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41.
42.
Tunneling between potential wells is considered as affected by random nonadiabatic change in the resonance condition. A general expression is derived for the transition probability on the assumption that the process involves only two states of the discrete spectrum. Detailed consideration is given to the case of an electron localized by the polarized layer it produces. 相似文献
43.
Burshtein AI 《The journal of physical chemistry. A》2006,110(51):13667-13675
The reversible electron transfer from donor to excited molecule (acceptor of electron) is shown to be the irreversible energy quenching, if it is completed by subsequent irreversible recombination radical-ions which are produced. The Stern-Volmer constant of fluorescence as well as the Markovian rate constant of triplet quenching are calculated analytically, assuming the electron transfer is contact. The multiple Rehm-Weller effect is shown to be peculiar to both constants. 相似文献
44.
The contact recombination from both singlet and triplet states of a radical pair is studied assuming that the spin conversion is carried out by the fast transversal relaxation and Delta g mechanism. The alternative HFI mechanism is neglected as being much weaker in rather large magnetic fields. The magnetic-field-dependent quantum yields of the singlet and triplet recombination products, as well as of the free radical production, are calculated for any initial spin state and arbitrary separation of radicals in a pair. The magnetic field effect is traced and its diffusional (viscosity) dependence is specified. 相似文献
45.
46.
The double-channel recombination and separation of the photochemically created singlet radical pair is investigated, taking into account the spin conversion in a zero magnetic field and the arbitrary initial distance between the radicals. The quantum yields of the singlet and triplet products and the free radicals production are found analytically, assuming that the recombination of the diffusing radicals occurs at contact. All the yields are related to the singlet and triplet populations of the recombining radical pair, subjected to spin conversion and contact exchange interaction. The general analytical expressions for the quantum yields are specified for the particular limits of the weak and strong exchange. They are greatly simplified in the case of polar solvents, especially at the contact start. A close similarity is obtained with the results of a previously developed incoherent model of spin conversion, provided that the conversion rate is appropriately related to the hyperfine coupling constant. 相似文献
47.
A nonadiabatic quasi-classical impact theory of the Q-band shape for isotropic and anisotropic Raman scattering by linear rotors has been developed. With our previous results this allows us to obtain upper and lower estimates of the contribution of collisional rotational relaxation to the Raman line broadening. 相似文献
48.
I. A. Machkarovskaya K. Ya. Burshtein V. A. Petrosyan 《Russian Chemical Bulletin》1993,42(11):1800-1805
By semiempirical MNDO and AM1 methods it was shown that electron transfer on the chloro-and bromomethane molecules of the general formula CHnHal4–n (n=1–3) results either in a kinetically independent particle, i.e., a radical anion, or in C-Hal-bond cleavage with the formation of Hal– and the respective radical. The enthalpy, activation energy of the reactions, and data on the geometry of the radical anion obtained show that the increasing the number of halogen atoms in the initial molecule and decreasing the solvent polarity favor radical anion stabilization. It was established that the cleavage of the C-H-bond in the radical anion is not favored energetically. Fragmentation at the C-H-bond can proceed according to the mechanism of dissociative electron capture by halomethane molecule only with additional factors favoring this reaction.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 1886–1892, November, 1993. 相似文献
49.
Gladkikh V Burshtein AI Feskov SV Ivanov AI Vauthey E 《The Journal of chemical physics》2005,123(24):244510
The recombination dynamics of ion pairs generated upon electron transfer quenching of perylene in the first singlet excited state by tetracyanoethylene in acetonitrile is quantitatively described by the extended unified theory of photoionization/recombination. The extension incorporates the hot recombination of the ion pair passing through the level-crossing point during its diffusive motion along the reaction coordinate down to the equilibrium state. The ultrafast hot recombination vastly reduces the yield of equilibrated ion pairs subjected to subsequent thermal charge recombination and separation into free ions. The relatively successful fit of the theory to the experimentally measured kinetics of ion accumulation/recombination and free ion yield represents a firm justification of hot recombination of about 90% of primary generated ion pairs. 相似文献
50.