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951.
Waluyo I Huang C Nordlund D Weiss TM Pettersson LG Nilsson A 《The Journal of chemical physics》2011,134(22):224507
X-ray absorption spectroscopy (XAS) and small angle x-ray scattering (SAXS) were utilized to study the effect of fluoride (F(-)) anion in aqueous solutions. XAS spectra show that F(-) increases the number of strong H-bonds, likely between F(-) and water in the first hydration shell. SAXS data show a low-Q scattering intensity increase similar to the effect of a temperature decrease, suggesting an enhanced anomalous scattering behavior in F(-) solutions. Quantitative analysis revealed that fluoride solutions have larger correlation lengths than chloride solutions with the same cations but shorter compared to pure water. This is interpreted as an increased fraction of tetrahedral low-density structures in the solutions due to the presence of the F(-) ions, which act as nucleation centers replacing water in the H-bonding network and forming stronger H-bonds, but the presence of the cations restricts the extension of strong H-bonds. 相似文献
952.
A novel synthetic data generation methodology is described for use in the development of pattern recognition classifiers that are employed for the automated detection of volatile organic compounds (VOCs) during infrared remote sensing measurements. The approach used is passive Fourier transform infrared spectrometry implemented in a downward-looking mode on an aircraft platform. A key issue in developing this methodology in practice is the need for example data that can be used to train the classifiers. To replace the time-consuming and costly collection of training data in the field, this work implements a strategy for taking laboratory analyte spectra and superimposing them on background spectra collected from the air. The resulting synthetic spectra can be used to train the classifiers. This methodology is tested by developing classifiers for ethanol and methanol, two prevalent VOCs in wide industrial use. The classifiers are successfully tested with data collected from the aircraft during controlled releases of ethanol and during a methanol release from an industrial facility. For both ethanol and methanol, missed detections in the aircraft data are in the range of 4 to 5%, with false positive detections ranging from 0.1 to 0.3%. 相似文献
953.
Cross-coupling of mesylated phenol derivatives with various potassium alkoxymethyltrifluoroborates has been achieved. The corresponding aryl and heteroaryl alkoxymethyl compounds have been obtained with equal facility with both electron-rich and electron-poor substituents on the activated alcohol. 相似文献
954.
Xiao Zhou Yali Lu Wenjing Wang Babak Borhan Gavin E. Reid 《Journal of the American Society for Mass Spectrometry》2010,21(8):1339-1351
Protein surface accessible residues play an important role in protein folding, protein-protein interactions and protein-ligand
binding. However, a common problem associated with the use of selective chemical labeling methods for mapping protein solvent
accessible residues is that when a complicated peptide mixture resulting from a large protein or protein complex is analyzed,
the modified peptides may be difficult to identify and characterize amongst the largely unmodified peptide population (i.e.,
the ‘needle in a haystack’ problem). To address this challenge, we describe here the development of a strategy involving the
synthesis and application of a novel ‘fixed charge’ sulfonium ion containing lysine-specific protein modification reagent,
S,S′-dimethylthiobutanoylhydroxysuccinimide ester (DMBNHS), coupled with capillary HPLC-ESI-MS, automated CID-MS/MS, and data-dependant
neutral loss mode MS3 in an ion trap mass spectrometer, to map the surface accessible lysine residues in a small model protein, cellular retinoic
acid binding protein II (CRABP II). After reaction with different reagent:protein ratios and digestion with Glu-C, modified
peptides are selectively identified and the number of modifications within each peptide are determined by CID-MS/MS, via the
exclusive neutral loss(es) of dimethylsulfide, independently of the amino acid composition and precursor ion charge state
(i.e., proton mobility) of the peptide. The observation of these characteristic neutral losses are then used to automatically
‘trigger’ the acquisition of an MS3 spectrum to allow the peptide sequence and the site(s) of modification to be characterized. Using this approach, the experimentally
determined relative solvent accessibilities of the lysine residues were found to show good agreement with the known solution
structure of CRABP II. 相似文献
955.
Indigo is one of the oldest dyes manufactured chemically and is mostly used in textile, food, and pharmaceutical industries.
However, owing to the environmental hazards posed by the chemical production, the present scenario in the field stipulates
a biosynthesis alternative for indigo production. The present study describes an indigenously isolated naphthalene-degrading
strain Pseudomonas sp. HOB1 producing a blue pigment when indole was added in the growth medium. This blue pigment was analyzed by high-pressure
thin-layer chromatography and other spectroscopic techniques which revealed it to be the indigo dye. Pseudomonas sp. HOB1 showed ability to produce 246 mg indigo liter−1 of the medium. The K
m for the enzyme naphthalene dioxygenase which is involved in indigo formation is 0.3 mM, and V
max was as high as 50 nmol min−1 mg dry biomass−1. The bacterial indigo dye was further successfully applied for dyeing cotton fabrics. The high indigo productivity of Pseudomonas sp. HOB1 using naphthalene as growth substrate and its applicability on cotton fabrics, therefore, stems the probability
of using this culture for commercial indigo production. 相似文献
956.
