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41.
Gilberto Gonzalez Avalos Rene Galindo Orozco 《Mathematical and Computer Modelling of Dynamical Systems: Methods, Tools and Applications in Engineering and Related Sciences》2013,19(1):38-57
A procedure is proposed to obtain the linearization of a class of non-linear physical systems using bond graphs. Also, a junction structure of a non-linear bond graph considering linearly dependent and independent state variables is described. From the junction structure of the non-linear bond graph a procedure to build a linearized bond graph is presented. Finally, an example of a Programmable Universal Manipulation Arm (PUMA) manipulator is given. 相似文献
42.
S. Aubin J. A. Behr R. Collister V. V. Flambaum E. Gomez G. Gwinner K. P. Jackson D. Melconian L. A. Orozco M. R. Pearson D. Sheng G. D. Sprouse M. Tandecki J. Zhang Y. Zhao 《Hyperfine Interactions》2013,214(1-3):163-171
We present a method for measuring the nuclear anapole in a string of francium isotopes. The anapole is a parity non-conserving electromagnetic moment that enables parity-forbidden transitions between ground state hyperfine levels of an atom. The experiment is run by the FrPNC collaboration and relies on a beam of artificially-produced francium from the ISAC facility at TRIUMF. 相似文献
43.
Zhongqi He Rachel L. Sleighter Patrick G. Hatcher Shasha Liu Fengchang Wu Haixuan Zou O. Modesto Olanya 《Journal of mass spectrometry : JMS》2019,54(8):655-666
Soluble extractives in wood function to protect living trees from destructive agents and also contribute to wood color and fragrance. Some extractive components have biological activities with medical applications. They also play important roles in wood processing and related applications. To increase the knowledge of wood chemistry, maple and oak were extracted by water. Ultraviolet/visible (UV/vis) spectroscopy indicated the presence of a phenolic compound, resorcinol, in maple extractives having higher molecular mass and more aromatic components than oak extractives. Negative and positive electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI FT‐ICR‐MS) identified thousands of formulas in the two samples in the m/z range of 200 to 800. They mainly fall into the lignin‐like, carbohydrate‐like, and tannin‐like compound categories. The top 25 peaks (ie, formulas) with the highest relative magnitude in negative ESI represented nearly 50% of the summed total spectral magnitude of all formulas assigned in the maple and oak extractives. Furthermore, the base peak (ie, most abundant peak) accounted for about 14% of the total abundance in each wood sample. Literature comparisons identified 17 of 20 formulas in the top five peaks of the four spectra as specific bioactive compounds in trees and other plants, implying the potential to explore utilization of maple and oak extractives for functional and medicinal applications. The various profiling of the top 25 peaks from the two samples also suggested the possible application of FT‐ICR‐MS for detecting chemical markers useful in profiling and identification of wood types and sources. 相似文献
44.
Lucía Aristizabal Mariana Ángel Camila Orozco Pablo Ruiz Jairo Quijano Rafael Notario 《Structural chemistry》2018,29(3):897-907
In spite of the several experimental and computational studies on the thermal decomposition of allyl ethers and allyl sulfides, there are still disagreements on aspects of the reaction mechanism, such as the true nature of the transition states and the grade of synchronicity of the reactions. This work presents a computational study of the gas-phase thermolysis reaction of allyl ethers and allyl sulfides substituted at α-carbon, at the M05-2X/6-31+G(d,p) level of theory and a temperature range from 586.15 to 673.15 K. The substituent groups were methyl, ethyl, n-propyl, i-propyl, allyl, benzyl and acetonyl. It was found that the sulfides react faster than the homologous ethers and that the substituent groups with the capacity of delocalize charge increase the reaction rate. Through natural bond orbital calculations, the transition states were characterized. The synchronicities and atomic charges of the studied reactions were determined. A computational study at the G3 level of theory on the thermochemistry of allyl ethers and sulfides was also carried out. 相似文献
45.
Brandaleze Elena Bazán Vanesa Orozco Ivana Valentini Marcelo Gomez Giuliana 《Journal of Thermal Analysis and Calorimetry》2018,133(1):435-441
Journal of Thermal Analysis and Calorimetry - Rhenium production from copper and molybdenum sulphides involves the use of a pyrometallurgical process. In traditional pyrometallurgy processes, gases... 相似文献
46.
