全文获取类型
收费全文 | 1640篇 |
免费 | 45篇 |
国内免费 | 5篇 |
专业分类
化学 | 1353篇 |
晶体学 | 23篇 |
力学 | 19篇 |
数学 | 39篇 |
物理学 | 256篇 |
出版年
2022年 | 9篇 |
2021年 | 14篇 |
2020年 | 16篇 |
2019年 | 21篇 |
2018年 | 17篇 |
2017年 | 9篇 |
2016年 | 27篇 |
2015年 | 39篇 |
2014年 | 38篇 |
2013年 | 84篇 |
2012年 | 75篇 |
2011年 | 63篇 |
2010年 | 53篇 |
2009年 | 48篇 |
2008年 | 92篇 |
2007年 | 119篇 |
2006年 | 102篇 |
2005年 | 74篇 |
2004年 | 93篇 |
2003年 | 73篇 |
2002年 | 84篇 |
2001年 | 42篇 |
2000年 | 39篇 |
1999年 | 34篇 |
1998年 | 20篇 |
1997年 | 24篇 |
1996年 | 22篇 |
1995年 | 12篇 |
1994年 | 17篇 |
1993年 | 16篇 |
1992年 | 24篇 |
1991年 | 17篇 |
1989年 | 12篇 |
1988年 | 9篇 |
1987年 | 7篇 |
1986年 | 7篇 |
1985年 | 27篇 |
1984年 | 20篇 |
1983年 | 11篇 |
1982年 | 14篇 |
1981年 | 27篇 |
1980年 | 22篇 |
1979年 | 21篇 |
1978年 | 17篇 |
1977年 | 10篇 |
1976年 | 7篇 |
1975年 | 13篇 |
1974年 | 8篇 |
1973年 | 7篇 |
1969年 | 7篇 |
排序方式: 共有1690条查询结果,搜索用时 15 毫秒
31.
32.
33.
34.
Q. B. Wang K. Masumoto K. Bessho H. Matsumura T. Miura T. Shibata 《Journal of Radioanalytical and Nuclear Chemistry》2007,273(1):55-58
For evaluation of radioactivity induced in the concrete samples from accelerator facilities, the residual radioactivity in
concrete sample, collected from seven accelerator facilities, was determined by γ-ray spectrometry. The tritium was extracted
by the heating method using an IR furnace, and measured with a liquid scintillation counter. It was found that the major radioisotopes
activated mainly by neutrons in the concrete samples were 152Eu, 60Co, 134Cs and 3H. The concentrations of radioactivities induced by thermal neutron capture are the highest at a depth of 10 cm in the concrete
wall. The correlation between tritium, 60Co and 152Eu activity was investigated by measuring many concrete samples for seven accelerator facilities. The results indicate that
their activities are strongly correlated with each other. So it would also be concluded that the total activity in shielding
concrete could be estimated on the basis of the activities of 60Co and 152Eu. 相似文献
35.
Okada Y Yokozawa M Akiba M Oishi K O-kawa K Akeboshi T Kawamura Y Inokuma S Nakamura Y Nishimura J 《Organic & biomolecular chemistry》2003,1(14):2506-2511
A variety of aromatic compounds with both activating and deactivating substituents were brominated with sodium monobromoisocyanurate (SMBI) 1, diethyl ether, diethyl ether-methanesulfonic acid, trifluoroacetic acid, or sulfuric acid were employed as solvents. Thus nitrobenzene was conveniently brominated in sulfuric acid, benzene was readily monobrominated in diethyl ether-methanesulfonic acid, and phenol was selectively brominated at the ortho position under mild conditions in refluxing diethyl ether. With substituents that are easily protonated, trifluoroacetic acid may be employed as solvent in the reaction with 1, in contrast NBS was ineffective in trifluoroacetic acid. This renders 1 a superior reagent relative to NBS. In addition to aromatics, alkenes, ketones and esters were also brominated with 1. Diethyl malonate was brominated with 1 and then subjected to a Bingel reaction with NaH to afford the desired methanofullerene in reasonable yield. 相似文献
36.
A novel class of activators, dialkyl(cyanomethyl)ammonium tetrafluoroborates 1a-c, has been developed and applied to the condensations of diastereopure 5'-O-tert-butyldiphenylsilylthymidine 3'-cyclic phosphoramidites 3a-d with 3'-O-tert-butyldimethylsilylthymidine (4a). Among them, the condensation of 3a with 4a in the presence of 1a completed within 5 min and gave only one diastereoisomer of the corresponding phosphite 5a. After sulfurization and deprtection, almost diastereopure (Rp)-TpsT 7 was obtained (d.r. = 99:1). Next the 5'-O-(DMTr)nucleoside 3'-phosphoramidites 8a-d containing thymine, N6-benzoyladenine, N4-benzoylcytosine, and N2-phenylacetylguanine have been synthesized and allowed to condense with 3'-O-protected thymidine and 2'-deoxyadenosine. The 5'-O-DMTr group and the N-acyl groups of the nucleobases were compatible with the reaction conditions and the condensations completed quickly with excellent diastereoselectivity. 相似文献
37.
