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31.
Michelle Gonçalves Mothé Cheila Gonçalves Mothé Carlos Henrique Monteiro de Carvalho Marcia Cristina Khalil de Oliveira 《Journal of Thermal Analysis and Calorimetry》2013,113(2):525-531
Present study investigates thermal behavior of two heavy crude oils with different °API values by simultaneous thermogravimetry–differential scanning calorimetry–fourier transform infrared spectroscopy (TG–DSC–FTIR), and an evaluation of the chemical element levels present in the oils’ ashes was done by energy dispersive X-ray fluorescence spectrometry. TG and DSC curves were obtained for two samples in nitrogen atmosphere. Among all inorganic components evaluated, the highest concentration in the two oils was SO3. Thus this study may contribute to a better understanding of the thermal behavior of heavy crude oils and their composition. 相似文献
32.
Vanessa F. M. Carvalho Daniela V. Giacone Leticia V. Costa‐Lotufo Edilberto Rocha Silveira Luciana B. Lopes 《Biomedical chromatography : BMC》2019,33(2)
This study reports the development of a simple and reproducible method, with high rates of recovery, to extract the cytotoxic agent piplartine from skin layers, and a sensitive and rapid UV‐HPLC method for its quantification. Considering the potential of piplartine for topical treatment of skin cancer, this method may find application for formulation development and pharmacokinetics studies to assess cutaneous bioavailability. Porcine skin was employed as a model for human tissue. Piplartine was extracted from the stratum corneum (SC) and remaining viable skin layers (VS) using methanol, vortex homogenization and bath sonication, and subsequently assayed by HPLC using a C18 column, and 1:1 (v/v) acetonitrile–water (adjusted to pH 4.0 with acetic acid 0.1%) as mobile phase. The quantification limit of piplartine was 0.2 μg/mL (0.6 μm ), and the assay was linear up to 5 μg/mL (15.8 μm ), with within‐day and between‐days assay coefficients of variation and relative errors <15%. Piplartine recovery from SC and VS varied from 86 to 96%. The method was suitable to assay samples from skin penetration studies, enabling detection of differences in cutaneous delivery in different skin compartments resulting from treatment with various formulations and time periods. 相似文献
33.
Diana Meneses Souza Luciana Lucas Machado Angelo Henrique Lira Machado 《Tetrahedron letters》2019,60(28):1811-1813
The first total synthesis of (±)-floribundane B is reported. Johnson-Claisen rearrangement of a Morita-Baylis-Hillman adduct assembled all of the stereochemical features of this secoiridoid. The formal synthesis of (±)-oleocanthal and the synthesis of a chemical constituent of olive press juice is also reported. 相似文献
34.
Knowledge of the element content of biological systems is important in enabling understanding of uptake mechanisms and physiological response to stress conditions. In this work concentrations of mineral elements in sycamore (Acer pseudoplatanus L.) cells grown in the presence of cadmium have been analysed and compared with concentrations in control cells. Energy-dispersive X-ray fluorescence (EDXRF) was used to quantify the nutrients K, Ca, Mn, Fe, Cu, and Zn present in the cells. The reproducibility and accuracy of the technique were demonstrated by analysis of biological reference materials. Exposure of sycamore cells to cadmium had induced variation in the content of some elements. Mn, Cu, Zn, and, particularly, Fe concentrations in cells exposed to Cd were higher than those found in control cells. Ca is adsorbed on the cell walls and the concentration of K is not affected by the presence of Cd. 相似文献
35.
36.
