全文获取类型
收费全文 | 8098篇 |
免费 | 1279篇 |
国内免费 | 1209篇 |
专业分类
化学 | 6084篇 |
晶体学 | 94篇 |
力学 | 525篇 |
综合类 | 104篇 |
数学 | 989篇 |
物理学 | 2790篇 |
出版年
2024年 | 33篇 |
2023年 | 161篇 |
2022年 | 328篇 |
2021年 | 313篇 |
2020年 | 351篇 |
2019年 | 340篇 |
2018年 | 292篇 |
2017年 | 279篇 |
2016年 | 390篇 |
2015年 | 360篇 |
2014年 | 462篇 |
2013年 | 610篇 |
2012年 | 706篇 |
2011年 | 755篇 |
2010年 | 496篇 |
2009年 | 497篇 |
2008年 | 590篇 |
2007年 | 489篇 |
2006年 | 414篇 |
2005年 | 378篇 |
2004年 | 287篇 |
2003年 | 243篇 |
2002年 | 231篇 |
2001年 | 201篇 |
2000年 | 162篇 |
1999年 | 157篇 |
1998年 | 136篇 |
1997年 | 129篇 |
1996年 | 132篇 |
1995年 | 121篇 |
1994年 | 105篇 |
1993年 | 82篇 |
1992年 | 79篇 |
1991年 | 65篇 |
1990年 | 50篇 |
1989年 | 36篇 |
1988年 | 29篇 |
1987年 | 30篇 |
1986年 | 14篇 |
1985年 | 22篇 |
1984年 | 8篇 |
1983年 | 7篇 |
1982年 | 3篇 |
1981年 | 5篇 |
1980年 | 1篇 |
1975年 | 1篇 |
1974年 | 1篇 |
1959年 | 1篇 |
1957年 | 3篇 |
1936年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
161.
GuoHongLI YueMaoSHEN KeQinZHANG 《中国化学快报》2005,16(3):359-361
A novel saponin was isolated from the transformed products of ginsenoside Rh1 by Bacillus subtilis. It‘s structure was determined to be 3-O-β-D-glucopyranosyl-6-O-β-D-glucopyranosyl-20 (S)-protopanaxatriol on the basis of the spectral data. 相似文献
162.
163.
164.
Qin XZ 《Journal of the American Society for Mass Spectrometry》2002,13(4):371-377
Compound 1 [N-[1(R)-[(1,2-dihydro-1-methylsulfonylspiro[3H-indole-3,4'-piperidin]-1'-yl)carbonyl]-2-(phenylmethyloxy)ethyl]-2-amino-2-methylpropanamide](MW 528) is an orally-active growth hormone secretagogue (GHS). As part of a continual effort to analyze the ESI/MS and MSn data of novel drugs, the ESI/MS and MS/MS data of protonated 1 (m/z 529) are analyzed and reported here. The analyses reveal that under low-energy collision-induced dissociation (CID) in an ion trap or a quadrupole collision cell, protonated 1 undergoes a gas-phase rearrangement to form protonated 3 (m/z 357) which competes with the y- and b-type product ions during the amide bond cleavages of protonated 1. It is proposed that when the b-type ion is formed by cleavage of the piperidine amide bond, piperidine (a neutral species) and the b-ion (a cation) form an ion-neutral complex. In this complex, piperidine functions as a nucleophile to attack the benzylic carbon of the b-ion, and the protonated ether group in the b-ion acts as a leaving group, which results in the migration of the benzylic group to the piperidine amine to form protonated 3. Protonated 2 (an analog of 1) was studied under the same experimental conditions. The results show that protonated 2 undergoes a similar rearrangement to form protonated 3. While this rearrangement is a relatively minor fragmentation process for protonated 1, it is a predominant process for protonated 2. This phenomenon is explained in terms of the proposed ion-neutral-complex mechanism. 相似文献
165.
中药一枝黄花、黄连、天麻、蛇床子中8种微量元素的测定 总被引:13,自引:2,他引:13
采用原子吸收光谱仪对一枝黄花、黄连、天麻、蛇床子中Fe、Ca、Mg、Mn、Cr、Cu、Zn、Pb八种无机元素的含量进行了测定,为进一步研究其药理和用途提供基础。 相似文献
166.
In Situ IR Spectroscopic Studies on Molybdenum Nitride Catalysts: Active Sites and Surface Reactions
Recent IR spectroscopic studies on the surface properties of fresh Mo2N/-Al2O3 catalyst are presented in this paper. The surface sites of fresh Mo2N/-Al2O3, both Mo+ (0<<2) and N sites, are probed by CO adsorption. Two characteristic IR bands were observed at 2045 and 2200 cm-1, due to linearly adsorbed CO on Mo and N sites, respectively. The surface N sites are highly reactive and can react with adsorbed CO to form NCO species. Unlike adsorbed CO on reduced passivated one, the adsorbed CO on fresh Mo2N/-Al2O3 behaves similarly to that of group VIII metals, suggesting that fresh nitride resembles noble metals. It is found that the surface of Mo nitrides slowly transformed into sulfide under hydrotreating conditions, which could be the main reason for the activity drop of molybdenum nitride catalysts in the presence of sulfur-containing species. Some surface reactions, such as selective hydrogenation of 1,3-butadiene, isomerization of 1-butene, and hydrodesulfurization of thiophene, were studied on both fresh and reduced passivated Mo2N/-Al2O3 catalysts using IR spectroscopy. The mechanisms of these reactions are proposed. The adsorption and reaction behaviors of these molecules on fresh molybdenum nitride also resemble those on noble metals, manifesting the unique properties of fresh molybdenum nitride catalysts. Mo and N sites are found to play different roles in the adsorption and catalytic reactions on the fresh Mo2N/-Al2O3 catalyst. Generally, Mo sites are the main active sites for the adsorption and reactions of adsorbates; N sites are not directly involved in catalytic reactions but they modify the electronic properties of Mo sites. 相似文献
167.
Laiyuan Chen Liwu Lin Qin Xin Pinliang Ying Mojie Cheng Zhusheng Xu Tao Zhang 《Reaction Kinetics and Catalysis Letters》1995,56(2):267-272
It has been observed by FT-IR spectroscopy that both kinds of Brönsted acid protons present in HZSM-5 zeolite may be involved in the adsorption of methane at low temperature (173 K) and exchange with CH4 or CD4 at high temperature (>500°C). The sites which can adsorb methane at low temperature are the active sites for methane conversion at high temperature. Over HZSM-5 zeolite, the activation of methane is suggested to occur via a heterolytic cleavage of C–H bond with the assistance of protons. 相似文献
168.
169.
170.
Lanthanum hexaboride nanowires produced by chemical vapor deposition are single-crystalline and grown along the [111] direction. Streaks appearing in the electron diffraction spots indicate the lateral direction perpendicular to the nanowire growth axis. 相似文献