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141.
Fumitaka Akiyama Shiichiro Teranishi Yuzo Fujiwara Hiroshi Taniguchi 《Journal of organometallic chemistry》1977,140(1):C7-C9
A new aromatic substitution reaction of styrene by arylamines such as aniline, (unp)-toluidine, (unp)-anisidine, (unp)-chloroaniline, and (unp)-nitroaniline in the presence of palladium(II) acetate has been found to give (E)-stilbene, (E)-(unp)-methylstilbene, (E)-(unp)-methoxystilbene, (E)-(unp)-chlorostilbene, and (E)-(unp)-nitrostilbene, respectively, in modest yields. 相似文献
142.
Mystery solved: Using heterologous expression, the activities of two enzymes exclusively belonging to the kanamycin biosynthetic pathway have been identified in vitro. A distinctive reaction mechanism to produce kanamycin is proposed and the previously unknown catalytic deamination activity of KanJ dioxygenase is uncovered. 相似文献
143.
A fission track technique was used as a sample preparation method for subsequent isotope abundance ratio analysis of individual uranium containing particles with secondary ion mass spectrometry (SIMS) to measure the particles with higher enriched uranium efficiently. A polycarbonate film containing particles was irradiated with thermal neutrons and etched with 6 M NaOH solution. Each uranium containing particle was then identified by observing fission tracks created and a portion of the film having a uranium containing particle was cut out and put onto a glassy carbon planchet. The polycarbonate film, which gave the increases of background signals on the uranium mass region in SIMS analysis, was removed by plasma ashing with 200 W for 20 min. In the analysis of swipe samples having particles containing natural (NBL CRM 950a) or low enriched uranium (NBL CRM U100) with the fission track–SIMS method, uranium isotope abundance ratios were successfully determined. This method was then applied to the analysis of a real inspection swipe sample taken at a nuclear facility. As a consequence, the range of 235U/238U isotope abundance ratio between 0.0276 and 0.0438 was obtained, which was higher than that measured by SIMS without using a fission track technique (0.0225 and 0.0341). This indicates that the fission track–SIMS method is a powerful tool to identify the particle with higher enriched uranium in environmental samples efficiently. 相似文献
144.
Takeyasu Tasaka Jianwei Wu Hiroaki Okamoto Vladimir F. Petrov Shunsuke Takenaka 《Molecular Crystals and Liquid Crystals》2013,570(1):727-732
Abstract This paper describes the liquid the crystalline properties of 4-(4-alkoxy-phenoxycarbonyl)phenyl 4-bromo-3-alkoxy-(2), 4-cyano-3-alkoxybenzoates(3), and 2-methyl-3-alkoxybenzoates(4). 2 and 3 are essentially smectogenic, while 4 are nematogenic. The difference in the mesomorphic properties is discussed in terms of their molecular geometrical characteristics estimated by a semi-empirical molecular orbital calculation. 相似文献
145.
[reaction: see text] Highly enantioselective Reformatsky reaction of ketones was accomplished using cinchona alkaloids as chiral ligands. Chelation with the sp(2)-nitrogen adjacent to the reactive carbonyl center contributed the enantioface discrimination for the high enantioselectivities. 相似文献
146.
Gando Y Fukuda S Fukuda Y Ishitsuka M Itow Y Kajita T Kameda J Kaneyuki K Kobayashi K Koshio Y Miura M Moriyama S Nakahata M Nakayama S Namba T Obayashi Y Okada A Ooyabu T Saji C Sakurai N Shiozawa M Suzuki Y Takeuchi H Takeuchi Y Totsuka Y Yamada S Desai S Earl M Kearns E Messier MD Stone JL Sulak LR Walter CW Goldhaber M Barszczak T Casper D Gajewski W Kropp WR Mine S Liu DW Smy MB Sobel HW Vagins MR Gago A Ganezer KS Hill J Keig WE Ellsworth RW Tasaka S Kibayashi A Learned JG Matsuno S 《Physical review letters》2003,90(17):171302
We present the results of a search for low energy nu(e) from the Sun using 1496 days of data from Super-Kamiokande-I. We observe no significant excess of events and set an upper limit for the conversion probability to nu(e) of the 8B solar neutrino. This conversion limit is 0.8% (90% C.L.) of the standard solar model's neutrino flux for total energy=8-20 MeV. We also set a flux limit for monochromatic nu(e) for E(nu(e))=10-17 MeV. 相似文献
147.
148.
Izumi Y Kiyotaki F Yagi N Vlaicu AM Nisawa A Fukushima S Yoshitake H Iwasawa Y 《The journal of physical chemistry. B》2005,109(31):14884-14891
X-ray absorption fine structure combined with X-ray fluorescence spectrometry was applied to various V+TiO2 hybrid samples. Emitted V K alpha1 fluorescence from the sample was selectively counted by using a high-energy-resolution (0.4 eV) spectrometer equipped with a Ge(331) crystal. Two advantages of this method, extremely high signal/background ratio and the compatibility of measurements in the atmosphere of reaction gas (in situ study in relation to heterogeneous catalysis), were effective at the V K-edge. Structure transformation of the V sites was spectroscopically followed for the V/TiO2 catalyst. The monooxo tetrahedral vanadate site was demonstrated to exist at 473 K. It transformed into dispersed species of 5-fold coordination in ambient air and further into polymeric VO(x) species in 0.85 kPa of water at 290 K. In the presence of 3.2 kPa of 2-propanol, dissociative adsorption of 2-propanol on the dispersed V species was strongly suggested at 290-473 K. In situ structure changes of V sites on TiO2 were reported by means of XAFS for the first time. The V(V) sites for the V/TiO2 catalysts were essentially identical with those for V supported on mesoporous (high-surface-area) TiO2 and V-TiO2 sample prepared by the sol-gel method. However, predominant V(IV) sites were found for mesoporous V-TiO2. The V(IV) sites substituted on the Ti sites of TiO2. When the molar ratio of V/Ti increased from 1/100 to 1/5.0, major octahedral V sites in the TiO2 matrix looked to transform into tetrahedral ones. 相似文献
149.
Mori M Nojiri MM Hirata KS Kihara K Oyama Y Suzuki A Takahashi K Yamada M Takei H Koga M Miyano K Miyata H Fukuda Y Hayakawa T Inoue K Ishida T Kajita T Koshio Y Nakahata M Nakamura K Sakai A Sato N Shiozawa M Suzuki J Suzuki Y Totsuka Y Koshiba M Nishijima K Kajimura T Suda T Suzuki AT Hara T Nagashima Y Takita M Yokoyama H Yoshimoto A Kaneyuki K Takeuchi Y Tanimori T Tasaka S Nishikawa K 《Physical review D: Particles and fields》1993,48(12):5505-5518
150.
Tada H Matsui H Shiota F Nomura M Ito S Yoshihara M Esumi K 《Chemical communications (Cambridge, England)》2002,(16):1678-1679
A heterosupramolecular photocatalyst consisting of TiO2 and a cationic surfactant bilayer formed on the surface has achieved a very high level of activity in the oxidation of 2-naphthol through the cooperation of the inorganic and organic components. 相似文献