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81.
R. -D. Herzberg S. Moon S. Eeckhaudt P. T. Greenlees P. A. Butler T. Page A. V. Afanasjev N. Amzal J. E. Bastin F. Becker M. Bender B. Bruyneel J. F. C. Cocks I. G. Darby O. Dorvaux K. Eskola J. Gerl T. Grahn C. Gray-Jones N. J. Hammond K. Hauschild P. -H. Heenen K. Helariutta A. Herzberg F. Hessberger M. Houry A. Hürstel R. D. Humphreys G. D. Jones P. M. Jones R. Julin S. Juutinen H. Kankaanp?? H. Kettunen T. L. Khoo W. Korten P. Kuusiniemi Y. LeCoz M. Leino A. -P. Lepp?nen C. J. Lister R. Lucas M. Muikku P. Nieminen M. Nyman R. D. Page T. Page J. Pakarinen A. Pritchard P. Rahkila P. Reiter M. Sandzelius J. Saren Ch. Schlegel C. Scholey Ch. Theisen W. H. Trzaska J. Uusitalo A. Wiens H. J. Wollersheim 《The European Physical Journal A - Hadrons and Nuclei》2009,42(3):333-337
In-beam gamma-ray and conversion electron spectroscopic studies have been performed on the 253 No nucleus. A strongly coupled rotational band has been identified and the improved statistics allows an assignment of the band structure as built on the $\ensuremath 9/2^-[734]_{\nu}$ ground state. The results agree with previously known transition energies but disagree with the tentative structural assignments made in earlier work. 相似文献
82.
There are many reports1 of the pyrolysis of fluorinated organic compounds, including the defluorination of cyclic fluorocarbons over iron to give aromatic compounds. Extending this technique we have investigated the flow pyrolysis of some readily accessible unsaturated fluorocarbons, such as I, II, and III, and found these to be synthetically useful routes to fluorinated dienes, cyclobutenes, and furans. Pyrolyses were carried out using a nitrogen flow over platinum, iron or caesium fluoride heated at 430–700°. The various products can all be rationalized in terms of intermediate allylic radicals, and the solid substrate influences which allylic radicals are formed.We are also investigating the chemistry of those now accessible compounds, such as IV, V, and VI, and some of the preliminary results are described. For example the fluoride ion induced dimerisation of IV gave two major products VII and VIII via a particular interesting mechanism. 相似文献
83.
Material optimisation for AlGaN/GaN HFET applications 总被引:1,自引:0,他引:1
Z. Bougrioua I. Moerman N. Sharma R. H. Wallis J. Cheyns K. Jacobs E. J. Thrush L. Considine R. Beanland J. -L. Farvacque C. Humphreys 《Journal of Crystal Growth》2001,230(3-4):573-578
An optimisation of some growth parameters for the epitaxy of AlGaN–GaN based heterostructure field effect transistors (HFET) at low pressure in a new 3 * 2″ MOVPE reactor is presented. Some possible processes for the growth of semi-insulating buffers have been identified and are described. TEM analysis shows that the insulating character is not due to a high density of dislocations, whereas SIMS analysis shows that classical impurity (Si, O and C) concentrations are in the same range as in conductive undoped layers. Further studies are needed to identify the traps responsible for the compensation of the GaN layers. The properties of the two-dimensional electron gas (2DEG) located at the AlGaN–GaN interface can be tuned by modifying the characteristics of the AlGaN layer and of the insulating buffer. The best mobility (1500 cm2 V−1 s−1 for n6×1012 cm−2) is obtained when using a thick buffer layer, whereas the sheet carrier density is found to increase with the Al content in the undoped supply layer and reaches 1.1×1013 cm−2 for a composition of 24%. 相似文献
84.
In this paper, a theoretical study of heat transfer to a fluid of vanishing viscosity in laminar flow in a pipe is made. The constant wall temperature boundary condition is considered in order to facilitate comparison with other classical solutions. Using velocity profiles of simple geometrical shape, the dependence of the heat transfer on velocity distribution is illustrated. Because of the nature of the idealised flow and heat transfer models, the theoretical results are applicable to all axisymmetric flows. Accordingly, some account of the possible effects of swirl on heat transfer in real flows is given.
