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81.
82.
A single-step synthesis for ring-fluorinated 4H-1,4-benzothiazines is reported by the condensation and oxidative cyclization of β-diketones with 2-amino-5-fluorobenzenethiol. The reaction is believed to proceed via an enaminoketone system. 相似文献
83.
The synthesis of 6-halogenated 4H-1,4-benzothiazines is reported by the condensation and oxidative cyclization of 4-substituted 2-aminobenzenethiols (I, R = Cl, Br) with β-diketones in presence of DMSO. The ir, nmr and mass spectral studies are included. 4-Substituted 2-aminobenzenethiols were also prepared by an improved and direct method. 相似文献
84.
Suppose u is the solution of the initial value problem Suppose n ≥ 1 is odd, f and g are supported in a ball B with boundary S, and one of f or g is zero. We derive identities relating the norm of f or g to the norm of the trace of u on S × [0,∞) . These identities are derived using integral geometric and multiplier methods. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
85.
86.
Lu Q Keskar G Ciocan R Rao R Mathur RB Rao AM Larcom LL 《The journal of physical chemistry. B》2006,110(48):24371-24376
Density gradient centrifugation is a high-resolution technique for the separation and characterization of large molecules and stable complexes. We have analyzed various nanotube structures by preparative centrifugation in sodium metatungstate-water solutions. Bundled, isolated and acid-treated single-walled nanotubes (SWNTs) and multiwall nanotubes (MWNTs) formed sharp bands at well-defined densities. The structure of the material in each band was confirmed by transmission electron microscopy and Raman spectroscopy. Our data suggest respective densities of 1.87, 2.13, 1.74, and 2.1 g/cm(3) for bundled, isolated, and acid-treated SWNTs and MWNTs. These measured results compare well with their calculated densities. 相似文献
87.
Rakesh Sohal Grzegorz Lupina Olaf Seifarth Peter Zaumseil Christian Walczyk Thomas Schroeder 《Surface science》2010,604(3-4):276-282
Process compatible high-k dielectric thin films are one of the key solutions to develop high performance metal–insulator–metal (MIM) structures for future microelectronic devices. Engineered cerium–aluminate (CexAl2–xO3) thin films were deposited on titanium nitride metal electrodes by electron-beam co-evaporation of ceria and alumina in a molecular beam deposition chamber. X-ray photoelectron spectroscopy clearly reveals that Ce cations can be stabilized in the 3+ valence state in CexAl2–xO3 up to x = 0.7 by accommodation in the alumina host matrix. Higher Ce content was observed to result in cerium dioxide segregation in cerium aluminate matrix, probably due to the chemical tendency of Ce cations to exist rather in the 4+ than in the 3+ state. Electrical characterization of the X-ray amorphous Ce0.7Al1.3O3 films reveals a dielectric constant value of about 11 and leakage current lower than 10?4 A/cm2. No parasitic low-k interface formation between the high-k Ce0.7Al1.3O3 film and the TiN metal electrode is detected. 相似文献
88.
Chawla Sheetal Rawal Rachna Sonia Ramrati Pundir C. S. 《Journal of nanoparticle research》2013,15(9):1-9
Highly dispersed platinum nanoparticles were deposited on gram quantities of non-functionalized multiwalled carbon nanotubes (MWCNTs) by atomic layer deposition (ALD) in a fluidized bed reactor at 300 °C. (Methylcyclopentadienyl) trimethylplatinum and oxygen were used as precursors. The results of TEM analysis showed that ~1.3 nm Pt nanoparticles were highly dispersed on non-functionalized MWCNTs. The porous structures of MWCNTs did not change with the deposition of Pt nanoparticles. For comparison, the commercial 3 wt% Pt/C catalyst was also characterized. The ALD-prepared Pt/MWCNT was used for the hydrogenation of xylose to xylitol. The ALD-prepared Pt/MWCNT showed the best catalytic performance with 100 % conversion of xylose and 99.3 % selectivity to xylitol, compared to commercially available Pt/C, Ru/C, and Raney Ni catalysts. The stability of ALD produced Pt/MWCNT catalyst was higher than that of the commercial Pt/C, due to the presence of surface defects on the MWCNTs and the strong metal–support interaction for the ALD-prepared Pt/MWCNT catalyst. 相似文献
89.
Sundeep Kaur Manjal Shelly Pathania Rohit Bhatia Ramandeep Kaur Kapil Kumar Ravindra K. Rawal 《Journal of heterocyclic chemistry》2019,56(9):2318-2332
In current scenario, heterocyclic compounds' role in medicinal chemistry has been tremendously increased as they possess wide number of pharmacological activities. One of the common heterocycles include indole skeleton with well‐established biological significance in field of medicinal chemistry. Fusion of indole nucleus with pyrrole heterocycle constitutes pyrroloindole scaffold, which further modifies the existing properties of indole alone. Pyrroloindole is a privileged scaffold found in various types of bioactive entities including natural compounds and exhibits wide variety of pharmacological activities like muscle relaxant, antifungal, antitumor, and antibiotic. Therefore, it is considered as attractive template for drug discovery. From several years, numbers of synthetic strategies have been reported for the synthesis of pyrroloindole and its derivatives, including also natural compounds such as amauromine, yuremamine, and chimonanthines. Here, in this review, we have tried to compile various synthetic strategies of pyrroloindole and its derivatives. 相似文献
90.
Rakesh Dontha Tian‐Cheng Zhu Yunjun Shen Michael Wrle Xin Hong Simon Duttwyler 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(52):19183-19189
The lithiacarborane [Li?CB11H11]? plays a central role in carborane chemistry, as it is a key intermediate to achieve the selective functionalization of the monocarba‐closo‐dodecaborate [CB11H12]? for applications in various fields. Also, it is an organometallic species of fundamental interest because it represents a 3D analogue of phenyllithium featuring an exo C?Li bond in addition to the delocalized negative endo charge of the spherical cluster. For the first time, the elusive and highly reactive endo/exo formal dianion [CB11H11]2? has been isolated as its lithiate as well as zincate in pure form and fully characterized. DFT calculations corroborate the experimental findings and underscore the remarkably high reactivity of the lithiacarborane. Subsequent derivatizations demonstrate the relevance of its initial clean formation. 相似文献