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81.
We count derangements, involutions and unimodal elements in the wreath product C
r
≀ S
n
by the numbers of excedances, fixed points and 2-cycles. Properties of the generating functions, including combinatorial
formulas, recurrence relations and real-rootedness are studied. The results obtained specialize to those on the symmetric
group S
n
and on the hyperoctahedral group B
n
when r = 1, 2, respectively. 相似文献
82.
B. Manz P. S. Chow L. F. Gladden 《Journal of magnetic resonance (San Diego, Calif. : 1997)》1999,136(2):226
A modified version of the echo-planar imaging technique incorporating a Carr–Purcell train of 180° rf pulses (PEPI) has been implemented on a standard spectrometer. It is demonstrated that artifacts in the image due to cumulative errors in the rf field can be reduced by replacing each 180° pulse by a composite sequence of three rf pulses. Artifact-free 3D images at 94 μm voxel resolution are obtained within 15 min. This technique has been applied to study the drying process in an initially water-saturated model porous medium with characteristicT*2of order 700 μs. 相似文献
83.
Silviu Polosan Tahsin J. Chow Taiju Tsuboi 《Journal of Physical Organic Chemistry》2008,21(4):315-320
Electronic states and their energies are calculated for a mixed‐ligand Ir(III) compound, (5‐chloro‐8‐hydroxyquinoline) bis(2‐phenylpyridyl) iridium (called IrQ(ppy)2‐5Cl) using time‐dependent density functional theory (TDDFT) calculations and are compared with the experimental result. A good agreement is obtained between the calculated and measured absorption spectra. The d‐πQ* molecular orbital transition gives the lowest‐energy triplet state absorption band. Its energy is estimated as 1.84 eV (671 nm), which is close to the absorption band position of 1.86 eV (666 nm) observed for IrQ(ppy)2‐5Cl doped in 4,4′‐N,N′‐dicarbazole‐biphenyl (CBP) host and of 1.88 eV (660 nm) observed for IrQ(ppy)2‐5Cl doped in polystyrene (PS). The second triplet state absorption band is caused by d‐πppy transition. Its position is calculated as 2.51 eV (494 nm). The dipole moment is estimated as 3.45 D, which is lower than the dipole moment of fac‐Ir(ppy)3. This is understood by a reduced charge transfer between Ir(III) and quinoline ligand. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
84.
CAOYi-Gang W.K.Chow 《理论物理通讯》2004,42(4):619-622
We investigate the depinning of two-dlmensional fluids interacting with quenched disorder, based on Langevin simulations. For weak disorder the fluids depin elastically and flow in an ordered state. A power-law scaling fit between velocity and driving force can be obtained for the onset of motion in the elastic regime. This is in good agreement with that of colloid, charge density wave, and superconducting vortex systems. With an increasing strength of the disorder, we find a sharp crossover to plastic depinning, accompanied by a substantial increase in the depinning force. The scaling fit obtained in the elastic regime becomes invalid when plastic flow occurs. In the plastic regime, the fluids flow in channels and the hexatic order decays exponentially with drives. 相似文献
85.
This paper presents the experimental characterization of the in-plane deformation field at any depth within a granular support medium (GSM) called Carbomer 940 using digital image correlation (DIC) and particle image velocimetry (PIV). A method was developed to produce a 2D plane of randomly shaped speckles within the GSM for DIC. Four different needle diameters and four different speeds were used as test specimens representative of those utilized for 3D printing of soft matter in the GSM. The results can be used to determine dimensional tolerances and assessing interactions between multiple injection needles and acceptable spacing. The displacements in the direction of needle motion (u) and transverse (v) were obtained. Subsequently, the magnitudes were determined as a function of distance from the needle path and time history. Results show that near the needle there is a region of yielded/fluidized material and away from the needle path the material acts like a viscoelastic solid. Permanent deformation decreases with increased distance from the path and recovery is enhanced by reversing back through the path. 相似文献
86.
Anxun Zheng Chang Shen Prof. Qian Tang Dr. Cheng-Bin Gong Dr. Cheuk-Fai Chow 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(41):9643-9649
Herein, a catalytic chemosensing assay (CCA), based on a bimetallic complex, [RuII(bpy)2(CN)2]2(CuII)2 (bpy=2,2′-bipyridine), is described. This complex integrates a task-specific catalyst (CuI-catalyst) and a signaling unit ([RuII(bpy)2(CN)2]) to specifically hydrolyze methyl parathion, a highly toxic organophosphate (OP) pesticide. The bimetallic complex catalyzed the hydrolysis of the phosphate ester to generate o,o-dimethyl thiophosphate (DTP) anion and 4-nitrophenolate. Intrinsically, 4-nitrophenolate absorbed UV/Vis light at λmax=400 nm, creating the first level of the chemosensing signal. DTP interacted with the original complex to displace the chromophore, [RuII(bpy)2(CN)2], which was monitored by spectrofluorometry; this was classified as the second level of chemosensing signal. By integrating both spectroscopic and spectrofluorometric signals with a simple AND logic gate, only methyl parathion was able to provide a positive response. Other aromatic and aliphatic OP pesticides (diazinon, fenthion, meviphos, terbufos, and phosalone) and 4-nitrophenyl acetate provided negative responses. Furthermore, owing to the metal-catalyzed hydrolysis of methyl parathion, the CCA system led to the detoxification of the pesticide. The CCA system also demonstrated its catalytic chemosensing properties in the detection of methyl parathion in real samples, including tap water, river water, and underground water. 相似文献
87.
