全文获取类型
收费全文 | 49352篇 |
免费 | 17526篇 |
国内免费 | 1009篇 |
专业分类
化学 | 58703篇 |
晶体学 | 101篇 |
力学 | 1748篇 |
综合类 | 85篇 |
数学 | 2298篇 |
物理学 | 4952篇 |
出版年
2024年 | 443篇 |
2023年 | 4351篇 |
2022年 | 1765篇 |
2021年 | 2799篇 |
2020年 | 5009篇 |
2019年 | 2600篇 |
2018年 | 2678篇 |
2017年 | 921篇 |
2016年 | 5992篇 |
2015年 | 5933篇 |
2014年 | 5429篇 |
2013年 | 5755篇 |
2012年 | 3913篇 |
2011年 | 1935篇 |
2010年 | 3898篇 |
2009年 | 3878篇 |
2008年 | 1618篇 |
2007年 | 1214篇 |
2006年 | 603篇 |
2005年 | 479篇 |
2004年 | 372篇 |
2003年 | 316篇 |
2002年 | 268篇 |
2001年 | 233篇 |
2000年 | 233篇 |
1999年 | 217篇 |
1998年 | 223篇 |
1997年 | 234篇 |
1996年 | 196篇 |
1995年 | 303篇 |
1994年 | 232篇 |
1993年 | 311篇 |
1992年 | 166篇 |
1991年 | 141篇 |
1990年 | 125篇 |
1989年 | 108篇 |
1988年 | 118篇 |
1980年 | 113篇 |
1979年 | 96篇 |
1978年 | 99篇 |
1977年 | 163篇 |
1976年 | 182篇 |
1975年 | 188篇 |
1974年 | 196篇 |
1973年 | 111篇 |
1972年 | 153篇 |
1971年 | 123篇 |
1970年 | 208篇 |
1969年 | 126篇 |
1968年 | 133篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
891.
Yashao Chen Jinhong Yi Qiang Gao Xiaoling Zhou Yanling Luo Peng Liu 《Plasma Chemistry and Plasma Processing》2013,33(6):1153-1165
To improve the biocompatibility of poly(tetrafluoroethylene-co-hexafluoropropylene) (FEP) film, a technique based on Ar plasma pretreatment and UV-induced grafting polymerization was used to immobilize carboxymethyl chitosan (CMCS) on the FEP film surfaces. Initially Ar plasma was used to treat FEP film. Then, plasma treated FEP film was modified via UV-induced grafting polymerization with hydrophilic acrylic acid (AAc) monomer. The following immobilization of CMCS on the FEP-pAAc surface was carried out via an amidation reaction. The change of chemical composition and surface morphology of FEP film were characterized by attenuated total reflectance Fourier transform infrared (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), scanning electronic microscopy (SEM) and atomic force microscopy (AFM). Results of water contact angles measurement showed that the hydrophilicity of the surface has improved significantly after surface modification. Furthermore, methyl thiazolyl tetrazolium (MTT) assay and cell morphology analysis confirmed that mouse fibroblasts (L929 cells) attachment and proliferation were improved remarkably on the modified FEP surface. These results suggest that CMCS were successfully employed to surface engineering FEP film, and enhanced its cell biocompatibility. The approach presented here may be exploited for surface modification of biomaterials. 相似文献
892.
Kongkai Zhu Junyan Lu Zhongjie Liang Xiangqian Kong Fei Ye Lu Jin Heji Geng Yong Chen Mingyue Zheng Hualiang Jiang Jun-Qian Li Cheng Luo 《Journal of computer-aided molecular design》2013,27(3):247-256
New Delhi metallo-β-lactamase-1 (NDM-1) has emerged as a major global threat to human health for its rapid rate of dissemination and ability to make pathogenic microbes resistant to almost all known β-lactam antibiotics. In addition, effective NDM-1 inhibitors have not been identified to date. In spite of the plethora of structural and kinetic data available, the accurate molecular characteristics of and details on the enzymatic reaction of NDM-1 hydrolyzing β-lactam antibiotics remain incompletely understood. In this study, a combined computational approach including molecular docking, molecular dynamics simulations and quantum mechanics/molecular mechanics calculations was performed to characterize the catalytic mechanism of meropenem catalyzed by NDM-1. The quantum mechanics/molecular mechanics results indicate that the ionized D124 is beneficial to the cleavage of the C–N bond within the β-lactam ring. Meanwhile, it is energetically favorable to form an intermediate if no water molecule coordinates to Zn2. Moreover, according to the molecular dynamics results, the conserved residue K211 plays a pivotal role in substrate binding and catalysis, which is quite consistent with previous mutagenesis data. Our study provides detailed insights into the catalytic mechanism of NDM-1 hydrolyzing meropenem β-lactam antibiotics and offers clues for the discovery of new antibiotics against NDM-1 positive strains in clinical studies. 相似文献
893.
Chiral N-[1-benzyl-2-hydroxyethyl]-3-[2-oxo-pyrrole]propionamide (C16H22N2O3) was obtained unexpectedly from the reaction of oxazoline involving pyrrolidone with copper acetate monohydrate, and the structure was characterized by NMR, IR, elemental analysis, and X-ray analysis. 相似文献
894.
