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71.
The current renaissance in main group chemistry has been fuelled by the remarkable array of fundamentally interesting yet synthetically applicable low oxidation state p-block compounds that have appeared over the last decade. Their syntheses generally require the ready availability of low oxidation state element halide precursors. In the case of gallium this is provided by the simple to prepare reagent, "GaI", which since it was first reported in 1990, has been utilised in areas as varied as organic synthesis and gallium cluster construction. This article tracks the history of this extraordinary material and highlights its synthetic diversity; hopefully allowing the reader to envisage its application to aspects of their own research fields. 相似文献
72.
We have designed and built a chirped-pulse parametric-amplifier system that utilizes a 10 Hz, 300 ps, Nd:YAG pump laser system; a 1.575 microm fiber oscillator and amplifier as the signal source; and rubidium titanyl phosphate and potassium titanyl arsenate nonlinear crystals. We obtained 260 fs, 30 mJ pulses centered at 1.550 microm, representing a gain of > 10(9) and a peak power of 100 GW. To our knowledge, these are the highest energy and peak power pulses ever produced in the 1.5-2.0 microm region 相似文献
73.
74.
The spatial, spectral, and temporal properties of self-focusing 798-nm 100-fs pulses in air are experimentally measured with high-resolution, single-shot techniques at a set propagation distance of 10.91 m. The data, obtained with an initially collimated Gaussian beam, show significant evolution of spatial narrowing as well as temporal and spectral changes at intensities lower than those required for significant ionization of air. 相似文献
75.
Macrocyclic inhibitors of the NS3 protease as potential therapeutic agents of hepatitis C virus infection 总被引:3,自引:0,他引:3
76.
Lainton JA Allen MC Burton M Cameron S Edwards TR Harden G Hogg R Leung W Miller S Morrish JJ Rooke SM Wendt B 《Journal of combinatorial chemistry》2003,5(4):400-407
Efficient and general procedures have been developed for the solution-phase preparation of substituted morpholine derivatives, and a library has been produced around generic structure 1. This library was designed with proprietary modeling software for use as a general screening library. The 30 R1 reagents were phenols, and the 275 R2 reagents were taken from five different reagent classes, giving a variety of product classes in the final library of 8250 potential products. All of the library members were generated from a common intermediate, mesylate (5), which was synthesized efficiently, in bulk, in three steps from N-benzylethanolamine (2). High-throughput chemistry using robotics was carried out to produce the 7907 library members, which were individually characterized by reversed-phase LC/MS analysis. 相似文献
77.
Hopkins JM Bowdridge M Robertson KN Cameron TS Jenkins HA Clyburne JA 《The Journal of organic chemistry》2001,66(17):5713-5716
Reactions of the nucleophilic carbene 1,3-dimesityl-imidazol-2-ylidene (1) with diazofluorene, diphenyldiazomethane, and azidotrimethylsilane were examined. Specifically, carbene 1 reacts with diazofluorene and diphenyldiazomethane to give addition products (azines: 3 and 4, respectively). Compounds 3 and 4 were further characterized in the solid-state by single-crystal X-ray crystallographic studies. [3 (a = 9.7936(6) A, b = 10.0529(7) A, c = 16.251(1) A, alpha = 75.765(1) degrees, beta = 79.711(1) degrees, gamma = 64.321(1) degrees, Z = 2, space group P1); 4 (a = 11.681(3) A, b = 11.861(4) A, c = 21.186(3) A, alpha = 90 degrees, beta = 97.05(2) degrees, gamma = 90 degrees, Z = 4, space group P2(1)/n)]. The structural parameters of 3 and 4 are discussed with reference to previously characterized symmetrical and unsymmetrical azines. Structural data suggest that charge separation is possible in 3. 相似文献
78.
N. S. Kelsall C. E. Svensson S. Fischer D. E. Appelbe R. A. E. Austin D. P. Balamuth G. C. Ball J. A. Cameron M. P. Carpenter R. M. Clark M. Cromaz M. A. Deleplanque R. M. Diamond P. Fallon D. F. Hodgson R. V. F. Janssens D. G. Jenkins G. J. Lane C. J. Lister A. O. Macchiavelli C. D. O’Leary D. G. Sarantities F. S. Stephens D. C. Schmidt D. Seweryniak K. Vetter J. C. Waddington R. Wadsworth D. Ward A. N. Wilson A. V. Afanasjev S. Frauendorf I. Ragnarsson 《The European Physical Journal A - Hadrons and Nuclei》2003,20(1):131-132
High-spin states have been studied in 72Kr and 72Br using the 40Ca + 40Ca and 36Ar + 40Ca reactions at 164 and 145 MeV, respectively. The properties and configurations of the high-spin bands observed have been interpreted using unpaired cranked Nilsson-Strutinsky (CNS), and for 72Kr, paired cranked relativistic Hartree-Bogoliubov (CRHB) calculations. In 72Kr a new band has been identified that has the properties expected for the doubly aligned S-band configuration. In 72Br the previously known bands have been extended to higher spin. This has lead to a re-interpretation of the configurations.Received: 31 October 2002, Published online: 24 February 2004PACS:
21.10.Re Collective levels - 23.20.Lv
transitions and level energies - 27.50. + e
相似文献
79.
Anomalous pulse-width narrowing with first-order compensation of polarization mode dispersion 总被引:2,自引:0,他引:2
We present analytical and experimental results to demonstrate the narrowing of pulses transmitted through optical fibers, with polarization mode dispersion compensated for to first order in frequency. The compensation technique splits the optical signal at the fiber output into polarization components that are aligned with the output principal states of polarization, and only one of the two components is subsequently detected. It is shown that it is possible with this compensation technique to have output pulses that are narrower than the input pulses. Pulse narrowing can also be found when the optical signal is split into orthogonal polarization components that are not principal states of polarization. 相似文献
80.
Ahmed M. Eissa Michael J.P. Smith Artur Kubilis Jackie A. Mosely Neil R. Cameron 《Journal of polymer science. Part A, Polymer chemistry》2013,51(24):5184-5193
Copper‐catalyzed azide‐alkyne cycloaddition (CuAAC) was used to prepare glycosylated polyethylene (PE)–poly(ethylene glycol) (PEG) amphiphilic block copolymers. The synthetic approach involves preparation of alkyne‐terminated PE‐b‐PEG followed by CuAAC reaction with different azide functionalized sugars. The alkyne‐terminated PE‐b‐PEG was prepared by etherification reaction between hydroxyl‐terminated PE‐b‐PEG (Mn ~ 875 g mol?1) and propargyl bromide and azidoethyl glycosides were prepared by glycosylation of 2‐azidoethanol. Atmospheric pressure solids analysis probe‐mass spectrometry was used as a novel solid state characterization tool to determine the outcome of the CuAAC click reaction and end‐capping of PE‐b‐PEG by the azidoethyl glycoside group. The aqueous solution self‐assembly behavior of these amphiphilic glycosylated polymers was explored by TEM and dye solubilization studies. Carbohydrate‐bearing spherical aggregates with the ability to solubilize a hydrophobic dye were observed. The potential of these amphiphilic glycosylated polymers to self‐assemble via electro‐formation into giant carbohydrate‐bearing polymersomes was also investigated using confocal fluorescence microscopy. An initial bioactivity study of the carbohydrate‐bearing aggregates is furthermore presented. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 5184–5193 相似文献