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31.
The discharge initiation mechanism of nanosecond dielectric barrier discharges in open air has been clarified with time-dependent measurement of the discharge electric field by electric-field-induced coherent Raman scattering and optical emission. Our experimental observations have revealed that, in the prebreakdown phase of a nanosecond dielectric barrier discharge, the externally applied fast-rising electric field is strongly enhanced near the cathode due to large accumulation of space charge, which then strongly enhances ionization near the cathode. Once a sufficiently large number of ionizations take place, the location of peak ionization forms a front and propagates toward the cathode with strong optical emission, which establishes the discharge. This process is essentially different from the well-known Townsend mechanism for slower discharges. 相似文献
32.
Arihiro Kanazawa Shokyoku Kanaoka Sadahito Aoshima 《Journal of polymer science. Part A, Polymer chemistry》2010,48(4):916-926
Cationic polymerization of isobutyl vinyl ether (IBVE) was examined using a variety of metal oxides in conjunction with IBVE–HCl adduct as a cationogen in toluene at 0 °C. Iron oxides (α‐Fe2O3, γ‐Fe2O3, and Fe3O4) induced living polymerization in the presence of an added base, ethyl acetate or 1,4‐dioxane, to give polymers with very narrow molecular weight distributions (MWDs). Conversely, with other metal oxides such as Ga2O3, In2O3, ZnO, Co3O4, and Bi2O3, polymers with bimodal MWDs, including long‐lived species along with uncontrolled higher molecular weight portions, were produced in the presence of an added base. A small amount of nBu4NCl or 2,6‐di‐tert‐butylpyridine (DTBP) suppressed the uncontrolled portion to induce controlled reactions with Ga2O3, In2O3, and ZnO. The roles of these reagents are discussed in terms of the nature of the active sites of the catalyst surface and the polymerization mechanisms. In addition, the reusability of the catalyst, the effect of stirring before and during polymerization, and the estimation of the number of active sites are also described. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 916–926, 2010 相似文献
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This paper presents a low-capacity cation-exchange chromatography method for the analysis of UV-absorbing dipeptides and amino acids. A newly marketed low-capacity cation-exchange column packed with sulfo-functionalized highly cross-linked macroreticular poly(ethylstyrene-divinylbenzene) copolymer was used for the simultaneous determination of imidazole amino acids, aromatic amino acids, and creatinine in urine samples. A dual-mode binary gradient chromatography method was established using two solvents, A: 15 mM H3PO4/5 mM ethylenediamine and B: 15 mM H3PO4/5 mM ethylenediamine/40 (v/v) % CH3CN at 40 °C, with an optimized time program for changing the delivery ratio of A/B and the flow rate. Good chromatograms were obtained within an acceptable cycle time of 25 min. The quantification data were satisfactory for all analytes, showing the relative standard deviations (RSD) of retention times between 0.08 and 1.68 %; RSDs of area intensities between 0.23 and 2.60 %; and linear regression lines with r 2 more than 0.9994. The method could determine the creatinine ratios of the diagnostic markers on the single chromatographic run, which enabled to discriminate disease from health. For example, the creatinine ratios for phenylketonuria were significantly higher than those for controls. The method can provide highly cost-efficient information or useful knowledge for clinical and pharmaceutical studies. 相似文献
35.
Nakamura K Kanazawa K Kobayashi N 《Chemical communications (Cambridge, England)》2011,47(36):10064-10066
We have demonstrated electroswitchable emission and coloration using a novel composite material containing luminescent europium(III) complex Eu(hfa)(3)(H(2)O)(2) and diheptyl viologen HV(2+). The photoluminescence of the Eu(III) complex was controlled by the electrochemical coloration of HV(2+)via intermolecular energy transfer mechanisms. 相似文献
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K. Matsuta T. Minamisono M. Mihara M. Fukuda Shengyun Zhu Y. Masuda K. Hatanaka Daqing Yuan Yongnan Zheng Yi Zuo Ping Fang Dongmei Zhou T. Ohtsubo T. Izumikawa S. Momota D. Nishimura R. Matsumiya A. Kitagawa S. Sato M. Kanazawa M. Torikoshi T. Nagatomo Y. Nojiri T. Suzuki Xizhen Zhang J. R. Alonso T. J. M. Symons S. Kawasaki S. C. Jeong Y. Watanabe K. Minamisono 《Hyperfine Interactions》2013,220(1-3):21-28
We report our studies in various fields of Physics through nuclear moments utilizing the β-NMR technique, including material sciences, nuclear structures and fundamental symmetries. Especially, we focus on the recent progress in the studies on the electronic structure in Pt through Knight shifts of various impurities, lattice locations of impurities, electric field gradients, the analysis of nuclear spin in terms of its components, anomaly in the spin expectation value for 9C-9Li mirror pair, the G-parity conservation law, and the Ramsey resonance on UCN for future neutron EDM measurements. 相似文献
39.
Tomomi Kanazawa Kohei Ono Masashi Yamazaki Shiho Cho Fumiyoshi Takano 《Applied Surface Science》2008,254(23):7918-7920
We propose a reactive ion etching (RIE) process of an L10-FePt film which is expected as one of the promising materials for the perpendicular magnetic recording media. The etching was carried out using an inductively coupled plasma (ICP) RIE system and an etching gas combination of CH4/O2/NH3 was employed. The L10-FePt films were deposited on (1 0 0)-oriented MgO substrates using a magnetron sputtering system. The etching masks of Ti were patterned on the FePt films lithographically. The etch rates of ∼16 and ∼0 nm/min were obtained for the FePt film and the Ti mask, respectively. The atomic force microscopy (AFM) analyses provided the average roughness (Ra) value of 0.95 nm for the etched FePt surface, that is, a very flat etched surface was obtained. Those results show that the highly selective RIE process of L10-FePt was successfully realized in the present study. 相似文献
40.
Prof. Isao Fujii Dr. Makoto Hashimoto Kaori Konishi Akiko Unezawa Haruka Sakuraba Kenta Suzuki Harue Tsushima Miho Iwasaki Satsuki Yoshida Akane Kudo Rina Fujita Aika Hichiwa Koharu Saito Dr. Takashi Asano Dr. Jun Ishikawa Dr. Daigo Wakana Dr. Yukihiro Goda Ayumi Watanabe Mamoru Watanabe Yui Masumoto Dr. Junichiro Kanazawa Dr. Hajime Sato Prof. Masanobu Uchiyama 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(22):8542-8548
Shimalactones A and B are neuritogenic polyketides possessing characteristic oxabicyclo[2.2.1]heptane and bicyclo[4.2.0]octadiene ring systems that are produced by the marine fungus Emericella variecolor GF10. We identified a candidate biosynthetic gene cluster and conducted heterologous expression analysis. Expression of ShmA polyketide synthase in Aspergillus oryzae resulted in the production of preshimalactone. Aspergillus oryzae and Saccharomyces cerevisiae transformants expressing ShmA and ShmB produced shimalactones A and B, thus suggesting that the double bicyclo-ring formation reactions proceed non-enzymatically from preshimalactone epoxide. DFT calculations strongly support the idea that oxabicyclo-ring formation and 8π-6π electrocyclization proceed spontaneously after opening of the preshimalactone epoxide ring through protonation. We confirmed the formation of preshimalactone epoxide in vitro, followed by its non-enzymatic conversion to shimalactones in the dark. 相似文献