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41.
Dominic Lingenfelser 《Applied Surface Science》2007,253(15):6563-6569
A method is introduced to investigate organic functionalizations on silicon by laser-induced thermal desorption (LITD), where well-ordered Si(1 1 1)-(1 × 1):H(D) surfaces are used to determine the desorption temperature as a function of laser fluence. To demonstrate the potential of this technique silicon surfaces with ultrathin oxide layers were functionalized with organic end groups. The species desorbed with focused XeCl laser pulses were monitored at an oblique angle and their time-of-flight (TOF) distributions were measured with a quadrupole mass analyzer after electron impact ionization. By assuming a negligible contribution of the oxide and organic layers to the heating effect, the TOF temperatures measured for Si(1 1 1)-(1 × 1):H(D) could be used to determine the mass of the desorbed species. Detailed results are presented for dimethylsilyl (DMS), bromomethyldimethylsilyl (BMDMS), and chloromethyldimethylsilyl (CMDMS) terminated surfaces which were prepared by silanization with suitable chloro and disilazane compounds. While for the DMS termination dimethylsilanol (76 u) is desorbed as a single species, clearly identifying the terminating group, in the case of BMDMS and CMDMS further fragmentation of the end group occurs at the surface. 相似文献
42.
Jing Jin Mark Prochaska Dominic Rochefort David K. Kim Lin Zhuang Francis J. DiSalvo R.B. van Dover Héctor D. Abruña 《Applied Surface Science》2007,254(3):653-661
We used a high-throughput method to screen for direct methanol fuel cell anode electrocatalysts in the Pt-Bi-Pb system. Previous studies showed that PtBi and PtPb (both NiAs structure type) were active electrocatalysts for the oxidation of formic acid, but only PtPb was active in oxidizing methanol. We synthesized thin films with continuous composition spreads of the three elements by magnetron sputtering at deposition temperatures from ambient to 510 °C. A fluorescence method was then used to identify compositions that were active toward methanol oxidation. Only films deposited between temperatures of 160 and 400 °C showed electrocatalytic activity. The areas that were active for methanol oxidation showed predominantly the NiAs structure type according to XRD, with optimal activity for compositions near PtBi0.01Pb0.53. 相似文献
43.
Stefan Eibl Andrew Fitch Michela Brunelli Alexander Dominic Evans Philip Pattison Marie Plazanet Mark Robert Johnson Christiane Alba‐Simionesco Helmut Schober 《Acta Crystallographica. Section C, Structural Chemistry》2009,65(6):o278-o280
The title compound, C10H18, a decalin stereoisomer, crystallizes with Z′ = 0.5 in the space group P21/n. The trans‐decalin molecule is located on an inversion centre with both rings in a chair conformation, making for a quasi‐flat overall shape. Despite the absence of hydrogen bonds, it crystallizes easily. In this work the unknown crystal structure of trans‐decalin has been solved and refined using X‐ray powder diffraction data. 相似文献
44.
Stuart C. Wimbush Dominic Walsh Simon R. Hall 《Physica C: Superconductivity and its Applications》2010,470(7-8):373-377
We have recently demonstrated that through a sol–gel route, superconductor crystallization in the presence of simple biopolymers results in a drastic alteration of morphology, producing technologically useful nanowires and porous architectures. Morphological control is of the utmost importance to bulk high-temperature superconductors, as grain boundaries act as weak links in limiting the achievable critical current density (Jc). Here we show that, as expected, the incorporation of nanoparticulate barium zirconate (BaZrO3) species into a biopolymer-mediated synthetic protocol for YBa2Cu3O7?δ (Y123) leads to a significantly improved in-field Jc compared to that observed in a sample without BaZrO3 additions. To ameliorate degradation of the BaZrO3 species in this protocol, we demonstrate that by drawing the precursor sol into fibers, a microtape architecture is able to be formed, leading to lengthy, anisotropic structures having enhanced Jc through the retention of the BaZrO3 species. 相似文献
45.
Georgiana Roman-Gusetu Karen C. Waldron Dominic Rochefort 《Journal of chromatography. A》2009,1216(47):8270-8276
Microencapsulation is used here as a new technique to immobilize enzymes in a microreactor coupled off-line to capillary electrophoresis (CE), allowing the determination of enzymatic reaction products. The redox enzyme laccase was encapsulated using the method of interfacial cross-linking of poly(ethyleneimine) (PEI). The 50 μm diameter capsules were slurry packed from a suspension into a capillary-sized reactor made easily and quickly from a short length of 530 μm diameter fused-silica tubing. The volume of the bed of laccase microcapsules in the microreactor was in the order of 1.1 μL through which 50 μL of the substrate o-phenylenediamine (OPD) was flowed. The oxidation product 2,3-diaminophenazine (DAP) and the remaining OPD were quantified by CE in a pH 2.5 phosphate buffer. Peak migration time reproducibility was in the order of 0.4% RSD and peak area reproducibility was less than 1.7% RSD within the same day. Using the OPD peak area calibration curve, a conversion efficiency of 48% was achieved for a 2-min oxidation reaction in the microreactor. 相似文献
46.
