全文获取类型
收费全文 | 28069篇 |
免费 | 3721篇 |
国内免费 | 3143篇 |
专业分类
化学 | 20386篇 |
晶体学 | 366篇 |
力学 | 1392篇 |
综合类 | 241篇 |
数学 | 3525篇 |
物理学 | 9023篇 |
出版年
2023年 | 440篇 |
2022年 | 486篇 |
2021年 | 697篇 |
2020年 | 915篇 |
2019年 | 932篇 |
2018年 | 797篇 |
2017年 | 763篇 |
2016年 | 1126篇 |
2015年 | 1147篇 |
2014年 | 1361篇 |
2013年 | 1914篇 |
2012年 | 2279篇 |
2011年 | 2517篇 |
2010年 | 1764篇 |
2009年 | 1738篇 |
2008年 | 1938篇 |
2007年 | 1763篇 |
2006年 | 1580篇 |
2005年 | 1393篇 |
2004年 | 1109篇 |
2003年 | 883篇 |
2002年 | 809篇 |
2001年 | 701篇 |
2000年 | 568篇 |
1999年 | 529篇 |
1998年 | 478篇 |
1997年 | 419篇 |
1996年 | 452篇 |
1995年 | 384篇 |
1994年 | 367篇 |
1993年 | 341篇 |
1992年 | 319篇 |
1991年 | 276篇 |
1990年 | 232篇 |
1989年 | 191篇 |
1988年 | 167篇 |
1987年 | 128篇 |
1986年 | 141篇 |
1985年 | 154篇 |
1984年 | 101篇 |
1983年 | 64篇 |
1982年 | 71篇 |
1981年 | 53篇 |
1980年 | 52篇 |
1979年 | 58篇 |
1978年 | 40篇 |
1976年 | 37篇 |
1975年 | 32篇 |
1974年 | 40篇 |
1973年 | 45篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
31.
32.
Zhipeng Lin Hao Zhang Guofeng Liang Yanqi Jin Hongbin Zeng Jiawang Li Jian Chen Weihong Zhang Fangyan Xie Yanshuo Jin Hui Meng 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(12):3112-3118
A composite of FeOOH nanocubes anchored on carbon ribbons has been synthesized and used as a cathode material for Li/O2 batteries. Fe2+ ion-exchanged resin serves as a precursor for both FeOOH nanocubes and carbon ribbons, which are formed simultaneously. The as-prepared FeOOH cubes are proposed to have a core–shell structure, with FeOOH as the shell and Prussian blue as the core, based on information from XPS, TEM, and EDS mapping. As a cathode material for Li/O2 batteries, FeOOH delivers a specific capacity of 14816 mA h g−1cathode with a cycling stability of 67 cycles over 400 h. The high performance is related to the low overpotential of the oxygen reduction/evolution reaction on FeOOH. The cube structure, the supporting carbon ribbons, and the -OOH moieties all contribute to the low overpotential. The discharge product Li2O2 can be efficiently decomposed in the FeOOH cathode after a charging process, leading to higher cycling stability. Its high activity and stability make FeOOH a good candidate for use in non-aqueous Li/O2 batteries. 相似文献
33.
Bei-Bei Guo Dr. Yue-Jian Lin Prof. Guo-Xin Jin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(41):9721-9727
Four flexible ligands with different lengths, degrees of flexibility, and steric bulk were synthesized and used to prepare metal-directed assemblies. Interestingly, minor differences among the ligands led to products with dramatically different topologies: a binuclear D -shaped macrocycle, tetranuclear rectangles, and hexanuclear trefoil knots. The interconversion of the trefoil-shaped complexes was also investigated. This contribution introduces a rare ligand-controlled trefoil–rectangle shape transformation in solution. 相似文献
34.
35.
Zhijian Fu Xingzhou Zhan Lin Luo Andreas Schadschneider Junmin Chen 《Physics letters. A》2019,383(16):1897-1906
Fatigue even increases the complexity of the pedestrian dynamics which is regarded as a kind of nonlinear system, and might have a significant negative impact on the crowd evacuation. However, it has never been investigated completely and properly. Thus, the fine discrete floor field cellular automata model is modified by integrating the fatigue function to explore the influence of fatigue on the crowd ascending evacuation. The simulation fits well with the empirical data and the observations quantitatively and qualitatively, indicating the model captures the main features of evacuation considering fatigue impact. As a prediction, without merging streams, compared with the case of walking in constant speed, when fatigue is considered, it takes 71.4% longer for all persons to enter the stairs and 87.2% longer to evacuate. With merging streams, fatigue has little impact on the inflow, while it makes the total evacuation time 84.2% longer. 相似文献
36.
Dr. Jun Zeng Dr. Zhichao Wang Dr. Xin Huang Dr. Sabine S. Eckstein Prof. Dr. Xiaohui Lin Prof. Dr. Hailong Piao Prof. Dr. Cora Weigert Dr. Peiyuan Yin Prof. Dr. Rainer Lehmann Prof. Dr. Guowang Xu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(21):5427-5432
Mass spectrometry (MS) driven metabolomics is a frequently used tool in various areas of life sciences; however, the analysis of polar metabolites is less commonly included. In general, metabolomic analyses lead to the detection of the total amount of all covered metabolites. This is currently a major limitation with respect to metabolites showing high turnover rates, but no changes in their concentration. Such metabolites and pathways could be crucial metabolic nodes (e.g., potential drug targets in cancer metabolism). A stable-isotope tracing capillary electrophoresis–mass spectrometry (CE-MS) metabolomic approach was developed to cover both polar metabolites and isotopologues in a non-targeted way. An in-house developed software enables high throughput processing of complex multidimensional data. The practicability is demonstrated analyzing [U-13C]-glucose exposed prostate cancer and non-cancer cells. This CE-MS-driven analytical strategy complements polar metabolite profiles through isotopologue labeling patterns, thereby improving not only the metabolomic coverage, but also the understanding of metabolism. 相似文献
37.
38.
Hui‐Min Lin Jian‐Rong Li Chao Mu Ao Li Xu‐Feng Liu Pei‐Hua Zhao Yu‐Long Li Zhong‐Qing Jiang Hong‐Ke Wu 《应用有机金属化学》2019,33(11)
Five monophosphine‐substituted diiron propane‐1,2‐dithiolate complexes as the active site models of [FeFe]‐hydrogenases have been synthesized and characterized. Reactions of complex [Fe2(CO)6{μ‐SCH2CH(CH3)S}] ( 1 ) with a monophosphine ligand tris(4‐methylphenyl)phosphine, diphenyl‐2‐pyridylphosphine, tris(4‐chlorophenyl)phosphine, triphenylphosphine, or tris(4‐fluorophenyl)phosphine in the presence of the oxidative agent Me3NO·2H2O gave the monophosphine‐substituted diiron complexes [Fe2(CO)5(L){μ‐SCH2CH(CH3)S}] [L = P(4‐C6H4CH3)3, 2 ; Ph2P(2‐C5H4N), 3 ; P(4‐C6H4Cl)3, 4 ; PPh3, 5 ; P(4‐C6H4F)3, 6 ] in 81%–94% yields. Complexes 2 – 6 have been characterized by elemental analysis, spectroscopy, and X‐ray crystallography. In addition, electrochemical studies revealed that these complexes can catalyze the reduction of protons to H2 in the presence of HOAc. 相似文献
39.
40.