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11.
C.A. Fields F.W.N. De Boer J.J. Kraushaar R.A. Ristinen L.E. Samuelson E. Sugarbaker 《Nuclear Physics A》1981,363(2):311-321
The high-spin states in 90Nb have been studied by in-beam γ-ray spectroscopy using the 35 MeV 89Y(α, 3nγ)90Nb and 33 MeV 90Zr(3He, p2nγ)90Nb reactions. A new isomeric state with half-life 0.44±0.02 σs and Jπ = 11? has been located in this nucleus. The level scheme derived from these measurements is compared with shell-model calculations. 相似文献
12.
C.A. Fields F.W.N. De Boer D.E. Prull R.A. Ristinen L.E. Samuelson P.A. Smith E. Sugarbaker 《Nuclear Physics A》1981,366(1):38-60
Exclusive neutron spectra and angular distributions have been measured by n-γ coincidence techniques for reactions on 150Nd in the 25–44 MeV range. The results show that pre-equilibrium processes dominate low-energy light-ion induced reactions at certain beam energies. Analysis of the yrast γ-ray cascades in the residual nuclei shows that a well-defined minimum entry-state spin exists in final nuclei populated by pre-equilibrium processes. This in turn implies the existence of a minimum classical impact parameter for these reactions. These results are discussed in terms of phenomenological models of the reaction mechanisms. 相似文献
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R.E. Anderson R.L. Bunting J.D. Burch S.R. Chinn J.J. Kraushaar R.J. Peterson D.E. Prull B.W. Ridley R.A. Ristinen 《Nuclear Physics A》1975,242(1):75-92
The 106Pd(p, d)105Pd reaction has been studied at 22.9 MeV with an energy resolution of 13 keV. Angular distributions permitted the assignment of l-values and the extraction of spectroscopic factors for 13 states including several previously unresolved l = 2 transitions. The 106Pd(3He, d)107Ag reaction has also been studied at 32.8 MeV with a resolution of 20 keV. Angular distributions were obtained, l-values assigned and spectroscopic factors extracted for 14 levels including many not observed previously in a proton transfer reaction. The level structure of 105Pd and 107Ag is discussed particularly in terms of quasirotational bands. 相似文献
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LUDVÍK BENEŠ KLÁRA MELÁNOVÁ JAN SVOBODA VÍTĚZSLAV ZIMA 《Journal of inclusion phenomena and macrocyclic chemistry》2006,55(3-4):289-293
Intercalates of o-, m-, and p-toluidine into α-Zr(HPO4)2 · H2O were prepared and characterized by powder X-ray diffraction, thermogravimetric analysis and infrared spectroscopy. As follows from IR, toludine molecules are protonated in the interlayer space. Toluidine molecules are arranged in a bimolecular way in the intercalates containing more than 1.5 toluidine molecules per Zr atom. On the other hand, a monolayer of the toluidine molecules is supposed in the intercalates with less than one toluidine molecule per Zr atom. 相似文献
16.
Biomolecular homochirality, the origin of which is still a puzzle, has challenged scientists to design chemical systems that provide chiral molecules through absolute asymmetric synthesis and to amplify a small stereochemical bias in such systems. The photoresolution of the enantiomers of helical-shaped, sterically overcrowded alkene 1 with circularly polarized light and the transduction of the stereochemical information by triggering the helical arrangement of a large collection of achiral molecules in a twisted nematic liquid crystalline phase (2) are examples of control and amplification of chirality. 相似文献
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Numerous organic and inorganic laboratory standards were gathered from nine European and North American laboratories and were analyzed for their delta(18)O values with a new on-line high temperature pyrolysis system that was calibrated using Vienna standard mean ocean water (VSMOW) and standard light Antartic precipitation (SLAP) internationally distributed reference water samples. Especially for organic materials, discrepancies between reported and measured values were high, ranging up to 2 per thousand. The reasons for these discrepancies are discussed and the need for an exact and reliable calibration of existing reference materials, as well as for the establishment of additional organic and inorganic reference materials is stressed. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
19.
A review is presented of the calculation of photoionization spectra, particularly in the spectral range where electron autoionization of diatomic molecules takes place. In addition to some interesting results obtained over years that compare favourably with experiment, the emphasis here is put on the relation between the methods developed for the calculation of observables associated with the continuum energy spectrum of the electrons and the Alchemy system of programs. This system of programs serves as a basis for initial and intermediate calculations. The examples presented show that diatomic molecules not only in gas phase but also oriented in space or physisorbed at surfaces may be studied readily. 相似文献
20.
The (3He, d) reaction at a sufficiently high energy is considered to be a reliable single-proton stripping direct reaction. The data for the low-lying states produced by this reaction on 24Mg and 28Si are compared to the predictions of the strong-coupling rotational model. The agreement with the model predictions for 25Al is quite good, both for the single-proton spectroscopic factors in that nucleus and most particularly for the excitation of states in 25Al and 29P by two-step processes. 相似文献