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81.
G. H. Banwell J. R. Roberts B. J. Halkon S. J. Rothberg S. Mohr 《Experimental Mechanics》2014,54(4):527-537
The ‘feel’ of tennis rackets is of increasing importance to manufacturers seeking product differentiation in a context where further performance enhancements are prevented by a combination of mechanical limits and regulations imposed to protect the integrity of the sport. Vibrations excited during a shot contribute greatly to the perception of ‘feel’. Previous studies have been reported but none has covered the full set of mode families or the frequency range in this study. In-plane vibrations associated with the routine use of topspin shots in modern tennis have not been documented so far in the literature. To consider modal behaviour, multiple measurements during play conditions are required but this is practically impossible. This paper proposes an alternative approach and successfully relates a comprehensive modal analysis on a freely suspended racket to vibration measurements under play conditions. This is achieved through an intermediate stage comprising a necessarily more limited modal analysis on a hand-gripped racket and use of the mass modification modal analysis tool. This stage confirmed the prevailing view that hand-gripping can be considered as a mass modification distributed along the handle of the freely suspended racket but the associated mass was much lower than that of an actual hand and the hand also increased the damping ratio of frame modes significantly. Furthermore, in frame vibration measurements during forehand groundstrokes, a greater reduction in bending mode frequencies was observed, consistent with a mass-loading of around 25 % of the actual hand as a consequence of the tighter grip. In these play tests, the first two bending modes, the first torsional mode, the first eight stringbed modes, the first three hoop modes and the third in-plane bending mode were identified, with the stringbed modes being particularly prominent. 相似文献
82.
83.
Jorge Segovia Chen Chen Ian C. Cloët Craig D. Roberts Sebastian M. Schmidt Shaolong Wan 《Few-Body Systems》2014,55(1):1-33
Predictions obtained with a confining, symmetry-preserving treatment of a vector ? vector contact interaction at leading-order in a widely used truncation of QCD’s Dyson–Schwinger equations are presented for Δ and Ω baryon elastic form factors and the γN → Δ transition form factors. This simple framework produces results that are practically indistinguishable from the best otherwise available, an outcome which highlights that the key to describing many features of baryons and unifying them with the properties of mesons is a veracious expression of dynamical chiral symmetry breaking in the hadron bound-state problem. The following specific results are of particular interest. The Δ elastic form factors are very sensitive to m Δ. Hence, given that the parameters which define extant simulations of lattice-regularised QCD produce Δ-resonance masses that are very large, the form factors obtained therewith are a poor guide to properties of the Δ(1232). Considering the Δ-baryon’s quadrupole moment, whilst all computations produce a negative value, the conflict between theoretical predictions entails that it is currently impossible to reach a sound conclusion on the nature of the Δ-baryon’s deformation in the infinite momentum frame. Results for analogous properties of the Ω baryon are less contentious. In connection with the N → Δ transition, the Ash-convention magnetic transition form factor falls faster than the neutron’s magnetic form factor and nonzero values for the associated quadrupole ratios reveal the impact of quark orbital angular momentum within the nucleon and Δ; and, furthermore, these quadrupole ratios do slowly approach their anticipated asymptotic limits. 相似文献
84.
Heinz J. Robota Laura A. Richard Soumitra Deshmukh Steve LeViness Daniele Leonarduzzi Diarmid Roberts 《Catalysis Surveys from Asia》2014,18(4):177-182
Each process configuration for practicing the Fischer–Tropsch synthesis places demands particular to that configuration on the catalyst to be used. We discuss how a particular catalyst, prepared by the OMX (organic matrix combustion) method, when used in conjunction with the Velocys microchannel reactor system, results in a very stable, high performance Fischer–Tropsch synthesis system. With the ability to remove heat far more effectively than a conventional reactor system, this microchannel reactor requires a catalyst with much higher volumetric reactive site density. Further, with such a high volumetric reaction rate, mass transfer effects will be important in both the observed activity and selectivity of the operating catalyst. Nevertheless, the catalyst prepared using the OMX method exhibits an apparent turnover frequency which is considerably higher than reported for other catalysts in the literature. In addition to high activity, an economically useful catalyst must exhibit a stable, high selectivity for liquid products and be able to recover near-fresh performance using a regeneration approach which can be carried out with the catalyst in-place. An example of such a stable, multiply regenerated catalyst is given. Finally, further development has focused on a catalyst with even higher C5+ selectivity. 相似文献
85.
Electromagnetic processing was used to study the effects of electro-magneto forming on the dimensional control and thermal stability of sintered powder metal (PM) parts. The investigation was carried out on sinter-hardened, low chromium-molybdenum bainitic steel. The results show an increase in the microhardness of about 14% for the electromagnetic processed parts compared to the as-sintered parts. This was attributed to the 2% increase in the density, 17% and 29% reduction in the volume fraction of porosity and width of the bainitic lath, respectively, due to the electromagnetic processing. Dimensional characterization was carried out using a vertically aligned push-rod dilatometer. After four thermal cycles of heating and cooling, at a controlled rate of 5 °C/min to 1000 °C, the electromagnetic processed parts exhibited reduced dimensional change of about 44% lower than for the as-sintered parts. This is significantly important for applications that demand high dimensional tolerance and performance, especially at elevated temperatures. 相似文献
86.
