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301.
A net is a graph consisting of a triangle C and three more vertices, each of degree one and with its neighbour in C, and all adjacent to different vertices of C. We give a polynomial-time algorithm to test whether an input graph has an induced subgraph which is a subdivision of a net. Unlike many similar questions, this does not seem to be solvable by an application of the “three-in-a-tree” subroutine. 相似文献
302.
Zaia J Miller MJ Seymour JL Costello CE 《Journal of the American Society for Mass Spectrometry》2007,18(5):952-960
Carbohydrates of all classes consist of glycoform mixtures built on common core units. Determination of compositions and structures of such mixtures relies heavily on tandem mass spectrometric data. Analysis of native glycans is often necessary for samples available in very low quantities and for sulfated glycan classes. Negative tandem mass spectrometry (MS) provides useful product ion profiles for neutral oligosaccharides and is preferred for acidic classes. In previous work from this laboratory, site-specific influences of sialylation on product ion profiles in the negative mode were elucidated. The present results show how the interplay of two other acidic groups, uronic acids and sulfates, determines product ion patterns for chondroitin sulfate oligosaccharides. Unsulfated chondroitin oligosaccharides dissociate to form C-type ions almost exclusively. Chondroitin sulfate oligosaccharides produce abundant B- and Y-type ions from glycosidic bond cleavage with C- and Z-types in low abundances. These observations are explained in terms of competing proton transfer reactions that occur during the collisional heating process. Mechanisms for product ion formation are proposed based on tandem mass spectra and the abundances of product ions as a function of collision energy. 相似文献
303.
Mowat JP Miller SR Griffin JM Seymour VR Ashbrook SE Thompson SP Fairen-Jimenez D Banu AM Düren T Wright PA 《Inorganic chemistry》2011,50(21):10844-10858
The crystal structure of the small pore scandium terephthalate Sc(2)(O(2)CC(6)H(4)CO(2))(3) (hereafter Sc(2)BDC(3), BDC = 1,4-benzenedicarboxylate) has been investigated as a function of temperature and of functionalization, and its performance as an adsorbent for CO(2) has been examined. The structure of Sc(2)BDC(3) has been followed in vacuo over the temperature range 140 to 523 K by high resolution synchrotron X-ray powder diffraction, revealing a phase change at 225 K from monoclinic C2/c (low temperature) to Fddd (high temperature). The orthorhombic form shows negative thermal expansivity of 2.4 × 10(-5) K(-1): Rietveld analysis shows that this results largely from a decrease in the c axis, which is caused by carboxylate group rotation. (2)H wide-line and MAS NMR of deuterated Sc(2)BDC(3) indicates reorientation of phenyl groups via π flips at temperatures above 298 K. The same framework solid has also been prepared using monofunctionalized terephthalate linkers containing -NH(2) and -NO(2) groups. The structure of Sc(2)(NH(2)-BDC)(3) has been determined by Rietveld analysis of synchrotron powder diffraction at 100 and 298 K and found to be orthorhombic at both temperatures, whereas the structure of Sc(2)(NO(2)-BDC)(3) has been determined by single crystal diffraction at 298 K and Rietveld analysis of synchrotron powder diffraction at 100, 298, 373, and 473 K and is found to be monoclinic at all temperatures. Partial ordering of functional groups is observed in each structure. CO(2) adsorption at 196 and 273 K indicates that whereas Sc(2)BDC(3) has the largest capacity, Sc(2)(NH(2)-BDC)(3) shows the highest uptake at low partial pressure because of strong -NH(2)···CO(2) interactions. Remarkably, Sc(2)(NO(2)-BDC)(3) adsorbs 2.6 mmol CO(2) g(-1) at 196 K (P/P(0) = 0.5), suggesting that the -NO(2) groups are able to rotate to allow CO(2) molecules to diffuse along the narrow channels. 相似文献
304.
Andy BuckleyJonathan Butterworth Stefan GiesekeDavid Grellscheid Stefan HöcheHendrik Hoeth Frank KraussLeif Lönnblad Emily NursePeter Richardson Steffen SchumannMichael H. Seymour Torbjörn SjöstrandPeter Skands Bryan Webber 《Physics Reports》2011,504(5):145-233
We review the physics basis, main features and use of general-purpose Monte Carlo event generators for the simulation of proton-proton collisions at the Large Hadron Collider. Topics included are: the generation of hard scattering matrix elements for processes of interest, at both leading and next-to-leading QCD perturbative order; their matching to approximate treatments of higher orders based on the showering approximation; the parton and dipole shower formulations; parton distribution functions for event generators; non-perturbative aspects such as soft QCD collisions, the underlying event and diffractive processes; the string and cluster models for hadron formation; the treatment of hadron and tau decays; the inclusion of QED radiation and beyond Standard Model processes. We describe the principal features of the Ariadne, Herwig++, Pythia 8 and Sherpa generators, together with the Rivet and Professor validation and tuning tools, and discuss the physics philosophy behind the proper use of these generators and tools. This review is aimed at phenomenologists wishing to understand better how parton-level predictions are translated into hadron-level events as well as experimentalists seeking a deeper insight into the tools available for signal and background simulation at the LHC. 相似文献
305.
Carbon–Carbon Cross‐Coupling Reactions Catalyzed by a Two‐Coordinate Nickel(II)–Bis(amido) Complex via Observable NiI,NiII, and NiIII Intermediates 下载免费PDF全文
Michael I. Lipschutz Prof. T. Don Tilley 《Angewandte Chemie (International ed. in English)》2014,53(28):7290-7294
Recently, the development of more sustainable catalytic systems based on abundant first‐row metals, especially nickel, for cross‐coupling reactions has attracted significant interest. One of the key intermediates invoked in these reactions is a NiIII–alkyl species, but no such species that is part of a competent catalytic cycle has yet been isolated. Herein, we report a carbon–carbon cross‐coupling system based on a two‐coordinate NiII–bis(amido) complex in which a NiIII–alkyl species can be isolated and fully characterized. This study details compelling experimental evidence of the role played by this NiIII–alkyl species as well as those of other key NiI and NiII intermediates. The catalytic cycle described herein is also one of the first examples of a two‐coordinate complex that competently catalyzes an organic transformation, potentially leading to a new class of catalysts based on the unique ability of first‐row transition metals to accommodate two‐coordinate complexes. 相似文献