全文获取类型
收费全文 | 2582篇 |
免费 | 92篇 |
国内免费 | 16篇 |
专业分类
化学 | 1657篇 |
晶体学 | 48篇 |
力学 | 48篇 |
数学 | 270篇 |
物理学 | 667篇 |
出版年
2023年 | 15篇 |
2022年 | 31篇 |
2021年 | 38篇 |
2020年 | 43篇 |
2019年 | 41篇 |
2018年 | 54篇 |
2017年 | 41篇 |
2016年 | 86篇 |
2015年 | 65篇 |
2014年 | 75篇 |
2013年 | 169篇 |
2012年 | 166篇 |
2011年 | 206篇 |
2010年 | 102篇 |
2009年 | 120篇 |
2008年 | 151篇 |
2007年 | 158篇 |
2006年 | 128篇 |
2005年 | 97篇 |
2004年 | 103篇 |
2003年 | 83篇 |
2002年 | 84篇 |
2001年 | 52篇 |
2000年 | 46篇 |
1999年 | 29篇 |
1998年 | 17篇 |
1997年 | 22篇 |
1996年 | 22篇 |
1995年 | 21篇 |
1994年 | 22篇 |
1993年 | 20篇 |
1992年 | 18篇 |
1991年 | 13篇 |
1990年 | 24篇 |
1989年 | 29篇 |
1988年 | 17篇 |
1987年 | 12篇 |
1986年 | 18篇 |
1985年 | 16篇 |
1984年 | 22篇 |
1983年 | 17篇 |
1982年 | 14篇 |
1981年 | 26篇 |
1980年 | 17篇 |
1979年 | 16篇 |
1978年 | 21篇 |
1977年 | 17篇 |
1976年 | 19篇 |
1975年 | 18篇 |
1974年 | 11篇 |
排序方式: 共有2690条查询结果,搜索用时 15 毫秒
141.
142.
Po‐Sheng Chen Yi‐Chang Liu Chia‐Her Lin Bao‐Tsan Ko 《Journal of polymer science. Part A, Polymer chemistry》2010,48(16):3564-3572
Two novel sulfonate phenol ligands—3,3′‐di‐tert‐butyl‐2′‐hydroxy‐5,5′,6,6′‐tetramethyl‐biphenyl‐2‐yl 4‐X‐benzenesulfonate (X?CF3, LCF3 ‐H, and X?OCH3, LOMe ‐H)—were prepared through the sulfonylation of 3,3′‐di‐tert‐butyl‐5,5′,6,6′‐tetramethylbiphenyl‐2,2′‐diol with the corresponding 4‐substituted benzenesulfonyl chloride (1 equiv.) in the presence of excess triethylamine. Magnesium (Mg) complexes supported by sulfonate phenoxide ligands were synthesized and characterized structurally. The reaction of MgnBu2 with L‐H (2 equiv.) produces the four‐coordinated monomeric complexes ( LCF3 )2Mg ( 1 ) and ( LOMe )2Mg ( 2 ). Complexes 1 and 2 are efficient catalysts for the ring‐opening polymerization of ε‐caprolactone (ε‐CL) and trimethylene carbonate (TMC) in the presence of 9‐anthracenemethanol; complex 1 catalyzes the polymerization of ε‐CL and TMC in a controlled manner, yielding polymers with the expected molecular weights and narrow polydispersity indices (PDIs). In ε‐CL polymerization, the activity of complex 1 is greater than that of complex 2 , likely because of the greater Lewis acidity of Mg2+ metal caused by the electron‐withdrawing substitute trifluoromethyl (? CF3) at the 4‐position of the benzenesulfonate group. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3564–3572, 2010 相似文献
143.
Yoon Yeol Yoon Kil Yong Lee Kyung Seok Ko 《Journal of Radioanalytical and Nuclear Chemistry》2010,284(3):591-595
The contents of H-3 and C-14 in groundwater and surface waters around low and medium-level atomic waste repository site in
Korea were determined. The concentrations of C-14 were in the range 0.186–0.287 Bq/L. The H-3 concentration of the groundwaters
and surface waters were <0.06–5.75 and 1.22–4.74 Bq/L. The average H-3 contents of west, north and south direction were 1.18 ± 0.12,
1.11 ± 0.78 and 2.85 ± 2.66. H-3 and C-14 concentrations in the south direction were relatively higher than west and north
direction samples. The surface waters sampled from catchment were four times higher than average H-3 concentration in precipitation.
The concentrations of H-3 and C-14 within 5 km area samples were much higher than other samples. 相似文献
144.
145.
