全文获取类型
收费全文 | 4013篇 |
免费 | 166篇 |
国内免费 | 18篇 |
专业分类
化学 | 2783篇 |
晶体学 | 40篇 |
力学 | 95篇 |
数学 | 333篇 |
物理学 | 946篇 |
出版年
2023年 | 16篇 |
2022年 | 48篇 |
2021年 | 93篇 |
2020年 | 79篇 |
2019年 | 69篇 |
2018年 | 59篇 |
2017年 | 45篇 |
2016年 | 121篇 |
2015年 | 114篇 |
2014年 | 141篇 |
2013年 | 231篇 |
2012年 | 317篇 |
2011年 | 348篇 |
2010年 | 181篇 |
2009年 | 172篇 |
2008年 | 266篇 |
2007年 | 245篇 |
2006年 | 227篇 |
2005年 | 218篇 |
2004年 | 168篇 |
2003年 | 151篇 |
2002年 | 137篇 |
2001年 | 88篇 |
2000年 | 90篇 |
1999年 | 75篇 |
1998年 | 59篇 |
1997年 | 33篇 |
1996年 | 50篇 |
1995年 | 45篇 |
1994年 | 49篇 |
1993年 | 44篇 |
1992年 | 30篇 |
1991年 | 21篇 |
1990年 | 30篇 |
1989年 | 22篇 |
1988年 | 7篇 |
1987年 | 9篇 |
1986年 | 12篇 |
1985年 | 13篇 |
1984年 | 7篇 |
1983年 | 6篇 |
1982年 | 8篇 |
1981年 | 4篇 |
1980年 | 7篇 |
1979年 | 5篇 |
1977年 | 4篇 |
1976年 | 5篇 |
1975年 | 4篇 |
1974年 | 7篇 |
1973年 | 4篇 |
排序方式: 共有4197条查询结果,搜索用时 406 毫秒
151.
152.
Y. J. Cho C. R. Diminnie R. W. Freese E. Z. Andalafte 《Mathematische Nachrichten》1992,157(1):225-234
A triple (x, y, z) in a linear 2-normed space (X, ‖.,.‖) is called an isosceles orthogonal triple, denoted |(x, y, z), if |(.,.,.) is said to be homogeneous if |(x, y, z) implies |(ax, y, z) for all real a and it is additive if |(x1, y, z) and |(x2, y, z) imply that |(x1 + x2, y, z). In addition to developing some basic properties of |(.,.,.), this paper shows that under the assumption of strict convexity, every subspace of X of dimension ≤ 3 contains an isosceles orthogonal triple. Further, if (X, ‖.,.‖) is strictly convex and |(…,.) is either homogeneous or additive, then (X, ‖.,.‖) is a 2-inner product space. 相似文献
153.
154.
2‐Aminobenzyl alcohol undergoes oxidative cyclization with aryl(alkyl), alkyl(alkyl) and cyclic ketones in dioxane at 80° in the presence of a catalytic amount of RhCl(PPh3)3 along with KOH to afford the corresponding quinolines in good yields. The catalytic pathway seems to be proceeded via a sequence involving initial oxidation of 2‐aminobenzyl alcohol to 2‐aminobenzaldehyde by a rhodium catalyst, cross aldol reaction between 2‐aminobenzaldehyde and ketones, and cyclodehydration. 相似文献
155.
Sessler JL Cho WS Lynch V Král V 《Chemistry (Weinheim an der Bergstrasse, Germany)》2002,8(5):1134-1143
The synthesis and structural characterization of hybrid heterocalix[4]arene analogues containing pyrrole, benzene, methoxy-substituted benzene, and pyridine subunits is described. Macrocycles 1 and 2, examples of calix[2]benzene[2]pyrrole and calix[1]benzene[3]pyrrole systems, respectively, are synthesized by the condensation of pyrrole and an appropriate phenylbis(carbinol). Macrocycles 3 and 7, examples of calix[2]benzene[1]pyridine[1]pyrrole and calix[1]pyridine[3]pyrrole, respectively, are synthesized by the use of a carbene-based pyrrole-to-pyridine ring-expansion procedure. Single-crystal X-ray analysis reveals that compounds 1a, 1b, and 2b adopt 1,3-alternate conformations in the solid state, whereas compounds 3 and 7 display structures that are best described as "flattened partial cones" in terms of their conformation. (Series a refers to pure benzene-derived systems, whereas series b indicates macrocycles containing 5-methoxyphenyl subunits). In the solid state, the methoxy-functionalized macrocycles 1b and 2b, and the chloropyridine-containing macrocycle 7 exist as dimers. In the case of 1a and 7, these compounds interact with neutral solvent in the solid state. The conformations of the macrocycles in solution were explored by temperature-dependent proton NMR and NOESY spectral analysis. At 188 K, macrocycles 1a and 2a adopt flattened 1,3-alternate conformations, whereas macrocycles 3 and 7 exist in the form of flattened partial-cone conformations. Standard proton NMR titration analyses were carried out in the case of macrocycles 1a and 2a, and reveal that at least the second of these systems is capable of binding fluoride and chloride anions in CD(2)Cl(2) solution at room temperature (K(a)=571 and 17M(-1) in the case of 2a and F(-) and Cl(-), respectively). 相似文献
156.
