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81.
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83.
The 7-endo Friedel-Crafts cyclization of arylpropyl vinyloxiranes was found to proceed regio- and stereoselectively to afford polyfunctional seven-membered carbocycles in excellent yields. 相似文献
84.
The enantiomeric resolution of N-t-butyloxycarbonyl (N-t-Boc) amino acids D/L isomers by reversed-phase HPLC was investigated using cyclodextrins (CD's) as chiral selectors for the mobile phase. The use of a low pH (pH<4) for the mobile phase enabled the enantioseparation of N-t-Boc amino acids. The opposite elution order of D/L isomers was observed when hydroxypropyl-derivatized beta-CD was used instead of native beta-CD. A computer simulation of the enantioseparation showed that the ratio of the retention factors of the chiral selector and the sample determined the elution order and the resolution. When the retention factor of the chiral selector is smaller than that of the sample, an isomer having larger complex formation constant eluted faster. However, when the chiral selector had a larger retention factor than the sample, an opposite elution order of the isomers was obtained. The large difference in the retention factors between the chiral selector and the sample led to good enantiomeric separation. 相似文献
85.
Yoshimune Nonomura Takaharu Fujii Yuichiro Arashi Taku Miura Takashi Maeno Kaoru Tashiro Yasuhisa Kamikawa Rie Monchi 《Colloids and surfaces. B, Biointerfaces》2009,69(2):1-267
Water has a unique touch as well as characteristic physical properties. However, nobody knows the real identity of its touch. Here, we show that water creates a stick-slip feel when a small amount is rubbed using fingertip on an artificial skin that mimics the structure of human skin. The results of frictional analyses predict that this stick-slip feel is caused by a drastic change in frictional resistance. The present result is valuable for biologists and robot engineers as well as cognitive scientists and tribologists, because it is a new example of stick-slip phenomena on biological surfaces. The tactile texture of this most familiar material could also be applied to consumer products or virtual reality systems. 相似文献
86.
H. Arimoto T. Saku Y. Hirayama N. Miura 《Physica E: Low-dimensional Systems and Nanostructures》2000,6(1-4)
We observed a new type of hysteresis in cyclotron resonance spectra of two-dimensional electron gas confined in GaAs/AlGaAs multi quantum wells when we applied high magnetic fields tilted from the growth direction. Pulsed high magnetic fields up to 150 T were generated by the single turn coil technique. We investigated in detail the condition for the occurrence of the hysteresis which is a disagreement between two traces in the up- and down-sweeps of the pulsed magnetic fields. The dependencies of the hysteresis on the wavelength, sweep rate of the fields and temperature has led to the conclusion that the hysteresis is due to inequilibrium states in the up-sweep of tilted magnetic fields. The relaxation time from inequilibrium to equilibrium states was revealed to be of the order of microsecond. 相似文献
87.
Bis(trifluoromethanesulfonyl)amide (TFSA), hexafluorophosphate (PF(6)(-)), and iodide salts of 1-ferrocenyl-3-alkylimidazolium were prepared and their thermal and physical properties, including the dependence on alkyl chain length (methyl-hexadecyl), were investigated. The TFSA salts were highly viscous ionic liquids with melting points around room temperature. 1-Ferrocenyl-4-methyltriazolium salts were also prepared for comparison. The ferrocenylimidazolium and ferrocenyltriazolium cations showed redox waves for both the ferrocenyl moiety and the azolium moiety and exhibited corresponding charge-transfer bands at around 330 nm, which were analyzed using the Marcus-Hush model. Crystal structure determinations at low temperature revealed that the PF(6) and iodide salts form layerlike structures composed of ionic layers of the charged moieties. The TFSA salt exhibited short hydrogen-bond-like intermolecular contacts between the hydrogen atoms of the cation and oxygen atoms of the anion. 相似文献
88.
Shigekazu Ito Joji Miura Noboru Morita Masaaki Yoshifuji Anthony J. Arduengo 《Comptes Rendus Chimie》2010,13(8-9):1180-1184
A new class of 1,3-diphoshacyclobutane-2,4-diyls bearing alkylsulfanyl or arylsulfanyl groups together with the sterically demanding Mes* groups have been prepared as air-stable compounds.
89.
Takeshi Miura 《Central European Journal of Mathematics》2011,9(4):778-788
Let A and B be uniformly closed function algebras on locally compact Hausdorff spaces with Choquet boundaries Ch A and ChB, respectively. We prove that if T: A → B is a surjective real-linear isometry, then there exist a continuous function κ: ChB → {z ∈ ℂ: |z| = 1}, a (possibly empty) closed and open subset K of ChB and a homeomorphism φ: ChB → ChA such that T(f) = κ(f ∘φ) on K and T( f ) = k[`(fof)]T\left( f \right) = \kappa \overline {fo\phi } on ChB \ K for all f ∈ A. Such a representation holds for surjective real-linear isometries between (not necessarily uniformly closed) function algebras. 相似文献
90.
Farouq Ahmed Ryo NagumoRyuji Miura Suzuki AiHideyuki Tsuboi Nozomu HatakeyamaAkira Endou Hiromitsu TakabaMomoji Kubo Akira Miyamoto 《Applied Surface Science》2011,257(24):10503-10513
The notion of “active sites” is fundamental to heterogeneous catalysis. However, the exact nature of the active sites, and hence the mechanism by which they act, are still largely a matter of speculation. In this study, we have presented a systematic quantum chemical molecular dynamics (QCMD) calculations for the interaction of hydrogen on different step and terrace sites of the Pd (3 3 2) surface. Finally the dissociative adsorption of hydrogen on step and terrace as well as the influence of surface hydrogen vacancy for the dissociative adsorption of hydrogen has been investigated through QCMD. This is a state-of-the-art method for calculating the interaction of atoms and molecules with metal surfaces. It is found that fully hydrogen covered (saturated) step sites can dissociate hydrogen moderately and that a monovacancy surface is suitable for significant dissociative adsorption of hydrogen. However in terrace site of the surface we have found that dissociation of hydrogen takes place only on Pd sites where the metal atom is not bound to any pre-adsorbed hydrogen atoms. Furthermore, from the molecular dynamics and electronic structure calculations, we identify a number of consequences for the interpretation and modeling of diffusion experiments demonstrating the coverage and directional dependence of atomic hydrogen diffusion on stepped palladium surface. 相似文献