全文获取类型
收费全文 | 2330篇 |
免费 | 110篇 |
国内免费 | 12篇 |
专业分类
化学 | 1581篇 |
晶体学 | 36篇 |
力学 | 46篇 |
数学 | 364篇 |
物理学 | 425篇 |
出版年
2023年 | 16篇 |
2022年 | 33篇 |
2021年 | 47篇 |
2020年 | 33篇 |
2019年 | 42篇 |
2018年 | 42篇 |
2017年 | 29篇 |
2016年 | 86篇 |
2015年 | 86篇 |
2014年 | 84篇 |
2013年 | 114篇 |
2012年 | 164篇 |
2011年 | 173篇 |
2010年 | 114篇 |
2009年 | 99篇 |
2008年 | 152篇 |
2007年 | 139篇 |
2006年 | 132篇 |
2005年 | 103篇 |
2004年 | 82篇 |
2003年 | 73篇 |
2002年 | 76篇 |
2001年 | 32篇 |
2000年 | 43篇 |
1999年 | 27篇 |
1998年 | 22篇 |
1997年 | 17篇 |
1996年 | 35篇 |
1995年 | 21篇 |
1994年 | 26篇 |
1993年 | 26篇 |
1992年 | 30篇 |
1991年 | 25篇 |
1990年 | 25篇 |
1989年 | 15篇 |
1988年 | 18篇 |
1987年 | 21篇 |
1986年 | 8篇 |
1985年 | 15篇 |
1984年 | 12篇 |
1983年 | 5篇 |
1982年 | 15篇 |
1981年 | 5篇 |
1977年 | 5篇 |
1974年 | 4篇 |
1961年 | 4篇 |
1890年 | 7篇 |
1885年 | 4篇 |
1882年 | 5篇 |
1879年 | 3篇 |
排序方式: 共有2452条查询结果,搜索用时 31 毫秒
91.
Millet O Muhandiram DR Skrynnikov NR Kay LE 《Journal of the American Chemical Society》2002,124(22):6439-6448
New pulse sequences are presented for the measurement of the relaxation of deuterium double quantum, quadrupolar order, and transverse antiphase magnetization in (13)CH(2)D methyl groups of (15)N-, (13)C-labeled, fractionally deuterated proteins. Together with previously developed experiments for measuring deuterium longitudinal and transverse decay rates [Muhandiram, D. R.; Yamazaki, T.; Sykes, B. D.; Kay, L. E. J. Am. Chem. Soc. 1995, 117, 11536], these schemes allow measurement of the five unique decay constants of a single deuteron, providing an unprecedented opportunity to investigate side-chain dynamics in proteins. All five deuterium relaxation rates have been measured for deuterons in the methyl groups of the B1 immunoglobulin binding domain of peptostreptococcal protein L and the N-terminal SH3 domain from the protein drk. Since values of the spectral density function at only three different frequencies contribute to the five relaxation rates, the self-consistency of the relaxation data is readily established. Very good agreement is obtained between calculated parameters describing the amplitudes and time scales of motion when different subsets of the relaxation data are employed. 相似文献
92.
Coronado E Gómez-García CJ Nuez A Romero FM Rusanov E Stoeckli-Evans H 《Inorganic chemistry》2002,41(18):4615-4617
The combination of hexacyanoferrate(III) anions, [Fe(CN)(6)](3)(-), with nickel(II) complexes derived from the chiral ligand trans-cyclohexane-1,2-diamine (trans-chxn) affords the enantiopure layered compounds [Ni(trans-(1S,2S)-chxn)(2)](3)[Fe(CN)(6)](2).2H(2)O (1) and [Ni(trans-(1R,2R)-chxn)(2)](3)[Fe(CN)(6)](2).2H(2)O (2). These chiral systems behave as ferromagnets (T(c) = 13.8 K) with a relatively high coercive field (H(c) = 0.17 T) at 2 K. They also exhibit an unusual magnetic behavior at low temperatures that has been attributed to the dynamics of the magnetic domains in the ordered phase. 相似文献
93.
Andrs Zelcer Zulema D. Chaia Fabio D. Cukiernik Oscar E. Piro Eduardo E. Castellano 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(3):m144-m146
The title compound, catena‐poly[[tetrakis(μ‐decanoato‐κ2O:O′)diruthenium(II,III)(Ru—Ru)]‐μ‐octanesulfonato‐κ2O:O′], [Ru2(C10H19O2)4(C8H17O3S)], is an octanesulfonate derivative of the mixed‐valence complex diruthenium tetradecanoate. The equatorial carboxylate ligands are bidentate, bridging two Ru atoms to form a dinuclear structure. Each of the two independent dinuclear metal complexes in the asymmetric unit is located at an inversion centre. The octanesulfonate anion bridges the two dinuclear units through axial coordination. The alkyl chains of the carboxylate and sulfonate ligands are arranged in a parallel manner. The global structure can be seen as infinite chains of polar moieties separated by a double layer of non‐polar alkyl groups, without interdigitation of the alkyl chains. 相似文献
94.
The solid phase extraction as a solvent-free method for the analysis of oil and grease in waters was studied. The use of
a PTFE surface as a solid phase allows the retention of the volatile fraction of oil and grease, and further analysis of carbon–hydrogen
bonds using infrared spectroscopy can be done on the surface.
