全文获取类型
收费全文 | 1881篇 |
免费 | 89篇 |
国内免费 | 26篇 |
专业分类
化学 | 1390篇 |
晶体学 | 25篇 |
力学 | 71篇 |
数学 | 204篇 |
物理学 | 306篇 |
出版年
2024年 | 14篇 |
2023年 | 24篇 |
2022年 | 81篇 |
2021年 | 114篇 |
2020年 | 76篇 |
2019年 | 74篇 |
2018年 | 73篇 |
2017年 | 52篇 |
2016年 | 104篇 |
2015年 | 58篇 |
2014年 | 70篇 |
2013年 | 107篇 |
2012年 | 133篇 |
2011年 | 148篇 |
2010年 | 94篇 |
2009年 | 93篇 |
2008年 | 85篇 |
2007年 | 81篇 |
2006年 | 67篇 |
2005年 | 64篇 |
2004年 | 45篇 |
2003年 | 29篇 |
2002年 | 34篇 |
2001年 | 12篇 |
2000年 | 11篇 |
1999年 | 8篇 |
1998年 | 9篇 |
1997年 | 17篇 |
1996年 | 17篇 |
1995年 | 14篇 |
1994年 | 5篇 |
1993年 | 20篇 |
1992年 | 7篇 |
1991年 | 10篇 |
1988年 | 7篇 |
1987年 | 5篇 |
1986年 | 9篇 |
1985年 | 11篇 |
1984年 | 17篇 |
1983年 | 6篇 |
1982年 | 10篇 |
1981年 | 6篇 |
1980年 | 9篇 |
1979年 | 6篇 |
1978年 | 8篇 |
1976年 | 7篇 |
1975年 | 7篇 |
1973年 | 7篇 |
1972年 | 6篇 |
1965年 | 4篇 |
排序方式: 共有1996条查询结果,搜索用时 15 毫秒
991.
Ashraf A. Aly Alan B. Brown Mohamed Abdel‐Aziz Gamal El‐Din A. A. Abuo‐Rahma Mohamed F. Radwan Mohamed Ramadan Amira M. Gamal‐Eldeen 《Journal of heterocyclic chemistry》2012,49(4):726-731
Reaction of 3‐aroyl‐1‐arylthioureas with dimethyl but‐2‐ynedioate in dichloromethane and catalyzed by triphenylphosphine at ?5°C led to (Z)‐methyl 2‐[(Z)‐2‐(4‐aroylimino)‐4‐oxo‐3‐aryl‐1,3‐thiazolidin‐5‐ylidene]acetates in good yields. The mechanism is discussed. X‐ray structure analysis of one thiazolidine derivative is described. Antitumor and antioxidant activities have been investigated. One derivative of 1,3‐thiazolidine showed moderate antiproliferative in vitro activity against hepatocellular carcinoma Hep‐G2, whereas another 1,3‐thiazolidine introduced effective antioxidant activity compared to ascorbic acid. 相似文献
992.
Alexander P. Filippov Alina I. Amirova Elena V. Belyaeva Elena B. Tarabukina Natalia A. Sheremetyeva Aziz M. Muzafarov 《Macromolecular Symposia》2012,316(1):43-51
Summary: Hyperbranched polycarbosilane with terminal butyl groups is obtained by chemical modification of hyperbranched polyallylcarbosilane using the reaction of hydrosilylation with methyldichlorosilane, followed by treatment of the polychlorosilyl derivative with butyllithium. Its hydrodynamic and conformational properties are studied by the methods of light scattering, sedimentation-diffusion analysis, and viscosimetry in dilute solutions of methyl-tert-butyl ether, hexane, THF, chloroform, and toluene. The results obtained are compared with the data for the initial polyallylcarbosilane and carbosilane dendrimer with butyl terminal groups. It is demonstrated that branching regularity is the decisive factor determining the solution properties at fixed degree of the branching. 相似文献
993.
Md. Masum Haider Tahmina Ferdous Syed S. Duha 《Central European Journal of Physics》2014,12(9):701-706
The nonlinear propagation of small but finite amplitude dust-ion-acoustic solitary waves in a magnetized, collisionless dusty plasma is investigated theoretically. It has been assumed that the electrons are trapped following the vortex-like distribution and that the negatively and positively charged ions are mobile with the presence of charge fluctuating stationary dusts, where ions mass provide the inertia and restoring forces are provided by the thermal pressure of hot electrons. A reductive perturbation method was employed to obtain a modified Korteweg-de Vries (mK-dV) equation for the first-order potential and a stationary solution is obtained. The effect of the presence of trapped electrons, negatively and positively charged ions and arbitrary charged dust grains are discussed. 相似文献
994.
