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51.
Toshiki Yoshizawa Michika Onoda Takeshi Ueki Ryota Tamate Aya Mizutani Akimoto Ryo Yoshida 《Angewandte Chemie (International ed. in English)》2020,59(10):3871-3875
Various biological behaviors are fueled by “respiration”, which is an example of catabolism. So far, we have reported various self‐oscillating soft materials exhibiting bioinspired dynamic movements. These autonomous polymer systems are driven by the Belousov–Zhabotinsky (BZ) reaction, which is analogous to the tricarboxylic acid (TCA) cycle that is an integral part of respiration. However, in the BZ reaction, the external addition of an oxidizing agent is necessary to initiate the oxidation process, which is realized by intracellular moieties such as ubiquinone in living systems. Herein, we realized self‐oscillating micelles that are driven without the external addition of an oxidizing agent. This was achieved by embedding the oxidizing source into the structure of the self‐oscillating AB diblock copolymers. This strategy introduces a new function equivalent to intracellular oxidizing moieties, and is useful for the design of completely autonomous bioinspired materials. 相似文献
52.
Toshiki Sugimura Shinji Kajimoto Takakazu Nakabayashi 《Angewandte Chemie (International ed. in English)》2020,59(20):7755-7760
We propose a label‐free method for measuring intracellular temperature using a Raman image of a cell in the O?H stretching band. Raman spectra of cultured cells and the medium were first measured at various temperatures using a Raman microscope and the intensity ratio of the two regions of the O?H stretching band was calculated. The intensity ratio varies linearly with temperature in both the medium and cells, and the resulting calibration lines allow simultaneous visualization of both intracellular and extracellular temperatures in a label‐free manner. We applied this method to the measurement of temperature changes after the introduction of FCCP (carbonyl cyanide‐p‐trifluoromethoxyphenylhydrazone) in living cells. We observed a temperature rise in the cytoplasm and succeeded in obtaining an image of the change in intracellular temperature after the FCCP treatment. 相似文献
53.
Yasuo Horikawa Takeshi Takeda Toshiki Takizawa Taro Akazawa Ryota Fujio Tatsuo Fujimaki 《Journal of polymer science. Part A, Polymer chemistry》1996,34(7):1183-1188
The anionic polymerization of 1,3-butadiene using a novel metalloidal anion initiator, triallylstannyllithium (TALi)-allyllithium (ALi), was studied. The TALi-ALi initiated anionic polymerization of 1,3-butadiene gave the star polymer along with the linear polybutadiene (PBD). The star polymer consisted of three PBD branches and a central tin atom. What is striking is a fact that the number-average molecular weights (Mn) and molecular weight distribution of three PBD branches and linear PBD were almost identical. A reversible chain transfer polymerization mechanism, which includes the equilibrium between tri(macroallyl)-stannyllithium and macroallylic anion, is proposed. © 1996 John Wiley & Sons, Inc. 相似文献
54.
Ying An Masahiro Suzuki Toshiki Koyama Kenji Hanabusa Hirofusa Shirai Mei-Yu Huang Ying-Jan Jiang 《先进技术聚合物》1996,7(8):652-656
The palladium cluster protected by silica-supported, crosslinking, partially phosphorylated poly(vinyl alcohol) (P-PVA) was prepared from a crosslinking P-PVA–Pd(II) complex by reduction in alcohol. The P-PVA–Pd complex and the palladium cluster protected by P-PVA were analyzed by electron spectroscopy, X-ray photoelectron spectrometry and transmission electron microscopy. The complex formation between the Pd(II) ion and phosphoric acid groups in P-PVA was important in the formation of a fine palladium cluster. Palladium clusters protected by silica-supported crosslinking P-PVA were used as catalysts for the hydrogenation of nitrobenzene or acrylic acid at 30°C under atmospheric pressure. The palladium cluster protected by crosslinking P-PVA supported on silica was the most active catalyst, was stable and had no by-products, compared with the palladium cluster protected by silica-supported noncrosslinking P-PVA or PVA. 相似文献
55.
