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71.
We consider the dynamical stability of horizontal fluid layer, performing harmonic oscillations in vertical direction. The continued fractions approach allowed us to avoid the conventional restriction to the case of small viscosity and almost-resonant frequencies. Our numerical results cover a wide range of the parameters (viscosity, amplitude and frequency of the oscillation, and depth of the layer). To cite this article: V.I. Yudovich et al., C. R. Mecanique 332 (2004).  相似文献   
72.
A novel chiral selector, clindamycin succinate, was synthesized and first used as a chiral selector in capillary electrophoresis (CE). The chiral resolution ability of this kind of clindamycin derivation was studied by CE using some racemic drugs as model analytes. From the experimental results, it was found that both resolution and selectivity of the selector were dependent on the following parameters: concentration of chiral selectors, pH of the running buffer, temperature of the capillary column, applied voltage and organic modifier used. The results show that the chiral selector possesses high resolution toward some racemic drugs, including ofloxacin, chlorphenamine, tryptophan, propranolol, sotalol and metoprolol. Excellent chiral resolution of these tested drugs was achieved under the optimal conditions of 50 mM clindamycin succinate, 10% MeOH v/v, 50 mM Tris buffer, pH 4.0, at 22 kV and 20 °C within 25 min.  相似文献   
73.
For any formal Laurent series with coefficients cn lying in some given finite field, let x=[a0(x);a1(x),a2(x),…] be its continued fraction expansion. It is known that, with respect to the Haar measure, almost surely, the sum of degrees of partial quotients grows linearly. In this note, we quantify the exceptional sets of points with faster growth orders than linear ones by their Hausdorff dimension, which covers an earlier result by J. Wu.  相似文献   
74.
Authenticity assessment of flavoured strawberry foods was performed using headspace-solid phase microextraction (HS-SPME) coupled to gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS). An authenticity range was achieved, investigating on the carbon isotope ratio of numerous selected aroma active volatile components (methyl butanoate, ethyl butanoate, hex-(2E)-enal, methyl hexanoate, buthyl butanoate, ethyl hexanoate, hexyl acetate, linalool, hexyl butanoate, octyl isovalerate, γ-decalactone and octyl hexanoate) of organic Italian fresh strawberries. To the author's knowledge, this is the first time that all these components were investigated simultaneously by GC-C-IRMS on the same sample. The results were compared, when applicable, with those obtained by analyzing the HS-SPME extracts of commercial flavoured food matrices. In addition, one Kenyan pineapple and one fresh Italian peach were analyzed to determine the δ(13)C(VPDB) of the volatile components common to strawberry. The δ(13)C(VPDB) values are allowed to differentiate between different biogenetic pathways (C(3) and CAM plants) and more interestingly between plants of the same CO(2) fixation group (C(3) plants). Additional analyses were performed on all the samples by means of Enantioselective Gas Chromatography (Es-GC), measuring the enantiomeric distribution of linalool and γ-decalactone. It was found that GC-C-IRMS and Es-GC measurements were in agreement to detect the presence of non-natural strawberry aromas in the food matrices studied.  相似文献   
75.
The 200 MHz 1H NMR spectra of the analgesic, famprofazone, 1, have been studied in CDCl3 solution at ambient temperatures with the achiral lanthanide shift reagent (LSR) tris (6, 6, 7, 7, 8, 8, 8-heptaf luoro-2, 2-dimethyl-3, 5-octanedionato) europium (III), Eu(FOD)3, 2, for spectral simplification, and with the chiral LSR, tris [3-(heptafluoropropylhydroxymethylene) - (+) camphorato] europium (III), Eu (HFC)3, 3. Lanthanide induced shift (LIS) magnitudes suggested predominant LSR binding at the carbonyl oxygen. Substantial enantiomeric shift differences were observed for several nuclei of 1 with added 3 which could permit direct determinations of enantiomeric excess.  相似文献   
76.
