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111.
The quaternary copper chalcogenide Cu(2)ZnSnS(4) is an important emerging material for the development of low-cost and sustainable solar cells. Here we report a facile solution synthesis of stoichiometric Cu(2)ZnSnS(4) in size-controlled nanorod form (11 nm × 35 nm). The monodisperse nanorods have a band gap of 1.43 eV and can be assembled into perpendicularly aligned arrays by controlled evaporation from solution. 相似文献
112.
Raman microscopy is employed to spectroscopically image biological cells previously exposed to fluorescently labelled polystyrene nanoparticles and, in combination with K-means clustering and principal component analysis (PCA), is demonstrated to be capable of localising the nanoparticles and identifying the subcellular environment based on the molecular spectroscopic signatures. The neutral nanoparticles of 50 nm or 100 nm, as characterised by dynamic light scattering, are shown to be non-toxic to a human lung adenocarcinoma cell-line (A549), according to a range of cytotoxicity assays including Neutral Red, Alamar Blue, Coomassie Blue and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT). Confocal fluorescence microscopy identifies intracellular fluorescence due to the nanoparticle exposure, but the fluorescence distribution is spatially diffuse, potentially due to detachment of the dye from the nanoparticles, and the technique fails to unambiguously identify the distribution of the nanoparticles within the cells. Raman spectroscopic mapping of the cells in combination with K-means cluster analysis is used to clearly identify and localise the polystyrene nanoparticles in exposed cells, based on their characteristic spectroscopic signatures. PCA identifies the local environment as rich in lipidic signatures which are associated with localisation of the nanoparticles in the endoplasmic reticulum. The importance of optimised cell growth conditions and fixation processes is highlighted. The preliminary study demonstrates the potential of the technique to unambiguously identify and locate nonfluorescent nanoparticles in cells and to probe not only the local environment but also changes in the cell metabolism which may be associated with cytotoxic responses. 相似文献
113.
Gas giants are believed to form by the accretion of hydrogen-helium gas around an initial protocore of rock and ice. The question of whether the rocky parts of the core dissolve into the fluid H-He layers following formation has significant implications for planetary structure and evolution. Here we use ab initio calculations to study rock solubility in fluid hydrogen, choosing MgO as a representative example of planetary rocky materials, and find MgO to be highly soluble in H for temperatures in excess of approximately 10,000 K, implying the potential for significant redistribution of rocky core material in Jupiter and larger exoplanets. 相似文献
114.
Lawford Hugh G. Rousseau Joyce D. Tolan Jeffrey S. 《Applied biochemistry and biotechnology》2001,91(1-9):133-146
Iogen Corporation of Ottawa, Canada, has recently built a 50 t/d biomass-to-ethanol demonstration plant adjacent to its enzyme
production facility. Iogen has partnered with the University of Toronto to test the C6/C5 cofermentation performance characteristics
of National Renewable Energy Laboratory's metabolically engineered Zymomonas mobilis using its biomass hydrolysates. In this study, the biomass feedstock was an agricultural waste, namely oat hulls, which was
hydrolyzed in a proprietary two-stage process involving pretreatment with dilute sulfuric acid at 200–250°C, followed by cellulase
hydrolysis. The oat hull hydrolysate (OHH) contained glucose, xylose, and arabinose in a mass ratio of about 8:3:0.5. Fermentation
media, prepared from diluted hydrolysate, were nutritionally amended with 2.5 mL/L of corn steep liquor (50% solids) and 1.2
g/L of diammonium phosphate. The estimated cost for large-scale ethanol production using this minimal level of nutrient supplementation
was 4.4c/gal of ethanol. This work examined the growth and fermentation performance of xyloseutilizing, tetracycline-resistant,
plasmid-bearing, patented, recombinant Z. mobilis cultures: CP4:pZB5, ZM4:pZB5, 39676:pZB4L, and a hardwood prehydrolysate-adapted variant of 39676:pZB4L (designated asthe
“adapted” strain). In pH-stat batch fermentations with unconditioned OHH containing 6% (w/v) glucose, 3% xylose, and 0.75%
acetic acid, rec Zm ZM4:pZB5 gave the best performance with a fermentation time of 30h, followed by CP4:pZB5 at 48h, with
corresponding volumetric productivities of 1.4 and 0.89 g/(L·h), respectively. Based on the available glucose and xylose,
the process ethanol yield for both strains was 0.47 g/g (92% conversion efficiency). At 48 h, the process yield for rec Zm
39676:pZB4L and the adapted strain was 0.32 and 0.34 g/g, respectively. None of the test strains was able to fermentarabinose.
Acetic acid tolerance appeared to be a major determining factor in cofermentation performance. 相似文献
115.