Fabin Orozco John N. Low Justo Cobo Christopher Glidewell 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(7):o379-o381
In the title compound, C34H31N2O8PS, the intramolecular distances provide evidence for polarization of the molecular–electronic structure. The molecules are linked into complex chains of rings by three independent C—H...O hydrogen bonds. The significance of this study lies in its finding that two of the four carbonyl O atoms play no role in the hydrogen bonding, despite the large excess of potential hydrogen‐bond donors present. 相似文献
47.
Fabían Orozco Braulio Insuasty John N. Low Justo Cobo Christopher Glidewell 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(4):o220-o225
In each of 6‐amino‐3‐methyl‐2‐(morpholin‐4‐yl)‐5‐nitrosopyrimidin‐4(3H)‐one, C9H13N5O3, (I), morpholin‐4‐ium 4‐amino‐2‐(morpholin‐4‐yl)‐5‐nitroso‐6‐oxo‐1,6‐dihydropyrimidin‐1‐ide, C4H10NO+·C8H10N5O3−, (II), and 6‐amino‐2‐(morpholin‐4‐yl)‐5‐nitrosopyrimidin‐4(3H)‐one hemihydrate, C8H11N5O3·0.5H2O, (III), the bond distances within the pyrimidine components are consistent with significant electronic polarization, which is most marked in (II) and least marked in (I). Despite the high level of substitution, the pyrimidine rings are all effectively planar, and in each of the pyrimidine components, there are intramolecular N—H...O hydrogen bonds. In each compound, the organic components are linked by multiple N—H...O hydrogen bonds to form sheets of widely differing construction, and in compound (III) adjacent sheets are linked by the water molecules, so forming a three‐dimensional hydrogen‐bonded framework. This study also contains the first direct geometric comparison between the electronic polarization in a neutral aminonitrosopyrimidine and that in its ring‐deprotonated conjugate anion in a metal‐free environment. 相似文献
48.
Sayra L. Orozco Erick R. Bandala Camilo A. Arancibia-Bulnes Benito Serrano Raúl Surez-Parra Isaias Hernndez-Prez 《Journal of photochemistry and photobiology. A, Chemistry》2008,198(2-3):144-149
The effect of chloride, sulfate and nitrate anions on the color removal of water containing the azo-dye reactive blue 69 (RB69) in acidic solution, by using photo-assisted Fenton process with Fe(II)/H2O2 and Fe(III)/H2O2 systems was investigated. Experiments were conducted in a batch reactor irradiated during 5 h with a domestic 15 W lamp with emission in the visible spectra. Experimental results showed color disappearance in the first 5 min of reaction in the photo-assisted process for all of the different salts, greatly enhancing the reaction rate with respect to the corresponding systems under dark conditions. The exception of the general trend was the Fe2(SO4)3/H2O2/UV system, where the decolorization process is slower probably because the oxidative species generated by rupture of Fe(III)–peroxo complexes are less reactive. Total organic matter depletion and mineralization of the effluent were also tested during the experimental runs by means of total organic carbon (TOC) showing that, for most of the photo-assisted experiments high mineralization was reached after 3 h of reaction. 相似文献
49.
Orozco J Fernández-Sánchez C Mendoza E Baeza M Céspedes F Jiménez-Jorquera C 《Analytica chimica acta》2008,607(2):176-182
This work reports on the development of a graphite-polystyrene composite electrode of planar configuration, containing silver(II) oxide and copper(II) oxide catalysts (AgO-CuO), for the measurement of electrochemical oxygen demand (EOD). Optimisation studies of the composite composition as well as conditions for its processing on planar substrates and generation of an appropriate electrochemical active area resulted in the scalable fabrication of robust composite electrodes. These were evaluated with glucose as target analyte. They showed competitive low limits of detection in a linear concentration range from 5 mg L−1 to 1400 mg L−1 of O2. Besides, they were stable for at least one year. The determination of EOD in wastewater samples coming from production lines of parenteral food and winemaking was successfully carried out. 相似文献
50.
Grossman J.S. Orozco L.A. Simsarian J.E. Sprouse G.D. Zhao W.Z. 《Hyperfine Interactions》1999,120(1-8):657-660
We have performed precision measurements in a magneto-optical trap of the 7P1/2 hyperfine structure of the isotopes 209-210Fr. The ratio of these hyperfine constants to the previously measured 7S1/2 ground state values reveals a significant hyperfine anomaly. This anomaly results from the different radial dependence of
the electron density in the two atomic levels. The measurements are sensitive to changes in the radial distribution of the
neutron magnetism.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献