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Xestospongin A,B,C and D represent a new class of macrocyclic 1-oxaquinolizidines, have been isolated from Australian sponge Xestospongiaexigua. The structure of xestospongin C has been determined by X-ray analysis.  相似文献   
95.
A partial-wave analysis of the ω ωπ0-system produced in the π- p→ωπ0 n reaction at 38 GeV/c beam momentum has been performed. A new 5?- meson state,ρ 5(22350), with a massM=2330±35 MeV and a width Γ=400±100 MeV, is observed. The analysis also confirms the 1?- ρ(2150) meson, a radial-orbital excitation of the ρ(770), observed earlier by the GAMS Collaboration.  相似文献   
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This paper provides a characterization of the storage needs of a quadtree when used as an index to access large volumes of 2-dimensional data. It is shown that the page occupancy for data in random order approaches 33%. A precise mathematical analysis that involves a modicum of hypergeometric functions and dilogarithms, together with some computer algebra is presented.A brief survey of the analysis of storage usage in tree structures is included. The 33% ratio for quadtrees is to be compared to the figures for binary search trees (50%), tries (69%), and quadtries (46%).The research of this author was done while visiting INRIA, Rocquencourt, France under support from the Ministry of Education of Japanese Government.Work of this author was supported in part by the Basic Research Action of the E.C. under contract No. 3075 (Project ALCOM).  相似文献   
98.
Orientation relaxation of dissimilar chains in the molten miscible blends, poly(methyl methacrylate)/poly(vinylidene fluoride) and poly(methyl methacrylate)/poly(vinylidene fluoride-co-trifluoroethylene), were investigated by measuring (1) the change of infrared dichroic ratio with time after the uniaxial stretching of film specimens, (2) the shear stress relaxation spectrum, and (3) birefringence relaxation in shear. The dissimilar polymers showed an identical time variation of the normalized Hermans orientation function. The blend showed a relaxation spectrum with a single characteristic relaxation time τc, depending on the blend composition. The birefringence relaxed monotonically, remaining positive. These results suggest that the dissimilar polymers do not relax independently but cooperatively. This behavior may be induced by a constraint due to the specific interactions between the dissimilar polymers, e.g., weak hydrogen bonding. For the cooperative chain relaxation, a third power relationship was found; τce vprop; (M/Me),3 where τe and Me are the relaxation time and molecular weight of entanglement strand, respectively, and M is the number average molecular weight in the blend.  相似文献   
99.
On heating vibro-milled CdS containing the strained high-pressure rock salt phase, the excess energy was gradually liberated accompanied by the retransformation into more stable phases and the restoration of their crystallinity. Profiles of DSC curves, inter-relationships between thermal and crystallographical properties, the stability of each phase and the mechanism of the mechanochemical activation are discussed. A direct retransformation of the strained high-pressure phase was found to accompany the liberation of the excess energy.  相似文献   
100.
Multiple optimum solutions of a multistage allocation problem, well-known to chemical engineers, are analyzed. The number of local optima becomes greater with a decrease in the initial-condition value of the first stage or with an increase in the total stage number. The fact that this behavior is closely related to the flat portion of the profile of a curvef(x), which determines the objective function, is revealed. A construction method by Aris is used to give an excellent insight into this behavior. Moreover, the construction curves ensure that all stationary points are found. Finally, a theorem to discriminate local optima from stationary points, without evaluating second-order derivatives, is presented.The authors would like to thank Dr. I. Hashimoto and Dr. H. Nishitani for valuable discussions. Computations were carried out with the assistance of Messrs. H. Unno, H. Nakano, Y. Era, and Y. Ueno. The authors are indebted to the computing centers of Osaka University, Kyoto University, and Nagoya University for the use of their facilities.  相似文献   
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