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81.
Ratnakar SJ Woods M Lubag AJ Kovacs Z Sherry AD 《Journal of the American Chemical Society》2008,130(1):6-7
The chemical exchange saturation transfer (CEST) efficiency for a series Eu3+-based tetraamide complexes bearing p-substituents on a single coordinating pendant arm is highly sensitive to water exchange rates. The CEST effect increases in the order Me < MeO < F approximately CO2tBu < CN < H. These results show that CEST contrast can be modulated by changes in electron density at a single ligating atom, and this forms the basis of creating imaging agents that respond to chemical oxidation and reduction. 相似文献
82.
Excited-state absorption spectra for several coumarin derivatives adsorbed to aerosol particles provide linear solvation energy (LSE) relationships for the aerosol surfaces. This study focuses on NaCl and (NH4)2SO(4) particles as models for tropospheric aerosol. We investigate several others, including NH(4)Cl, NaBr, KI, Na(2)SO(4), NaNO(3), Al(2)O3, and CaCO(3), to establish trends and understand the factors that control polarity for surfaces. The Kamlet-Taft dipolarity/polarizability parameter, pi*, for these particles ranges from 0.73 to 1.69. The values are high compared to most homogeneous molecular solvents and are attributable to ion-dipole forces, especially at defect sites. We also find that the smaller values of pi* (1.01 for (NH4)2SO(4) and 0.73 for NH(4)Cl) correlate with appreciable hydrogen bond donor acidity in the surface (alpha = 0.23 and 1.06, respectively). Strong hydrogen bonds with the surface lead to a drop in overall polarity either by making interaction with very polar defect sites less likely or orienting the probe molecule away from the surface. Adsorbed water layers mainly alter the alpha value of the surface, but can have indirect effects on pi* by changing the interaction of the adsorbed molecule with the surface. 相似文献
83.
D. Habs O. Kester T. Sieber H. Bongers S. Emhofer P. Reiter P.G. Thirolf G. Bollen J. Aystö O. Forstner H. Ravn T. Nilsson M. Oinonen H. Simon J. Cederkall F. Ames P. Schmidt G. Huber L. Liljeby O. Skeppstedt K.G. Rensfelt F. Wenander B. Jonson G. Nyman R. von Hahn H. Podlech R. Repnow C. Gund D. Schwalm A. Schempp K.-U. Kühnel C. Welsch U. Ratzinger G. Walter A. Huck K. Kruglov M. Huyse P. Van den Bergh P. Van Duppen L. Weissman A.C. Shotter A.N. Ostrowski T. Davinson P.J. Woods J. Cub A. Richter G. Schrieder 《Hyperfine Interactions》2000,129(1-4):43-66
The Radioactive Beam Experiment REX-ISOLDE [1–3] is a pilot experiment at ISOLDE (CERN) testing the new concept of post acceleration
of radioactive ion beams by using charge breeding of the ions in a high charge state ion source and the efficient acceleration
of the highly charged ions in a short LINAC using modern ion accelerator structures. In order to prepare the ions for the
experiments singly charged radioactive ions from the on-line mass separator ISOLDE will be cooled and bunched in a Penning
trap, charge bred in an electron beam ion source (EBIS) and finally accelerated in the LINAC. The LINAC consists of a radiofrequency
quadrupole (RFQ) accelerator, which accelerates the ions up to 0.3 MeV/u, an interdigital H-type (IH) structure with a final
energy between 1.1 and 1.2 MeV/u and three seven gap resonators, which allow the variation of the final energy. With an energy
of the radioactive beams between 0.8 MeV/u and 2.2 MeV/u a wide range of experiments in the field of nuclear spectroscopy,
astrophysics and solid state physics will be addressed by REX-ISOLDE.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
84.
85.
86.
