全文获取类型
收费全文 | 12339篇 |
免费 | 2369篇 |
国内免费 | 2020篇 |
专业分类
化学 | 8837篇 |
晶体学 | 210篇 |
力学 | 796篇 |
综合类 | 150篇 |
数学 | 1329篇 |
物理学 | 5406篇 |
出版年
2024年 | 52篇 |
2023年 | 237篇 |
2022年 | 451篇 |
2021年 | 482篇 |
2020年 | 602篇 |
2019年 | 564篇 |
2018年 | 513篇 |
2017年 | 465篇 |
2016年 | 672篇 |
2015年 | 678篇 |
2014年 | 799篇 |
2013年 | 995篇 |
2012年 | 1267篇 |
2011年 | 1216篇 |
2010年 | 901篇 |
2009年 | 880篇 |
2008年 | 974篇 |
2007年 | 822篇 |
2006年 | 685篇 |
2005年 | 572篇 |
2004年 | 446篇 |
2003年 | 349篇 |
2002年 | 350篇 |
2001年 | 292篇 |
2000年 | 241篇 |
1999年 | 209篇 |
1998年 | 142篇 |
1997年 | 118篇 |
1996年 | 115篇 |
1995年 | 87篇 |
1994年 | 93篇 |
1993年 | 65篇 |
1992年 | 68篇 |
1991年 | 58篇 |
1990年 | 57篇 |
1989年 | 40篇 |
1988年 | 30篇 |
1987年 | 17篇 |
1986年 | 21篇 |
1985年 | 25篇 |
1984年 | 21篇 |
1983年 | 15篇 |
1982年 | 11篇 |
1981年 | 8篇 |
1979年 | 2篇 |
1977年 | 2篇 |
1974年 | 4篇 |
1972年 | 2篇 |
1966年 | 2篇 |
1957年 | 2篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
71.
Zhang H Zhou Y Zhang M Shen T Li Y Zhu D 《Journal of colloid and interface science》2002,251(2):443-446
A dyad-anthraquinone-methyl ester of fluorescein-and its model compound-butyl ester-were synthesized. The effects of photo-induced electron transfer from fluorescein to an organic anthraquinone acceptor and injection into inorganic colloidal TiO(2) were studied respectively. It is found that the photo-induced electron transferring to an organic acceptor is much faster than injecting into inorganic colloidal particles when fluorescein was excited by visible light. While inorganic colloidal TiO(2) was excited by UV, the electron of fluorescein will inject into TiO(2). 相似文献
72.
73.
Seong J Rohrbacher A Li ZR Janda KC Tao FM Spiegelman F Halberstadt N 《The Journal of chemical physics》2004,120(16):7456-7463
The potential energy surface of He2Ne+ has been reinvestigated using a combination of ab initio and diatomics-in-molecule (DIM) calculations. In contrast to the reports of two recent studies the ion is found to have an asymmetric linear He-Ne-He structure, with no barrier to formation from the separated atoms on the ground-state surface. The He-Ne+ bond lengths at the potential minimum are 1.51 and 1.81 A, and the total bonding energy is 0.717 eV. Comparing the He2Ne+ energy to that of HeNe+, the bonding energy for the second helium atom is 0.06 eV, about 10% of that of the first He atom. The saddle point between the two equivalent minima is a symmetric structure, 0.0074 eV above the potential minimum. A symmetric geometry becomes the overall potential minimum if the 2s hole on the Ne is excluded from the reference states of a multireference configuration interaction calculation. A DIM potential was created for the HenNe+ family of ions. The DIM potential is consistent with the asymmetric He2Ne+ ion serving as a core; it predicts a slightly more asymmetric geometry than the ab initio results. Additional helium atoms form five-membered rings around the bonds of the core ion to fill the first shell and then add to the ends of the cluster. The asymmetric core ion and the highly compact structure help to account for the lack of apparent shell structure in the mass spectrometry of HenNe+ clusters. Finally, we recommend that the value De=0.63+/-0.04 eV be adopted for the ground state of HeNe+. 相似文献
74.
