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41.
Jasquer A. Sehnem Priscila Milani Vanessa Nascimento Leandro H. Andrade Luciano Dorneles Antonio L. Braga 《Tetrahedron: Asymmetry》2010,21(8):997-1003
N-Trifluoracyl β-chalcogeno amides and N-perfluoracyl β-thio amide ligands were prepared by a simple and efficient reaction sequence. These new ligands were evaluated in palladium-catalyzed alkylation of rac-(E)-1,3-diphenyl-2-propenyl acetate in the presence of dimethyl malonate and an enantioselectivity of up to 99% was obtained. After catalysis, the fluorous ligand can be easily recovered by liquid–liquid extraction and reused without loss in the activity. 相似文献
42.
43.
Leandro E. Roth Enrique M. Valls Marcelo A. Villar 《Journal of polymer science. Part A, Polymer chemistry》2003,41(8):1099-1106
Model silicone networks obtained by curing linear poly(dimethylsiloxane) (PDMS) chains with end‐vinyl groups, (B2), with a polyfunctional silane‐terminated crosslinker of functionality f, (Af), through a hydrosilylation reaction have been widely used. In these networks, the principal characteristics of their ultimate molecular structure are strongly affected by the final extent of reaction reached during the crosslinking reaction. This work analyzes the effect of the initial concentration of the reactive end groups on the maximum attainable extent of reaction under normal bulk crosslinking conditions. This was accomplished by examining the reaction between linear B2 PDMS chains with difunctional and trifunctional silanes. The experimental results were fitted by an exponential equation to have an empirical equation able to predict the maximum extent of reaction to be obtained as a function of the initial concentration of reactive groups. Molecular parameters relevant to this study, such as the degree of polymerization, the weight‐average molecular weight for the A2 + B2 system, or the weight fraction of solubles for the A3 + B2 system, were calculated with a mean field theory (recursive approach). © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1099–1106, 2003 相似文献
44.
Vicenţiu D. Rădulescu Gelson C. G. dos Santos Leandro S. Tavares 《Mathematische Nachrichten》2023,296(6):2555-2574
This paper is concerned with the existence and multiplicity of solutions for a class of problems involving the Φ-Laplacian operator with general assumptions on the nonlinearities, which include both semipositone cases and critical concave convex problems. The research is based on the subsupersolution technique combined with a truncation argument and an application of the Mountain Pass Theorem. The results in this paper improve and complement some recent contributions to this field. 相似文献
45.
Leandro Arosio 《Journal of Geometric Analysis》2017,27(2):1178-1210
We prove the existence and the essential uniqueness of canonical models for the forward (resp., backward) iteration of a holomorphic self-map f of a cocompact Kobayashi hyperbolic complex manifold, such as the ball \(\mathbb {B}^q\) or the polydisc \(\Delta ^q\). This is done by performing a time-dependent conjugacy of the autonomous dynamical system defined by f, obtaining in this way a non-autonomous dynamical system admitting a relatively compact forward (resp., backward) orbit, and then proving the existence of a natural complex structure on a suitable quotient of the direct limit (resp., subset of the inverse limit). As a corollary we prove the existence of a holomorphic solution with values in the upper half-plane of the Valiron equation for a hyperbolic holomorphic self-map of the unit ball. 相似文献
46.
Kelly L. dos Santos CastroPaulo G. de Lima Leandro S.M. e MirandaRodrigo O.M.A. de Souza 《Tetrahedron letters》2011,52(32):4168-4171
A solvent mixture containing the ionic liquid derived from 4-picoline (C4MPyBF4) and water was tested for the Suzuki-Miyaura reaction under microwave irradiation. This solvent system led to very high conversions and clean reactions. When compared with the other more common ionic liquid, such as C4MImBF4, C4MPyBF4 proved to be superior. 相似文献
47.
A new approach for target quantitative analysis for comprehensive two-dimensional gas chromatography (GC × GC), interval Multi-way Partial Least Square (iNPLS) is presented and evaluated in this paper. In iNPLS, the two-dimensional chromatogram is split in small sections; each of these pieces is treated as an independent new chromatogram. Separated conventional NPLS calibration models for the concentration of the target analyte are built for each of the pieces of the whole chromatogram, and the best model is selected for quantitative analysis. An algorithm for iNPLS running on MatLab platform was written, preliminarily evaluated with using solutions of model compounds with different chemical properties and subsequently applied to quantify some allergens in perfume samples. The results were found to be adequate, and good precision and accuracy was obtained even for poorly resolved peaks. 相似文献
48.
A series of organochalcogenanes was synthesized and evaluated as protein tyrosine phosphatases (PTPs) inhibitors. The results indicate that organochalcogenanes inactivate the PTPs in a time- and concentration-dependent fashion, most likely through covalent modification of the active site sulfur-moiety by the chalcogen atom. Consequently, organochalcogenanes represent a new class of mechanism-based probes to modulate the PTP-mediated cellular processes. 相似文献
49.
Tertiary propargyl vinyl ethers armed with an electron-withdrawing group (amide or ester) at the tertiary propargylic position have been efficiently transformed into trisubstituted C(2)-chain functionalized furans. The metal-free domino transformation involves a microwave-assisted tandem [3,3]-propargyl Claisen rearrangement/5-exo-dig O-cyclization reaction. The manifold can be performed in a one-pot fashion from the primary components (1,2-ketoester/1,2-ketoamide or tertiary propargyl alcohols). 相似文献
50.
Pedroso MP Ferreira EC Hantao LW Bogusz S Augusto F 《Journal of separation science》2011,34(13):1547-1554
Combining qualitative data from the chromatographic structure of 2-D gas chromatography with flame ionization detection (GC×GC-FID) and that from gas chromatography-mass spectrometry (GC/MS) should result in a more accurate assignment of the peak identities than the simple analysis by GC/MS, where coelution of analytes is unavoidable in highly complex samples (rendering spectra unsuitable for qualitative purposes) or for compounds in very low concentrations. Using data from GC×GC-FID combined with GC/MS can reveal coelutions that were not detected by mass spectra deconvolution software. In addition, some compounds can be identified according to the structure of the GC×GC-FID chromatogram. In this article, the volatile fractions of fresh and dehydrated pineapple pulp were evaluated. The extraction of the volatiles was performed by dynamic headspace extraction coupled to solid-phase microextraction (DHS-SPME), a technique appropriate for slurries or solid matrices. Extracted analytes were then analyzed by GC×GC-FID and GC/MS. The results obtained using both techniques were combined to improve compound identifications. 相似文献