首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   21193篇
  免费   2501篇
  国内免费   2889篇
化学   16677篇
晶体学   307篇
力学   857篇
综合类   264篇
数学   2124篇
物理学   6354篇
  2024年   36篇
  2023年   190篇
  2022年   493篇
  2021年   536篇
  2020年   535篇
  2019年   619篇
  2018年   507篇
  2017年   471篇
  2016年   830篇
  2015年   883篇
  2014年   1088篇
  2013年   1508篇
  2012年   1785篇
  2011年   1826篇
  2010年   1344篇
  2009年   1282篇
  2008年   1625篇
  2007年   1459篇
  2006年   1340篇
  2005年   1121篇
  2004年   1047篇
  2003年   946篇
  2002年   1024篇
  2001年   787篇
  2000年   598篇
  1999年   465篇
  1998年   287篇
  1997年   294篇
  1996年   246篇
  1995年   220篇
  1994年   190篇
  1993年   184篇
  1992年   162篇
  1991年   119篇
  1990年   109篇
  1989年   93篇
  1988年   50篇
  1987年   54篇
  1986年   44篇
  1985年   38篇
  1984年   28篇
  1983年   21篇
  1982年   13篇
  1981年   17篇
  1980年   10篇
  1978年   11篇
  1977年   7篇
  1976年   9篇
  1974年   5篇
  1973年   7篇
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
31.
The crystal structures of two potential tumor imaging agents and therapeutic agents -copper(Ⅱ) complexes with salicylidene-tyrosinato Schiff base and nitrogen-donor chelating Lewis base, [Cu(sal-tyr)(bipy)] 1 and [Cu(sal-tyr)(phen)]2CH3OH 2 are presented. Our work is helpful to get deep understanding of novel 64Cu tumor imaging agents and therapeutic agents.  相似文献   
32.
Jensen and Toft 8 conjectured that every 2‐edge‐connected graph without a K5‐minor has a nowhere zero 4‐flow. Walton and Welsh 19 proved that if a coloopless regular matroid M does not have a minor in {M(K3,3), M*(K5)}, then M admits a nowhere zero 4‐flow. In this note, we prove that if a coloopless regular matroid M does not have a minor in {M(K5), M*(K5)}, then M admits a nowhere zero 4‐flow. Our result implies the Jensen and Toft conjecture. © 2005 Wiley Periodicals, Inc. J Graph Theory  相似文献   
33.
34.
(1,1—二硝基—2—叠氮基乙基)苯的合成及其热稳定性   总被引:1,自引:0,他引:1  
阎红  管晓培 《应用化学》1996,13(2):111-112
  相似文献   
35.
主要介绍了丝绸之路上多元文化的典型代表——艾德莱斯绸.文章重点介绍了艾德莱斯绸的历史和传说,扎经染色工艺,各类艾德莱斯绸的特点及典型的艾德莱斯绸图案.  相似文献   
36.
A hybrid emulsion polymerization was formulated for synthesizing Fe3O4/polystyrene composite latex. This system, containing binary droplets that are magnetic (Mag)‐droplets with a diameter of 100–200 nm and styrene (St)‐droplets with a diameter of 3–4 μm, was obtained by mixing Mag‐miniemulsion and St‐macroemulsion. With extremely low surfactants concentration (?critical micelle concentration, CMC), the nucleated loci are selectively controlled in the Mag‐droplets, as the result of smaller droplet size and larger surface ratio. Both water‐soluble potassium persulfate (KPS) and oil‐soluble 2,2′‐azobis(2‐isobutyronitrile) was adopted to initiate the polymerization. In the presence of KPS, magnetic polystyrene latices with particles size of 60–200 nm, narrow size distribution, and high magnetite content (86 wt % measured by TGA) were attained successfully. The synthesized magnetic Fe3O4/polystyrene latices assembled into well‐ordered hexagonal structure in the surface of a carbon supported copper grid. The influence of various parameters on various aspects of the as‐synthesized Fe3O4/polystyrene was investigated in detail: type of initiator on composite morphology, feed ratio of Mag‐miniemulsion and St‐macroemulsion on magnetite content, and hydrophobic agent or amount of surfactant on size and size distribution. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5285–5295, 2007  相似文献   
37.
Catalytic decomposition of NO over Cu-Os/13X has been carried out in a tubular fixed bed reactor at atmospheric pressure and the results were compared with literature data performed by high-throughput screening (HTS). The activity and durability of Cu-Os/13X prepared by conventional ion-exchange method have been investigated in the presence of H2O and SO2. It was found that Cu-Os/13X prepared by ion-exchange shows a high activity in a wide temperature range in selective catalytic reduction (SCR) of NO with C3H6 compared to Cu/13X, proving the existence of more NO adsorption site on Cu-Os/13X. However, Cu-Os/13X exhibited low activity in the presence of water, and was quite different from the result reported in literature. SO2 resistance is also low and does not recover its original activity when the SO2 was blocked in the feed gas stream. This result suggested that catalytic activity between combinatorial screening and conventional testing should be compared to confirm the validity of high-throughput screening.  相似文献   
38.
39.
The decay process J/ψ→p X X→p P,where p,p and P are the proton,antiproton and pseudoscalar states,respectively,has been studied in terms of the angular distribution and the generalized moment analysis methods.The result shows that we can identify the spin,but cannot determine the parity of the baryon resonance state X produced in the process J/ψ→p X X→p P.  相似文献   
40.
Porous zirconia particles are very robust material and have received considerable attention as a stationary phase support for HPLC. We prepared cellulose dimethylphenylcarbamate-bonded carbon-clad zirconia (CDMPCCZ) as a chiral stationary phase (CSP) for separation of enantiomers of a set of 14 racemic compounds in normal phase (NP) and reversed-phase (RP) liquid chromatography. Retention and enantioselectivity on CDMPCCZ were compared to those on CDMPC-coated zirconia (CDMPCZ) to see how the change in immobilization method of the chiral selector affects the retention and chiral selectivity. In NPLC, retention was longer and the number of resolved racemates was smaller on CDMPCCZ than on CDMPCZ. However, chiral selectivity factors for some resolved racemates were better on CDMPCCZ than on CDMPCZ. The longer retention on CDMPCCZ is likely due to strong, non-chiral discriminating interactions with the carbon layer on CDMPCZ. In RPLC only two racemates were resolved on CDMPCCZ, but retention times were shorter than, and resolutions were comparable to, those in NPLC, indicating a potential for improving chromatographic performance of the CDMPCCZ column in RPLC with optimized column preparation and separation conditions.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号