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Friction plays a key role in the efficiency and stability of the slip-controlled torque converter clutches. The effects of
friction on the dynamics and stability of a slip-controlled torque converter clutch system using a bifurcation-analysis-based
approach is presented in this paper. A three degree-of-freedom nonlinear driveline model with integral feedback action to
control the clutch slip speed has been utilized for this study. The clutch interface friction is dependent on the slip speed
and is a function of the static friction constant, μ
0, the low velocity friction constant μ
1, and the low velocity exponential rate, γ. Using one-parameter numerical continuation, local Hopf bifurcations of the subcritical type are observed as the friction
parameters μ
1 and γ were varied at low slip speeds. The continuation results are verified using simulations of the full nonlinear model. Stick-slip
and undesirable oscillations of the model inertia elements are observed for certain parameter values. As the slip speed is
increased, the bifurcation instability occurs at an increasingly higher value of μ
1 signifying an improved tolerance of negative friction gradient at higher slip speeds. Smaller exponential rates γ are tolerated at higher slip speeds before the bifurcation instability occurs. For the range of parameter values considered,
no bifurcations occur for a slip speeds higher than 3.4 and 4.5 rad/s with μ
1 and γ as the continuation parameters, respectively. These values of slip speeds are much lower than the system’s first mode of
torsional vibration of 16 Hz (≈100 rad/s). 相似文献
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117.
Venkatramani R Davis KL Wierzbinski E Bezer S Balaeff A Keinan S Paul A Kocsis L Beratan DN Achim C Waldeck DH 《Journal of the American Chemical Society》2011,133(1):62-72
We present evidence for a near-resonant mechanism of charge transfer in short peptide nucleic acid (PNA) duplexes obtained through electrochemical, STM break junction (STM-BJ), and computational studies. A seven base pair (7-bp) PNA duplex with the sequence (TA)(3)-(XY)-(TA)(3) was studied, in which XY is a complementary nucleobase pair. The experiments showed that the heterogeneous charge transfer rate constant (k(0)) and the single-molecule conductance (σ) correlate with the oxidation potential of the purine base in the XY base pair. The electrochemical measurements showed that the enhancement of k(0) is independent, within experimental error, of which of the two PNA strands contains the purine base of the XY base pair. 7-bp PNA duplexes with one or two GC base pairs had similar measured k(0) and conductance values. While a simple superexchange model, previously used to rationalize charge transfer in single stranded PNA (Paul et al. J. Am. Chem. Soc. 2009, 131, 6498-6507), describes some of the experimental observations, the model does not explain the absence of an enhancement in the experimental k(0) and σ upon increasing the G content in the duplexes from one to two. Moreover, the superexchange model is not consistent with other studies (Paul et al. J. Phys. Chem. B 2010, 114, 14140), that showed a hopping charge transport mechanism is likely important for PNA duplexes longer than seven base pairs. A quantitative computational analysis shows that a near-resonant charge transfer regime, wherein a mix of superexchange and hopping mechanisms are expected to coexist, can rationalize all of the experimental results. 相似文献
118.
Campylobacter jejuni is found in the intestines of poultry, cattle, swine, wild birds and pet animals and is the major cause of foodborne gastroenteritis in developed countries. We report the use of the receptor binding protein (RBP) of Campylobacter bacteriophage NCTC 12673 for the specific capture of Campylobacter jejuni bacteria using RBP-derivatized capturing surfaces. The Gp48 RBP was expressed as a glutathione S-transferase-Gp48 (GST-Gp48) fusion protein and immobilized onto surface plasmon resonance (SPR) surfaces using glutathione self-assembled monolayers (GSH SAM). Bovine serum albumin (BSA) was used to block any non-specific binding. Glutathione SAM leads to an oriented attachment of the protein, resulting in a two- to three-fold improvement of bacterial capture when compared to dithiobis(succinimidyl propionate) (DTSP) SAM-based unoriented attachment. The specificity of recognition was confirmed using Salmonella enterica subsp. enterica serovar Typhimurium as a negative control, which indeed showed negligible binding. The detection limit of the RBP-derivatized SPR surfaces was found to be 10(2) cfu/ml. Finally, GST-Gp48 was also immobilized onto magnetic beads that were successfully used to capture and pre-concentrate the host pathogen from suspension. 相似文献
119.