N. Mansourian-Hadavi T.O. MasonD. Ko K.R. Poeppelmeier 《Journal of solid state chemistry》2002,164(2):188-200
This work presents a modified defect model for pure and chemically substituted quadruple and quintuple pure perovskite layered cuprates, using data from the Jonker (thermopower vs ln conductivity) and Brouwer (log conductivity vs log pO2) analyses. The closely matched in-plane bond lengths of the blocking and the active layers in these structures promote ionic compensation rather than electronic compensation upon aliovalent p-type doping. A comprehensive defect model that takes into account all the major defect species in an ionically compensated quadruple or quintuple perovskite provides a better means for understanding the electrical behavior of these novel materials. The presented model allows for the calculation of effective dopant and the oxygen interstitial concentrations in these materials. 相似文献
146.
Link JM Reyes M Yager PM Anjos JC Bediaga I Göbel C Magnin J Massafferi A de Miranda JM Pepe IM dos Reis AC Carrillo S Casimiro E Cuautle E Sánchez-Hernández A Uribe C Vazquez F Agostino L Cinquini L Cumalat JP O'Reilly B Ramirez JE Segoni I Butler JN Cheung HW Gaines I Garbincius PH Garren LA Gottschalk E Kasper PH Kreymer AE Kutschke R Bianco S Fabbri FL Zallo A Cawlfield C Kim DY Rahimi A Wiss J Gardner R Kryemadhi A Chung YS Kang JS Ko BR Kwak JW Lee KB Park H Alimonti G Boschini M 《Physical review letters》2002,88(16):161801
A high statistics measurement of the Lambda(+)(c) lifetime from the Fermilab fixed-target FOCUS photoproduction experiment is presented. We describe the analysis technique with particular attention to the determination of the systematic uncertainty. The measured value of 204.6 +/- 3.4 (stat) +/- 2.5 (syst) fs from 8034 +/- 122 Lambda(+)(c)-->pK(-)pi(+) decays represents a significant improvement over the present world average. 相似文献
147.
Che-Chian Ko Thein Kyu Steven D. Smith 《Journal of Polymer Science.Polymer Physics》1995,33(3):517-525
Dynamics of phase separation in bisphenol-A polycarbonate (PC)/syndiotactic polymethyl methacrylate (sPMMA) blends has been investigated by means of time-resolved light scattering. Solvent-cast films of the PC/sPMMA blends were transparent, suggestive of miscible character. Several temperature jumps were carried out at a 50/50 PC/sPMMA composition from a homogeneous state (room temperature) into a two-phase regime. The process of phase separation first occurred for some considerable period, then it was followed by phase dissolution driven by chemical reaction. The thermodegradative reaction of sPMMA triggered the dissolution process by probably forming PC/sPMMA graft or random copolymers at the interface, which eventually resulted in a single phase. However, annealing at elevated temperatures for an extended period could lead to cross-linking, and thus a two-phase structure could be fixed permanently. The early stage of spinodal decomposition was interpreted in terms of the linearized Cahn-Hilliard theory. In the late stages of spinodal decomposition, the relationship between scattering peak wavenumber and time was found to obey a power law, but the exponents showed a strong dependence on temperature jumps. The temporal universal scaling failed due to the influence of the chemical reaction. © 1995 John Wiley & Sons, Inc. 相似文献
148.
Blahoslav Košťák 《Experimental Mechanics》1969,9(8):374-379
A new device for movement detection in joints is designed using the moiré technique. Archimedean spiral grids are used. A space displacement may be evaluated in two planes by vectors of known magnitudes and directions. An extremely simple design is proposed to provide stability for the system being installedin situ over long periods of time. 相似文献
149.
The deposit of carbon and oxygen adatoms on Mo(100) was characterized by AES and LEED. Carbon was introduced by the thermal cracking of ethylene; several ordered structures were observed as a function of coverage with carbon atoms residing on four-fold sites. The Mo(100)—O system exhibited two different sequences of LEED patterns depending on the adsorption temperature of oxygen. The effects of adsorbed carbon and oxygen on the chemisorption properties of Mo(100) was investigated by FDS. The presence of either carbon or oxygen severely hindered the ability of Mo(100) to dissociatively adsorb hydrogen or carbon monoxide. The amount of CO dissociated was directly related to the available four-fold sites on the carbide surfaces. The molecular adsorption of CO was not significantly affected by the adlayers. It was found that one monolayer of adsorbed oxygen reduced the binding energy of molecular CO considerably more than the same amount of adsorbed carbon. A continuous shift in the binding energy of CO with the C/O ratio on the surface was observed. 相似文献
150.
The heats of solution of alcohols in hexane can be considered as the energy necessary to break hydrogen bonds (H-bond). The amount of non H-bonded OH groups estimated from caloric data, are in good agreement with IR-spectroscopic data. Comparison of calorimetric and IR-spectroscopically determined H-bond energies permit the separation of intermolecular van der Waals effects from H-bond interactions. This separation shows that van der Waals interactions of alcohols or water should not be underestimated. 相似文献