Zs. Podolyák G.F. Farrelly P.H. Regan A.B. Garnsworthy S.J. Steer M. Górska J. Benlliure E. Casarejos S. Pietri J. Gerl H.J. Wollersheim R. Kumar F. Molina A. Algora N. Alkhomashi G. Benzoni A. Blazhev P. Boutachkov A.M. Bruce L. Caceres I.J. Cullen A.M. Denis Bacelar P. Doornenbal M.E. Estevez Y. Fujita W. Gelletly H. Geissel H. Grawe J. Gr?bosz R. Hoischen I. Kojouharov S. Lalkovski Z. Liu K.H. Maier C. Mihai D. Mücher B. Rubio H. Schaffner A. Tamii S. Tashenov J.J. Valiente-Dobón P.M. Walker P.J. Woods 《Physics letters. [Part B]》2009
87.
Ross L. Spencer Jaron KrogelJamie Palmer Adam PayneAndrew Sampson William SomersCharles N. Woods 《Spectrochimica Acta Part B: Atomic Spectroscopy》2009
The Direct Simulation Monte Carlo algorithm has been applied to the flow of neutral argon gas through the first vacuum stage of the Inductively Coupled Plasma Mass Spectrometer. Good agreement is found between the simulation results and the equations of fluid dynamics, including the approximate hemispherical sink model of Douglas and French. The simulation reveals details of boundary layer formation in the nozzle, including a reduction in the total flow through the nozzle of about 15% from the ideal value calculated by Douglas and French. 相似文献
88.
Optical computing 总被引:1,自引:0,他引:1
89.
Kawatkar SP Kuntz DA Woods RJ Rose DR Boons GJ 《Journal of the American Chemical Society》2006,128(25):8310-8319
The X-ray crystal structures of mannose trimming enzyme drosophila Golgi alpha-mannosidase II (dGMII) complexed with the inhibitors mannostatin A (1) and an N-benzyl analogue (2) have been determined. Molecular dynamics simulations and NMR studies have shown that the five-membered ring of mannostatin A is rather flexible occupying pseudorotational itineraries between 2T3 and 5E, and 2T3 and 4E. In the bound state, mannostatin A adopts a 2T1 twist envelope conformation, which is not significantly populated in solution. Possible conformations of the mannosyl oxacarbenium ion and an enzyme-linked intermediate have been compared to the conformation of mannostatin A in the cocrystal structure with dGMII. It has been found that mannostatin A best mimics the covalent linked mannosyl intermediate, which adopts a 1S5 skew boat conformation. The thiomethyl group, which is critical for high affinity, superimposes with the C-6 hydroxyl of the covalent linked intermediate. This functionality is able to make a number of additional polar and nonpolar interactions increasing the affinity for dGMII. Furthermore, the X-ray structures show that the environment surrounding the thiomethyl group of 1 is remarkably similar to the arrangements around the methionine residues in the protein. Collectively, our studies contradict the long held view that potent inhibitors of glycosidases must mimic an oxacarbenium ion like transition state. 相似文献
90.
Woods M Woessner DE Zhao P Pasha A Yang MY Huang CH Vasalitiy O Morrow JR Sherry AD 《Journal of the American Chemical Society》2006,128(31):10155-10162
Paramagnetic lanthanide(III) complexes that contain hyperfine-shifted exchangeable protons offer considerable advantages over diamagnetic molecules as chemical exchange saturation transfer (CEST) agents for MRI. As part of a program to investigate avenues to improve the sensitivity of such agents, the CEST characteristics of europium(III) macrocyclic complexes having appended hydroxyethyl groups were investigated. The CEST spectrum of the asymmetrical complex, EuCNPHC3+, shows five distinct peaks for each magnetically nonequivalent exchangeable proton in the molecule. The CEST spectra of this complex were fitted to NMR Bloch theory to yield exchange rates between each of six exchanging proton pools (five on the agent plus bulk water). Exchange between the Eu3+-bound hydroxyl protons and bulk water protons was slow in dry acetonitrile but accelerated incrementally upon stepwise addition of water. In pure water, exchange was too fast to observe a CEST effect. The utility of this class of europium(III) complex for CEST imaging applications is ultimately limited by the small chemical shifts induced by the hydroxyl-appended ligands of this type and the resulting small Deltaomega values for the exchangeable hydroxyl protons. 相似文献