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201.
The zero-order desorption kinetics is described for adsorbate systems in which three phases are in equilibrium and first-order desorption kinetics is assumed for the desorption from the topmost phase. The calculated results represent typical features of the observed zero-order desorption spectra. The possibility of specifying the phase boundaries from the thermal or isothermal desorption spectra is proposed. The relationship between the thermal or isothermal desorption processes and trajectories in the phase diagram is also discussed. 相似文献
202.
Masanori Ohya 《International Journal of Theoretical Physics》1998,37(1):495-505
The concept of complexity in InformationDynamics is discussed. The chaos degree defined by thecomplexities is applied to examine chaotic behavior oflogistic map. 相似文献
203.
We show analytically that in the presence of cubic and quintic nonlinearities above a certain critical power, multidimensional optical solitary waves could propagate stably in bulk media. To investigate the stability an analytical expression for the solitary-wave fields with an arbitrary transverse dimension is derived through the combined use of Galerkin’s method and self-consistent-field approximation. 相似文献
204.
The effects of foreign impurity ions in the conduction plane on the β″-Al2O3 lattice have been analyzed by molecular dynamics. As impurity ions, K and Ca ions were chosen and Na sites in the conduction plane were replaced with these ions. Results are summarized as follows: (1) The β″-Al2O3 lattice expands perpendicular to the conduction plane when K ions are doped; (2) Ca ions do not contribute to expansions of the β″-Al2O3 lattice; (3) both K and Ca ions reduce the mean square displacement of Na ions, which can be attributed to decreased Na ion diffusion. 相似文献
205.
Colloids for Catalysts: A Concept for the Preparation of Superior Catalysts of Industrial Relevance
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Dr. Jonathan Quinson Sara Neumann Tanja Wannmacher Laura Kacenauskaite Masanori Inaba Jan Bucher Francesco Bizzotto Dr. Søren B. Simonsen Dr. Luise Theil Kuhn Dajana Bujak Dr. Alessandro Zana Prof. Dr. Matthias Arenz Dr. Sebastian Kunz 《Angewandte Chemie (International ed. in English)》2018,57(38):12338-12341
Compared to conventional preparation methods for supported heterogeneous catalysts, the use of colloidal nanoparticles (NPs) allows for a precise control over size, size distribution, and distribution/location of the NPs on the support. However, common colloidal syntheses have restrictions that limit their applicability for industrial catalyst preparation. We present a simple, surfactant‐free, and scalable preparation method for colloidal NPs to overcome these restrictions. We demonstrate how precious‐metal NPs are prepared in alkaline methanol, how the particle size can be tuned, and how supported catalysts are obtained. The potential of these colloids in the preparation of improved catalysts is demonstrated by two examples from heterogeneous catalysis and electrocatalysis. 相似文献
206.
Yamamoto A Nakamura K Furukawa K Konishi Y Ogino T Higashiura K Yago H Okamoto K Otsuka M 《Chemical & pharmaceutical bulletin》2002,50(1):47-52
To find new tachykinin NK1 receptor antagonists from natural sources, we examined the tachykinin antagonist activity in the extracts of approximately 200 species of plants by the use of isolated guinea pig ileum. As a result, we discovered a novel and potent NK1 receptor antagonist in the extract of dried flowers of Matricaria chamomilla L. (chamomile). The structure of the antagonist was established as N1,N5,N10,N14-tetrakis[3-(4-hydroxyphenyl)-2-propenoyl]-1,5,10,14-tetraazatetradecane (tetracoumaroyl spermine, 1a). The Ki values of 1a, estimated from the inhibitory action on the substance P (SP)-induced contraction of the guinea pig ileum and the inhibition of the binding of [3H][Sar9, Met(O2)11]SP to human NK1 receptors, were 21.9 nM and 3.3 nM, respectively. 1a is the first potent NK1 receptor antagonist from natural sources and it has a unique structure of a polyacylated spermine. 1a was concentrated in pollen of Matricaria chamomilla L. and was also found in the extracts of flowers of other four species of Compositae. In addition, we found N1,N5,N10-tris[3-(4-hydroxyphenyl)-2-propenoyl]-1,5,10,14-tetraazatetradecane (2) as a new compound in the extract of flowers of Matricaria chamomilla L., which did not exhibit any tachykinin antagonist activity. A number of related compounds were synthesized, and the structure-activity relationship was studied. 相似文献
207.
Junji Mizukado Yasuhisa Matsukawa Heng-dao Quan Masanori Tamura Akira Sekiya 《Journal of fluorine chemistry》2005,126(3):365-369
ROCHF2-type fluorinated ethers were synthesized by the reaction of hexafluoropropene oxide (HFPO) with alcohol or phenol. In this reaction, although the insertion reaction of difluorocarbene to OH bond and the nucleophilic attack of alcohol or phenol to HFPO were competition, the insertion reaction proceeded predominantly to give fluorinated ether in the case of low nucleophilic alcohol or phenol. In addition, high reaction pressure is advantageous to the selectivity of the fluorinated ethers in the reaction of HFPO with (CF3)2CHOH or C6F5OH. 相似文献
208.
Hirokazu Tsukamoto Takamichi Suzuki Masanori Sato Yoshinori Kondo 《Tetrahedron letters》2007,48(48):8438-8441
Polystyrene-bound diethanolamine (PS-DEAM) work-up for a newly developed Pd(PPh3)4-catalyzed cleavage of allylic alkyl ethers using phenylboronic acid can effectively release Pd-free parent alcohols. Furthermore, chromatography-free deallylation can be conducted by using vinylboronic anhydride pyridine complex as an allyl scavenger with a catalytic amount of Pd(OAc)2 and 4-(diphenylphosphino)benzoic acid instead of Pd(PPh3)4 to yield the desired products in high purities and yields after removal of volatile byproducts and the phosphine-derived contaminants by evaporation and sequestration through acid-base interaction with PS-DEAM, respectively. 相似文献
209.
Kawasaki T Ogawa A Terashima R Saheki T Ban N Sekiguchi H Sakaguchi KE Sakamoto M 《The Journal of organic chemistry》2005,70(8):2957-2966
Hexahydropyrrolo[2,3-b]indoles 6 were synthesized in five steps from indolin-3-one 8 by a general and efficient method, in which elements of molecular diversity were readily added onto the 3a-position of the pyrrolo[2,3-b]indole ring system. Horner-Wadsworth-Emmons reaction of 2-allyloxyindolin-3-ones 7, derived from indolin-3-one 8 and a variety of allylic alcohols, smoothly proceeded with successive Claisen rearrangement to give the corresponding 3-allyl-3-cyanomethylindolin-2-ones 15. Indolin-2-ones 15 were converted into pyrrolo[2,3-b]indoles 6 using partial hydrolysis followed by reductive cyclization with LiAlH(4). Synthesis of N-methylated pyrrolo[2,3-b]indole derivatives 23 and 26 is also described. 相似文献
210.
The reactions of some diorganonickel(II) complexes with N-bromosuccinimide (NBS) resulted in facile bromine for hydrogen substitution in aromatic, alkynyl or alkenyl substituents, or in the addition of NBS to CC bonds. 相似文献