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91.
A novel avenue for oxazoles via Beckmann rearrangement of alpha-formyl ketoxime dimethyl acetals is described that indicates the possibility of a non-amino acid biosynthetic pathway in marine natural products. 相似文献
92.
Transverse wave generation mechanism in rotating detonation 总被引:2,自引:0,他引:2
Yuho Uemura A. Koichi Hayashi Makoto Asahara Nobuyuki Tsuboi Eisuke Yamada 《Proceedings of the Combustion Institute》2013,34(2):1981-1989
Detonation engines are expected to be included in a number of aerospace thrusters in the future. Several types of detonation engines are currently under examination, including the rotating detonation engine (RDE). Although the RDE has been explored experimentally, its rotating detonation propagation mechanism is not well understood. This paper clarifies the detonation mechanism and dynamics of the RDE by 2D and 3D simulation using compressible Euler equations with a full chemical reaction mechanism of H2/O2 and H2/Air, especially from the triple-point and transverse detonation points of view. A total variation diminishing (TVD) scheme is used for the mixture of H2/Air, and an advection upwind splitting method difference vector (AUSMDV) scheme is used for the mixture of H2/O2. The use of an AUSMDV scheme provides a much clearer detonation structure than does the TVD scheme. We focus on the complex interaction mechanism of the detonation front and burned mixture gases. We found out that at this interaction point, an unreacted gas pocket appears and ignites periodically to generate transverse waves at the detonation front and maintain detonation propagation. 相似文献
93.
MacDougall GJ Aczel AA Carlo JP Ito T Rodriguez J Russo PL Uemura YJ Wakimoto S Luke GM 《Physical review letters》2008,101(1):017001
We have performed zero-field muon-spin-relaxation measurements on single crystals of La(2-x)SrxCuO4 to search for spontaneous currents in the pseudogap state. By comparing measurements on materials across the phase diagram, we put strict upper limits on any possible time-reversal symmetry breaking fields that could be associated with the pseudogap. Comparison between experimental limits and the proposed circulating current states effectively eliminates the possibility that such states exist in this family of materials. 相似文献
94.
Prof. Dr. Hiroyoshi Takamura Takayuki Fujiwara Yohei Kawakubo Prof. Dr. Isao Kadota Prof. Dr. Daisuke Uemura 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(6):1979-1983
Stereoselective and streamlined synthesis of the proposed C79–C104 fragment 2 of symbiodinolide ( 1 ), a polyol marine natural product with a molecular weight of 2860, was achieved. In the synthetic route, the proposed C79–C104 fragment 2 was synthesized by utilizing a Julia–Kocienski olefination and subsequent Sharpless asymmetric dihydroxylation as key transformations in a convergent manner. Detailed comparison of the 13C NMR chemical shifts between the natural product and the synthetic C79–C104 fragment 2 revealed that the stereostructure at the C91–C99 carbon chain moiety of symbiodinolide ( 1 ) should be reinvestigated. 相似文献
95.
96.
An efficient synthesis of (-)-ternatin derivatives directed toward their SAR at the beta-OH-D-Leu(7) moiety and their biological activities against 3T3-L1 murine adipocytes are described. 相似文献
97.
Complanine, an inflammation-inducing substance isolated from the marine fireworm Eurythoe complanata
Nakamura K Tachikawa Y Kitamura M Ohno O Suganuma M Uemura D 《Organic & biomolecular chemistry》2008,6(12):2058-2060
The marine fireworm, Eurythoe complanata, is known as a dangerous animal for humans because it induces skin inflammation through its small setae. Here, the inflammation-inducing substance was successfully isolated from the whole body using a methanolic extraction, and the inflammatory activity was determined using a bioassay. The structure was spectroscopically revealed to be a trimethylammonium with an unsaturated carbon chain and was named complanine. Complanine enhanced PKC activity in combination with TPA in vitro. This may explain the molecular mechanism behind its inflammation-inducing activity. 相似文献
98.
The first enantioselective total synthesis of (+)-sarcodictyenone is described [4.3% overall yield from (5R,6R)-6-methyl-5-trimethylsily-2-cyclohexenone]. This work establishes the absolute stereochemistry of the natural product. 相似文献
99.
Yamazoe H Uemura T Tanabe T 《Langmuir : the ACS journal of surfaces and colloids》2008,24(16):8402-8404
Fabrication of micropatterned surfaces to organize and control cell adhesion and proliferation is an indispensable technique for cell-based technologies. Although several successful strategies for creating cellular micropatterns on substrates have been demonstrated, a complex multistep process and requirements for special and expensive equipment or materials limit their prevalence as a general experimental tool. To circumvent these problems, we describe here a novel facile fabrication method for a micropatterned surface for cell patterning by utilizing the UV-induced conversion of the cell adhesive property of albumin, which is the most abundant protein in blood plasma. An albumin-coated surface was prepared by cross-linking albumin with ethylene glycol diglycidyl ether and subsequent casting of the cross-linked albumin solution on the cell culture dish. While cells did not attach to the albumin surface prepared in this way, UV exposure renders the surface cell-adhesive. Thus, surface micropatterning was achieved simply by exposing the albumin-coated surface to UV light through a mask with the desired pattern. Mouse fibroblast L929 cells were inoculated on the patterned albumin substrates, and cells attached and spread in a highly selective manner according to the UV-irradiated pattern. Although detailed investigation of the molecular-level mechanism concerning the change in cell adhesiveness of the albumin-coated surface is required, the present results would give a novel facile method for the fabrication of cell micropatterned surfaces. 相似文献
100.
Unraveling Inter‐ and Intrachain Electronics in Polythiophene Assemblies Mediated by Coordination Nanospaces
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Michael W. A. MacLean Takashi Kitao Dr. Takeo Suga Prof. Dr. Motohiro Mizuno Prof. Dr. Shu Seki Dr. Takashi Uemura Prof. Susumu Kitagawa 《Angewandte Chemie (International ed. in English)》2016,55(2):708-713
Strong interchain interactions render unsubstituted polythiophene un‐fusible, non‐melting, and insoluble. Therefore, control of the packing structure, which has a profound effect on the optical and electronic properties of the polymer, has never been achieved. Unsubstituted polythiophene was prepared in the one‐dimensional channels of [La(1,3,5‐benzenetrisbenzoate)]n, where polymer chains form unprecedented assembly structures mediated by the host framework. It is noteworthy that the emission and carrier transport properties were drastically changed by varying the number of chains within a particular assembly. The response of the composite to additional guests is also examined as a method to use the composites as low‐concentration sensors. Our findings show that the encapsulation of polymer chains in host materials is a facile method for understanding the intrinsic properties of conjugated polymers, along with controlling and enhancing their functions. 相似文献