全文获取类型
收费全文 | 5869篇 |
免费 | 572篇 |
国内免费 | 443篇 |
专业分类
化学 | 1632篇 |
晶体学 | 56篇 |
力学 | 212篇 |
综合类 | 134篇 |
数学 | 2323篇 |
物理学 | 2527篇 |
出版年
2024年 | 15篇 |
2023年 | 53篇 |
2022年 | 116篇 |
2021年 | 113篇 |
2020年 | 122篇 |
2019年 | 142篇 |
2018年 | 155篇 |
2017年 | 173篇 |
2016年 | 199篇 |
2015年 | 158篇 |
2014年 | 334篇 |
2013年 | 444篇 |
2012年 | 308篇 |
2011年 | 360篇 |
2010年 | 301篇 |
2009年 | 368篇 |
2008年 | 423篇 |
2007年 | 401篇 |
2006年 | 338篇 |
2005年 | 284篇 |
2004年 | 261篇 |
2003年 | 271篇 |
2002年 | 218篇 |
2001年 | 176篇 |
2000年 | 175篇 |
1999年 | 149篇 |
1998年 | 128篇 |
1997年 | 133篇 |
1996年 | 123篇 |
1995年 | 78篇 |
1994年 | 53篇 |
1993年 | 47篇 |
1992年 | 40篇 |
1991年 | 31篇 |
1990年 | 29篇 |
1989年 | 16篇 |
1988年 | 22篇 |
1987年 | 15篇 |
1986年 | 20篇 |
1985年 | 15篇 |
1984年 | 16篇 |
1983年 | 6篇 |
1982年 | 21篇 |
1981年 | 9篇 |
1980年 | 3篇 |
1979年 | 11篇 |
1978年 | 8篇 |
1977年 | 1篇 |
1976年 | 1篇 |
1974年 | 1篇 |
排序方式: 共有6884条查询结果,搜索用时 31 毫秒
21.
Hiroto Kudo Nobuhito Ito Keiji Nakajima Masami Ochiai Tadatomi Nishikubo 《Journal of polymer science. Part A, Polymer chemistry》2007,45(19):4421-4429
The polyaddition of fluorine‐containing bis(epoxide)s and fluorine‐containing triazine di(aryl ether)s were examined to give the corresponding fluorine‐containing poly(cyanurate)s. It was observed that the synthesized fluoropolymers had good thermal stabilities and good film‐forming properties. The glass transition temperatures (Tg's) and refractive‐indices (nD's) of synthesized polymers were determined by differential scanning calorimetry and ellipsometry, respectively, and it was found that the values of Tg's and nD's were supported by their fluorine containing ratios and skeletons. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4421–4429, 2007 相似文献
22.
求线性规划初始可行基的新方法 总被引:9,自引:3,他引:6
本文提出一个求线性规划初始可行基的新算法,该算法不仅避免了人工变量,而且理论分析及初步的数值实验结果表明其效率更高。 相似文献
23.
24.
25.
M. A. Bertolim M. P. Mello K. A. de Rezende 《Transactions of the American Mathematical Society》2005,357(10):4091-4129
In this article the main theorem establishes the necessity and sufficiency of the Poincaré-Hopf inequalities in order for the Morse inequalities to hold. The convex hull of the collection of all Betti number vectors which satisfy the Morse inequalities for a pre-assigned index data determines a Morse polytope defined on the nonnegative orthant. Using results from network flow theory, a scheme is provided for constructing all possible Betti number vectors which satisfy the Morse inequalities for a pre-assigned index data. Geometrical properties of this polytope are described.
26.
n阶矩阵A称为完全正的,如果A有分解:A=BBT,其中B为元素非负矩阵,B的最小可能列数称为A的分解指数.本文考察低阶双非负矩阵在整数环上的完全正分解及其分解指数. 相似文献
27.
