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81.
Let I = [0, 1], c
1, c
2 ∈ (0, 1) with c
1 < c
2 and f : I⊸I be a continuous map satisfying:
are both strictly increasing and
is strictly decreasing. Let A = {x ∈ [0, c
1]∣f(x) = x},
a=max A, a
1 =max(A\{a}), and B = {x ∈ [c
2, 1]∣f(x) = x}, b=minB, b
1 =min(B\{b}). Then the inverse
limit (I, f) is an arc if and only if one of the following three conditions holds:
(1) If c
1 < f (c
1) ≤ c
2 (resp. c
1 ≤ f (c
2) < c
2), then f has a single fixed point, a period two orbit,
but no points of period greater than two or f has more than one fixed point but no points of other periods, furthermore, if A≠φ and B≠φ, then f (c
2) > a (resp. f (c
1) < b).
(2) If f (c
1) ≤ c
1 (resp. f (c
2) ≥ c
2), then f has more than one fixed point, furthermore, if B≠φ and A\ {a} ≠φ, f (c
2) ≥ a or if a
1 < f (c
2) < a, f
2 (c
2) > f (c
2), (resp. f has more than one fixed point, furthermore, if A≠φ and B\{b}≠φ, f (c
1) ≤ b or if b < f (c
2) < b
1, f
2 (c
1) < f (c
1)).
(3) If f (c
1) > c
2 and f (c
2) < c
1, then f has a single fixed point, a single period two orbit lying in I\(u, v) but no points of period greater than two, where u, v ∈ [c
1, c
2] such that f (u) = c
2 and f (v) = c
1.
Supported by the National Natural Science Foundation of China (No. 19961001, No. 60334020) and Outstanding Young Scientist
Research Fund. (No. 60125310) 相似文献
82.
Molality as a unit of measure for expressing 1H MRS brain metabolite concentrations in vivo 总被引:1,自引:0,他引:1
Knight-Scott J Haley AP Rossmiller SR Farace E Mai VM Christopher JM Manning CA Simnad VI Siragy HM 《Magnetic resonance imaging》2003,21(7):787-797
Absolute concentrations of cerebral metabolite in in vivo 1H magnetic resonance spectroscopy studies (1H-MRS) are widely reported in molar units as moles per liter of tissue, or in molal units as moles per kilogram of tissue. Such measurements require external referencing or assumptions as to local water content. To reduce the scan time, avoid assumptions that may be invalid under specific pathologies, and provide a universally accessible referencing procedure, we suggest that metabolite concentrations from 1H-MRS measurements in vivo be reported in molal units as moles per kilogram of tissue water. Using internal water referencing, a two-compartment water model, a simulated brain spectrum for peak identification, and a spectroscopic bi-exponential spin-spin relaxation segmentation technique, we measured the absolute concentrations for the four common 1H brain metabolites: choline (Cho), myo-inositol (mIno), phosphocreatine + creatine (Cr), and N-acetyl-aspartate (NAA), in the hippocampal region (n = 26) and along the Sylvian fissure (n = 61) of 35 healthy adults. A stimulated echo localization method (20 ms echo time, 10 ms mixing time, 4 s repetition time) yielded metabolite concentrations, uncorrected for metabolite relaxation or contributions from macromolecule resonances, that were expectantly higher than with molar literature values. Along the Sylvian fissure the average concentrations (coefficient of variation (CV)) in mmoles/kg of tissue water were 17.6 (12%) for NAA, 14.2 (9%) for Cr, 3.6 (13%) for Cho, and 13.2 (15%) for mIno. Respective values for the hippocampal region were 15.7 (20%), 14.7 (16%), 4.6 (19%), and 17.7 (26%). The concentrations of the two regions were significantly different (p = 0.001) for NAA, mIno, and Cho, a trend in agreement with previous studies. All gray matter Sylvian fissure CV values, except for NAA, were also in agreement with previous 1H-MRS gray matter studies. The reduced precision of the NAA concentration was attributed to overlapping signal contributions from glutamate and glutamine (Glx), suggesting that a detailed Glx model is critical for accurate quantitation of the NAA 2.02 ppm resonance. The reduced precision of the measurements in the hippocampal region was attributed to poor spectral resolution. 相似文献
83.
