores, (μ-p-CH3C6H4C2S) (μ-n-C3H7S)Fe2(CO)6Co2(CO)6, has been determined by X-ray diffraction method. The crystals are triclinic, space group P&1bar;, with a — 9.139(2), b=9.610(1), c-17.183(2) Å, α = 84.36(1), β-89.45(1), γ=88.15(1)°, V-1501.0 Å3; Z=2, Dc=1.74 g/cm3. R=0.072, Rw=0.081. The results of the structure determination show a cobalt-carbon cluster core formed through the reaction of (μ-p-CH3C6H4C2S)(μ-n-C3H7S)Fe2(CO)6 with Co2(CO)8. In the cobalt-carbon cluster core, the bond length of the original C≡C lengthened to 1.324 Å which is close to the typical value of carbon-carbon double bond. The groups connecting the carbons of the cluster core are in cis position and lie on the opposite side of cobalt atoms. In this complex, the conformation of —SC3H7 is e-type, while that of —SC2C6H4CH3 is a-type. 相似文献
48.
养殖池塘沉积物的重金属分布及污染特征 总被引:3,自引:0,他引:3
浙江省淅西北地区淡水养殖池塘沉积物重金属调查研究表明,养殖池塘沉积物中7种重金属元素分布不均衡,差异也较大,除Hg和Cr元素外,其余重金属元素已大大超过土壤本底值.虽然其实测含量都未超出国家规定的标准值范围,但沉积物中重金属元素对养殖水环境、养殖品种存在的潜在污染与危害值得关注.污染指数评价显示,养殖池塘沉积物中主要污染物质为Cu和Cr,而Hg、Pb污染程度相对较轻. 相似文献
49.
Zhong‐Zhen Yu Mingshu Yang Qingxin Zhang Chungui Zhao Yiu‐Wing Mai 《Journal of Polymer Science.Polymer Physics》2003,41(11):1234-1243
Nylon‐66 nanocomposites were prepared by melt‐compounding nylon‐66 with an alkyl ammonium surfactant pretreated montmorillonite (MMT). The thermal stability of the organic MMT powders was measured by thermogravimetric analysis. The decomposition of the surfactant on the MMT occurred from 200 to 500 °C. The low onset decomposition temperature of the organic MMT is one shortcoming when it is used to prepare polymer nanocomposites at high melt‐compounding temperatures. To provide greater property enhancement and better thermal stability of the polymer/MMT nanocomposites, it is necessary to develop MMT modified with more thermally stable surfactants. The dispersion and spatial distribution of the organic MMT layers in the nylon‐66 matrix were characterized by X‐ray diffraction. The organic MMT layers were exfoliated but not randomly dispersed in the nylon‐66 matrix. A model was proposed to describe the spatial distribution of the organic MMT layers in an injection‐molded rectangular bar of nylon‐66/organic MMT nanocomposites. Most organic MMT layers were oriented in the injection‐molding direction. Layers near the four surfaces of the bar were parallel to their corresponding surfaces; whereas those in the bulk differed from the near‐surface layers and rotated themselves about the injection‐molding direction. The influence of the spatial distribution of the organic MMT on crystallization of nylon‐66 was also investigated. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1234–1243, 2003 相似文献
50.
Leong‐Huat Gan Palaniswamy Ravi Bao Wei Mao Kam‐Chiu Tam 《Journal of polymer science. Part A, Polymer chemistry》2003,41(17):2688-2695
Polymerization of 2‐(diethylamino)ethyl methacrylate (DEAEMA) via homogeneous atom transfer radical polymerization under various reaction conditions is described. The effects of the initiators and solvents were examined. With 1,1,4,7,10,10‐hexamethyl triethylenetetramine/copper(I) chloride/p‐toluenesulfonyl chloride as the ligand/catalyst/initiator system in methanol, poly(DEAEMA) with a polydispersity index as low as 1.07 was synthesized. Kinetic studies demonstrated the polymerization was very well controlled and exhibited the living characteristic of the process. Well‐defined block copolymers of DEAEMA and tert‐butyl methacrylate (tBMA) were successfully synthesized. The copolymers could be synthesized with equally good results by starting with either p(DEAEMA) or p(tBMA) as the macroinitiators. However, only the macroinitiators terminated with chlorine should be used. The corresponding macroinitiators with bromine as a transferable group did not yield well‐defined copolymers. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2688–2695, 2003 相似文献