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排序方式: 共有85条查询结果,搜索用时 31 毫秒
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Tan C Atas E Müller JG Pinto MR Kleiman VD Schanze KS 《Journal of the American Chemical Society》2004,126(42):13685-13694
The conjugated polyelectrolyte PPESO3 features a poly(phenylene ethynylene) backbone substituted with anionic 3-sulfonatopropyloxy groups. PPESO3 is quenched very efficiently (KSV > 10(6) M(-1)) by cationic energy transfer quenchers in an amplified quenching process. In the present investigation, steady-state and picosecond time-resolved fluorescence spectroscopy are used to examine amplified quenching of PPESO3 by a series of cyanine dyes via singlet-singlet energy transfer. The goal of this work is to understand the mechanism of amplified quenching and to characterize important parameters that govern the amplification process. Steady-state fluorescence quenching of PPESO3 by three cationic oxacarbocyanine dyes in methanol solution shows that the quenching efficiency does not correlate with the Forster radius computed from spectral overlap of the PPESO3 fluorescence with the cyanines' absorption. The quenching efficiency is controlled by the stability of the polymer-dye association complex. When quenching studies are carried out in water where PPESO3 is aggregated, changes observed in the absorption and fluorescence spectra of 1,1',3,3,3',3'-hexamethylindotricarbocyanine iodide (HMIDC) indicate that the polymer templates the formation of a J-aggregate of the dye. The fluorescence dynamics in the PPESO3/HMIDC system were probed by time-resolved upconversion and the results show that PPESO3 to HMIDC energy transfer occurs on two distinctive time scales. At low HMIDC concentration, the dynamics are dominated by an energy transfer pathway with a time scale faster than 4 ps. With increasing HMIDC concentration, an energy pathway with a time scale of 0.1-1 ns is active. The prompt pathway (tau < 4 ps) is attributed to quenching of delocalized PPESO3 excitons created near the HMIDC association site, whereas the slow phase is attributed to intra- and interchain exciton diffusion to the HMIDC. 相似文献
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Ortiz W Krueger BP Kleiman VD Krause JL Roitberg AE 《The journal of physical chemistry. B》2005,109(23):11512-11519
We present a theoretical investigation of energy transfer in the phenylene ethynelene dendrimer known as the nanostar. Data from extensive molecular dynamics simulations are used to model the dynamical effects caused by torsional motion of the phenyl groups. We compare rate constants for energy transfer between the two-ring chromophore and the three-ring chromophore obtained via the F?rster model, the ideal dipole approximation (IDA), and the transition density cube (TDC) method, which has as its limit an exact representation of the Coulombic coupling. We find that the rate constants obtained with the TDC are extremely sensitive to the phenyl group rotation, whereas the constants computed with the F?rster model and the IDA are not. The implications of these results for the interpretation of recent pump-probe experiments on the nanostar are discussed in detail. Finally, we predict the temperature dependence of the rate constant for energy transfer. 相似文献
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Steven L. Kleiman 《代数通讯》2013,41(12):5677-5678
We consider the original version of the author's example of an algebraic scheme carrying an invertible sheaf arising from no Cartier divisor. 相似文献
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C. Saragovi F. Labenski de Kanter L. Kleiman R. Valentin C. Puglisi 《Hyperfine Interactions》1990,57(1-4):2285-2290
Several natural biotite samples were studied by M.E., electron microprobe and XRD. The M.E. parameters allow to group them
as oxybiotites, normal biotites, chloritized biotites and muscovitized biotites. Mechanisms of oxybiotite formation and processes
undergone by the rocks are discussed. 相似文献
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Isoperimetric inequalities are applied to a moving-boundaryproblem for doubly-connected domains. This problem occurs forexample in electrochemistry, in which case the domains in questionare the electrolyte of an electrolytic cell. The two electrodessurrounding the electrolyte are assumed to grow or dissolve,at different rates in general, by electrochemical reaction.We obtain optimal estimates showing, for example, that the leastchange in volume of each electrode always occurs in sphericalsymmetry. 相似文献
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Steven L. Kleiman 《Annali dell'Universita di Ferrara》2017,63(1):147-158
We prove a projection formula, expressing a relative Buchsbaum–Rim multiplicity in terms of corresponding ones over a module-finite algebra of pure degree, generalizing an old formula for the ordinary (Samuel) multiplicity. Our proof is simple in spirit: after the multiplicities are expressed as sums of intersection numbers, the desired formula results from two projection formulas, one for cycles and another for Chern classes. Similarly, but without using any projection formula, we prove an expansion formula, generalizing the additivity formula for the ordinary multiplicity, a case of the associativity formula. 相似文献