Madeleine A. Dallaston Christian J. Bettencourt Dr. Sharon Chow Joshua Gebhardt Jordan Spangler Dr. Martin R. Johnston Craig Wall Dr. Jason S. Brusnahan Prof. Craig M. Williams 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(41):9614-9618
Common oxidants used in chemical synthesis, including newly developed perruthenates, were evaluated in the context of understanding (and better appreciating) the sensitiveness and associated potential hazards of these reagents. Analysis using sealed cell differential scanning calorimetry (scDSC) facilitated Yoshida correlations, which were compared to impact sensitiveness and electrostatic discharge experiments (ESD), that enabled sensitiveness ranking. Methyltriphenylphoshonium perruthenate (MTP3, 8 ), isoamyltriphenylphosphonium perruthenate (ATP3, 7 ) and tetraphenylphosphonium perruthenate (TP3, 9 ) were found to be the most sensitive followed by 2-iodoxybenzoic acid (IBX, 2 ) and benzoyl peroxide (BPO, 10 ), whereas the most benign were observed to be Oxone ( 12 ), manganese dioxide (MnO2, 13 ), and N-bromosuccinimide (NBS, 17 ). 相似文献
88.
Wei Peng Jie Dong Han‐Bin Li Christine Chow Qiao‐Sheng Hu 《Journal of polymer science. Part A, Polymer chemistry》2019,57(14):1606-1611
Room temperature Suzuki cross‐coupling polymerization of aryl dibromides/diiodides with aryldiboronic acids/acid esters with t‐Bu3P‐coordinated 2‐phenylaniline‐based palladacycle complex, [2′‐(amino‐kN)[1,1′‐biphenyl]‐2‐yl‐kC]chloro(tri‐t‐butylphosphine)palladium, as a general precatalyst is described. Such room temperature Suzuki cross‐coupling polymerization is achieved by employing six equivalents or more of the base and affords polymers within an hour, with the yields and the molecular weights in general comparable to or higher than reported results that required higher reaction temperature and/or longer polymerization time. Our study provides a general catalyst system for the room temperature Suzuki cross‐coupling polymerization of aryl dibromides/diiodides with aryldiboronic acids/acid esters and paves the road for the investigation of employing other monodentate ligand‐coordinated palladacycle complexes including other electron‐rich monophosphine‐coordinated ones for room temperature cross‐coupling polymerizations. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1606–1611 相似文献
89.
Dr. Lidia A. Maslovskaya Dr. Andrei I. Savchenko Prof. Elizabeth H. Krenske Dr. Sharon Chow Tina Holt Dr. Victoria A. Gordon Dr. Paul W. Reddell Carly J. Pierce Prof. Peter G. Parsons Prof. Glen M. Boyle Prof. Andrei G. Kutateladze Prof. Craig M. Williams 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(51):11862-11867
Structurally unique halimanes EBC-232 and EBC-323, isolated from the Australian rainforest plant Croton insularis, proved considerably difficult to elucidate. The two diastereomers, which consist an unusual oxo-6,7-spiro ring system fused to a dihydrofuran, were solved by unification and consultation of five in silico NMR elucidation and prediction methods [i.e., ACDLabs, olefin strain energy (OSE), DP4, DU8+ and TD DFT CD]. Structure elucidation challenges of this nature are prime test case examples for empowering future AI learning in structure elucidation. 相似文献
90.
Bennett GR Cuneo ME Vesey RA Porter JL Adams RG Aragon RA Caird JA Landen OL Rambo PK Rovang DC Ruggles LE Simpson WW Smith IC Wenger DF 《Physical review letters》2002,89(24):245002
An inertial-confinement-fusion (ICF) concept using two 60-MA Z pinches to drive a cylindrical hohlraum to 220 eV has been recently proposed. The first capsule implosions relevant to this concept have been performed at the same physical scale with a lower 20-MA current, yielding a 70+/-5 eV capsule drive. The capsule shell shape implies a polar radiation symmetry, the first high-accuracy measurement of this type in a pulsed-power-driven ICF configuration, within a factor of 1.6-4 of that required for scaling to ignition. The convergence ratio of 14-21 is to date the highest in any pulsed-power ICF system. 相似文献