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41.
A Sedimentological Approach to Upscaling 总被引:1,自引:0,他引:1
Optimised upscaling in reservoir simulations requires the construction of realistic petrophysical properties that are representative of the heterogeneity in the sedimentary deposits. Reservoir heterogeneities are controlled by the arrangement of various hierarchies of sedimentary facies and their internal bounding surfaces. The conventional sedimentological approach to reservoir upscaling involves subdivision and ranking of various hierarchies of architectural units and associated bounding surfaces of the reservoir sequence according to their geological significance. This global upscaling approach produces realistic scaled up models that retain both the structural and non-structural heterogeneities of the original sedimentological models. Analyses of sedimentary sequences from various depositional environments indicate that the fractional Levy model can adequately describe the heterogeneity and scaling characteristics of individual genetic sediment sequences in the clastic sedimentary system without further subdividing and ranking of the heterogeneous sequences. The heterogeneous nature of each sedimentary system can be quantified by the Levy index parameter, whereas the maximum upscaling magnitude (or upscaling index) for a particular sequence can be determined from the Levy width parameter plot. Depositional modelling mimics the sedimentary processes in a range of scales and honours hierarchies of sedimentary facies and their bounding surfaces. It can be used effectively for upgridding and upscaling in accordance with the stratigraphic framework and sedimentological models. Both the fractional Levy model and the depositional modelling provide quantitative alternatives to the conventional global sedimentological upscaling approach. 相似文献
42.
43.
Mohamed Ghazzali Lars
hrstrm Per Lincoln Vratislav Langer 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(7):m243-m245
The title compound, [Ru(C12H8N2)3]2[Fe(NCS)4](ClO4)2, crystallizes in a tetragonal chiral space group (P41212) and the assigned absolute configuration of the optically active molecules was unequivocally confirmed. The Δ‐[RuII(phen)3]2+ complex cations (phen is 1,10‐phenanthroline) interact along the 41 screw axis parallel to the c axis, with an Ru...Ru distance of 10.4170 (6) Å, and in the ab plane, with Ru...Ru distances of 10.0920 (6) and 10.0938 (6) Å, defining a primitive cubic lattice. The Fe atom is situated on the twofold axis diagonal in the ab plane. The supramolecular architecture is supported by C—H...O interactions between the [RuII(phen)3]2+ cation and the disordered perchlorate anion. This study adds to the relatively scarce knowledge about intermolecular interactions between [Ru(phen)3]2+ ions in the solid state, knowledge that eventually may also lead to a better understanding of the solution state interactions of this species; these are of immense interest because of the photochemical properties of these ions and their interactions with DNA. 相似文献
44.
Christopher B. Smith Stephen F. Lincoln Max R. Taylor Kevin P. Wainwright 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(9):m358-m360
Crystallization of [Cd(S‐thpc12)](ClO4)2·H2O {S‐thpc12 is 1,4,7,10‐tetrakis[(S)‐2‐hydroxypropyl]‐1,4,7,10‐tetraazacyclododecane} in the presence of two equivalents of sodium picrate monohydrate (sodium 2,4,6‐trinitrophenolate monohydrate) diastereoselectively produces a neutral receptor complex, viz. the title compound, Λ‐[Cd(C20H44N4O4)](C6H2N3O7)2·CH3CN. In this complex, two picrate anions hydrogen bond, via their phenolate moieties, to the pendant hydroxyl groups of the receptor which, together with the four N atoms, themselves bond to CdII in an approximately cubic arrangement. One picrate anion hydrogen bonds to all four hydroxyl groups, one of which also acts as the sole hydrogen‐bond donor to the second picrate anion. 相似文献
45.
The high temperature 13C NMR spectra of the methyl esters of deuteroporphyrin-IX and protoporphyrin-IX, and octaethylporphyrin show sharp discrete signals for the inner macrocycle carbon resonances. The temperature dependence of these shifts is discussed. 相似文献
46.
47.
CM Thaker S Rayaprol Krushna Mavani DS Rana MS Sahasrabudhe SI Patil DG Kuberkar 《Pramana》2002,58(5-6):1035-1039
The effect of simultaneous substitution of a fluctuating cation and a divalent cation in LaMnO3 perovskite modifies the properties of the material to exhibit large valence colossal magnetoresistance (CMR) effect. A good
example of these properties is (La1−2x
Pr
x
Ca
x
)MnO3 (LPCMO) type CMR material. In this communication it is reported that, with the increase in x (for x=0.1, 0.15, 0.2), the T
c varies between 100 and 120 K with improvisation in metal-insulator transition. Interestingly, resistance increases with x from few hundred ohms to few kilo ohms with corresponding decrease in the unit cell volume. The results of the studies using
X-ray diffraction (XRD), electrical resistivity, magnetoresistance and ac susceptibility measurements on LPCMO samples for
understanding the structural, transport and magnetic properties are discussed in detail. 相似文献
48.
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50.
Ch. Anjaiah M. Nagamani Ch. Abraham Lincoln D. Ashok 《Russian Journal of General Chemistry》2018,88(10):2149-2153
An efficient microwave-assisted synthesis of 3-(arylsulfanyl)-4-hydroxy-2H-chromen-2-ones by condensation of arenesulfonohydrazides with 4-hydroxy-2H-chromen-2-one in the presence of iodine is described. The synthesized compounds were characterized by spectral data (IR, 1H and 13C NMR, and mass spectra and elemental analyses) and were tested for their in vitro antimicrobial activity against bacterial and fungal organisms. 相似文献