Victoria A. Roberts Elaine E. Thompson Michael E. Pique Martin S. Perez L. F. Ten Eyck 《Journal of computational chemistry》2013,34(20):1743-1758
Computational docking is a useful tool for predicting macromolecular complexes, which are often difficult to determine experimentally. Here, we present the DOT2 software suite, an updated version of the DOT intermolecular docking program. DOT2 provides straightforward, automated construction of improved biophysical models based on molecular coordinates, offering checkpoints that guide the user to include critical features. DOT has been updated to run more quickly, allow flexibility in grid size and spacing, and generate an infinitive complete list of favorable candidate configurations. Output can be filtered by experimental data and rescored by the sum of electrostatic and atomic desolvation energies. We show that this rescoring method improves the ranking of correct complexes for a wide range of macromolecular interactions and demonstrate that biologically relevant models are essential for biologically relevant results. The flexibility and versatility of DOT2 accommodate realistic models of complex biological systems, improving the likelihood of a successful docking outcome. © 2013 Wiley Periodicals, Inc. 相似文献
87.
Juan L. Navia Richard A. Roberts Robert E. Wingard Jr 《Journal of carbohydrate chemistry》2013,32(4-5):465-480
Abstract A study of the selectivity of metal chelate-directed benzoylation of sucrose dianion, relative to unchelated sucrose anion, was conducted as part of a study on new synthetic approaches to the high-potency sweetener sucralose. Ionic complexes of sucrose with various metal ions were prepared in DMF and the resulting complexes reacted at low temperature with benzoic anhydride. Cobalt and manganese salts directed esterification mostly to the 3′-OH on the fructosyl portion. Unchelated sucrose anion and other metals favored esterification at the 2-OH of the glucosyl portion. Migration of the benzoate ester along the glucose portion was observed in the direction O-2 to O-6 at moderate temperature, but at higher temperature transannular migration was observed from the glucose to the fructose ring. Reaction mixtures were analyzed by HPLC and monobenzoates identified by retention times relative to standards. Six of eight possible monobenzoates of sucrose were isolated from mixtures and identified by their 1H NMR spectra. 相似文献
88.
We demonstrate a high-power, narrowband pulsed source at 390 nm by two stages of frequency doubling in periodically poled MgO:LiNbO(3) and periodically poled KTiOPO(4) of an amplified, passively mode-locked fiber laser. With a frequency quadrupling efficiency of 5.5% and a 0.1 nm bandwidth, the 250 mW ultraviolet source is a suitable compact pump source for many entanglement-based quantum information processing tasks. 相似文献
89.
Enzyme Design from the Bottom Up: An Active Nickel Electrocatalyst with a Structured Peptide Outer Coordination Sphere 下载免费PDF全文
Dr. Matthew L. Reback Dr. Garry W. Buchko Dr. Brandon L. Kier Bojana Ginovska‐Pangovska Dr. Yijia Xiong Dr. Sheri Lense Dr. Jianbo Hou Dr. John A. S. Roberts Dr. Christina M. Sorensen Dr. Simone Raugei Dr. Thomas C. Squier Dr. Wendy J. Shaw 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(6):1510-1514
Catalytic, peptide‐containing metal complexes with a well‐defined peptide structure have the potential to enhance molecular catalysts through an enzyme‐like outer coordination sphere. Here, we report the synthesis and characterization of an active, peptide‐based metal complex built upon the well‐characterized hydrogen production catalyst [Ni(PPh2NPh)2]2+ (PPh2NPh=1,3,6‐triphenyl‐1‐aza‐3,6‐diphosphacycloheptane). The incorporated peptide maintains its β‐hairpin structure when appended to the metal core, and the electrocatalytic activity of the peptide‐based metal complex (≈100,000 s?1) is enhanced compared to the parent complex ([Ni(PPh2NAPPA)2]2+; ≈50,500 s‐1). The combination of an active molecular catalyst with a structured peptide provides a scaffold that permits the incorporation of features of an enzyme‐like outer‐coordination sphere necessary to create molecular electrocatalysts with enhanced functionality. 相似文献
90.
Wing Ying Chow Brendan P. Norman Norman B. Roberts Lakshminarayan R. Ranganath Christian Teutloff Robert Bittl Melinda J. Duer James A. Gallagher Hartmut Oschkinat 《Angewandte Chemie (International ed. in English)》2020,59(29):11937-11942
Alkaptonuria (AKU) is a rare disease characterized by high levels of homogentisic acid (HGA); patients suffer from tissue ochronosis: dark brown pigmentation, especially of joint cartilage, leading to severe early osteoarthropathy. No molecular mechanism links elevated HGA to ochronosis; the pigment's chemical identity is still not known, nor how it induces joint cartilage degradation. Here we give key insight on HGA‐derived pigment composition and collagen disruption in AKU cartilage. Synthetic pigment and pigmented human cartilage tissue both showed hydroquinone‐resembling NMR signals. EPR spectroscopy showed that the synthetic pigment contains radicals. Moreover, we observed intrastrand disruption of collagen triple helix in pigmented AKU human cartilage, and in cartilage from patients with osteoarthritis. We propose that collagen degradation can occur via transient glycyl radicals, the formation of which is enhanced in AKU due to the redox environment generated by pigmentation. 相似文献