Li Luo Kathrin Häfliger Dan Xie Markus Niederberger 《Journal of Sol-Gel Science and Technology》2013,65(1):28-35
Homogeneous transparent conducting Sn:ZnO films on fused silica substrates were prepared by dip-coating from nanoparticle dispersions, while the nanocrystalline Sn:ZnO particles with different dopant concentrations were synthesized by microwave-assisted non-aqueous sol–gel process using Sn(IV) tert-butoxide and Zn(II) acetate as precursors and benzyl alcohol as solvent. The dopant concentration had a great impact on the electrical properties of the films. A minimum resistivity of 20.3 Ω cm was obtained for a porous Sn:ZnO film with initial Sn concentration of 7.5 mol% after annealing in air and post-annealing in N2 at 600 °C. The resistivity of this porous film could further be reduced to 2.6 and 0.6 Ω cm after densified in Sn:ZnO and Al:ZnO reaction solution, respectively. The average optical transmittance of a 400-nm-thick Sn:ZnO film densified with Sn:ZnO after the two annealing steps was 91%. 相似文献
895.
Li‐Wei Zhao Hui‐Min Shi Zhe An Jiu‐Zhao Wang Prof. Jing He 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(37):12350-12355
Effectively enhancing the enantioselectivity is a persistent challenge in heterogeneous asymmetric catalysis. Here, the validity of a layered double hydroxides (LDH) nanosheet as an efficient planar substituent to enhance the enantioselectivity has been investigated theoretically; first in vanadium‐catalyzed asymmetric epoxidation of allylic alcohols, and then in zinc‐catalyzed direct asymmetric aldol addition. The computational predication is further confirmed experimentally in zinc‐catalyzed direct asymmetric aldol addition by controlling the location of catalytic sites. 相似文献
896.
Wenbo Wu Dr. Guohua Xu Prof. Conggang Li Prof. Gui Yu Prof. Yunqi Liu Prof. Cheng Ye Prof. Jingui Qin Prof. Zhen Li 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(21):6874-6888
Through the combination of the divergent and convergent approaches, coupled with the utilization of the powerful Sharpless “click‐chemistry” reaction, two series of sulfonyl‐based high‐generation NLO dendrimers were conveniently prepared with high purity and in satisfactory yields. Thanks to the perfect three‐dimensional (3D) spatial isolation from the highly branched structure and the isolation effect of the exterior benzene moieties and the interior triazole rings, these dendrimers exhibited large second harmonic generation coefficient (d33) values up to 181 pm V?1, which, to the best of our knowledge, is the highest value so far for polymers containing sulfonyl‐based chromophore moieties. Meanwhile, compared with the nitro‐chromophore‐based analogues, their optical transparency and NLO stability were improved in a large degree, due to the lower dipole moment (μ) and the special main‐chain structure of sulfonyl‐based chromophore in these dendrimers. 相似文献
897.
Dr. Yang Chen Dr. Elzbieta Trzop Jesse D. Sokolow Prof. Dr. Philip Coppens 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(49):16651-16655
The structures of three newly synthesized phosphonate‐substituted polyoxotitanates are reported. The Ti/O core of [Ti4O(OEt)12(PhenylPO3)] ( 1 ) is the building block for two larger phosphonate‐substituted nanoclusters, [Ti25O26(OEt)36(PhenylPO3)6] ( 2 ) and [Ti26O26(OEt)39(PhenylPO3)6]Br ( 3 ). All compounds exhibit a not previously recognized triply bridging binding mode of the phosphonate anchor with short connecting Ti? O bonds, the average of which is 2.010(7) Å. Comparison with previously reported work suggests that the binding mode of the phosphonate anchor is strongly dependent on the structure of the underlying substrate. 相似文献
898.
899.
Prof. Dr. Sjoerd Harder Dominik Naglav Dr. Christian Ruspic Prof. Dr. Claudia Wickleder Dr. Matthias Adlung Dr. Wilfried Hermes Dr. Matthias Eul Prof. Dr. Rainer Pöttgen Dr. Daniel B. Rego Prof. Dr. Frederic Poineau Prof. Dr. Kenneth R. Czerwinski Prof. Dr. Rolfe H. Herber Prof. Dr. Israel Nowik 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(37):12173-12173
900.
A. Sudheer Kumar Vikas D. Ghule S. Subrahmanyam Prof. Dr. Akhila K. Sahoo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(2):509-518
Various thermally stable energetic polynitro‐aryl‐1,2,3‐triazoles have been synthesized through Cu‐catalyzed [3+2] cycloaddition reactions between their corresponding azides and alkynes, followed by nitration. These compounds were characterized by analytical and spectroscopic methods and the solid‐state structures of most of these compounds have been determined by using X‐ray diffraction techniques. Most of the polynitro‐bearing triazole derivatives decomposed within the range 142–319 °C and their heats of formation and crystal densities were determined from computational studies. By using the Kamlet–Jacobs empirical relation, their detonation velocities and pressures were calculated from their heats of formation and crystal densities. Most of these newly synthesized compounds exhibited high positive heats of formation, good thermal stabilities, reasonable densities, and acceptable detonation properties that were comparable to those of TNT. 相似文献