A very sensitive and reversible optical chemical sensor based on a novel tetradentate Schiff base namely N.N/bis(2-aminothiophenol)benzene-1,2-dicarboxaldehyde (ATBD) immobilized within a plasticized PVC film for Hg2+ determination is described. At optimum conditions (i.e. pH 6.0), the proposed sensor displayed a linear response to Hg2+ over 1.0?×?10?10 ? 1.0?×?10?2 mol L?1 with a limit of detection of 7.23?×?10?11 mol L?1 (0.0145 μgL?1). Moreover, the results revealed that, under batch condition, the sensor is fully reversible within a response time?~?35 s. In addition to its high stability and reproducibility, the sensor showed good selectivity towards Hg2+ ion with respect to common metal cations. The sensor was successfully applied for determination of Hg2+ ion in some real samples, including hair, urine and well water samples. The results were in good correlation with the data obtained using cold vapor atomic absorption spectrometry. 相似文献
995.
Surface modified adsorbent mesoporous silicate MCM-41 has been prepared by grafting thiol containing functional group onto mesoporous silicate MCM-41. XRD, N2 adsorption/desorption measurements, SEM, FT-IR, thermogravimetry and elemental analysis have been made to confirm the ordered mesoporous framework and the functionalization of the thiol groups. Sorption of 18 metal ions on this sorbent have been studied and discussed. Chromatographic separation of Rb(I)–U(VI)–Sr(II)–Zr(IV), has been achieved on column of this sorbent. 相似文献
996.
Mohy S. Mansour Hisham Imam Khaled A. Elsayed Wafaa Abbass 《Spectrochimica Acta Part B: Atomic Spectroscopy》2009,64(10):1079
One of the most recently applied laser-based techniques in combustion environment is the laser-induced breakdown spectroscopy (LIBS). The technique has been extensively and successfully applied to elemental concentration measurements in solids and liquids. The LIBS signal is much weaker in gases and hence more work is required for quantitative measurements in flames. In the present work we used two orthogonal Nd:YAG lasers that operate at the fundamental wavelength with laser pulse energy of about 100 mJ/pulse. A Princeton-Instruments IMAX ICCD camera attached to a PI-Echelle spectrometer was used for signal detection. The lasers are focused using two 5-cm lenses. Several calibration points have been collected in well defined and homogeneous mixtures of air and fuel in order to be used as references for the measurements in turbulent partially premixed flames. This work shows that the application of the LIBS technique in a turbulent combustion environment is feasible and signal is enhanced by applying an orthogonal dual-pulse arrangement for air–fuel. 相似文献
997.
Iver Lauermann Dr. Timo Kropp Damien Vottier Ahmed Ennaoui Wolfgang Eberhardt Prof. Dr. Emad F. Aziz Dr. 《Chemphyschem》2009,10(3):532-535
Bridging the gap between high‐vacuum soft X‐ray absorption spectroscopy and real systems under ambient conditions probes chemical reactions in situ during deposition and annealing processes. The origin of highly efficient buffer layers in Zn(S,O) is the complex formation between Zn2+ and the S?C group of thiourea (see schematic), which allows ligand‐to‐metal and metal‐to‐ligand charge transfer (LMCT and MLCT).
998.
Francesco Ricci Nadia Zari Felice Caprio Simona Recine Aziz Amine Danila Moscone Giuseppe Palleschi Kevin W. Plaxco 《Bioelectrochemistry (Amsterdam, Netherlands)》2009,76(1-2):208
E-DNA sensors are a reagentless, electrochemical oligonucleotide sensing platform based on a redox-tag modified, electrode-bound probe DNA. Because E-DNA signaling is linked to hybridization-linked changes in the dynamics of this probe, sensor performance is likely dependent on the nature of the self-assembled monolayer coating the electrode. We have investigated this question by characterizing the gain, specificity, response time and shelf-life of E-DNA sensors fabricated using a range of co-adsorbates, including both charged and neutral alkane thiols. We find that, among the thiols tested, the positively charged cysteamine gives rise to the largest and most rapid response to target and leads to significantly improved storage stability. The best mismatch specificity, however, is achieved with mercaptoethanesulfonic and mercaptoundecanol, presumably due to the destabilizing effects of, respectively, the negative charge and steric bulk of these co-adsorbates. These results demonstrate that a careful choice of co-adsorbate chemistry can lead to significant improvements in the performance of this broad class of electrochemical DNA sensors. 相似文献
999.
1000.
A novel approach to the electrochemical determination of heavy metals in tap water using anodic stripping voltammetry was developed using screen-printed electrodes modified with gold films. After optimisation of the experimental conditions, the screen-printed electrodes modified with gold films displayed excellent linear behaviour in the examined concentration range from 2 to 16 µg L-1 mercury and lead in 50 mM HCl with a detection limit of 1.5 µg L-1 and 0.5 µg L-1 for mercury and lead, respectively. In order to decrease the working range down to less than 1 µg L-1, a preconcentration step based on the use of magnetic particles modified with thiols was introduced into the protocol. Applying optimum binding conditions, the assay using screen-printed electrodes modified with gold films displayed excellent linear behaviour in the concentration range 0.1 to 0.8 µg L-1 in 50 mM HCl. The detection limit after a 120 s deposition time for mercury and lead were 0.08 µg L-1 and 0.02 µg L-1, respectively. The method has been applied to the determination of mercury and lead traces in tap water 相似文献