J. T. Hoeft M. Polcik D. I. Sayago M. Kittel R. Terborg R. L. Toomes J. Robinson D. P. Woodruff M. Pascal G. Nisbet C. L. A. Lamont 《Surface science》2003,540(2-3):441-456
The local adsorption geometry of CO adsorbed in different states on Ni(1 0 0) and on Ni(1 0 0) precovered with atomic hydrogen has been determined by C 1s (and O 1s) scanned-energy mode photoelectron diffraction, using the photoelectron binding energy changes to characterise the different states. The results confirm previous spectroscopic assignments of local atop and bridge sites both with and without coadsorbed hydrogen. The measured Ni–C bondlengths for the Ni(1 0 0)/CO states show an increase of 0.16 ± 0.04 Å in going from atop to bridge sites, while comparison with similar results for Ni(1 1 1)/CO for threefold coordinated adsorption sites show a further lengthening of the bond by 0.05 ± 0.04 Å. These changes in the Ni–CO chemisorption bondlength with bond order (for approximately constant adsorption energy) are consistent with the standard Pauling rules. However, comparison of CO adsorbed in the atop geometry with and without coadsorbed hydrogen shows that the coadsorption increases the Ni–C bondlength by only 0.06 ± 0.04 Å, despite the decrease in adsorption energy of a factor of 2 or more. This result is also reproduced by density functional theory slab calculations. The results of both the experiments and the density functional theory calculations show that CO adsorption onto the Ni(1 0 0)/H surface is accompanied by significant structural modification; the low desorption energy may then be attributed to the energy cost of this restructuring rather than weak local bonding. 相似文献
28.
Vincent S. Smentkowski John T. Yates Jr. Xiaojie Chen William A. Goddard III 《Surface science》1997,370(2-3):209-231
The radiation-induced decomposition of C4F9I and CF3I overlayers at 119 K on diamond (100) surfaces has been shown to be an efficient route to fluorination of the diamond surface. X-ray photoelectron spectroscopy has been used for photoactivation as well as for studying the photodecomposition of the fluoroalkyl iodide molecules, the attachment of the photofragments to the diamond surface, and the thermal decomposition of the fluoroalkyl ligands. Measured chemical shifts agree well with ab initio calculations of both C 1s and F 1s binding energies. It is found that chemisorbed CF3 groups on diamond (100) decompose by 300 K whereas C4F9 groups decompose over the range 300 to 700 K and this reactivity difference is rationalized on steric grounds. Both of these thermal decomposition processes produce surface C---F bonds on the diamond. The surface C---F species thermally decompose over a wide temperature range extending up to 1500 K. Hydrogen passivation of the diamond surface is ineffective in preventing free radical attack from the photodissociated products of the fluoroalkyl iodides; I atoms produced photolytically abstract H from surface C---H bonds to yield hydrogen iodide at 119 K allowing diamond fluorination. The attachment of chemisorbed F species to the diamond (100) surface causes band bending as the surface states are occupied as a result of chemisorption. This results in a shift to higher binding energy of the diamond-related C 1s levels present in the surface and subsurface regions which are sampled by XPS on the diamond. The use of photoactivation of fluoroalkyl iodides for the fluorination of diamond surfaces provides a convenient route compared to other methods involving the action of atomic F, molecular F2, XeF2 and F-containing plasmas. 相似文献
29.
Linear and nonlinear optical properties of racemic (±)2-(α-methylbenzylamino)-5-nitropyridine ((±)MBANP) single crystals have been comprehensively investigated and compared with those of the enantiomorph (–)2-(α-methylbenzylamino)-5-nitropyridine ((–)MBANP) crystals. (±)MBANP crystal exhibits very high chemical and physical stability, but relatively small nonlinear optical coefficients (d31 = 6.8 pm/V, d32 = 4.7 pm/V, d33 = 0.84 pm/V). A comparison between the nonlinear optical coefficients of (±)MBANP and (–)MBANP demonstrates the validity of the oriented-gas model in molecular crystals that neglects all the contributions from intermolecular interaction. 相似文献
30.