全文获取类型
收费全文 | 32482篇 |
免费 | 4392篇 |
国内免费 | 3663篇 |
专业分类
化学 | 23748篇 |
晶体学 | 398篇 |
力学 | 1608篇 |
综合类 | 276篇 |
数学 | 3977篇 |
物理学 | 10530篇 |
出版年
2024年 | 88篇 |
2023年 | 518篇 |
2022年 | 924篇 |
2021年 | 962篇 |
2020年 | 1065篇 |
2019年 | 1073篇 |
2018年 | 936篇 |
2017年 | 873篇 |
2016年 | 1293篇 |
2015年 | 1329篇 |
2014年 | 1568篇 |
2013年 | 2183篇 |
2012年 | 2591篇 |
2011年 | 2818篇 |
2010年 | 1974篇 |
2009年 | 1915篇 |
2008年 | 2189篇 |
2007年 | 1930篇 |
2006年 | 1751篇 |
2005年 | 1562篇 |
2004年 | 1254篇 |
2003年 | 1048篇 |
2002年 | 1059篇 |
2001年 | 887篇 |
2000年 | 724篇 |
1999年 | 660篇 |
1998年 | 574篇 |
1997年 | 485篇 |
1996年 | 559篇 |
1995年 | 449篇 |
1994年 | 413篇 |
1993年 | 371篇 |
1992年 | 351篇 |
1991年 | 303篇 |
1990年 | 259篇 |
1989年 | 207篇 |
1988年 | 180篇 |
1987年 | 144篇 |
1986年 | 151篇 |
1985年 | 169篇 |
1984年 | 104篇 |
1983年 | 69篇 |
1982年 | 76篇 |
1981年 | 58篇 |
1980年 | 55篇 |
1979年 | 61篇 |
1978年 | 40篇 |
1976年 | 37篇 |
1974年 | 41篇 |
1973年 | 45篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
991.
Changyuan Lu Side Yao Wenfeng Wang Yongpeng Tong Weizhen Lin Tingwen Rong Nianyun Lin 《中国科学B辑(英文版)》1998,41(3):259-265
Fullerols of C60 and of C70 [C60(OH)n, C70(OH)m], water-soluble fullerene derivatives, unlike some other fullerene derivatives (such as C60 (C4H6O), C60 (C3H7N) and C60 [C(COOEt)2]x), do not result in excited triplet state but in ionization via monophotonic process in aqueous solutions with 248 nm laser.
The quantum yields of formation of hydrated electron (Φe
−) are determined to be 0.08 and 0.11 for fullerols of C60 and of C70 respectively at room temperature (ca. 15°C) with KI solution used as reference. By laser flash photolysis and oxidation of
sulfate radical anion SO4
−, the fullerol radical cation or neutral radical of C60 is confirmed to be existent and the transient absorption spectra of fullerol radical cation of C70 are observed for the first time.
Project supported by the National Natural Science Foundation of China 相似文献
992.
993.
The interaction between diethylenetriaminepentaacetic acid (DTPA or HsZ) and Ce(III) and Th(IV) ions has been investigated spectrophotometrically in aqueous solution at an ionic strength of 0.1 and for various temperatures. It has been found that the Ce(III)-DTPA chelate (1:1) exhibited a characteristic absorption maximum at 297 nm, and the optimum pH range is between 3.4 to 4.4. The absorption of Ce(III)-DTPA chelate is considerably diminished by adding small amounts of Th(IV) ions. This phenomenon was used to evaluate the formation constant of Th(IV)-DTPA chelate (1:1). The formation constants and the thermodynamic properties characterizing the formation of the chelates have been calculated at 25°. The results are as follows: 相似文献
994.