Tao Song Corey N. W. Lam Dominic C. M. Ng Galina Orlova Julia Laskin De-Cai Fang Ivan K. Chu 《Journal of the American Society for Mass Spectrometry》2009,20(6):972-984
The dissociation of [CuII(L)His]•2+ complexes [L=diethylenetriamine (dien) or 1,4,7-triazacyclononane (9-aneN3)] bears a strong resemblance to the previously reported behavior of [CuII(L)GGH]•2+ complexes. We have used low-energy collision-induced dissociation experiments and density functional theory (DFT) calculations
at the B3LYP/6-31+G(d) level to study the macrocyclic effect of the auxiliary ligands on the formation of His•+ from prototypical [CuII(L)His]•2+ systems. DFT revealed that the relative energy barriers of the same electron-transfer (ET) dissociation pathways of [CuII(9-aneN3)His]•2+ and [CuII(dien)His]•2+ are very similar, with the ET reactions of [CuII(9-aneN3)His]•2+ leading to the generation of two distinct His•+ species; in contrast, the proton transfer (PT) dissociation pathways of [CuII(9-aneN3)His]•2+ and [CuII(dien)His]•2+ differ considerably. The PT reactions of [CuII(9-aneN3)His]•2+ are associated with substantially higher barriers (>13 kcal/mol) than those of [CuII(dien)His]•2+. Thus, the sterically encumbered auxiliary 9-aneN3 ligand facilitates ET reactions while moderating PT reactions, allowing the formation of hitherto nonobservable histidine
radical cations. 相似文献
47.
Dominic G. B. Edelen 《International Journal of Theoretical Physics》1989,28(6):633-649
Realization of the Poincaré groupP
10 as a subgroup ofGL(5,R) that maps a 4-dimensional affine set into itself has been shown to lead to a direct Yang-Mills gauging process. This paper discusses the differences between direct gauge theory forP
10 and previously published works. These differences are fundamental, both physically and mathematically, and lead to marked departures from previous concepts and interpretations. The translation subgroup is correctly gauged; the metric structure and metric compatibility are derived from the gauging process rather than assumed; spin structures are automatically incorporated in a consistent manner; the local holonomy group is shown to be the component of the Lorentz group connected to the identity; the geometric analog of Yang-Mills minimal coupling precludes dependence of the free gauge field Lagranian on torsion; and the theory reduces exactly to general relativity when the momentumenergy complex is symmetric and all matter fields are spin-free. Gravitational effects on neutral test particles are shown to arise from the compensating 1-forms for local action of Lorentz boosts. The compensating 1-forms for local action of the translation subgroup may be interpreted as space-time dislocations, while the compensating 1-forms for the rotation subgroup can be viewed as space-time disclinations. Unfortunately, there are no clear physical meanings that can be ascribed to space-time dislocations or disclinations. 相似文献
48.
49.
Wai Yi Kelly Chan T. W. Dominic Chan Peter B. O’Connor 《Journal of the American Society for Mass Spectrometry》2010,21(6):1012-1015
Electron-transfer dissociation (ETD) with supplemental activation of the doubly charged deamidated tryptic digested peptide
ions allows differentiation of isoaspartic acid and aspartic acid residues using the c + 57 or z • − 57 peaks. The diagnostic peak clearly localizes and characterizes the isoaspartic acid residue. Supplemental activation
in ETD of the doubly charged peptide ions involves resonant excitation of the charge reduced precursor radical cations and
leads to further dissociation, including extra backbone cleavages and secondary fragmentation. Supplemental activation is
essential to obtain a high quality ETD spectrum (especially for doubly charged peptide ions) with sequence information. Unfortunately,
the low-resolution of the ion trap mass spectrometer makes detection of the diagnostic peak, [M-60], for the aspartic acid
residue difficult due to interference with side-chain loss from arginine and glutamic acid residues. 相似文献
50.
Siriani DF 《Optics letters》2011,36(5):701-703
Coupled waveguides, such as those used as optical filters, switches, or couplers, are investigated in the context of coherence theory. A stochastic source is introduced to the standard coupled-mode model. Decay in the power transferred between the waveguides as a function of distance is predicted. Application of this result in the form of an interferometric spectrometer is explored. 相似文献