Cho YL Rudkevich DM Shivanyuk A Rissanen K Rebek J 《Chemistry (Weinheim an der Bergstrasse, Germany)》2000,6(20):3788-3796
The synthesis and spectroscopic characterization of self-assembling calix[4]arene based capsules 1a.1a and 1b.1b are described. These compounds feature four urea substituents at the upper rims and four secondary amide fragments at the lower rims that can participate in inter- and intramolecular hydrogen bonding in apolar solution. Communication between the calixarene rims in 1a, b influences the self-assembled cavity's size and shape. Specifically. dimerization results in a perfect cone conformation of the calixarene skeleton in 1a, b and stabilizes a seam of intramolecular amide C=O...H-N hydrogen bonds at the lower rim. This seam is cycloenantiomeric, with either clockwise or counterclockwise arrangements of the head-to-tail amides. Complexation of Na+-cation breaks hydrogen bonds at the lower rim but maintains the capsular assembly. Encapsulation properties of 1a.1a and 1b.1b were studied in nonpolar solvents and their binary mixtures as well as through heterodimerization experiments. The presence of amide groups at the lower rim causes notable differences in the capsule's binding affinities when compared to the corresponding tetraester capsules 1c.1c and 1d.1d. In the monomeric state calixarenes 1a, b are in a pinched cone conformation. The solid state X-ray crystallographic studies with monomeric 1a reveal only two intramolecular C=O...H-N hydrogen bonds between the adjacent amides at the lower rim, and an extensive network of intermolecular hydrogen bonds between urea groups at the upper rim. 相似文献
157.
A new synthesis of 6‐carbomethoxy‐1,2,3,5‐tetrahydroirnidazo[2,3‐b][1,3]benzodiazocines 13 by the intramolecular cycloaddition reaction of methyl 2‐(1‐aziridinylmethyl)‐3‐(2‐ureidophenyl)propenoates 10 under Appel's dehydration conditions is described. The latter were readily obtained from 2‐nitrobenzalde‐hyde with methyl acrylate through the Baylis‐Hillman reaction. 相似文献
158.
Fouling Mitigation in a Heat Exchanger: High Cycles of Concentration for a Cooling-Tower Application
The purpose of the present study is to investigate the effect of a physical water treatment (PWT) technology on fouling mitigation in a simulated cooling tower operating at high cycles of concentration. Hard water was produced by evaporating pure water in a circulating open cooling tower, where dissolved calcium carbonate ions became concentrated with time. Heat transfer tests were conducted in a rectangular channel by varying the cycle of concentration (COC) from 5 to 10, and fouling resistances were measured over 270 hrs for each case with and without the PWT treatment. Another test was conducted with no blowdown case with and without the PWT treatment. The fouling resistance at 5 cycles with the PWT treatment was about 70% less than that in the case without the PWT treatment at the end of 270-hr tests. Even at 10 cycles, the PWT treatment reduced the fouling resistance by 60% from the value for the no treatment case. Thus, one can conclude that the PWT technology can help circulating cooling-tower water at relatively high COC for significant freshwater conservation, while keeping fouling resistances below industry standards. 相似文献
159.
Shahid Muhammad Kim Kwangsoo Kim Guinyun Naik Haladhara Zaman Muhammad Lee Young-Ouk Cho Young-Sik 《Journal of Radioanalytical and Nuclear Chemistry》2017,311(3):1971-1981
Journal of Radioanalytical and Nuclear Chemistry - We measured excitation functions for the production of the 108m,108g,109g,110m,110g,111gIn, the 109g,111mCd, and the 105g,106m,110m,111gAg in... 相似文献
160.