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71.
The growth morphology of crystals of zinc tris(thiourea) sulphate (ZTS) is investigated experimentally, and computed using
the Hartman-Perdok approach. Attachment energies of the observed habit faces are calculated for determining their relative
morphological importance. A computer code is developed for carrying out these calculations. A special procedure is adopted
for computing the cohesive energy of a slice of the structure parallel to any rational crystallographic plane. For estimating
the cohesive energies, formal charges on the experimentally determined atomic positions in the molecules of ZTS are calculated
by ab initio molecular-orbital computations, with wave functions obtained by the Hartree-Fock procedure. Fairly good agreement with the
observed crystal morphology is obtained for a model of growth mechanism in which ZTS is assumed to exist in solution sa szinc
tris(thiourea) ions and sulphate ions. 相似文献
72.
Fractional Linear Multistep Methods for Abel-Volterra Integral Equations of the First Kind 总被引:1,自引:0,他引:1
Fractional powers of linear multistep methods are suggestedfor the numerical solution of weakly singular Volterra integralequations of the first kind. The proposed methods are convergentof the order of the underlying multistep method. The stabilityproperties are directly related to those of the multistep method. 相似文献
73.
We estimate the growth order in n of the Taylor coefficientsof bounded univalent functions in the unit disk. Our estimatedepends on the norm of the Grunsky operator. In particular,we improve the known results for coefficients of quasiconformallyextendible univalent functions. 1991 Mathematics Subject Classification30C50, 30C75, 30C55. 相似文献
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75.
M.P. Combes P. Berthet R. Frascaria CH.F. Perdrisat B. Tatischeff N. Willis J. Banaigs J. Berger A. Codino J. Duflo F. Plouin E. Aslanides F. Hibou O. Bing R. Beurtey M. Boivin D. Hutcheon Y. Le Bornec J. Yonnet 《Nuclear Physics A》1984,431(4):703-712
A search for isoscalar dibaryonic resonances by means of missing-mass spectra in the d + d → d + X reaction has been attempted using deuteron beams of T = 2.29,2.00 and 1.65 GeV. The results do not show any evidence for a narrow peak with a limit of for a 15 MeV width or a broad enhancement which could be unambiguously attributed to a dibaryonic resonance. 相似文献
76.
Clauwaert KM Van Bocxlaer JF Major HJ Claereboudt JA Lambert WE Van den Eeckhout EM Van Peteghem CH De Leenheer AP 《Rapid communications in mass spectrometry : RCM》1999,13(14):1540-1545
This paper describes the investigation of the potential of a quadrupole orthogonal acceleration time-of-flight mass spectrometer (Q-TOF) equipped with an atmospheric pressure ionisation interface for quantitative measurements of small molecules separated by reversed phase liquid chromatography. To this end, the detection limits and linear dynamic range in particular were studied in an LC/MS/MS experiment using 3,4-methylenedioxymethamphetamine standards and 3,4-methylenedioxyethylamphetamine for internal standardisation. In a second phase, the experiment was repeated with real biological extracts (whole blood, serum, and vitreous humour). A calibration for 3,4-methylenedioxymethamphetamine and its metabolite 3,4-methylenedioxyamphetamine was prepared in each of these matrices again using 3,4-methylenedioxyethylamphetamine as internal standard. The resulting quantitative data were compared with those obtained by liquid chromatography with fluorescence detection for the same extracts. The Q-TOF results revealed excellent sensitivity and a linear dynamic range of nearly four decades (2-10 000 pg on-column, r(2) = 0.9998, 1/x weighting). Furthermore, all the calibration curves prepared in biological material were superimposable, LC/MS/MS and LC-fluorescence, and the quantitative results for actual samples compared very favourably. It was concluded that the Q-TOF achieves a linear dynamic range for quantitative LC/MS/MS work exceeding that of fluorescence detection and at much better absolute sensitivity. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
77.
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option. 相似文献
78.