Sanjay S. Latthe Hiroaki Imai V. Ganesan Charles Kappenstein A. Venkateswara Rao 《Journal of Sol-Gel Science and Technology》2010,53(2):208-215
Optically transparent silica films were prepared at room temperature (~27°C) by keeping the molar ratio of TEOS:MeOH:H2O (0.001 M NH4F) constant at 1:19.29:6.20, respectively. A surface chemical modification of the films was done with alkylchlorosilanes at
different concentrations from 0 to 1 vol. % and aging times varied from half to 2 h. The DMCS and TMCS surface modified silica
films showed the static water contact angle of 146° and 162°, respectively. When the DMCS and TMCS modified films were cured
at temperatures higher than 240 and 275°C, respectively, the films became superhydrophilic. Further, the humidity study was
carried out at a relative humidity of 90% at 30°C temperature over 60 days. We characterized the water repellent silica films
by Fourier transform infrared spectroscopy, scanning electron microscopy, atomic force microscopy, % of optical transmission,
humidity tests and contact angle measurements. 相似文献
957.
Nives Škrlj Vladka Čurin Šerbec Marko Dolinar 《Applied biochemistry and biotechnology》2010,160(6):1808-1821
Prion diseases are incurable neurodegenerative diseases that affect both humans and animals. The infectious agent is a pathogenic
form of the prion protein that accumulates in brain as amyloids. Currently, there is neither cure nor reliable preclinical
diagnostics on the market available. The growing number of reports shows that passive immunisation is one of the most promising
strategies for prion disease therapy, where antibodies against prions may prevent and even cure the infection. Since antibodies
are large molecules and, thus, might not be suitable for the therapy, different antibody fragments are a good alternative.
Therefore, we have designed and prepared single-chain antibody fragments (scFvs) derived from the PrPSc-specific murine monoclonal antibody V5B2. Using a new expression vector pMD204, we produced scFvs in two opposing chain orientations
in the periplasm of Escherichia coli. Both recombinant antibody fragments retained the specificity of the parent antibody and one of these exhibited binding properties
comparable to the corresponding murine Fab fragments with the affinity in nM range. Our monovalent antibody fragments are
of special interest in view of possible therapeutic reagents for prion diseases as well as for development of a new generation
of diagnostics. 相似文献
958.
Francisco López-Suevos Christian Eyholzer Nico Bordeanu Klaus Richter 《Cellulose (London, England)》2010,17(2):387-398
Suspensions of commercial refined beech pulp (RBP) were further processed through mechanical disintegration (MD-RBP), chemical
modification (CM-RBP) and through chemical modification followed by mechanical disintegration (CM-MD-RBP). Nanocomposites
were prepared by compounding a poly(vinyl acetate) (PVAc) latex adhesive with increasing contents of the different types of
nanofibrils, and the resulting nanocomposites were analyzed by dynamic mechanical analysis (DMA). Also, the suitability of
using the CM-RBP fibrils to formulate PVAc adhesives for wood bonded assemblies with improved heat resistance was studied.
The presence of cellulose nanofibrils had a strong influence on the viscoelastic properties of PVAc latex films. For all nanocomposites,
increasing amounts of cellulose nanofibrils (treated or untreated) led to increasing reinforcing effects in the glassy state,
but especially in the PVAc and PVOH glass transitions. This reinforcement primarily resulted from interactions between the
cellulose fibrils network and the hydrophilic PVOH matrix that led to the complete disappearance of the PVOH glass transition
(tan δ peak) for some fibril types and contents. At any given concentration in the PVOH transition, the CM-MD-RBP nanofibrils
provided the highest reinforcement, followed by the MD-RBP, CM-RBP and the untreated RBP. Finally, the use of the CM-RBP fibrils
to prepare PVAc reinforced adhesives for wood bonding was promising since, even though they generally performed worse in dry
and wet conditions, the boards showed superior heat resistance (EN 14257) and passed the test for durability class D1. 相似文献
959.
Inhibition effect of imidazole derivative 1,7′-dimethyl-2′-propyl-1H,3′H-2,5′-bibenzo[d]imidazole (DPBI) against mild steel corrosion in 1 M HCl solutions was evaluated using the conventional mass loss method,
potentiodynamic polarization, linear polarization, and electrochemical impedance spectroscopy. The mass loss results showed
that DPBI is an excellent corrosion inhibitor; electrochemical polarizations data revealed the mixed mode of inhibition; and
the results of electrochemical impedance spectroscopy showed that the change in the impedance parameters, charge transfer
resistance, and double layer capacitance with the change in the concentration of the inhibitor is due to the adsorption of
the molecule leading to the formation of a protective layer on the surface of mild steel. The inhibition action of this compound
was assumed to occur via adsorption on the steel surface through the active centers of the molecule. 相似文献
960.
Jia-Zheng Lu Yi-fan Du Bin Wu Jin-Wang Huang Jing Jiang 《Transition Metal Chemistry》2010,35(4):451-456
A fluorescein–porphyrin hybrid (Fl-PTPP) has been synthesized and characterized by UV/Vis, IR, 1H NMR, ES-MS and elemental analysis. The supramolecular self-assembly of Fl-PTPP with the copper(II) complex of 5-(p-amino-phenyl)-10,15,20-triphenylporphyrin, (CuAPTPP), by hydoxyl-amino type hydrogen bonding was studied using vapor pressure
osmometry (VPO) measurements, ES-MS, UV/Vis, 1H NMR and fluorescence spectroscopic titration. The data indicate formation of a (Fl-PTPP)–CuAPTPP supramolecular complex.
Fluorescence strengthening character was observed in a spectroscopic titration experiment for the Fl-PTPP/CuAPTPP system.
The association constant of the supramolecular complex was calculated from the fluorescence titration data, and found to be
less than that of a carboxyl–carboxyl type hydrogen-bonding system. 相似文献