Chung‐Der Chen Andrew P. J. Brunskill Stan S. Hall Roger A. Lalancette Hugh W. Thompson 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(9):1148-1151
α‐Oxobenzeneacetic (phenylglyoxylic) acid, C8H6O3, adopts a transoid dicarbonyl conformation in the solid state, with the carboxyl group rotated 44.4 (1)° from the nearly planar benzoyl moiety. The heterochiral acid‐to‐ketone catemers [O?O = 2.686 (3) and H?O = 1.78 (4) Å] have a second, longer, intermolecular O—H?O contact to a carboxyl sp3 O atom [O?O = 3.274 (2) and H?O = 2.72 (4) Å], with each flat ribbon‐like chain lying in the bc plane and extending in the c direction. In α‐oxo‐2,4,6‐trimethylbenzeneacetic (mesitylglyoxylic) acid, C11H12O3, the ketone is rotated 49.1 (7)° from planarity with the aryl ring and the carboxyl group is rotated a further 31.2 (7)° from the ketone plane. The solid consists of chiral conformers of a single handedness, aggregating in hydrogen‐bonding chains whose units are related by a 31 screw axis, producing hydrogen‐bonding helices that extend in the c direction. The hydrogen bonding is of the acid‐to‐acid type [O?O = 2.709 (6) and H?O = 1.87 (5) Å] and does not formally involve the ketone; however, the ketone O atom in the acceptor molecule has a close polar contact with the same donor carboxyl group [O?O = 3.005 (6) and H?O = 2.50 (5) Å]. This secondary hydrogen bond is probably a major factor in stabilizing the observed cisoid dicarbonyl conformation. Several intermolecular C—H?O close contacts were found for the latter compound. 相似文献
116.
Thomas Marley 《manuscripta mathematica》2001,104(4):519-525
Let R be a commutative Noetherian local ring of dimension d, I an ideal of R, and M a finitely generated R-module. We prove that the set of associated primes of the local cohomology module H
i
I
(M) is finite for all i≥ 0 in the following cases: (1) d≤ 3; (2) d= 4 and $R$ is regular on the punctured spectrum; (3) d= 5, R is an unramified regular local ring, and M is torsion-free. In addition, if $d>0$ then H
d
− 1
I
(M) has finite support for arbitrary R, I, and M.
Received: 31 October 2000 / Revised version: 8 January 2001 相似文献
117.
Hugh W. Thompson Roger A. Lalancette Andrew P. J. Brunskill 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(5):632-633
The hemihydrate of the title diketo acid, C24H36O4·0.5H2O, forms hydrogen‐bonded carboxyl dimers related by a C2 axis at crystallographic sites on the a and b edges of the chosen cell [O?O = 2.643 (7) and 2.716 (7) Å]. The ketone ends of the molecules approach each other at sites near (½,½,½), (½,0,½), (0,0,½) and (0,½,½) in an interleaved arrangement incorporating partial‐occupancy water hydrogen bonded to the B‐ring ketone. 相似文献
118.
Shulin Zhao Chandan Prasad Hugh J. F. Robertson Y.-M. Liu 《Analytical and bioanalytical chemistry》2001,369(3-4):220-224
A capillary electrophoresis (CE) method with laser induced fluorescence (LIF) detection is described for quantification of enterostatin (Val-Pro-Asp-Pro-Arg), a pentapeptide involved in appetite regulation and insulin secretion. Enterostatin and two other pentapeptides belonging to the enterostatin family (i.e. Ala-Pro-Gly-Pro-Arg and Val-Pro-Gly-Pro-Arg) were well separated from each other. The peptides were fluorescently tagged with naphthalene-2,3- dicarboxaldehyde (NDA) and separated by micellar electrokinetic chromatography (MEKC) in the presence of methanol as an organic modifier. Coupled with LIF detection, the method had a detection limit of 4.8 × 10–6 M for enterostatin. The relative standard deviation was to be 4.0% from five determinations of enterostatin at 37.2 μM in a human cerebrospinal fluid (CSF) sample. Twenty-three human CSF samples were analyzed. The level of enterostatin ranged from 24 μM to 51 μM with a mean (± SEM) value of 41.7 ± 2.0 μM. 相似文献
119.
Alan Barcon Andrew P. J. Brunskill Roger A. Lalancette Hugh W. Thompson Allan J. Miller 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(3):325-328
The crystal structure of (±)-4-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (C11H10O3) involves projection of the carboxyl group nearly orthogonal to the aromatic plane and hydrogen bonding of the acid groups by centrosymmetric pairing across the a edge and the center of the chosen cell [O⃛O = 2.705 (2) Å]. Intermolecular C—H⃛O=C close contacts to translationally related molecules are found for both the ketone (2.55 Å) and the acid (2.67 Å). In (±)-1-oxo-1,2,3,4-tetrahydronaphthalene-2-acetic acid (C12H12O3), the aggregation involves centrosymmetric carboxyl dimers mutually hydrogen bonded across the bc face and the a edge of the chosen cell [O⃛O = 2.674 (2) Å]. A 2.60 Å close C—H⃛O=C contact is found to the carboxyl group of centrosymmetrically related molecule. 相似文献
120.
Alcorta M Rehm KE Back BB Bedoor S Bertone PF Deibel CM DiGiovine B Esbensen H Greene JP Hoffmann CR Jiang CL Lighthall JC Marley ST Pardo RC Paul M Rogers AM Ugalde C Wuosmaa AH 《Physical review letters》2011,106(17):172701
The structure of (15)C, with an s(1/2) neutron weakly bound to a closed-neutron shell nucleus (14)C, makes it a prime candidate for a one-neutron halo nucleus. We have for the first time studied the cross section for the fusion-fission reaction (15)C+(232)Th at energies in the vicinity of the Coulomb barrier and compared it to the yield of the neighboring (14)C+(232)Th system measured in the same experiment. At sub-barrier energies, an enhancement of the fusion yield by factors of 2-5 was observed for (15)C, while the cross sections for (14)C match the trends measured for (12,13)C. 相似文献