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Miles G. Nicholls 《The Journal of the Operational Research Society》1985,36(2):137-145
In this paper, an absorbing Markov chain representing the stocks and flows of undergraduate students in a tertiary education faculty is established.In order to assist faculty planners in achieving specific goals, a direct control model in fixed time is developed that allows a partial specification of the distribution of students within the system based on the concept of stated ratios. The attainment and maintenance of this objective, together with a given system size for each planning period, is attempted through recruitment control, as this is the most appropriate control mechanism in an educational institution. The unique specification of the distributional objective makes for considerable ease of planning.The development of a useful sensitivity analysis modus operandi, along with a new efficient solution algorithm to the direct control model, further enhances its applicability for faculty planning. 相似文献
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Douglas F. Foster Barry S. Nicholls Anthony K. Smith 《Journal of organometallic chemistry》1982,236(3):395-402
Reactions of Rh6(CO)16 with bis(diphenylphosphino)methane (dppm) gave Rh6(CO)14(dppm), Rh6(CO)12(dppm)2, or Rh6(CO)10(dppm)3, depending upon the reaction conditions. Rh4(CO)10(dppm) may be obtained from the reaction of Rh4(CO)12 with dppm, but this derivative rapidly decomposes in solution to give Rh4(CO)8(dppm)2, Rh6(CO)14(dppm), and Rh6(CO)12(dppm)2. Ir4(CO)10(dppm) and Ir4(CO)8(dppm)2 have also been prepared, and their structures are discussed on the basis of infrared and 31P NMR spectroscopic data. 相似文献
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Ranganathan Bharadwaj Andreas Windemuth S. Sridharan Barry Honig Anthony Nicholls 《Journal of computational chemistry》1995,16(7):898-913
We propose a fast implementation of the boundary element method for solving the Poisson equation, which approximately determines the electrostatic field around solvated molecules of arbitrary shape. The method presented uses computational resources of order O(N) only, where N is the number of elements representing the dielectric boundary at the molecular surface. The method is based on the Fast Multipole Algorithm by Rokhlin and Greengard, which is used to calculate the Coulombic interaction between surface elements in linear time. We calculate the solvation energies of a sphere, a small polar molecule, and a moderately sized protein. The values obtained by the boundary element method agree well with results from finite difference calculations and show a higher degree of consistency due to the absence of grid dependencies. The boundary element method can be taken to a much higher accuracy than is possible with finite difference methods and can therefore be used to verify their validity. © 1995 by John Wiley & Sons, Inc. 相似文献
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R.W Nicholls 《Chemical physics letters》1981,79(2):317-320
The properties of continuum wavefunctions for the regions of Morse potentials above the dissociation limit are discussed in the context of photodissociation processes of diatomic molecules. 相似文献
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The roles of template complexation and ligand binding conditions on recognition in bupivacaine molecularly imprinted polymers 总被引:3,自引:0,他引:3
A model for the molecular basis for ligand recognition in bupivacaine imprinted methacrylic acid-ethylene glycol dimethacrylate co-polymers has been developed based upon a series of (1)H-NMR studies in conjunction with HPLC and radioligand binding analyses. (1)H-NMR studies indicated that functional monomer-template complexes survive the polymerisation process, at least up until the stage of gelation. Polymers were synthesised and characterised by surface area analysis (BET), FT-IR and SEM. A combination of zonal and frontal chromatographic studies in aqueous and non-polar media indicate that selectivity arises from a combination of hydrophobic and electrostatic interactions. However, in the concentration regime employed for LC-based studies, ligand recognition in aqueous media was shown to be predominantly non-specific and hydrophobic in character. Radioligand binding studies, in lower ligand binding concentration regimes, permitted closer examination of the higher affinity binding sites. It was shown that the presence of a polar modifier in a non-polar solvent, or an organic modifier in water, produced enhanced selectivity. Variable temperature studies showed that the temperature of binding influences selectivity as well as the apparent number of sites available and that this effect is different in organic and aqueous environments. This indicates that the system studied is more complex in character than is generally appreciated. A comparison of the techniques employed here indicates that although chromatographic studies provide a valuable first-round screen for polymer-ligand selectivities, the level of detail obtainable using radioligand binding studies (lower concentrations and true equilibrium binding) makes them superior for detailed evaluations of molecularly imprinted polymers. 相似文献
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Abstract— The triplet state of tryptophan in the solid environments of a polyvinyl alcohol) (PVA) film and the protein wool keratin has been studied by emission and absorption spectroscopy at room temperature. The decay kinetics of the triplet state vary depending on the conditions under which the study is made. The observation of second order kinetics suggests triplet-triplet interactions play a major role in the deactivation of the tryptophan triplet state in PVA films plasticised by the presence of water vapour. For wool keratin in the presence of air the major mechanism appears to be a first order reaction between tryptophan residues and oxygen. The actual effects of moisture and oxygen on the tryptophan triplet state are discussed. 相似文献