Hirofusa Shirai Kenji Hanabusa Toshiki Koyama Hisanaga Tsuiki Etsuko Masuda 《Macromolecular Symposia》1992,59(1):155-162
The oxidation of HO-CH2-CH2-SH (RSH) by molecular oxygen and Fe(III)- as well as Co(II)-multicarboxyphthalocyanine and the mechanism in homogeneous aqueous system were investigated. As application to enzyme-like heterogeneous catalysts, Fe(III)-as well as Co(II)-octacarboxyphthalocyanine were supported on amorphous enriched rayon staple fiber and their enzyme-like activities were estimated. These fibers were applicated to new odor-removers acting as artificial enzyme systems. 相似文献
56.
Yasushi Koyama Ichiro Takatsuka Munetaka Nakata Mitsuo Tasumi 《Journal of Raman spectroscopy : JRS》1988,19(1):37-49
Raman and infrared spectra in the region of 1800-150 cm−1 were recorded for a set of cis-trans isomers of d̃-carotene, i.e. the all-trans, 7-cis, 9-cis, 13-cis and 15-cis isomers. Spectral comparison revealed Raman and infrared key bands which (1) distinguish stretched or terminal-bent configurations (all-trans, 7-cis and 9-cis) from central-bent configurations (13-cis and 15-cis), and (2) distinguish unmethylated 7-cis and 15-cis configuratios. Keybands (1) include Raman bands at 1160 and 1140 cm−1 and infrared bands at 825 and 775 cm−1 (the intensity varies with the position of the cis-bend) Key bands (2) include Raman bands at 1274 and 962 cm−1 and an infrared band at 741 cm−1 (characteristic of the 7-cis configuration), and also a Raman band at 1247 cm−1 and an infrared band at 775 cm−1 (characteristic of the 15-cis configuration). The normal modes for the key bands were determined by a set of normal coordinate calculations for the isomeric configurations of a simplified model of d̃-carotene. The key bands were mainly related to the C H in-plane bendings, coupled with the CC or C C stretching, or to the C H out-of-plane wagging vibrations, some of which coupled with the CC torsion. 相似文献
57.
58.
Chaotic mixing generated by acoustic streaming 总被引:2,自引:0,他引:2
The acoustic mixer presented in this paper is a closed cylinder containing chemical solutions. The ultrasound was generated in a water bath outside of the cylinder. The mixing efficiency was measured by using a laser-photodiode system and by mixing iodine and sodium thiosulfate. Iodine solution has a light brown color which becomes transparent if the solution is mixed with sodium thiosulfate. The unmixed regions of the solution in the container remain dark. Starch was used to make the solution darker. Considering the relative position between the cylinder and the transducer, it was shown that displacements parallel to the axes of the streaming have little effect on the mixing speed. Indeed, the distance of the cylinder from the center of the streaming is more important to obtain ideal mixing performances. The frequency and size of the transducers has been investigated too and little effect was found. In contrast, the wave amplitude seems to be the biggest factor in obtaining rapid mixing. 相似文献
59.
The effect of inelastic scattering on the electron reflection in multi-quantum barriers (MQBs) has been examined using the damped resonant tunnelling model for the first time. The electron reflectivity in the virtual barrier region for unstrained GalnAs/InP MQB deteriorates below 100% by about 10% for phase relaxation time of 0.22ps. We propose a strain-compensated GalnAs/GalnP MQB which not only has virtual barrier 4 times as high as that of an unstrained MQB, but whose reflectivity deterioration is reduced to less than 5% in comparison with 10% for unstrained MQB for the same phase relaxation time. We have also successfully grown a Ga0.25In0.75As (1.5% compressive) well/Ga0.25In0.75P (1.2% tensile) barrier short-period superlattice with six wells by chemical beam epitaxy, which exhibits the possibility of fabrication of the strain-compensated MQBs. 相似文献
60.
Partially oxidized free-standing porous silicon films show a strongly superlinear increase in photoluminescence (PL) intensity above a threshold cw excitation intensity of 10 W/cm2. The PL-intensity increase can be expressed by a power law with n9 as a function of the excitation intensity. The PL-peak wavelength of this emission is slightly redshifted from that at low-excitation levels. These changes are fully reversible and reproducible, but not observed in samples on substrate. We attribute this behavior to thermal reexcitation of carriers trapped at the dangling bond states in initially nonluminescent Si nanocrystallites. 相似文献