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排序方式: 共有482条查询结果,搜索用时 281 毫秒
41.
H. Kira Y. Sakaguchi T. Oku J. Suzuki M. Nakamura M. Arai K. Kakurai Y. Endo Y. Arimoto T. Ino H.M. Shimizu T. Kamiyama K. Tsutsumi K. Ohoyama H. Hiraka K. Yamada L.-J. Chang 《Physica B: Condensed Matter》2011,406(12):2433-2435
We have begun the development of an in-situ spin-exchange optical pumping (SEOP) system aiming to use it as a neutron spin filter for incident beam polarization at the Japan Proton Accelerator Research Complex (J-PARC). To use it, it is recommended that the optics be adjusted easily, have high stability, and have a small size. In this paper we improved our previous SEOP system aiming to use it in J-PARC and performed a neutron beam test at the JRR-3 NOP beamline to see the performance of the neutron spin filter (NSF). The polarization of the 3He gas reached 73%. This paper gives the present status of the development of in-situ SEOP system in J-PARC. 相似文献
42.
43.
S Matsuo N Sakaguchi E Obuchi K Nakano R C Perera T Watanabe T Matsuo H Wakita 《Analytical sciences》2001,17(1):149-153
Ni L- and Ti L-edge as well as Ti K-edge X-ray absorption experiments for TiO2 thin films and Ni-doped TiO2 thin films coated on glass plates were performed using synchrotron radiation to investigate the structures around Ni and Ti ions in the films. The obtained spectra were compared with the results of theoretical calculations. It has consequently been found that the spectral features were affected by a change in the oxidizing form of Ni ions due to hydrogen reduction, by the charge variation and/or slight orbital splitting of Ti ions, and by the magnitude of the interaction between the center Ti ion and neighboring Ti ions. 相似文献
44.
Kazuya Tanaka Aya Sakaguchi Yutaka Kanai Haruo Tsuruta Atsushi Shinohara Yoshio Takahashi 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(3):1927-1937
We analyzed 137Cs in aerosols, rock, soil and river suspended sediment collected after the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident. Based on the results, we discuss the post-event behavior and transportation of radiocesium in the environment from the air into ground and river systems. First, radionuclides were emitted from the FDNPP as airborne ‘hot’ particles, which contained water-soluble fractions of radiocesium. Radiocesium was still present in a water-soluble fraction after deposition on the ground. Subsequent interaction of the ‘hot’ particles with water (e.g. rainfall) dissolved and strongly fixed the radiocesium on rock and soil particles, thus changing the radiocesium into insoluble forms. The distribution of ‘hot spots’ was possibly controlled by the initial position of deposition on the ground. Consequently, ‘hot spots’ were studded on the rock surface rather than being uniformly distributed. The distribution of radiocesium in river suspended particles was not homogeneous during water transportation, reflecting the heterogeneity of radiocesium in rock and soil. Leaching experiments demonstrated that radiocesium in rock, soil and river suspended sediment was fairly insoluble, showing that the adsorption reaction is irreversible. The micro-scale heterogeneous distribution of radiocesium in aerosols, soil and suspended particles was due to the presence of ‘hot’ particles in aerosols. Dissolution of radiocesium in the ‘hot’ particles in the aerosols and subsequent irreversible adsorption onto the soil particle complex are responsible for the preservation of the heterogeneity both in soil and in river suspended particles. 相似文献
45.
Takahiro Nakae Ryuji Ohnishi Yoshiharu Kitahata Tatsuya Soukawa Hisako Sato Shigeki Mori Tetsuo Okujima Hidemitsu Uno Hiroshi Sakaguchi 《Tetrahedron letters》2012,53(13):1617-1619
6,13-Diiododibenzo[a,h]anthracene and 5,8-diiodopicene were synthesized by AuCl-catalyzed double cyclization. The highly selective reaction yielded a new class of peri-halogenated fused aromatics. 相似文献
46.
Beker H. Bøggild H. Boissevain J. Cherney M. Dodd J. Esumi S. Fabjan C. W. Fields D. E. Franz A. Hansen K. H. Holzer B. Humanic T. Jacak B. Jayanti R. Kalechofsky H. Kobayashi T. Kvatadze R. Lee Y. Y. Leltchouk M. Lörstad B. Maeda N. Medvedev A. Miake Y. Miyabayashi A. Murray M. Nagamiya S. Nishimura S. Noteboom E. Pandey S. U. Piuz F. Polychronakos V. Potekhin M. Poulard G. Sakaguchi A. Sarabura M. Shigaki K. Simon-Gillo J. Sletten H. Sondheim W. Sugitate T. Sullivan J. P. Sumi Y. van Hecke H. Willis W. J. Wolf K. 《Zeitschrift fur Physik C Particles and Fields》1994,64(2):209-217
K+K+ and K–K– correlations from S+Pb collisions at 200 GeV/c per nucleon and K+K+ correlations from p+Pb collisions at 450 GeV/c per nucleon, are presented as measured by the focusing spectrometer of the NA44 experiment at CERN. Multidimensional fits are performed in order to characterize the kaon-emission volume, which is found to be smaller than the pion-emission volume. 相似文献
47.
