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41.
This paper deals with the inversive congruential method with power of two modulusm for generating uniform pseudorandom numbers. Statistical independence properties of the generated sequences are studied based on the distribution of triples of successive pseudorandom numbers. It is shown that there exist parameters in the inversive congruential method such that the discrepancy of the corresponding point sets in the unit cube is of an order of magnitude at leastm
–1/3. The method of proof relies on a detailed analysis of certain rational exponential sums. 相似文献
42.
43.
This article completes and simplifies earlier results on the derivation of best linear, or affine, unbiased estimates in the general Gauss-Markov model with a singular dispersion matrix and additional restrictions under very general conditions. We provide the class of all linear representations of the best affine unbiased estimator with precise statements concerning its indeterminacy. 相似文献
44.
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47.
Marty W. DeGroot Chhatra Khadka Harald Rösner John F. Corrigan 《Journal of Cluster Science》2006,17(1):97-110
The thermolysis of the zinc trimethylsilylchalcogenolate complexes (N,N′-tmeda)Zn(ESiMe3)2 (E = S, 1; E = Se, 2) and (3,5-Me2-C5H3N)2Zn(ESiMe3)2 (E = S, 3; E = Se, 4) has been investigated. Solid-state thermal decomposition of complexes 1–4 above 250°C results in the formation of hexagonal ZnS and cubic ZnSe, respectively, via the liberation of TMEDA (1–2) or 3,5-lutidine (3–4) and E(SiMe3)2. Solid-state or solution thermolysis of these complexes up to 200°C produces nanocrystalline ZnS and ZnSe materials whose surface is protected by either coordinated TMEDA or 3,5-lutidine ligands. The progress of the step-wise solid-state decomposition of these complexes was monitored by thermogravimetric and single differential thermal analysis and volatile decomposition products in both solution and solid-state experiments were identified by GC/MS.Dedicated to Professor Brian F. G. Johnson on the occasion of his retirement. 相似文献
48.
Walter Feit 《Israel Journal of Mathematics》1993,82(1-3):141-156
LetK be a field and letG be a finite group.G isK-admissible if there exists a Galois extensionL ofK withG=Gal(L/K) such thatL is a maximal subfield of a centralK-division algebra. This paper contains a characterization of those number fields which areQ
16-admissible. This is the same class of number fields which are 2A
6=SL(2, 9) and 2A
7 admissible.
Dedicated to John Thompson to celebrate his Wolf Prize in Mathematics 1992 相似文献
49.
Harald Hofberger 《Archiv der Mathematik》1993,61(3):238-240
Ohne Zusammenfassung 相似文献
50.
Diemar A. Plattner Andreas Brunner Max Dobler Hans-Martin Müller Walter Petter Peter Zbinden Dieter Seebach 《Helvetica chimica acta》1993,76(5):2004-2033
Cyclic Oligomers of (R)-3-Hydroxybutanoic Acid: Preparation and Structural Aspects The oligolides containing three to ten (R)-3-hydroxybutanoate (3-HB) units (12-through 40-membered rings 1–8 ) are prepared from the hydroxy acid itself, its methyl ester, its lactone (‘monolide’), or its polymer (poly(3-HB), mol. wt. ca. 106 Dalton) under three sets of conditions: (i) treatment of 3-HB ( 10 ) with 2,6-dichlorobenzoyl chloride/pyridine and macrolactonization under high dilution in toluene with 4-(dimethylamino)pyridine (Fig. 3); (ii) heating a solution (benzene, xylene) of the β-lactone 12 or of the methyl ester 13 from 3-HB with the tetraoxadistanna compound 11 as trans-esterification catalyst (Fig. 4); (iii) heating a mixture of poly(3-HB) and toluene-sulfonic acid in toluene/1,2-dichloroethane for prolonged periods of time at ca. 100° (Fig. 6). In all three cases, mixtures of oligolides are formed with the triolide 1 being the prevailing component (up to 50% yield) at higher temperatures and with longer reaction times (thermodynamic control, Figs. 3–6). Starting from rac-β-lactone rac- 12 , a separable 3:1 to 3:2 mixture of the l,u- and the l,l-triolide diasteroisomers rac- 14 and rac- 1 , respectively, is obtained. An alternative method for the synthesis of the octolide 6 is also described: starting from the appropriate esters 15 and 17 and the benzyl ether 16 of 3-HB, linear dimer, tetramer, and octamer derivatives 18–23 are prepared, and the octamer 23 with free OH and CO2H group is cyclized (→ 6 ) under typical macrolactonization conditions (see Scheme). This ‘exponential fragment coupling protocol’ can be used to make higher linear oligomers as well. The oligolides 1–8 are isolated in pure form by vacuum distillation, chromatography, and crystallization, an important analytical tool for determining the composition of mixtures being 13C-NMR spectroscopy (each oligolide has a unique and characteristic chemical shift of the carbonyl C-atom, with the triolide 1 at lowest, the decolide 8 at highest field). The previously published X-ray crystal structures of triolide 1 , pentolide 3 , and hexolide 4 (two forms), as well as those of the l,u-triolide rac- 14 , of tetrolide ent- 2 , of heptolide 5 , and of two modifications of octolide 6 described herein for the first time are compared with each other (Figs. 7–10 and 12–15, Tables 2 and 5–7) and with recently modelled structures (Tables 3 and 4, Fig. 11). The preferred dihedral angles τ1 to τ4 found along the backbone of the nine oligolide structures (the hexamer and the larger ones all have folded rings!) are mapped and statistically evaluated (Fig. 16, Tables 5–7). Due to the occurrence of two conformational minima of the dihedral angle O? CO? CH2? CH (τ3 = + 151 or ?43°), it is possible to locate two types of building blocks for helices in the structures at hand: a right-handed 31 and a left-handed 21 helix; both have a ca. 6 Å pitch, but very different shapes and dispositions of the carbonyl groups (Fig. 17). The 21 helix thus constructed from the oligolide single-crystal data is essentially superimposable with the helix derived for the crystalline domains of poly(3-HB) from stretched-fiber X-ray diffraction studies. The absence of the unfavorable (E)-type arrangements around the OC? OR bond (‘cis-ester’) from all the structures of (3-HB) oligomers known so far suggests that the model proposed for a poly(3-HB)-containing ion channel (Fig. 2) must be modified. 相似文献