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   812篇
  免费   52篇
  国内免费   39篇
化学   278篇
晶体学   9篇
力学   9篇
综合类   3篇
数学   91篇
物理学   513篇
  2021年   6篇
  2020年   10篇
  2019年   5篇
  2018年   12篇
  2017年   6篇
  2016年   12篇
  2015年   13篇
  2014年   14篇
  2013年   21篇
  2012年   25篇
  2011年   53篇
  2010年   26篇
  2009年   21篇
  2008年   47篇
  2007年   50篇
  2006年   50篇
  2005年   41篇
  2004年   29篇
  2003年   21篇
  2002年   24篇
  2001年   23篇
  2000年   23篇
  1999年   15篇
  1998年   8篇
  1997年   6篇
  1996年   32篇
  1995年   31篇
  1994年   21篇
  1993年   29篇
  1992年   27篇
  1991年   15篇
  1990年   19篇
  1989年   12篇
  1988年   6篇
  1987年   10篇
  1986年   12篇
  1985年   13篇
  1984年   8篇
  1983年   9篇
  1982年   6篇
  1981年   6篇
  1980年   8篇
  1979年   4篇
  1978年   7篇
  1977年   4篇
  1976年   8篇
  1975年   9篇
  1974年   6篇
  1973年   9篇
  1972年   7篇
排序方式: 共有903条查询结果,搜索用时 15 毫秒
21.
高效液相色谱氮杂冠醚键合固定相的合成及性能研究   总被引:2,自引:0,他引:2  
我们曾用γ-氯丙基键合硅胶(CPS),在氢化钠(NaH)作用下合成了3-(氮杂-18-冠-6)丙基键合固定相(BCP)[1].该固定相对碱基、核苷酸、硝基苯酚等有较好的分离选择性,但由于NaH对硅胶基质腐蚀作用较大,导致BCP柱效及渗透性较低.本文采...  相似文献   
22.
23.
24.
G.H. Barnett  B. Evans  K.M. Smith 《Tetrahedron》1975,31(21):2711-2717
Treatment of porphyrins with thallium(III) trifluoroacetate in the presence of trifluoroacetic acid results in uncontrolled oxidation at the macrocyclic meso-positions, presumably via radical processes. For example, a mixture of the thallium(III) α γ-dioxoporphodimethene (4a; R = Et), the αβγ-trioxo compound (3), and octaethylxanthoporphyrinogen (6) is obtained when octaethylporphyrin (1; R = Et) is oxidised in the presence of air. More controlled oxidation is achieved when the meso-trifluoroacetoxyporphyrin complexes (8a, b) or metallo-oxophlorins (7a, b) are treated with mild bases in air, the major products being metallo-αγ-dioxoporphodimethenes (4b, c).β-Hydroxy-α-oxophlorins (16) are isolated and characterised for the first time; aspects of the chemistry of this novel oxygenated porphyrin system are reported.  相似文献   
25.
Topoglidis E  Lutz T  Willis RL  Barnett CJ  Cass AE  Durrant JR 《Faraday discussions》2000,(116):35-46; discussion 67-75
We have investigated the use of nanoporous TiO2 films as substrates for protein immobilisation. Such films are of interest due to their high surface area, optical transparency, electrochemical activity and ease of fabrication. These films moreover allow detailed spectroscopic study of protein/electrode electron transfer processes. We find that protein immobilisation on such films may be readily achieved from aqueous solutions at 4 degrees C with a high binding stability and no detectable protein denaturation. The nanoporous structure of the film greatly enhances the active surface area available for protein binding (by a factor of up to 850 for an 8 microns thick film). We demonstrate that the redox state of proteins such as immobilised cytochrome-c (Cyt-c) and haemoglobin (Hb) may be modulated by the application of an electrical bias potential to the TiO2 film, without the addition of electron transfer mediators. The binding of Cyt-c on the TiO2 films is investigated as a function of film thickness, protein concentration, protein surface charge and ionic strength. We demonstrate the potential use of immobilised Hb on such TiO2 films for the detection of dissolved CO in aqueous solutions. We further show that protein/electrode electron transfer may be initiated by UV bandgap excitation of the TiO2 electrode. Both photooxidation and photoreduction of the immobilised proteins can be achieved. By employing pulsed UV laser excitation, the interfacial electron transfer kinetics can be monitored by transient optical spectroscopy, providing a novel probe of protein/electrode electron transfer kinetics. We conclude that nanoporous TiO2 films may be useful both for basic studies of protein/electrode interactions and for the development of novel bioanalytical devices such as biosensors.  相似文献   
26.
High-field asymmetric waveform ion mobility spectrometry (FAIMS) was used to separate gas-phase conformers of bovine ubiquitin produced by electrospray ionization. These conformers were sampled by a triple quadrupole mass spectrometer where energy-loss experiments, following the work of Douglas and co-workers, were used to determine their cross sections. The measured cross sections for some conformers were readily altered by the voltages applied to the interface ion optics, therefore very gentle mass spectrometer interface conditions were required to preserve gas-phase conformers separated by FAIMS. Cross sections for 19 conformers (charge states +5 through +13) were measured. Two conformers for the +12 charge state, which were readily separated in FAIMS, were found to have similar cross sections. Based on a method to calibrate the collision gas thickness, the cross sections measured using the FAIMS/energy-loss method were compared with literature values determined using drift tube ion mobility spectrometry. The comparison illustrated that the conformers of bovine ubiquitin that were identified using drift tube ion mobility spectrometry were also observed using the FAIMS device.  相似文献   
27.
28.
29.
8,8"-Biflavonoidsareantw0rtantclass0fbiflavonoids.Asasystematicresearchofthe8,8"-biflav0noids,wehavepreviouslyreportedthestudyonthereactionof2'-hydroxychaloneswithl2-H2SO4-DMSOsystem.'InthispaPer,thesynthesisof5,5",7,7',-tetTameth0xy-8,8"-biflavonela2,4,4",7,7"-tetramethoxy-8,8"-biflavone1b',4',4",,5,5,',7,7"-hexamethoxy-8,8"-biflav0ne1c4and4,4"-dibenZyl0xy-5,5",7,7"-tetramothoxy-8,8"-biflavoneldisreported.ThesyntheticmethodisshownintheSchemebelow.2-Hydroxyacet0phenonescondensedwithsubsti…  相似文献   
30.
酸性化合物在十二胺-N; N-二亚甲基膦酸改性氧化锆固定相上的分离;氧化锆;色谱固定相;十二胺-N; N-二亚甲基膦酸  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