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1.
We describe a general method that enables us to obtain all the singular terms of helicity amplitudes of n-parton processes at one loop. The algorithm uses helicity amplitudes at tree level and simple color algebra. We illustrate the method by calculating the singular part of the one-loop helicity amplitudes of all 2 → 3 parton subprocesses. The results are used to derive the soft gluon limit of the cross sections of all 2 → 4 parton scattering subprocesses which provide a useful initial condition for the angular ordering approximation to coherent multiple soft gluon emission, incorporated in existing Monte Carlo simulation programs. 相似文献
2.
Marshall M. Siegel Keiko Tabei Frank Lambert Leonard Candela Bart Zoltan 《Journal of the American Society for Mass Spectrometry》1998,9(11):1196-1203
The atmospheric pressure ionization (API) source for a commercial mass spectrometer was modified to operate as a dual source in both the electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) techniques by simultaneously utilizing the electrospray probe and the corona discharge needle. A switching box was designed to operate in either manual or programmable modes to permit rapid switching between ionization techniques without changing sources, probes, or breaking vacuum. The source can be operated using the following ionization techniques: ESI only, APCI only, ESI/APCI simultaneously, and ESI/APCI alternatingly. The optimum operating conditions for these ionization techniques were similar to the manufacturer’s original specifications except that the APCI flow rate was lower (~50 µL/min versus 1000 µL/min) and externally heated nebulizing gas was found to be desirable. A four-component mixture, introduced by flow injection, was used to demonstrate the versatility of the dual ESI/APCI source. 相似文献
3.
Junjun Wu Lu Gem Gao Zoltan Varga Xuefei Xu Wei Ren Donald G. Truhlar 《Angewandte Chemie (International ed. in English)》2020,59(27):10826-10830
Faced with the contradictory results of two recent experimental studies [Jara‐Toro et al., Angew. Chem. Int. Ed. 2017 , 56, 2166 and Chao et al., Angew. Chem. Int. Ed. 2019 , 58, 5013] of the possible catalytic effect of water vapor on CH3OH + OH reaction, we report calculations that corroborate the conclusion made by Chao et al. and extend the rate constant evaluation down to 200 K. The rate constants of the CH3OH + OH reaction catalyzed by a water molecule are computed as functions of temperature and relative humidity using high‐level electronic structure and kinetics calculations. The Wuhan–Minnesota Scaling (WMS) method is used to provide accurate energetics to benchmark a density functional for direct dynamics. Both high‐frequency and low‐frequency anharmonicities are included. Variational and tunneling effects are treated by canonical variational transition state theory with multidimensional small‐curvature tunneling. And, most significantly, we include multistructural effects in the rate constant calculations. Our calculations show that the catalytic effect of water vapor is not observable at 200–400 K. 相似文献
4.
C. Camy-Peyret J.-M. Flaud J.-Y. Mandin R.A. Toth 《Journal of Molecular Spectroscopy》1978,70(3):361-373
The intensities of about 90 lines of the ν1 + ν2 and ν2 + ν3 bands of H218O have been measured using a Fourier transform spectrum of natural water vapor. The constants involved in the rotational expansion of the transformed transition moment operators corresponding to these bands have been determined through a fit of these line intensities. The constants obtained are used to compute the whole spectrum of the ν1 + ν2 and ν2 + ν3 bands of H218O providing reliable line positions and intensities. For lines involving perturbed levels a comparison is given with the results obtained for H216O and it is shown that the results for one isotopic species cannot be transferred directly to another one. 相似文献
5.
R.A. Toth L.R. Brown V. Malathy Devi 《Journal of Quantitative Spectroscopy & Radiative Transfer》2008,109(6):906-921
A new spectroscopic database for carbon dioxide in the near infrared is presented to support remote sensing of the terrestrial planets (Mars, Venus and the Earth). The compilation contains over 28,500 transitions of 210 bands from 4300 to 7000 cm−1 and involves nine isotopologues: 16O12C16O (626), 16O13C16O (636), 16O12C18O (628), 16O12C17O (627), 16O13C18O (638), 16O13C17O (637), 18O12C18O (828), 17O12C18O (728) and 18O13C18O (838). Calculated line positions, line intensities, Lorentz half-width and pressure-induced shift coefficients for self- and air-broadening are taken from our recent measurements and are presented for the Voigt molecular line shape. The database includes line intensities for 108 bands measured using the McMath-Pierce Fourier transform spectrometer located on Kitt Peak, Arizona. The available broadening parameters (half-widths and pressure-induced shifts) of 16O12C16O are applied to all isotopologues. Broadening coefficients are computed using empirical expressions that have been fitted to the experimental data. There are limited data for the temperature dependence of widths and so no improvement has been made for those parameters. The line intensities included in the catalog vary from 4×10−30 to 1.29×10−21 cm−1/(molecule cm−2) at 296 K. The total integrated intensity for this spectral interval is 5.9559×10−20 cm−1/(molecule cm−2) at 296 K. 相似文献
6.