Aoyagi Y Saitoh Y Ueno T Horiguchi M Takeya K Williams RM 《The Journal of organic chemistry》2003,68(18):6899-6904
Lipase TL-mediated kinetic resolution of (+/-)-5-benzyloxy-1-tert-butyldimethylsilyloxy-2-pentanol (5) at low temperature proceeded to give the corresponding (S)-alcohol 5 and (R)-acetate 6 in quantitative yields with high enantiomeric purity. The addition of bases such as pyridine, DMAP, 2,4- and 2,6-lutidines, or triethylamine considerably enhanced the rate of kinetic resolution. The alcohol (S)-5 and the acetate (R)-6 were converted to piperazic acid derivatives (R)- and (S)-3, respectively, via the intramolecular Mitsunobu reaction as a key step. 相似文献
84.
Synthesis of a new insoluble polymer-supported chiral alcohol auxiliary and its first application to nucleophilic addition to ketenes 总被引:2,自引:0,他引:2
Akkari R Calmes M Mai N Rolland M Martinez J 《The Journal of organic chemistry》2001,66(17):5859-5865
The preparation of a new optically active alcohol with a carboxylic function that allowed its attachment to an amine-functionalized insoluble polymer is described. Its first use as a polymer supported chiral auxiliary is demonstrated by asymmetric transformation of two racemic aryl propionic acids via ketene formation (95-96% ee). 相似文献
85.
Low density lipoprotein-cholesterol (LDL-c) concentration measured by a homogeneous enzymatic assay was reported to correlate well with the modified beta-quantification assay, especially in samples with high triglyceride (TG) concentration. In this study, we evaluated a homogeneous enzymatic assay, Cholestest-LDL assay system, in hypertriglycemic patient samples, and found that 56% (9/16) of serum samples with intermediate TG concentrations (2.27-4.52 mmol/L) showed more than 10% discrepancy with concentration by the modified beta-quantification assay. Such serum samples originated from patients with hyperglycemia of type II a (three cases), type II b (two cases), type III (one case), and type IV (six cases). Differential staining of cholesterol and triglyceride after agarose gel electrophoresis revealed that these serum samples contained significant amounts of intermediate fractions between pre-beta- and beta-lipoproteins. Since lipoprotein (a), which migrates between pre-beta- and beta-lipoproteins, is not correlated with the discrepancy, we believe the intermediate fraction consists of intermediate density lipoprotein (IDL) and a chylomicron remnant. A part of IDL and chylomicron remnant, which contain a significant amount of triglyceride, might be measured as LDL-c by the homogeneous enzymatic assay, but not by the modified beta-quantification assay. 相似文献
86.
87.
B. Ittermann M. Füllgrabe M. Heemeier F. Kroll F. Mai K. Marbach P. Meier D. Peters G. Welker W. Geithner S. Kappertz S. Wilbert R. Neugart P. Lievens U. Georg M. Keim 《Hyperfine Interactions》2000,129(1-4):423-441
β-active probe nuclei are implanted in nominally undoped ZnSe crystals. β-radiation detected nuclear magnetic resonance (β-NMR)
studies are described for two different probe nuclei, 8Li and 12B. This way, the implantation behavior of two “opposite”dopants, one acceptor (Li) and one donor (B) can be characterized
by the same microscopic technique. Such characterizations are attempted in terms of the structure of intermediate or final
lattice sites, defect charge states, or the kinetics of defect reactions and site changes.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
88.
89.
90.
A. Gautier C. Mai G. Lockemann H. B. Bishop und Zoltan de Vamossy 《Fresenius' Journal of Analytical Chemistry》1906,45(12):767-768
Ohne Zusammenfassung 相似文献