Three-dimensional open frameworks [Co2(nicotinate)4(mu-H2O)]-CH3CH2OH-H2O, 1, and [Ni2(nicotinate)4(mu-H2O)]-CH3CH2OH-H2O, 2, were obtained by hydro(solvo)thermal reactions between 3-cyanopyridine and cobalt(II) nitrate and nickel(II) perchlorate, respectively. Both 1 and 2 exhibit complicated 3-D structures based on [M2(nicotinate)4(mu-H2O)] (M = Co or Ni) building blocks and possess open channels that are occupied by removable solvent molecules. 3-D open frameworks [M2L4(mu-H2O)]-HL-(H2O)x (where M = Co, x = 2, 3, and M = Ni, x = 1, 4, and L = trans-3-(3-pyridyl)acrylate) were similarly prepared with trans-3-(3-pyridyl)acrylic acid in place of 3-cyanopyridine. Compounds 3 and 4 are isostructural and exhibit network topologies similar to that of 1 with open channels occupied by disordered trans-3-(3-pyridyl)acrylic acid and water guest molecules. Crystal data for 1: triclinic space group Ponebar, a = 10.534(1) A, b = 11.907(1) A, c = 14.046(1) A, alpha = 106.645(1) degrees, beta = 101.977(1) degrees, gamma = 112.078(1) degrees, and Z = 4. Crystal data for 2: tetragonal space group P4/ncc, a = 20.089(1) A, c = 14.016(1) A, and Z = 4. Crystal data for 3: monoclinic space group C2/c, a = 14.082(2) A, b = 15.278(2) A, c = 18.537(2) A, beta = 105.360(2) degrees, and Z = 2. Crystal data for 4: monoclinic space group C2/c, a = 14.082(1) A, b = 15.250(1) A, c = 18.606(1) A, beta = 106.747(1) degrees, and Z = 2. 相似文献
995.
A new activation method has been developed for electroless copper plating on silicon wafer based on palladium chemisorption on SAMs of APTS without SnCl2 sensitization and roughening condition.A closely packed electroless copper film with strong adhesion is successfully formed by AFM observation.XPS study indicates that palladium chemisorption occurred via palladium chloride bonding to the pendant amino group of the SAMs. 相似文献
996.
Wang Zhong-Ming Lin Hua-Kuan Zhou Zhi-Fen Zhu Shou-Rong Chen Yun-Ti Murmann R. Kent 《Transition Metal Chemistry》2000,25(5):562-567
The kinetics of the reaction of CH2O with a quasi-aromatic metal complex (1,1,2,8,9,9-hexamethyl-4,6-dioxa-5-hydro-3,7,10,14-tetraazacyclotetradecane-2,7,10,12-tetraene)copper(II), [Cu(PnAO)-6H]0 (AH), have been studied spectrophotometrically under neutral conditions in 1/3(v/v) MeOH–H2O. The Cu, 2N, 3C quasi-aromatic heterocyclic ring in AH is highly reactive towards CH2O at the central-aromatic-carbon atom, C(12) and the following reaction mechanism is proposed.
The compounds AH, A—CH2OH and A—CH2—A were isolated and identified by i.r spectroscopy and by elemental analysis. The kinetic data supported the proposed reaction sequence. All reactions were second order overall. The rate constants and corresponding activation parameters for every step were obtained and are discussed. 相似文献
997.
The amount of silicon sample used in instrumental neutron activation analysis (INAA) is generally less than twenty grams and the detection limits are in the range of ppb to ppt. The detection limits can be decreased further in several ways. Increasing neutron flux density, extending irradiation period and/or using more effective detector can improve the detection limits to some extent. Increasing sample weight, however, is a more feasible way to decrease the detection limits by a factor of hundreds with no new investment in existing irradiation/counting systems. In this work, two 8-inch high-purity silicon samples were analyzed by INAA to evaluate the validity and limitations of this concept in respect to neutron flux inhomogeneity, neutron shielding and -ray counting efficiency. 相似文献
998.
使用MS 80型Calvet微量热计, 在25 ℃, 0.1mol·dm~(-3)(NaClO_4)的50%(V/V)二氧六环溶液中, 测定了镍(Ⅱ)-N,N′-双(对位取代苯基)乙二胺二元及镍(Ⅱ)-2,2′-联吡啶-N,N′-双(对位取代苯基)乙二胺三元体系的生成热和N,N′-双(对位取代苯基)乙二胺的质子化热, 发现在二元和三元配合物的生成热、生成熵与配体的质子化热及质子化熵之间存在较好的线性关系。 相似文献
999.
1000.