Yoshizawa M Nagao M Umemoto K Biradha K Fujita M Sakamoto S Yamaguchi K 《Chemical communications (Cambridge, England)》2003,(15):1808-1809
Despite their structural similarity, triangular tetradentate ligands 2b and 2c experience different assembly pathways on complexation with (en)Pd(NO3)2 to give M8L4 tetrahedral (3) and open cone (4) structures, respectively, due to steric restriction by side chains at the corner or on the edge of the ligands. 相似文献
38.
A novel synthetic basic resolving agent, cis-1-aminobenz[f]indan-2-ol (ABI), was rationally designed by introducing effective CH/pi interaction sites to cis-1-aminoindan-2-ol (AI), whose chiral recognition ability has been reported from our laboratory. ABI was applicable to a wide variety of racemic arylalkanoic acids and showed moderate to excellent chiral recognition ability, which was obviously higher than that of AI. The fundamental and important role of CH/pi interactions, such as tunable CH(sp(2))/pi and CH(sp(3))/pi interactions, in the chiral recognition by ABI was revealed by X-ray crystallographic study. 相似文献
39.
Evaluation of the adsorption affinity of proteins to calcium hydroxyapatites by desorption and pre-adsorption methods 总被引:1,自引:0,他引:1
Kazuhiko Kandori Aya Fujiwara Megumi Mukai Akemi Yasukawa Tatsuo Ishikawa 《Colloids and surfaces. B, Biointerfaces》1998,11(6):313-320
The adsorption affinity of bovine serum albumin (BSA) and lysozyme (LSZ) to calcium hydroxyapatite (CaHAP) was evaluated by desorption and two step adsorption methods. These experiments were carried out at 15°C in a 1×10−4 mol dm−3 KCl solution of pH 6.0. BSA molecules were scarcely desorbed, exhibiting an irreversible adsorption of BSA, though LSZ slightly desorbed. This result supports our previous findings that LSZ adsorbs weakly onto phosphate ions exposed on ac or bc faces of CaHAP while BSA adsorbs strongly onto positively charged sites on ac or bc faces of CaHAP. The amount of adsorbed LSZ was markedly increased by the pre-adsorption of BSA, where LSZ was adsorbed onto BSA-covered CaHAP. On the other hand, the amount of adsorbed BSA was not changed by the pre-adsorption of LSZ. In both pre-adsorption systems it was confirmed by an HPLC method that no protein molecule pre-adsorbed was desorbed after the post-adsorption procedure. Therefore, it was interpreted that the enhancement of adsorption of positively charged LSZ is induced by an electrostatic attractive force through pre-adsorption of negatively charged BSA molecules with a high coverage. However, since the coverage of LSZ onto CaHAP is considerably low, no stimulation of BSA adsorption occurred on the LSZ-covered surface. The formation of double protein adsorbed layers consisting of pre- and post-adsorbed proteins was proposed. 相似文献
40.
A comparison of the adsorption of saliva proteins and some typical proteins onto the surface of hydroxyapatite 总被引:1,自引:0,他引:1
K. Kawasaki M. Kambara H. Matsumura W. Norde 《Colloids and surfaces. B, Biointerfaces》2003,32(4):321-334
Adsorption of protein from saliva on hydroxyapatite was compared with adsorption of several typical proteins with different electric charges, i.e. lysozyme, human serum albumin, β-lactoglobulin and ovalbumin. Adsorbed amounts of these proteins were determined and electrophoretic mobilities of protein-covered hydroxyapatite particles were measured, at different values for the adsorbed mass and, therefore, at various degrees of surface coverage. Also, adsorption kinetics were investigated by streaming potential measurements of a hydroxyapatite surface in contact with a protein solution, allowing monitoring of changes in the zeta-potential of the protein-covered hydroxyapatite surface in real time. The adsorbed amounts show that, as compared to most of the other proteins, the saliva proteins have remarkably low adsorption affinity. The measured values for the electrophoretic mobilities indicate that the positively charged proteins in the saliva mixture preferentially adsorb onto the negatively charged hydroxyapatite surface; this is most pronounced at low protein concentration in solution (i.e. at low coverage of the surface by the protein). Preferential uptake of the positively charged saliva proteins during the initial stages of the adsorption process is also concluded from the results of the kinetics experiments. Preferential adsorption of positive proteins is somewhat suppressed by the presence of Ca2+ ions in the medium. The results suggest that an acquired pellicle on a tooth in an oral environment contains a significant fraction of positively charged proteins. The positively charged proteins in the pellicle reduce the zeta-potential at the tooth surface to low values; consequently, electrostatic forces are expected to play only a minor role in the interaction with other components (e.g. bacterial cells). 相似文献