Kouji Kuramochi Ryo Takeuchi Masaharu Takemura Kengo Sakaguchi Susumu Kobayashi Fumio Sugawara 《Tetrahedron》2006,62(34):8006-8015
Synthesis of plakevulin A and structure-activity relationships of its related compounds against DNA polymerases is described. We have achieved a total synthesis and revised the structure of plakevulin A. Several analogues including untenone A, manzamenone A, and optically active plakevulin A, were prepared and tested with an enzyme inhibition assay for mammalian DNA polymerases. The effect of the methyl ester moiety, and the substituents at the 1- and 4-positions of plakevulin A on DNA polymerase activities are discussed. 相似文献
48.
Takuya OkadaKazuhiko Sakaguchi Tetsuro ShinadaYasufumi Ohfune 《Tetrahedron letters》2011,52(44):5744-5746
The stereoselective total synthesis of (−)-funebrine from 2-butyn-1-ol was described. The crucial steps in the synthesis involved the stereoselective enolate Claisen rearrangement of the (S)-α-acyloxy-α-alkynylsilane 8, the Au-catalyzed regio- and stereoselective lactonization of the allenylsilane 7, and the Paal-Knorr pyrrole condensation using an unsymmetrical 1,4-diketone 4b. 相似文献
49.
Masato HigashinoNaoko Ikeda Tetsuro ShinadaKazuhiko Sakaguchi Yasufumi Ohfune 《Tetrahedron letters》2011,52(3):422-425
A novel silyl group-directed anti-SN2′ reaction of allylic alcohols under Mitsunobu reaction conditions is described. The Mitsunobu reaction of α-hydroxy-α-alkenylsilanes with a TBS or TIPS group gave the anti-SN2′ product, in which regio- and stereochemical outcomes of the reaction depended on the steric bulkiness of the silyl group. 相似文献
50.
Kojima T Nakayama K Sakaguchi M Ogura T Ohkubo K Fukuzumi S 《Journal of the American Chemical Society》2011,133(44):17901-17911
Ruthenium(II)-acetonitrile complexes having η(3)-tris(2-pyridylmethyl)amine (TPA) with an uncoordinated pyridine ring and diimine such as 2,2'-bipyridine (bpy) and 2,2'-bipyrimidine (bpm), [Ru(II)(η(3)-TPA)(diimine)(CH(3)CN)](2+), reacted with m-chloroperbenzoic acid to afford corresponding Ru(II)-acetonitrile complexes having an uncoordinated pyridine-N-oxide arm, [Ru(II)(η(3)-TPA-O)(diimine)(CH(3)CN)](2+), with retention of the coordination environment. Photoirradiation of the acetonitrile complexes having diimine and the η(3)-TPA with the uncoordinated pyridine-N-oxide arm afforded a mixture of [Ru(II)(TPA)(diimine)](2+), intermediate-spin (S = 1) Ru(IV)-oxo complex with uncoordinated pyridine arm, and intermediate-spin Ru(IV)-oxo complex with uncoordinated pyridine-N-oxide arm. A Ru(II) complex bearing an oxygen-bound pyridine-N-oxide as a ligand and bpm as a diimine ligand was also obtained, and its crystal structure was determined by X-ray crystallography. Femtosecond laser flash photolysis of the isolated O-coordinated Ru(II)-pyridine-N-oxide complex has been investigated to reveal the photodynamics. The Ru(IV)-oxo complex with an uncoordinated pyridine moiety was alternatively prepared by reaction of the corresponding acetonitrile complex with 2,6-dichloropyridine-N-oxide (Cl(2)py-O) to identify the Ru(IV)-oxo species. The formation of Ru(IV)-oxo complexes was concluded to proceed via intermolecular oxygen atom transfer from the uncoordinated pyridine-N-oxide to a Ru(II) center on the basis of the results of the reaction with Cl(2)py-O and the concentration dependence of the consumption of the starting Ru(II) complexes having the uncoordinated pyridine-N-oxide moiety. Oxygenation reactions of organic substrates by [Ru(II)(η(3)-TPA-O)(diimine)(CH(3)CN)](2+) were examined under irradiation (at 420 ± 5 nm) and showed selective allylic oxygenation of cyclohexene to give cyclohexen-1-ol and cyclohexen-1-one and cumene oxygenation to afford cumyl alcohol and acetophenone. 相似文献