Roy AS Biswas MK Weyhermüller T Ghosh P 《Dalton transactions (Cambridge, England : 2003)》2011,40(1):146-155
Two bis(unsymmetrical diimine) complexes of (L(NO(2))(?1))(L(NO(2))(?2))M(II)Cl(2) family with M = Fe and Mn, are reported (L(NO(2))(?) = (E)-3-nitro-N-(pyridine-2-ylmethylene)aniline; ? = dihedral angle between the diimine unit including pyridine ring and the phenyl ring planes). Pure tcc-(L(NO2)(33.6))(L(NO2)(79.3))Fe(II)Cl(2)·0.5H(2)O (1) and tcc-(L(NO2)(32.0))(L(NO2)(79.4))Mn(II)Cl(2)·0.5H(2)O (2) isomers have been successfully isolated in high yields and characterized by elemental analyses, variable temperature magnetic susceptibility measurements, IR, mass, UV-vis and M?ssbauer spectra including the single-crystal X-ray structure determinations that identified strong intermolecular non-bonding interactions in lattice (tcc refers to trans-cis-cis positions with respect to pyridine N-imine N-Cl donors). Geometries optimizations of all possible tcc, ttt, ctc, ccc and cct isomers of iron at the B3LYP/DFT level in gas-phase have shown that the tcc-isomer incorporating two non-equivalent ligands as in (L(NO(2))(42))(L(NO(2))(61))Fe(II)Cl(2), 1 (g), is stabilized by 6-20 kJ mol(-1) compared to other isomers where two ligands are equivalent. The frozen methanol glasses of 1 and 2 are luminescent at 77 K (1: λ(ext) = 370, λ(em) = 521 nm, χ(2) = 1.3, τ(avg) = 0.57 ns; 2: λ(ext) = 368, λ(em) = 524 nm, χ(2) = 1.1, τ(avg) = 0.90 ns). The DFT calculations have identified four closely spaced localized π(*) orbitals comprising of two non-equivalent ligands as UPMOs. The features contrast the tcc-isomer of (L(?))(2)Fe(II)Cl(2) (3), congener of 1 without -NO(2) substitution and non-emissive (bpy)(2)Fe(II)Cl(2) (4) where two ligands are equivalent. TD-DFT calculations have assigned intra-ligand (IL) and ligand to ligand charge transfer (LLCT) dominated excited states as the origin of luminescence of 1 and 2. 相似文献
120.
Mohana Krishna Reddy Mudiam Rajeev Jain Virendra K. Dua Amit Kumar Singh V. P. Sharma R. C. Murthy 《Analytical and bioanalytical chemistry》2011,401(5):1699-1705
A simple and rapid analytical method based on in-matrix ethyl chloroformate (ECF) derivatization has been developed for the
quantitative determination of bisphenol-A (BPA) in milk and water samples. The samples containing BPA were derivatised with
ECF in the presence of pyridine for 20 s at room temperature, and the non-polar derivative thus formed was extracted using
polydimethylsiloxane solid-phase microextraction (SPME) fibres with thicknesses of 100 μm followed by analysis using gas chromatography–mass
spectrometry. Three alkyl chloroformates (methyl, ethyl and isobutyl chloroformate) were tested for optimum derivatisation
yields, and ECF has been found to be optimum for the derivatisation of BPA. Several parameters such as amount of ECF, pyridine
and reaction time as well as SPME parameters were studied and optimised in the present work. The limit of detection for BPA
in milk and water samples was found to be 0.1 and 0.01 μg L−1, respectively, with a signal-to-noise ratio of 3:1. The limit of quantitation for BPA in milk and water was found to be 0.38
and 0.052 μg L−1, respectively, with a signal-to-noise ratio of 10:1. In conclusion, the method developed was found to be rapid, reliable
and cost-effective in comparison to silylation and highly suitable for the routine analysis of BPA by various food and environmental
laboratories. 相似文献