MingTaoLIANG DeXinWANG 《中国化学快报》2002,13(3):199-200
Some dehydropeptide analogues were directly synthesized by the reaction of unsaturated oxazolones with free amino acids. 相似文献
75.
Tao Miao 《Tetrahedron letters》2007,48(1):95-99
The immobilization of copper in organic-inorganic hybrid materials catalyzing the Ullmann reaction has been described. Phenols reacted with aryl iodides, aryl bromides and aryl chlorides smoothly in the presence of a 3-(2-aminoethylamino)propyl functionalized silica gel immobilized copper catalyst. The protocol involved the use of DMSO as the solvent, and potassium fluoride as the base. The reactions generated the corresponding cross-coupling products in good to excellent yields. Furthermore, the silica-supported copper could be recovered and recycled by a simple filtration of the reaction solution and used for 10 consecutive trials without loss of its reactivity. 相似文献
76.
77.
A series of 1-(2,4-dichlorophenoxyacetoxy)alkylphosphonic acid dimethyl esters 5 and its corresponding phosphonate monosalts 6 were synthesized as potential herbicide. The phosphonate monosalts can be prepared from 1-(2,4-dichlorophenoxyacetoxy)alkylphosphonic acid dimethyl esters 5, which were synthesized by the condensation of O,O-dimethyl-1-hydroxyalkylphosphonates with dichlorophenoxyacetic chloride. This method provides a simple and efficient procedure for the synthesis of phosphonate derivatives containing sensitive groups to acid, base or water such as carboxylate ester bond; and the herbicidal activity of title compounds was evaluated in a set of experiments in greenhouse. Most of the compounds exhibited notable herbicidal activity. 相似文献
78.
Six new ent‐abietane diterpenoids, rubescensins I–M ( 1 – 5 ) and P ( 6 ), along with two related acetonide derivatives ( 7 and 8 ), were isolated from Isodon rubescens. Their structures were elucidated by detailed spectroscopic analysis. Compound 5 is the first N‐containing diterpenoid from the genus Isodon, exhibiting notable cytotoxicity against human tumor K562 cells. 相似文献
79.
Quan HAN Hong Tao YAN* Zhen Jie QIAN Department of Chemistry Northwest University Xi抋n 《中国化学快报》2002,13(12)
Thermal lens spectrometry (TLS) is an excellent tool for trace analysis1. TLS allows the detection of absorbances of 10-7~10-8, concentration of ≈ 10-11 mol稬-1 and the analysis of 10-15 L volumes with ≈10-2 absorbing molecules2. Kinetic analysis is playing an increasingly important part in modern analytical chemistry. Therefore, TLS shows much promise in combination with kinetic analysis. However, there are few data on TLS applications in kinetic analysis method so far3~4. A ne… 相似文献
80.
Yuichiro Hori Miyako Nishiura Tomomi Tao Reisuke Baba Steven D. Bull Kazuya Kikuchi 《Chemical science》2021,12(7):2498
Reversible enzymatic post-translational modification of the ε-amino groups of lysine residues (e.g. N-acylation reactions) plays an important role in regulating the cellular activities of numerous proteins. This study describes how enzyme catalyzed N-deprotection of lysine residues of non-fluorescent peptide-coumarin probes can be used to generate N-deprotected peptides that undergo spontaneous O- to N-ester transfer reactions (uncatalyzed) to generate a highly fluorescent N-carbamoyl peptide. This enables detection of enzyme catalyzed N-deacetylation, N-demalonylation, N-desuccinylation and N-demethylation reactions activities towards the N-modified lysine residues of these probes using simple ‘turn on’ fluorescent assays.We developed “turn-on” fluorescent probes that detect enzymatic lysine deacylation and demethylation critical for epigenetic and other cellular phenomena, using intramolecular O- to N-ester transfer reactions. 相似文献