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1.
Simen Gjelseth Antonsen Arne Joakim C. Bunkan Tomas Mikoviny Yngve Stenstrøm Armin Wisthaler 《Molecular physics》2020,118(15)
The kinetics of the O3, OH and NO3 radical reactions with diazomethane were studied in smog chamber experiments employing long-path FTIR and PTR-ToF-MS detection. The rate coefficients were determined to be k CH2NN+O3?=?(3.2?±?0.4)?×?10?17 and k CH2NN+OH?=?(1.68?±?0.12)?×?10?10 cm3 molecule?1 s?1 at 295?±?3?K and 1013?±?30 hPa, whereas the CH2NN?+?NO3 reaction was too fast to be determined in the static smog chamber experiments. Formaldehyde was the sole product observed in all the reactions. The experimental results are supported by CCSD(T*)-F12a/aug-cc-pVTZ//M062X/aug-cc-pVTZ calculations showing the reactions to proceed exclusively via addition to the carbon atom. The atmospheric fate of diazomethane is discussed. 相似文献
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Ghorbani Bahram Ebrahimi Armin Skandarzadeh Fatemeh Ziabasharhagh Masoud 《Journal of Thermal Analysis and Calorimetry》2021,145(3):925-953
Journal of Thermal Analysis and Calorimetry - The natural gas entering the liquefaction cycle usually consists of nitrogen, ethane, propane and also heavier hydrocarbons which are economically... 相似文献
5.
Wolfgang J. Fischer Armin Zankel Christian Ganser Franz J. Schmied Hartmuth Schroettner Ulrich Hirn Christian Teichert Wolfgang Bauer Robert Schennach 《Cellulose (London, England)》2014,21(1):251-260
Besides the determination of the force and the energy needed to break individual fibre to fibre joints, the investigation of the formerly bonded area (FBA) is of essential importance to learn more about the failure mechanisms of fibre–fibre bonds in general. In this study the surfaces of paper fibres and the FBA of fibre–fibre joints after the determination of the breaking force as well as the bonding energy were analysed by means of low voltage scanning electron microscopy and atomic force microscopy. A comparison between the contact zone of fibres broken at different loading rates as well as under cyclic loading showed that there seems to be no significant difference in the appearance of the FBA in these cases. Only minor delamination of the cell wall could be found in the bonding zone, which indicates no mechanical interlocking of fibrils in the bonding zone. Furthermore, it is shown that some glues used for specimen preparation of fibre–fibre bond strength measurement are forming a glue film on the fiber surface and migrate into the bonding region. 相似文献
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Collocation discretization for an integral equation in ocean acoustics with depth‐dependent speed of sound 下载免费PDF全文
Armin Lechleiter Tobias Rienmüller 《Mathematical Methods in the Applied Sciences》2017,40(5):1608-1624
We analyze two collocation schemes for the Helmholtz equation with depth‐dependent sonic wave velocity, modeling time‐harmonic acoustic wave propagation in a three‐dimensional inhomogeneous ocean of finite height. Both discretization schemes are derived from a periodized version of the Lippmann‐Schwinger integral equation that equivalently describes the sound wave. The eigenfunctions of the corresponding periodized integral operator consist of trigonometric polynomials in the horizontal variables and eigenfunctions to some Sturm‐Liouville operator linked to the background profile of the sonic wave velocity in the vertical variable. Applying an interpolation projection onto a space spanned by finitely many of these eigenfunctions to either the unknown periodized wave field or the integral operator yields two different collocation schemes. A convergence estimate of Sloan [J. Approx. Theory, 39:97–117, 1983] on non‐polynomial interpolation allows to show converge of both schemes, together with algebraic convergence rates depending on the smoothness of the inhomogeneity and the source. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
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Dr. Andreas Eitzinger Justus Reitz Patrick W. Antoni Prof. Dr. Herbert Mayr Dr. Armin R. Ofial Jun.-Prof. Max M. Hansmann 《Angewandte Chemie (International ed. in English)》2023,62(40):e202309790
A series of mesoionic, 1,2,3-triazole-derived N-heterocyclic olefins (mNHOs), which have an extraordinarily electron-rich exocyclic CC-double bond, was synthesized and spectroscopically characterized, in selected cases by X-ray crystallography. The kinetics of their reactions with arylidene malonates, ArCH=C(CO2Et)2, which gave zwitterionic adducts, were investigated photometrically in THF at 20 °C. The resulting second-order rate constants k2(20 °C) correlate linearly with the reported electrophilicity parameters E of the arylidene malonates (reference electrophiles), thus providing the nucleophile-specific N and sN parameters of the mNHOs according to the correlation lg k2(20 °C)=sN(N+E). With 21<N<32, the mNHOs are much stronger nucleophiles than conventional NHOs. Some mNHOs even excel the reactivity of mono- and diacceptor-substituted carbanions. It is exemplarily shown that the reactivity parameters thus obtained allow to calculate the rate constants for mNHO reactions with further Michael acceptors and predict the scope of reactions with other electrophilic reaction partners including carbon dioxide, which gives zwitterionic mNHO-carboxylates. The nucleophilicity parameters N correlate linearly with a linear combination of the quantum-chemically calculated methyl cation affinities and buried volumes of mNHOs, which offers a valuable tool to tailor the reactivities of strong carbon nucleophiles. 相似文献
9.
Christian Balischewski Hyung-Seok Choi Karsten Behrens Alkit Beqiraj Thomas Körzdörfer André Geßner Dr. Armin Wedel Prof. Dr. Andreas Taubert 《ChemistryOpen》2021,10(2):272-295
Metal sulfides are among the most promising materials for a wide variety of technologically relevant applications ranging from energy to environment and beyond. Incidentally, ionic liquids (ILs) have been among the top research subjects for the same applications and also for inorganic materials synthesis. As a result, the exploitation of the peculiar properties of ILs for metal sulfide synthesis could provide attractive new avenues for the generation of new, highly specific metal sulfides for numerous applications. This article therefore describes current developments in metal sulfide nanoparticle synthesis as exemplified by a number of highlight examples. Moreover, the article demonstrates how ILs have been used in metal sulfide synthesis and discusses the benefits of using ILs over more traditional approaches. Finally, the article demonstrates some technological challenges and how ILs could be used to further advance the production and specific property engineering of metal sulfide nanomaterials, again based on a number of selected examples. 相似文献
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Regioselective Ring‐Opening Polymerization of a Polyhydroxycarboxylic Acid for the Synthesis of a Nanoscale Carrier Material with pH‐Dependent Stability and Sustained Drug Release 下载免费PDF全文
Dipl.‐Chem. Alexander Ewe Dr. Anita Jansen de Salazar Dipl.‐Phys. Katharina Lemmnitzer Michael Marsch Prof. Dr. Achim Aigner Prof. Dr. Armin Geyer 《Angewandte Chemie (International ed. in English)》2015,54(21):6364-6369
Synthetic polyesters are usually composed of monohydroxycarboxylic acids to avoid the problem of regioselectivity during ring‐opening polymerization. In contrast, the linear polyester BICpoly contains four secondary OH groups and is nevertheless esterified regioselectively at only one of these positions. Neither the synthesis of the tricyclic monomers nor the ring‐opening polymerization requires protecting groups, making BICpoly an attractive novel and biocompatible polymer. BICpoly nanoparticles can be loaded with low‐molecular weight drugs or coated onto surfaces as thin films. The release of loaded compounds makes BICpoly an attractive depot for drug release, as shown herein by loading BICpoly with dyes or the cytostatic drug doxorubicin. BICpoly is distinguishable from other polymers by its characteristic pH‐dependent degradation. 相似文献