High resolution measurement of the linewidths of HCl broadened by CO2 and N2 and CO broadened by CO2 have been performed in both the 1-0 and 2-0 bands of HCl and the 2-0 band of CO. The data were analyzed by the direct and the peak absorption methods. Values of the linewidths obtained by the two methods are in good agreement. For |m| ≤ 3, for the case of HCl + CO2, the agreement is good for the values obtained in both bands of HCl. However for |m| > 3, the HCl + CO2 linewidths in the 1-0 band are smaller than the corresponding lines in the 2-0 band by as much as 11% for |m| = 9. Lines (|m| ≤ 3) of the 1-0 and 2-0 bands of HCl broadened by CO2 were also analyzed in terms of the super-Lorentzian line profile proposed by Varanasi, S. K. Sarangi, and G. D. T. Tejwani (J. Quan. Spectr. Radiative Transfer12, 857 (1972)) and the Lorentzian profile. The results indicate that near the line center (within 3γ), the shape of HCl + CO2 lines are Lorentzian. 相似文献
7.
8.
Studies of the vibrational spectra of matrix-isolated M+NO
3
–
ion pairs have been extended to glassy aprotic solvents. The deuterated form of the solvents DMSO, THF, and ACN have windows through the 7- nitrate ionv
3(e) mode infrared region, so it was possible to clearly observe the splitting of the degeneracy of this mode,v
3, produced by the contacting, but solvated, alkali metal cation. Primary attention has been directed to the extent to which this splitting is reduced relative to the argon matrix values. This reduction, which reflects electron-density transfer from the solvating molecules to the ion pairs, is comparable to that observed for H2O and NH3 matrices as the splitting is reduced to 20–35% of the argon-matrix values. The extent of reduction ofv
3 for the different solvents has been related to Gutmann's donicity number scale with the correlation holding well for solvent molecules of comparable size, DMSO, THF and DMF, but breaking down for the smaller linear ACN, apparently because of more molecules in the cation solvation sphere. The matrix data have also been used, through comparison with spectra for saturated liquid solutions of Li+NO
3
–
, to show that the contact ion pair is the dominant species in liquid THF and ACN, whereas the ions are largely solvent separated in DMSO. 相似文献
9.
Balazs Kobzi Erno Kuzmann Zoltan Homonnay Stjepko Krehula Mira Ristic Shiro Kubuki 《Journal of Radioanalytical and Nuclear Chemistry》2018,316(2):579-586
Tin silicate glass without SnOx nanoparticles (SiO2·SnOx), a silica glass containing only SnOx nanoparticles (SiO2·SnOxNP) and the improved product, which combines the tin silicate glass with SnOx nanoparticles (SiO2·SnOx·SnOxNP) was prepared. For the structural analysis 119Sn Mössbauer spectroscopy and X-ray diffraction were applied. The 119Sn Mössbauer spectra showed that the SiO2·SnOx·SnOxNP sample had the largest SnII content (12.0%). It also had an outstanding methylene blue degradation with the first-order rate value with (18?±?2) × 10?3 min?1 with visible light irradiation. 相似文献
10.
Anita Toth Eszter Riethmuller Krisztina Vegh Agnes Alberti Szabolcs Beni Agnes Kery 《Natural product research》2018,32(17):2058-2061
Quantitative phytochemical characterisation of the chief flavonoid aglycones in the hydrolysed Lysimachia extracts revealed the dominance of kaempferol, quercetin and myricetin in L. vulgaris, L. nummularia, L. punctata, L. christinae, L. ciliata and L. clethroides, respectively. Due to the significant radical scavenging capacity of the samples, the contribution of the individual aglycones to the total antioxidant activity became of interest. Therefore, a HPLC method coupled to pre-column DPPH scavenging assay was developed. Differences in the six Lysimachia species’ phenolic composition regarding their participation to the antioxidant activity were revealed. The participation of the three investigated flavonoids to the radical quenching activity was the highest (91.2%) in the L. vulgaris sample, the lowest in L. christinae sample with 29.6%. In L. vulgaris sample, the 76.3% contribution of quercetin to the scavenger capacity was the highest peak area decrement ratio among the investigated samples. 相似文献