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951.
The first examples of metallodendritic spiranes have been obtained via incorporation of single terpyridine units within each dendritic quadrant. 相似文献
952.
The thermal vapor transport of nitrogen-rich carbon nitride powders produces carbon nitride films on substrates that retain significant nitrogen content, have conjugated bond character, and show blue photoluminescent emission near 450 nm. 相似文献
953.
Removal of or replacement of one of two phenylethyl sidearms on azalariats leads to clear evidence for cation-pi interactions with the remaining sidearm. 相似文献
954.
Razavet M Borg SJ George SJ Best SP Fairhurst SA Pickett CJ 《Chemical communications (Cambridge, England)》2002,(7):700-701
Iron(I) in biology?: one-electron oxidation of an (Fe(I)-Fe(I)) carbonyl cyanide precursor bearing a proximal thioether group leads to an (Fe(I)-Fe(II)) bridging carbonyl transient with spectral features similar to the di-iron sub-site of the CO inhibited paramagnetic centre of all-iron hydrogenase. 相似文献
955.
956.
Reactions of aldehydes with 2 equiv of alkyne in the presence of TiX(4) (X = Cl, Br) regioselectively generated 1,5-dihalo-1,4-dienes in moderate to good yields with high (E,Z)-stereoselectivity. [reaction: see text] 相似文献
957.
Miller TJ Farquar HD Sheybani A Tallini CE Saurage AS Fronczek FR Hammer RP 《Organic letters》2002,4(6):877-880
[reaction: see text] The thiazole C-nucleoside analogue was synthesized by the Hantzsch cyclization method to form the thiazole ring and was then converted to the thiazole N-oxide C-nucleoside analogue by peracid oxidation of the heterocycle nitrogen. Incorporation of the thiazole and thiazole N-oxide phosphoramidites into DNA was successful though significant deoxygenation of the N-oxide occurred during DNA assembly. The mechanism proposed for the reduction of the thiazole N-oxide to thiazole involves the formation of an N-oxide phosphite ester. 相似文献
958.
Thalladi VR Schwartz A Phend JN Hutchinson JW Whitesides GM 《Journal of the American Chemical Society》2002,124(33):9912-9917
A new physical model based on mesoscale self-assembly is developed to simulate indentation fracture in crystalline materials. Millimeter-scale hexagonal objects exhibiting atom-like potential functions were designed and allowed to self-assemble into two-dimensional (2D) aggregates at the interface between water and perfluorodecalin. Indentation experiments were performed on these aggregates, and the stresses and strains involved in these processes were evaluated. The stress field in the aggregates was analyzed theoretically using the 2D elastic Hertz solution. Comparison of the experimental results with theoretical analysis revealed that fracture develops in regions subjected to high shear stress and some, albeit low, tensile stress. The potential for the broader application of the model is illustrated using indentation of assemblies with point defects and adatoms introduced at predetermined locations, and using a two-phase aggregate simulating a compliant film on a stiff substrate. 相似文献
959.
Sculimbrene BR Morgan AJ Miller SJ 《Journal of the American Chemical Society》2002,124(39):11653-11656
Peptide-based catalysts have been found that catalyze the enantiodivergent phosphorylation of a meso myo-inositol-derived triol (1). The sequential screening of random peptide libraries, followed by the evaluation of a focused library, led to the identification of two peptides (2 and 24) that are complementary in producing enantiomeric D-myo-inositol-1-phosphate and D-myo-inositol-3-phosphate derivatives. The catalysts were then used to complete efficient total syntheses of both D-I-1P and D-I-3P in optically pure form. Additional information is gleaned from relative rate experiments that unambiguously show the catalysts to afford enantioselection through rate accelerative pathways with respect to simple achiral alkylimidazole catalysts. Furthermore, solvent effect studies show that the two enantiodivergent catalysts exhibit different tolerances of polar media. The systematic discovery of site-selective catalysts establishes a basis for future studies of chiral catalysts that differentiate unique functional groups in polyfunctional molecules. 相似文献
960.
Eckhart E Gan KK Gwon C Hart T Honscheid K Hufnagel D Kagan H Kass R Pedlar TK Thayer JB Von Toerne E Wilksen T Zoeller MM Muramatsu H Richichi SJ Severini H Skubic P Dytman SA Mueller JA Nam S Savinov V Chen S Hinson JW Lee J Miller DH Pavlunin V Shibata EI Shipsey IP Cronin-Hennessy D Lyon AL Park CS Park W Thorndike EH Coan TE Gao YS Liu F Maravin Y Stroynowski R Artuso M Boulahouache C Bukin K Dambasuren E Khroustalev K Mountain R Nandakumar R Skwarnicki T Stone S Wang JC Mahmood AH 《Physical review letters》2002,89(25):251801
We report on a search for charmless hadronic B decays to the three-body final states K(0)(S)h(+)pi(-), K(+)h(-)pi(0), K(0)(S)h(+)pi(0) (h(+/-) denotes a charged pion or kaon), and their charge conjugates, using 13.5 fb(-1) of integrated luminosity produced near sqrt[s]=10.6 GeV, and collected with the CLEO detector. We observe the decay B-->K0pi(+)pi(-) with a branching fraction (50(+10)(-9)(stat.)+/-7(syst.))x10(-6) and the decay B-->K(*+)(892)pi(-) with a branching fraction (16(+6)(-5)(stat.)+/-2(syst.))x10(-6). 相似文献