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81.
LI GuangShun ZHOU XiaoHong ZHANG ShuangQuan ZHANG YuHu & MENG Jie Institute of Modern Physics Chinese Academy of Sciences Lanzhou China Graduate University of Chinese Academy of Sciences Beijing School of Physics SK Laboratory of Nuclear Physics & Technology Peking University Beijing 《中国科学:物理学 力学 天文学(英文版)》2011,(Z1)
Theoretical calculations have been performed for the ν9/2+[624](i13/2) and ν7/2-[503](f7/2) bands of 185Pt in the framework of particle-rotor model. The band properties of signature splitting and configuration mixing have been analyzed. The level energy and signature splitting before the band crossing can be well interpreted by introducing triaxiality. The positive-parity yrast band is pro posed to be dominated by the ν9/2+[624](i13/2) component, while the negative-parity band shows strong mixing of ν7/2-[5... 相似文献
82.
E. G. Richardson 《Colloid and polymer science》1937,81(1):87-88
Zusammenfassung Mit Bezug auf kürzlich in der Kolloid-Zeitschrift veröffentlichte Arbeiten wird die Theorie der Analyse der Partikelgröße mittels Sedimentation und Photozelle diskutiert. Es wird darauf hingewiesen, daß der Verfasser schon im Jahre 1934 einen ähnlichen Apparat beschrieben hat. Es wird gezeigt, wie man eine ununterbrochene Verteilungskurve der Partikeldurchmesser eines Dispersoids bekommen kann.Übersetzt von H. A. Wannow (Leipzig). 相似文献
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Jonathan P. Williams Julie Ann Lough Iain Campuzano Keith Richardson Peter J. Sadler 《Rapid communications in mass spectrometry : RCM》2009,23(22):3563-3569
We report the development of an enhanced algorithm for the calculation of collision cross‐sections in combination with Travelling‐Wave ion mobility mass spectrometry technology and its optimisation and evaluation through the analysis of an organoruthenium anticancer complex [(η6‐biphenyl)RuII(en)Cl]+. Excellent agreement was obtained between the experimentally determined and theoretically determined collision cross‐sections of the complex and its major product ion formed via collision‐induced dissociation. Collision cross‐sections were also experimentally determined for adducts of this ruthenium complex with the single‐stranded oligonucleotide hexamer d(CACGTG). Ion mobility tandem mass spectrometry measurements have allowed the binding sites for ruthenium on the oligonucleotide to be determined. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
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Simon J. Holder Geraldine G. Durand Chert‐Tsun Yeoh Elodie Illi Nicholas J. Hardy Tim H. Richardson 《Journal of polymer science. Part A, Polymer chemistry》2008,46(23):7739-7756
A series of ABA amphiphilic triblock copolymers possessing polystyrene (PS) central hydrophobic blocks, one group with “short” PS blocks (DP = 54–86) and one with “long” PS blocks (DP = 183–204) were synthesized by atom transfer radical polymerization. The outer hydrophilic blocks were various lengths of poly(oligoethylene glycol methyl ether) methacrylate, a comb‐like polymer. The critical aggregation concentrations were recorded for certain block copolymer samples and were found to be in the range circa 10−9 mol L−1 for short PS blocks and circa 10−12 mol L−1 for long PS blocks. Dilute aqueous solutions were analyzed by transmission electron microscopy (TEM) and demonstrated that the short PS block copolymers formed spherical micelles and the long PS block copolymers formed predominantly spherical micelles with smaller proportions of cylindrical and Y‐branched cylindrical micelles. Dynamic light scattering analysis results agreed with the TEM observations demonstrating variations in micelle size with PS and POEGMA chain length: the hydrodynamic diameters (DH) of the shorter PS block copolymer micelles increased with increasing POEGMA block lengths while maintaining similar PS micellar core diameters (DC); in contrast the values of DH and DC for the longer PS block copolymer micelles decreased. Surface‐pressure isotherms were recorded for two of the samples and these indicated close packing of a short PS block copolymer at the air–water interface. The aggregate solutions were demonstrated to be stable over a 38‐day period with no change in aggregate size or noticeable precipitation. The cloud point temperatures of certain block copolymer aggregate solutions were measured and found to be in the range 76–93 °C; significantly these were ∼11 °C higher in temperature than those of POEGMA homopolymer samples with similar chain lengths. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7739–7756, 2008 相似文献
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Preston S. P.; Jensen O. E.; Richardson G. 《The Quarterly Journal of Mechanics and Applied Mathematics》2008,61(1):1-24
We consider the axisymmetric deformation of an initially spherical,porous vesicle with incompressible membrane having finite resistanceto in-plane shearing, as the vesicle is compressed between parallelplates. We adopt a thin-shell balance-of-forces formulationin which the mechanical properties of the membrane are describedby a single dimensionless parameter, C, which is the ratio ofthe membrane's resistance to shearing to its resistance to bending.This results in a novel free-boundary problem which we solvenumerically to obtain vesicle shapes as a function of plateseparation, h. For small deformations, the vesicle contactseach plate over a small circular area. At a critical value ofplate separation, hTC, there is a transcritical bifurcationfrom which a new branch of solutions emerges, representing buckledvesicles which contact each plate along a circular curve. Forthe values of C investigated, we find that the transcriticalbifurcation is subcritical and that there is a further saddle-nodebifurcation (fold) along the branch of buckled solutions ath = hSN (where hSN > hTC). The resulting bifurcation structureis commensurate with a hysteresis loop in which a sudden transitionfrom an unbuckled solution to a buckled one occurs as h is decreasedthrough hTC and a further sudden transition, this time froma buckled solution to an unbuckled one, occurs as h is increasedthrough hSN. We find that hSN and hTC increase with C, thatis, vesicles that resist shear are more prone to buckling. 相似文献
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