Nomenclature =(k/c) Thermal diffusivity - C, C 1, C2, C3, Cn Constants - c Specific heat at constant pressure - D=(2rw) Diameter - k Thermal conductivity - M n Root of Bessel Equation,J 0(Mn)=0 - r Radius - T Temperature - u, Velocity, average velocity - x Axial distance - X, R Function ofx, (r) alone - n (= 2M n/r w 2 ) Eigen value - Dynamic viscosity - (=/) Kinematic viscosity - Density - (=(T-T w)/(T1-Tw)) Dimensionless temperature - (=(T–T w)/(T 1–T w)) Nusselt number - Pe (=Re·Pr) Péclet number - Pr (= c/k) Prandtl number - Re(=2rw·v) Reynolds number Suffixes b Bulk - 1 Inlet - w wall 相似文献
Zusammenfassung Es handelt sich um eine theoretische Untersuchung des Wärmeübergangs in laminarer Rohrströmung bei verschwindender Viskosität. Zum Vergleich mit anderen klassischen Lösungen wurde konstante Wandtemperatur als Randbedingung vorgegeben. Unter Benutzung von Geschwindigkeitsprofilen einfacher Geometrie wurde deren Einfluß auf den Wärmeübergang ermittelt. Diese Ergebnisse sind wegen der gewählten Strömungs- und Wärmeübergangsmodelle auf alle achsensymmetrischen Strömungen anwendbar. Die mögliche Wirkung einer Wirbelströmung auf den Wärmeübergang wird diskutiert.
Nomenclature =(k/c) Thermal diffusivity - C, C 1, C2, C3, Cn Constants - c Specific heat at constant pressure - D=(2rw) Diameter - k Thermal conductivity - M n Root of Bessel Equation,J 0(Mn)=0 - r Radius - T Temperature - u, Velocity, average velocity - x Axial distance - X, R Function ofx, (r) alone - n (= 2M n/r w 2 ) Eigen value - Dynamic viscosity - (=/) Kinematic viscosity - Density - (=(T-T w)/(T1-Tw)) Dimensionless temperature - (=(T–T w)/(T 1–T w)) Nusselt number - Pe (=Re·Pr) Péclet number - Pr (= c/k) Prandtl number - Re(=2rw·v) Reynolds number Suffixes b Bulk - 1 Inlet - w wall 相似文献
85.
Titanium dioxide was deposited from aqueous suspension onto cellulosic surfaces.Titania was sourced from Degussa (P25TM,70:30 anatase:rutile).Dry uptake of particles was shown to be rapid and dominant with one-third of the deposition occurring in less than 30 s and over one-half in the first minute.Isotherms were recorded to compare the rate of titanium deposition on dry and pre-wetted cotton.In the dry case uptake reached a maximum in 30 min whereas in the pre-wetted case the uptake was seen to continue beyond 180 min.A broad trend of higher deposition occurring at lower pH was seen,corresponding to the region where surface charges were opposite and thus attractive.Dry pickup was less significant at high pH.The response to varying ionic strength was complex and was attributed to the combined effect of charge screening,particle aggregation and consequent particle entrapment or occlusion.Titania deposition into the interstices of woven cotton sheets resulted in the formation of inorganic,nanoparticulate skeletons which could be isolated by controlled combustion of the cellulose and thus cotton was suggested to have potential for the templated synthesis of high surface area semiconductor materials. 相似文献
86.
87.
88.
Lucchese B Humphreys KJ Lee DH Incarvito CD Sommer RD Rheingold AL Karlin KD 《Inorganic chemistry》2004,43(19):5987-5998
The ligand TMPA (tris(2-pyridylmethyl)amine) and its copper complexes have played a prominent role in recent (bio)inorganic chemistry studies; the copper(I) complex [CuI(TMPA)(CH3CN)]+ possesses an extensive dioxygen reactivity, and it is also known to effect the reductive dechlorination of substrates such as dichloromethane and benzyl and allyl chlorides. In this report, we describe a set of new analogues of TMPA, ligand 6TMPAOH, binucleating Iso-DO, and trinucleating SYMM. Copper(I) complexes with these ligands and a previously described binucleating ligand DO react with chloroform, resulting in reductive dechlorination and production of [CuIIx(L)Clx]x+ (x = 1, 2, or 3). X-ray crystal structures of [CuII(6TMPAOH)Cl]PF6, [CuII2(Iso-DO)Cl2](PF6)2, [CuII2(DO)Cl2](PF6)2, and [Cu3(SYMM)Cl3](PF6)3 are presented, and the compounds are also characterized by UV-vis and EPR spectroscopies as well as cyclic voltammetry. The steric influence of a pyridyl 6-substituent (in the complexes with 6TMPAOH, Iso-DO, and SYMM) on the solid state and solution structures and redox potentials are compared and contrasted to those chlorocopper(II) complexes with a pyridyl 5'-substituent (in [CuII2(DO)Cl2](PF6)2 and in [CuII(TMPA)Cl]+). Some insights into the reductive dechlorination process have been obtained by using 2H NMR spectroscopy in following the reaction of [Cu2(Iso-DO)(CH3CN)2](PF6)2 with CDCl3, in the presence or absence of a radical trap, 2,4-di-tert-butylphenol. 相似文献
89.
90.