Various oils and grease samples were tested: n-hexadecane, n-tetradecane, n-nonadecane, n-docosane, isooctane, diesel oil
and gasoline. Temperatures from 25° to 90 °C and a range of heating times were checked for extraction.
Precision tests showed relative standard deviation values of around 10% in several samples of the same concentration. Calibration
lines of n-hexadecane showed high correlation coefficients from 0.9 to 30 mg/l. Recoveries for the various oils using different
calibration lines showed values from 90 to 110%.
The method described here is fast and clean, and allows reproducible measurements of oil and grease in water that do not require
the use of a solvent.
Received March 1, 2001; accepted August 15, 2001; published online July 15, 2002 相似文献
95.
G. Gallego Ferrer J. M. Soria Meliá J. Hernández Canales J. M. Meseguer Dueñas F. Romero Colomer M. Monleón Pradas J. L. Gómez Ribelles P. Pissis G. Polizos 《Colloid and polymer science》2005,283(6):681-690
A series of interpenetrated polymer networks (IPNs) in which the first component is a porous poly(ethyl methacrylate) (PEMA) hydrophobic network and the second one is a poly(2-hydroxyethyl acrylate) (PHEA) hydrophilic network were synthesized. Equilibrium sorption isotherms can be reduced to a single master curve for all the IPNs when the water absorbed is expressed per gram of PHEA in them. The equilibrium water sorption in immersion is always much smaller than that of pure PHEA. This feature is due to the confining effect of the stiff PEMA matrix. The plasticizing effect of the absorbed water on the PHEA phase was characterized using thermally stimulated depolarization currents, dynamic-mechanical analysis and dielectric relaxation spectroscopy. The results show that the shift of the main relaxation peak towards lower temperatures is unaffected by the presence of the PEMA matrix, and only depends on the water content per gram of PHEA in the IPN. 相似文献
96.
Gonzalo Astray Juan F. Gálvez Juan C. Mejuto Oscar A. Moldes Iago Montoya 《Journal of computational chemistry》2013,34(5):355-359
In this article, an artificial neural network to predict the flash point of 95 esters was implemented. Four variables were used for its development. A neural network with 4‐5‐8‐5‐1 topology was encountered to gain the best agreement of the experimental results with those predicted (square correlation coefficient (R2) and root mean square error were 0.99 and 5.46 K for the training phase and 0.96 and 13.02 K for the testing set). © 2012 Wiley Periodicals, Inc. 相似文献
97.
The renewal of the urban waterfronts has become a major focus of attention for politicians and decision makers in the city’s management programs. The recognition of the patterns that define the waterfronts’ identity is essential to select new strategies of intervention for the environmental recovery. In order to create adequate environments for everyday life within a sustainable development, new links between human senses, human perception and design need to be created. Within this wide approach, the landscape and the soundscape play a significant role and can become a key driving force in the implementation of the changes. New techniques have to be tested to identify the sonic and visual parameters capable to explain the specificity of a waterfront. With this purpose, an artificial neural network (ANN) was developed, and the relative importance of the input variables was evaluated. The collected database was also analysed by multiple linear regression (MLR) to compare the outcomes of both models. The urban waterfront of Naples (Italy) was chosen as case study. The results obtained show that the performance of the neural network is better than the one of the linear regression (rANN = 0.949, rMLR = 0.639). The interpretation of the relative importance method is also quite satisfactory in the ANN. 相似文献
98.
The microwave spectrum has been investigated for the molecule of Benzenesulphonyl chloride within the 8–18 Ghz frequency region. Several a and b type bands corresponding to the Cl35 and Cl37 Isotopes were observed and assigned. We have also used the CNDO/2 method in order to estimate some molecular parameters and the dipole moment. The theoretical calculation and the experimental data have been joined to derive a reliable structure of the molecule concluding that the Cl is located on the plane of the benzene ring. 相似文献
99.
100.
Multiaxial mechanical behavior of aramid fibers and identification of skin/core structure from single fiber transverse compression testing 下载免费PDF全文
Judith Wollbrett‐Blitz Sébastien Joannès Rémi Bruant Christophe Le Clerc Marc Romero De La Osa Anthony Bunsell Alba Marcellan 《Journal of Polymer Science.Polymer Physics》2016,54(3):374-384
The transverse and longitudinal mechanical properties of aramid fibers like Kevlar? 29 (K29) fibers are strongly linked to their highly oriented structure. Mechanical characterization at the single fiber scale is challenging especially when the diameter is as small as 15 µm. Longitudinal tensile tests on single K29 fibers and single fiber transverse compression test (SFTCT) have been developed. Our approach consists of coupling morphological observations and mechanical experiments with SFTCT analysis by comparing analytical solutions and finite element modeling. New insights on the analysis of the transverse direction response are highlighted. Systematic loading/unloading compression tests enable to experimentally determine a transverse elastic limit. Taking account of the strong anisotropy of the fiber, the transverse mechanical response sheds light on a skin/core architecture. More importantly, results suggest that the skin of the fiber, typically representing a shell of one micrometer in thickness, has a transverse apparent modulus of 0.2 GPa. That is around more than fifteen times lower than the transverse modulus of 3.0 GPa in the core. By comparison, the measured longitudinal modulus is about 84 GPa. The stress distribution in the fiber is explored and the critical areas for damage initiation are discussed. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 374–384 相似文献