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41.
Arkom Kaewrawang Akimitsu Morisako 《Journal of magnetism and magnetic materials》2010,322(14):2043-2046
Strontium ferrite (SrM) thin films were deposited on thermally oxidized silicon wafer with Au underlayer. Gold underlayers were prepared at various substrate temperatures by using a magnetron sputtering system. C-axis oriented SrM perpendicular films and preferred (1 1 1) orientation of underlayer have confirmed by X-ray diffraction patterns. The intensity of (1 1 1) diffraction line for Au and that of (0 0 l) diffraction line for strontium ferrite decrease with increase in substrate temperature (Tu) The maximum coercivity and remanent squareness ratio in perpendicular direction, at Tu of 500 °C, are 5.4 kOe and 0.68, respectively. The strength of the intergranular interaction of SrM magnetic particles is described by the parameter Δm. The SrM/Au films prepared at Tu above 100 °C have smaller Δm peak values than that for SrM/Au films prepared at Tu of room temperature. This behavior is related to low magnetostatic coupling between the magnetic particles separated by the non-magnetic amorphous phase. 相似文献
42.
Negishi Y Tsunoyama H Suzuki M Kawamura N Matsushita MM Maruyama K Sugawara T Yokoyama T Tsukuda T 《Journal of the American Chemical Society》2006,128(37):12034-12035
We report herein the X-ray magnetic circular dichroism (XMCD) at the Au L2,3 edges of a series of Au clusters protected by glutathione (GSH). The samples used here included AuN(SG)M with (N, M) = (10, 10), (15, 13), (18, 14), (22, 16), (25, 18), (29, 20), (39, 24) and a sodium gold(I) thiomalate (SGT) as a reference. Magnetic moments per cluster were found to be increased with size, whereas those per Au-S bond were nearly constant. This finding suggests that a localized hole created by Au-S bonding at the gold/glutathione interface, rather than the quantum size effect, is responsible for the spin polarization of gold clusters. 相似文献
43.
We report on the first synthesis of alkanethiolate-protected Au55 (11 kDa), which has been a "missing" counterpart of Schmid's Au55(PR3)12Cl6. Au:SCx clusters (x = 12, 18) were prepared by the reaction of alkanethiol (CxSH) with polymer-stabilized Au clusters ( approximately 1.3 nm) and subsequently incubated in neat CxSH. The resulting clusters were successfully fractionated by recycling gel permeation chromatography into Au approximately 38:SCx and Au approximately 55:SCx and identified by laser-desorption ionization mass spectrometry. The Au approximately 55:SCx clusters exhibited structured optical spectra, suggesting molecular-like properties. The thiolate monolayers were found to be liquid-like on the basis of the IR spectrum and the monolayer thickness, which was estimated from the hydrodynamic diameter. 相似文献
44.
Maeyama T Negishi Y Tsukuda T Yagi I Mikami N 《Physical chemistry chemical physics : PCCP》2006,8(7):827-833
Size-dependent features of the electron localization in negatively charged formamide clusters (FAn-, n = 5-21) have been studied by photodetachment spectroscopy. In the photoelectron spectra for all the sizes studied, two types of bands due to different isomers of anions were found. The low binding energy band peaking around 1 eV is assigned to the solvated electron state by relative photodetachment cross-section measurements in the near-infrared region. It is suggested that nascent electron trapping is dominated by formation of the solvated electron. The higher energy band originates from the covalent anion state generated after a significant relaxation process, which exhibits a rapid increase of electron binding energy as a function of the cluster size. A unique behavior showing a remarkable band intensity of the higher energy band was found only for n = 9. 相似文献
45.
5-Methylcytosine was distinguished from cytosine using the large difference of their osmium oxidation rates, and this reaction was applied to detection of the cytosine methylation status at a specific site of a long sequence using the formation of a bulge structure by hybridization with a guide DNA. 相似文献
46.
Jun Akimitsu Jiro Amano Masaki Yoshinari Michio Kokubun Tatsuya Iwasaki Satoshi Okuma Nobuhiko Nishida Kusuo Nishiyama Nobuo Mori 《Hyperfine Interactions》1994,85(1):187-192
We report SR measurements of Pr2CuO4– and (Pr2–xCex)CuO4– single crystals in the temperature range 4.2K300K. Two spin reorientation phase transitions were observed, although neutron scattering experiment could not detect these phase transitions. These allow us to conclude that magnetic moments of the Cu atoms order in an antiferromagnetic noncollinear cross like structure including a hidden canting spin arrangement. 相似文献
47.
Okamoto A Tainaka K Nishiza K Saito I 《Journal of the American Chemical Society》2005,127(38):13128-13129
We have developed a nucleotide modified by a pyrene derivative with dual fluorescence. The dual fluorescence of the fluorophore, which was incorporated into DNA, was effectively controlled at ambient temperature according to DNA structural status. Our nucleoside with dual fluorescence is effective as a conceptually new probe for monitoring DNA hybridization by the color change without multilabeling with fluorescent dyes. 相似文献
48.
Naoki Kamo Tomoya Kujirai Hitoshi Kurumizaka Hiroshi Murakami Gosuke Hayashi Akimitsu Okamoto 《Chemical science》2021,12(16):5926
The application of organometallic compounds for protein science has received attention. Recently, total chemical protein synthesis using transition metal complexes has been developed to produce various proteins bearing site-specific posttranslational modifications (PTMs). However, in general, significant amounts of metal complexes were required to achieve chemical reactions of proteins bearing a large number of nucleophilic functional groups. Moreover, syntheses of medium-size proteins (>20 kDa) were plagued by time-consuming procedures due to cumbersome purification and isolation steps, which prevented access to variously decorated proteins. Here, we report a one-pot multiple peptide ligation strategy assisted by an air-tolerant organoruthenium catalyst that showed more than 50-fold activity over previous palladium complexes, leading to rapid and quantitative deprotection on a protein with a catalytic amount (20 mol%) of the metal complex even in the presence of excess thiol moieties. Utilizing the organoruthenium catalyst, heterochromatin factors above 20 kDa, such as linker histone H1.2 and heterochromatin protein 1α (HP1α), bearing site-specific PTMs including phosphorylation, ubiquitination, citrullination, and acetylation have been synthesized. The biochemical assays using synthetic proteins revealed that the citrullination at R53 in H1.2 resulted in the reduced electrostatic interaction with DNA and the reduced binding affinity to nucleosomes. Furthermore, we identified a key phosphorylation region in HP1α to control its DNA-binding ability. The ruthenium chemistry developed here will facilitate the preparation of a variety of biologically and medically significant proteins containing PTMs and non-natural amino acids.Chemical protein synthesis assisted by an organoruthenium catalyst streamlined the production of heterochromatin factors bearing various patterns of epigenetic modifications, and their biological significance was elucidated. 相似文献
49.
50.
Souma S Komatsu H Takahashi T Kaji R Sasaki T Yokoo Y Akimitsu J 《Physical review letters》2003,90(2):027202
We report high-resolution angle-resolved photoemission spectroscopy (ARPES) on CaB6. The band structure determined by ARPES shows a 1 eV energy gap at the X point between the valence and the conduction bands. We found a small electron pocket at the X point, whose carrier number is estimated to be (4-5) x 10(19) cm(-3), in good agreement with the Hall resistivity measurement with the same crystal. The experimental results are discussed in comparison with band structure calculations and theoretical models for the high-temperature ferromagnetism. 相似文献