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排序方式: 共有254条查询结果,搜索用时 15 毫秒
21.
H. Hayashi Y. Akita O. Suematsu M. Shibata M. Asai T. K. Sato S. Ichikawa I. Nishinaka Y. Nagame A. Osa K. Tsukada T. Ishii Y. Kojima A. Taniguchi 《The European Physical Journal A - Hadrons and Nuclei》2007,34(4):363-370
Q
β values of the neutron-rich isotopes of 160-165Eu and 163Gd were measured for the first time using a total absorption bismuth germanate (BGO) detector, and previously obtained data
on 158, 159Pm , 159, 161Sm and 166Tb were re-analyzed. These radioactive sources were prepared by an on-line mass separator (Tokai-ISOL) following the 238U (p,f reaction. The deduced Q
β values are the following: 6085(80)keV for 158Pm , 3805(65)keV for 159Sm , 5460(140)keV for 159Pm , 4705(60)keV for 160Eu , 5065(130)keV for 161Sm , 3705(60)keV for 161Eu , 5575(60)keV for 162Eu , 4690(70)keV for 163Eu , 3170(70)keV for 163Gd , 6430(70)keV for 164Eu , 5800(120)keV for 165Eu , and 4695(70)keV for 166Tb . Moreover, the deduced mass excesses and two-neutron separation energies ( S
2n values) were compared with those of the atomic mass evaluations and theoretical predictions. 相似文献
22.
T. Shizuma M. Kidera E. Ideguchi A. Odahara H. Tomura S. Suematsu T. Kuroyanagi Y. Gono S. Mitarai J. Mukai T. Komatsubara K. Furuno K. Heiguchi 《Zeitschrift für Physik A Hadrons and Nuclei》1994,348(1):25-29
Theβ + decay of86Mo has been firstly investigated by means ofβγ spectroscopy. The86Mo nuclei were produced by fusion-evaporation reactions of54 Fe (35Cl, 1 p2n) and58Ni (32S,2p 2n) at beam energies of 103 and 120 MeV, respectively. Threeγ rays of 47.3, 49.8 and 187.0 keV were unambiguously identified to follow theβ + decay of86Mo by results ofXγ andβγ coincidence and cross-bombardment. A half life and a maximumβ +-ray energy of86Mo were determined to be 19.6±1.1 s and 3.9±0.4 MeV, respectively. A decay scheme of86Mo is proposed in this article. Furthermore, a decay of86Nb has been studied using the same combinations of projectiles and targets, and a newβ-decaying isomer86m Nb was observed with a half life of 56.3±8.3 s. 相似文献
23.
The mechanism of the gold nanocluster‐catalyzed aerobic homocoupling of arylboronic acids has been elucidated by means of DFT calculations with Au20? as a model cluster for the Au:[poly(N‐vinylpyrrolidin‐2‐one)] catalyst. We found that oxygen affects the adsorption of phenylboronic acid and, by lowering the energy barrier, a water molecule enhances dissociation of the C?B bond, which is probably the rate‐determining step. The key role of oxygen is in activating the surface of the gold cluster by generating Lewis acidic sites for adsorption and activation of the phenylboronic acid, leading to the formation of biphenyl through a superoxo‐like species. Moreover, the oxygen adsorbed on the Au nanocluster can act as an oxidant for phenylboronic acid, giving phenol as a byproduct. As shown by NBO analysis, the basic aqueous reaction medium facilitates the reductive elimination process by weakening the Au?C bond, thereby enhancing the formation of biphenyl. The coupling of phenyl and reductive elimination of biphenyl occur at the top or facet site with low‐energy‐barrier through spillover of phenyl group on Au NC. The present findings are useful for the interpretation or design of other coupling reactions with Au NC. 相似文献
24.
Gold/Palladium Alloy for Carbon–Halogen Bond Activation: An Unprecedented Halide Dependence
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Dr. Raghu Nath Dhital Dr. Karan Bobuatong Prof. Dr. Masahiro Ehara Prof. Dr. Hidehiro Sakurai 《化学:亚洲杂志》2015,10(12):2669-2676
New catalytic activity of gold/palladium alloy nanoclusters (NCs) for carbon–halogen bond activation is demonstrated. In the case of an aryl chloride, the inclusion of gold in a bimetallic catalyst is indispensable to achieve the coupling reactions. Gold has the unique effect of stabilizing palladium, such that Pd2+ leached from clusters by means of spillover of chloride during oxidative addition. The thus‐formed spillover intermediate further reacts heterogeneously in both Ullmann and Suzuki‐type coupling reactions through a new type of mechanism. In the case of an aryl bromide, Ullmann coupling occurs through the spillover of bromide, similar to that of aryl chloride. However, a significant fraction of palladium also leached, which diminished the Ullmann coupling activity of the aryl bromide and, as a result, the order of reactivity was ArCl>ArBr. With regard to the activation of the C?Br bond towards a Suzuki‐type reaction, the inclusion of a higher gold content in gold/palladium clusters stabilized palladium to prevent the leaching of Pd2+ from the clusters by means of spillover of bromide. The spillover intermediate reacts heterogeneously with PhB(OH)2, palladium‐rich gold/palladium, or pure palladium clusters; the oxidative addition of ArBr favors the extraction of palladium from the clusters, yielding Pd2+ intermediates. The extracted intermediates react homogenously (Pd2+/Pd0 catalysis) with PhB(OH)2, which results in the higher selectivity of the cross‐coupling product. An initial step to observe such unprecedented halide dependency, together with the dynamic behavior of palladium on the surface of gold is the oxidative addition of Ar?X. A detailed insight into the first oxidative addition process was also examined by quantum chemical calculations. 相似文献
25.
