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排序方式: 共有108条查询结果,搜索用时 31 毫秒
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S. Grace V. Meera S. A. Balakrishnan H. D. Sarma 《Journal of Radioanalytical and Nuclear Chemistry》1997,224(1-2):83-87
A study for separation and sequential recovery of uranium and plutonium from nitric acid solutions by extraction chromatography using tributyl phosphate (TBP)/Amberlite XAD7 as stationary phase is presented. Distribution ratios of actinides, lanthanides and fission products were obtained. The column capacity was investigated and actinides retention conditions were established. Finally, U-Pu sequential separation was studied as well as the U and Pu recovery yields from nitric solutions containing Am/fission products were determined. 相似文献
23.
We report the infrared and Raman studies of titanium doped vitreous silica glasses for a number of titanium concentrations. The vibrational modes associated with the randomly oriented chains of SiO4 tetrahedra show broadenings and shifts. The LO-TO splitting of some Raman active modes decreases with increasing titanium concentration. This is attributed to the decrease in long-range coulomb fields associated with the chains of SiO4 tetrahedra which are broken by the titanium atoms. The results are discussed in the context of random network models. An increase in the average intertetrahedral angle of the SiO4 network is calculated from the data. This explains the anomalous decrease in the density of TiO2---SiO2 glasses with increasing titanium content. We identify two new modes associated with the distorted titanium tetrahedra. A polarized Raman mode at 1115 cm−1 which is infrared inactive and an unpolarized Raman mode at 945 cm−1 which is infrared active are observed. 相似文献
24.
The well-studied X-ray-edge problem is revisited using the sea-boson method. This approach is contrasted with the well-known theories of Mahan, Nozières and De Dominicis (MND). The present approach does not use the sudden approximation and the holes carry a momentum label unlike in the MND theory. We focus on the case of doped semiconductors rather than metals. The problem of electrons in a partially filled conduction band and holes in the initially hole-depleted valence band is recast in the sea-boson language. The resulting hamiltonian is shown to be equivalent to the electron-phonon hamiltonian with the excitons taking on the role of electrons and intra-conduction band particle-hole excitations known as ‘conductrons’ taking on the role of phonons. It is shown that the excitonic pole in the computed absorption spectra is replaced by a branch cut with a simple radical leading to a broadening of the exicton line due to these many-body effects. A critical comparison is made with the MND theory as well as with relevant experiments. 相似文献
25.
Generation of fluorescent adducts of malondialdehyde and amino acids: toward an understanding of lipofuscin 总被引:2,自引:0,他引:2
Chowdhury PK Halder M Choudhury PK Kraus GA Desai MJ Armstrong DW Casey TA Rasmussen MA Petrich JW 《Photochemistry and photobiology》2004,79(1):21-25
Lipofuscin is a yellow-brown, highly fluorescent pigment that undergoes an age-related progressive accumulation in animal cells, mainly in postmitotic cells. It is a heterogeneous, high-molecular weight material associated with proteins, lipids and nucleic acids. Lipofuscin is implicated in many aspects of human health, including aging, oxidative stress, macular degeneration, lipid peroxidation, atherosclerosis, dementia (Alzheimer's Disease) and diseases associated with prions. Although the fluorescent properties of lipofuscin have long been recognized, neither histologists nor chemists have yet isolated the pigments themselves or characterized their optical properties. We have prepared lipofuscinlike species by reacting malondialdehyde (MDA) with cysteine (Cys). MDA:Cys adducts 3:2 and 2:2 are two of those that have been identified among the many that were present in the reaction. Whereas previous attempts to synthesize lipofuscinlike species resulted in compounds that were either nonfluorescent or emitted principally in the blue, the MDA:Cys adducts reported in this study are not only fluorescent but also emit over a broader range. 相似文献
26.
This paper is motivated by a link between algebraic proof complexity and the representation theory of the finite symmetric groups. Our perspective leads to a new avenue of investigation in the representation theory of Sn. Most of our technical results concern the structure of “uniformly” generated submodules of permutation modules. For example, we consider sequences
of submodules of the permutation modules M(n−k,1k) and prove that if the sequence Wn is given in a uniform (in n) way – which we make precise – the dimension p(n) of Wn (as a vector space) is a single polynomial with rational coefficients, for all but finitely many “singular” values of n. Furthermore, we show that dim(Wn)<p(n) for each singular value of n≥4k. The results have a non-traditional flavor arising from the study of the irreducible structure of the submodules Wn beyond isomorphism types. We sketch the link between our structure theorems and proof complexity questions, which are motivated by the famous NP vs. co-NP problem in complexity theory. In particular, we focus on the complexity of showing membership in polynomial ideals, in various proof systems, for example, based on Hilbert's Nullstellensatz. 相似文献
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Dr. Michael H. Holthausen Meera Mehta Prof. Dr. Douglas W. Stephan 《Angewandte Chemie (International ed. in English)》2014,53(25):6538-6541
The dicationic imidazolium‐phosphonium salt [(SIMes)PFPh2][B(C6F5)4]2 has been prepared and shown to exhibit remarkable Lewis acidity in stoichiometric reactions and acting as an effective Lewis acid catalyst for the hydrodefluorination of fluoroalkanes and the hydrosilylation of olefins. 相似文献
29.
High quality assays are needed in drug discovery to reduce the high attrition rate of lead compounds during primary screening. Capillary electrophoresis (CE) represents a versatile micro-separation technique for resolution of enzyme-catalyzed reactions, including substrate(s), product(s), cofactor(s) and their stereoisomers, which is needed for reliable characterization of biomolecular interactions in free solution. This review article provides a critical overview of new advances in CE for drug screening over the past five years involving biologically relevant enzymes of therapeutic interest, including transferases, hydrolases, oxidoreductases, and isomerases. The basic principles and major configurations in CE, as well as data processing methods needed for rigorous characterization of enzyme inhibition are described. New developments in functional screening of small molecules that modulate the activity of disease-related enzymes are also discussed. Although inhibition is a widely measured response in most enzyme assays, other important outcomes of ligand interactions on protein structure/function that impact the therapeutic potential of a drug will also be highlighted, such as enzyme stabilization, activation and/or catalytic uncoupling. CE offers a selective platform for drug screening that reduces false-positives while also enabling the analysis of low amounts of complex sample mixtures with minimal sample handling. 相似文献
30.