The partial hydrogenation of benzene to cyclohexene by nanoscale ruthenium catalysts in imidazolium ionic liquids 总被引:3,自引:0,他引:3
Silveira ET Umpierre AP Rossi LM Machado G Morais J Soares GV Baumvol IJ Teixeira SR Fichtner PF Dupont J 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(15):3734-3740
The controlled decomposition of an Ru(0) organometallic precursor dispersed in 1-n-butyl-3-methylimidazolium hexafluorophosphate (BMI.PF(6)), tetrafluoroborate (BMI.BF(4)) or trifluoromethane sulfonate (BMI.CF(3)SO(3)) ionic liquids with H(2) represents a simple and efficient method for the generation of Ru(0) nanoparticles. TEM analysis of these nanoparticles shows the formation of superstructures with diameters of approximately 57 nm that contain dispersed Ru(0) nanoparticles with diameters of 2.6+/-0.4 nm. These nanoparticles dispersed in the ionic liquids are efficient multiphase catalysts for the hydrogenation of alkenes and benzene under mild reaction conditions (4 atm, 75 degrees C). The ternary diagram (benzene/cyclohexene/BMI.PF(6)) indicated a maximum of 1 % cyclohexene concentration in BMI.PF(6), which is attained with 4 % benzene in the ionic phase. This solubility difference in the ionic liquid can be used for the extraction of cyclohexene during benzene hydrogenation by Ru catalysts suspended in BMI.PF(6). Selectivities of up to 39 % in cyclohexene can be attained at very low benzene conversion. Although the maximum yield of 2 % in cyclohexene is too low for technical applications, it represents a rare example of partial hydrogenation of benzene by soluble transition-metal nanoparticles. 相似文献
37.
Daniel M. Silveira Pedro A. S. Salgueiro M. Filomena G. F. C. Cam?es Ricardo J. N. Bettencourt da Silva 《Accreditation and quality assurance》2012,17(2):115-127
Tear gases are the most widely used non-lethal weapons, both by security forces and by the general public. The pepper spray,
whose active agent is capsaicin, is the only self-defence aerosol allowed in Portugal, where capsaicin concentration must
be below 5 g/100 mL. The cost-effective evaluation of the compliance of self-defence weapons with legislation involves the
use of two measurement procedures with increasing quantitative capability. Samples are first assessed by preliminary measurement
procedure based on single-point GC–MS calibration. Whenever the measurement uncertainty from this assessment makes evaluation
inconclusive, the evaluation of sample compliance using multi-point GC–MS calibration is performed. Metrological models including
sound criteria for the evaluation of sample compliance with legislation were developed for both measurement procedures. Such
models include the evaluation of the impact of instrumental performance, calibration model, sample dilution and standards
preparation on measurement uncertainty. The relative expanded uncertainty, in the studied range (capsaicin 3–7 g/100 mL),
of measurements supported in single-point calibrations ranged from 10 to 22% and the ones supported on multi-point calibrations
from 8 to 12% depending on capsaicin concentration and daily GC–MS repeatability. Measurements are fit for the intended use
since they present a relative expanded uncertainty smaller than a target value of 30, or 15%, for measurements supported in
single- or multi-point calibrations, respectively. 相似文献
38.
Alliny F. Naves Henrique T. C. Fernandes Ana P. S. Immich Luiz H. Catalani 《Journal of polymer science. Part A, Polymer chemistry》2013,51(18):3881-3891
The search for materials produced from renewable sources aiming at the substitution of petroleum‐based derivates is an area of intense investigation. In this work, the enzymatic copolymerization of isosorbide or isomannide with diethyl adipate and fractions of different unsaturated diesters (diethyl itaconate, diethyl fumarate, diethyl glutaconate, and diethyl hydromuconate) were examined using CAL‐B as catalyst. The polyesters prepared using one‐step syntheses were characterized by SEC, NMR, and MALDI‐TOF MS. In addition, syntheses with linear diols were carried out in bulk to evaluate the reactivity of cyclic diols in producing unsaturated polyesters using enzymatic catalysis, as well as to evaluate the occurrence of addition side reactions on the double bonds. Isosorbide and isomannide yielded unsaturated polymers with values in the order of 4,000‐16,000 when fumarate or glutaconate esters were added in 5 mol % ratio against adipate. In all cases MALDI‐TOF confirmed the presence of unsaturated units. Although these polyesters have unreacted double bonds they are prone to crosslinking and ready to further functionalization, like anchoring bioactive molecules. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 3881–3891 相似文献
39.
40.
Dihalocarbenes generated under phase transfer conditions add to cis and trans vinylic selenides to give the corresponding 1,1-dihalo-2-selenocyciopropanes with retention of configuration. 相似文献