Dr. Shinichiro Fuse Ayako Ikebe Kazuya Oosumi Tomoya Karasawa Keisuke Matsumura Dr. Miho Izumikawa Dr. Kohei Johmoto Dr. Hidehiro Uekusa Dr. Kazuo Shin‐ya Prof. Takayuki Doi Prof. Takashi Takahashi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(26):9454-9460
An asymmetric total synthesis of ent‐pyripyropene A was achieved by a convergent synthetic route. We used our originally developed TiIII‐catalyzed radical cyclization to construct an AB‐ring portion that consisted of a trans‐decalin skeleton with five contiguous stereogenic centers. The coupling between the AB‐ring and the DE‐ring portions, and a subsequent C‐ring cyclization, led to the total synthesis of ent‐pyripyropene A. An evaluation of the insecticidal activity of ent‐pyripyropene A against two aphid species revealed that ent‐pyripyropene A was 35–175 times less active than naturally occurring pyripyropene A. This result indicated that the biological target of pyripyropene A recognizes the absolute configuration of pyripyropene A. 相似文献
26.
Directing/Protecting‐Group‐Free Synthesis of Tetraaryl‐Substituted Pyrazoles through Four Direct Arylations on an Unsubstituted Pyrazole Scaffold
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Dr. Shinichiro Fuse Taiki Morita Dr. Kohei Johmoto Dr. Hidehiro Uekusa Dr. Hiroshi Tanaka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(41):14370-14375
A directing/protecting‐group‐free synthesis of 1,3,4,5‐tetraaryl‐substituted pyrazoles was achieved through four transition metal‐catalyzed direct arylations. Various pyrazoles with four different aryl rings were obtained using readily available reagents from an unsubstituted pyrazole. Two aryl‐substituted pyrazoles showed intense violet fluorescence, high quantum yields (Φf=0.68, 0.64), and large Stokes shifts (19000, 15200 cm?1). 相似文献
27.
We measured quantitative spectra of firefly (Photinus pyralis) bioluminescence in the presence of Zn2+ and other bivalent metal ions to investigate the effects of these metal ions on luciferin‐luciferase reaction. We studied the dependence of the quantum yield and spectrum on quantity and kind of bivalent metal ions. Adding various amounts of Mg2+, Mn2+ and Ca2+ produced virtually no change in the quantum yields or the spectra of bioluminescence. In contrast, increasing amounts of ions such as Zn2+ and Cd2+ decreased quantum yields and changed the bioluminescence color from yellow‐green to red. Quantitative analysis showed that the sensitivities of the quantum yield and color to various metal ions were in the order of Hg2+>Zn2+, Cd2+>Ni2+, Co2+, Fe2+≫Mg2+, Mn2+, Ca2+. We propose that the changes in quantum yield and spectrum caused by the metal ions are due to their effect on luciferase that surrounds oxyluciferin during its radioactive decay. We also found that having more metal ions accelerated bioluminescence reactions. The sensitivity of the reaction rate had no correlation with those of the quantum yield and spectrum. 相似文献
28.
Enantioenriched synthesis of cyclopropenes with a quaternary stereocenter, versatile building blocks
Uehara M Suematsu H Yasutomi Y Katsuki T 《Journal of the American Chemical Society》2011,133(2):170-171
Ir(salen) complexes were found to catalyze enantioselective cyclopropenation efficiently. Cyclopropenation can be carried out using either a donor/acceptor- or an acceptor/acceptor-substituted diazo compound such as α-aryl-α-diazoacetates, α-phenyl-α-diazophosphonate, 2,2,2-trifluoro-1-phenyl-1-diazoethane, and α-cyano-α-diazoacetamide as carbenoid precursors. The reactions provide highly enantioenriched cyclopropenes (84-98% ee) with a functionalized quaternary carbon as versatile building blocks. 相似文献
29.
30.
Ultrafine MgAl2O4 powder has been synthesized by a polymerized complex method. Heating of a precursor solution containing citric acid (CA), ethylene glycol (EG) and Mg and Al salts with a molar ratio of Mg/Al/CA/EG=1/2/8/32 at 180°C produced a transparent polymeric gel, which have been characterized by FT-IR spectroscopy and TG/DTA. The organic fraction was removed by controlled thermal treatments (350–1200°C) whereby the bimetallic oxide was formed. XRD analysis showed the presence of MgAl2O4 at 600°C. TEM observation showed that the spherical nanosized powders with good uniformity was obtained. Furthermore, these powders showed excellent sinterability, relative density up to 99.8% was achieved when sintered at 1550°C for 3 h in air without any sintering additive. 相似文献