氮和磷是水环境生物生长和繁殖必须的营养成分,影响水体初级生产力的水平,且水体富营养化水平与氮磷形态密切相关,随着水体环境的改变,沉积物会向水体释放氮磷,造成二次污染。同时,对外源氮磷污染来源的贡献进行定量识别,可有效管理和控制水体氮磷污染负荷。毗河和石亭江是沱江的重要支流,影响着长江母亲河的水质。采用钼锑抗分光光度法和连续提取法研究在枯水期和丰水期毗河和石亭江水体和表层沉积物中总氮(TN)、总磷(TP)及各形态氮磷的分布特性,对比不同土地利用类型河流氮磷行为特性及释放风险,并采用Multiple Linear Regression of the Absolute Principal Component Scores(APCS-MLR)受体模型进行氮磷污染源的识别和量化。研究结果表明:(1)研究区水体和表层沉积物中氮磷均处于不同程度的污染水平,水体枯水期TP的主要贡献者是颗粒态无机磷(PIP)和颗粒态有机磷(POP),而丰水期却是颗粒态无机磷(PIP)和溶解态无机磷(DIP),两水期水体中TN的主要贡献者是硝态氮(NO-3-N)和有机氮(ON)...  相似文献   
77.
The comparisons of five different chiral stationary phases (CSPs) based on 2,6-dinitro-4-trifluoromethylphenyl (DNP-TFM) ether substituted β-cyclodextrin are presented. The five CSPs differ from each other in the linkage/spacer chemistry, or on the position of the substituents on β-cyclodextrin, or in the sequence of the synthetic procedure. The results show that there are two optimum combinations: (1) DNP-TFM randomly substituted on the β-cyclodextrin as the chiral selector along with a carbamate linkage chain bonding it to the silica support; and (2) β-cyclodextrin derivatized by DNP-TFM substituents only on the C-2 and C-3 positions of the cyclodextrin with an ether linkage chain anchoring it to the silica gel. These two combinations show complementary separations for some enantiomers. The spacer chain effect is much more pronounced for the CSP based on the β-cyclodextrin derivatives with DNP-TFM substituents only on C-2 and C-3 positions than its randomly substituted counterpart. The sequence of derivatizing the cyclodextrin and attaching it to silica gel also affects its selectivity and efficiency. The β-cyclodextrin should be derivatized before it is linked to the silica gel.  相似文献   
78.
Chiral title compounds have been resolved by medium pressure liquid chromatography (MPLC) on triacetylcellulose in ethanol. Whereas a quantitative separation was achieved for16 and20, a recycling technique had to be applied to1,4,6,10 and15 leading to a 100% e.e. for1,6 and15 and to ca. 60% e.e. for4 and10.An unambiguous assignment of the chirality (+)-(R) a -(S) m for tricarbonylchromium-6,6-dimethyl-diphenicacid dimethylester (4) was deduced both from the photochemical decomplexation to (-)-5 with the known chirality (R) a (whose e.e. was determined by MPLC on triacetylcellulose) and by comparison of the1H-n.m.r. spectra of4 and5 thereby proving the structure 4 for the former.Other chiralities both for mono and bis(tricarbonylchromium)biphenyl complexes were established by chemical correlations and comparison of the CD spectra with those of key compounds.
Herrn Prof. Dr.H. Tuppy mit besten Wünschen zum 60. Geburtstag gewidmet.  相似文献   
79.
We define and describe a class of algebraic continued fractions for power series over a finite field. These continued fraction expansions, for which all the partial quotients are polynomials of degree one, have a regular pattern induced by the Frobenius homomorphism.This is an extension, in the case of positive characteristic, of purely periodic expansions corresponding to quadratic power series.  相似文献   
80.
设含幺交换环R对其乘法子集T的分式环为RT,交换幺半群S在其子半群∑处局部化为S∑本文证明了R[S]对于A的分环式环R[S]AM 构于半群环RT[S∑]。  相似文献   
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