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61.
Ailong Li Hideshi Ooka Nadge Bonnet Toru Hayashi Yimeng Sun Qike Jiang Can Li Hongxian Han Ryuhei Nakamura 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(15):5108-5112
Efficient, earth‐abundant, and acid‐stable catalysts for the oxygen evolution reaction (OER) are missing pieces for the production of hydrogen via water electrolysis. Here, we report how the limitations on the stability of 3d‐metal materials can be overcome by the spectroscopic identification of stable potential windows in which the OER can be catalyzed efficiently while simultaneously suppressing deactivation pathways. We demonstrate the benefits of this approach using gamma manganese oxide (γ‐MnO2), which shows no signs of deactivation even after 8000 h of electrolysis at a pH of 2. This stability is vastly superior to existing acid‐stable 3d‐metal OER catalysts, but cannot be realized if there is a deviation as small as 50‐mV from the stable potential window. A stable voltage efficiency of over 70 % in a polymer–electrolyte membrane (PEM) electrolyzer further verifies the availability of this approach and showcases how materials previously perceived to be unstable may have potential application for water electrolysis in an acidic environment. 相似文献
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63.
Hideshi Hattori Toshiyuki Uryu 《Journal of polymer science. Part A, Polymer chemistry》2000,38(5):887-894
Photochromic liquid‐crystalline copolymers consisting of a photochromic monomeric unit containing both a spironaphthoxazine group and an undecamethylene spacer, and a liquid‐crystalline monomeric unit containing both a cholesteryl group and a decamethylene spacer were prepared to investigate the effect of the thermal properties of the photochromic monomeric unit on the mesomorphic order of the side chain of the related copolymers. The photochromic liquid‐crystalline copolymers containing a photochromic liquid‐crystalline monomeric unit showed only a smectic phase. On the other hand, the photochromic liquid‐crystalline copolymers containing a photochromic non‐liquid‐crystalline monomeric unit showed a chiral nematic phase (cholesteric phase). The photochromic chiral nematic liquid‐crystalline copolymer containing 14 mol % photochromic monomeric unit reflected visible light around 104 °C. To lower the temperature range of reflection of visible light, cholesteryl oleyl carbonate was used as a chiral nematic plasticizer for the photochromic chiral liquid‐crystalline polymer systems. Photo‐induced pitch change of the mixture by means of UV irradiation was investigated and it was concluded that the pitch change observed under UV irradiation was mainly induced by thermal effect in the case of our system. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 887–894, 2000 相似文献
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Hideshi Hattori Toshiyuki Uryu 《Journal of polymer science. Part A, Polymer chemistry》1999,37(17):3513-3522
The novel photochromic liquid-crystalline polyacrylates containing a spirooxazine group were synthesized. The photochromic polymer containing (4-penta- methyleneoxy)biphenylene moiety at the 5-position of spironaphthoxazine showed nematic phase from 122.9 to 133.8°C. The photochromic polymer containing undeca- methylene instead of pentamethylene showed smectic phase from 93.1 to 169.7°C. On the other hand, the photochromic polymer containing both undecamethylene as a spacer and spironaphthoxazine-bound biphenylene moiety at 9′-position did not show any liquid crystallinity. All spirooxazine-containing liquid-crystalline polymers showed photochromism in the solid state at room temperature. Because the shape of the absorption spectra of the photochromic quenched liquid-crystalline polymer films was almost the same as those of the photochromic amorphous polymer films, the photochromic properties did not depend on the mesophase in the polymers examined. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 3513–3522, 1999 相似文献
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We developed the detection apparatus that equipped with the two-photomultiplier tubes for chemiluminescence from singlet oxygen. Singlet oxygen was generated with reaction between sodium hypochlorite and hydrogen peroxide. The chemiluminescence from singlet oxygen, the dimol light emission (ca. 634 nm) and the monomol light emission (ca. 1270 nm), was observed simultaneously for the same reaction cell. The effects of sodium azide as an antioxidant, human serum albumin, and α-amino acids on the chemiluminescence based on the both emissions were examined; the observed chemiluminescence could provide direct information with regard to the reaction between singlet oxygen and antioxidant/biomolecules. The apparent rate constants for quenching singlet oxygen in the presence of human serum albumin were calculated to be ca. 3.3 × 109 and ca. 8.8 × 108 M−1 s−1 for the dimol and monomol light emissions, respectively, under the present conditions. The chemiluminescence intensities of the dimol emission decreased in the presence of His, Asp, Phe, Ser, and Tyr, and that of the monomol decreased in the presence of Cys and Trp. The chemiluminescence observed in the presence of biomolcules was discussed together with the reactivities of sodium hypochlorite and hydrogen peroxide to biomolecules. 相似文献
68.
Thermal mode spectroscopy (TMS) has been recently proposed for accurately measuring thermal diffusivity of solids from a temperature decay rate of a specific thermal mode selected by three-dimensional (anti)nodal information [Phys. Rev. Lett., 117, 195901 (2016)]. In this paper, we find out the following advantages of TMS by use of perturbation analyses. First, TMS is applicable to the measurement of high-thermal diffusivity with a small-size specimen. Second, it is less affected by thermally resistive films on a specimen in the sense that the resistance at the interface does not affect the first-order correction of thermal diffusivity. Third, it can perform doubly accurate measurement of the thermal diffusivity specified at a thermal equilibrium state even if the diffusivity depends on temperature in the sense that the measurement can be performed within tiny temperature difference from the given state and that the decay rate of the slowest decaying mode is not affected by the dependence. 相似文献
69.
Hirofumi Okuda Shigeru Matsushima Hideshi Sugiura Kenji Yamada Shunsuke Hamada Yoshihiro Nishida Naoki Ishiguro 《Magnetic resonance imaging》2014
Objective
Equivalent cross-relaxation rate imaging (ECRI) is an MRI technique used to evaluate qualitative changes in protein-water interactions. We aimed to prospectively evaluate the utility of ECRI for classification of adipocytic tumors.Materials and Methods
Institutional Review Board approval was obtained and all patients provided informed consent. Study participants included 40 patients with adipocytic tumors who were diagnosed with lipomas (n = 22), atypical lipomatous tissue/well-differentiated liposarcoma (ALT/WDL; n = 9), myxoid/round cell liposarcoma (MyL; n = 6), and dedifferentiated liposarcoma (DDL; n = 3), and 20 control patients for whom subcutaneous fat in the buttock or thigh was analyzed.Results
Mean ECR values of lipomas, ALT/WDL, and subcutaneous fat were low, and those of MyL and DDL were high. Mean ECR values of MyL and DDL were significantly higher than those of ALT/WDL. The cut-off value was 5.1%. There was a positive correlation between ECR value, pathological grade, and cell density in adipocytic tumors.Conclusion
The ECR value positively correlates with pathological grade and cell density of adipocytic tumors. Our findings suggest that ECRI is a useful method for preoperative evaluation of adipocytic tumors. 相似文献70.
The first nickel-catalyzed C-H bond arylation of azoles with phenol derivatives is described. The new Ni(cod)(2)/dcype catalytic system is active for the coupling of various phenol derivatives such as esters, carbamates, carbonates, sulfamates, triflates, tosylates, and mesylates. With this C-H/C-O biaryl coupling, we synthesized a series of privileged 2-arylazoles, including biologically active alkaloids. Moreover, we demonstrated the utility of the present reaction for functionalizing estrone and quinine. 相似文献