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1.
Dr. Konrad Natterer 《Monatshefte für Chemie / Chemical Monthly》1885,6(1):519-522
Ohne Zusammenfassung 相似文献
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N. M. Agababyan I. V. Ajinenko Yu. A. Belokopytov K. S. Belous H. Boettcher F. Botterweck M. M. Chapkin P. V. Chliapnikov F. Crijns A. De Roeck E. A. De Wolf K. Dziunikowska A. M. F. Endler A. Eskreys Z. C. Garutchava P. van Hal T. Haupt A. I. Katargin W. Kittel S. S. Megrabyan F. Meijers A. B. Micha?owska V. I. Nikolaenko K. Olkiewicz V. M. Ronjin R. Rosmalen H. M. T. Saarikko L. Scholten E. K. Shabalina J. Stepaniak O. G. Tchikilev V. A. Uvarov F. Verbeure R. Wischnewski S. A. Zotkin Y. V. Yarba EHS-NA Collaboration 《Zeitschrift fur Physik C Particles and Fields》1990,46(3):387-395
We report on a study of ρ0, ρ+, ω, \(\bar K^{*0} (892)\) andK *0 (892) inclusive production in π+ p interactions at 250 GeV/c, for ρ+, \(\bar K^{*0} (892)\) for the first time in a π+ p experiment. The data are compared withK + p data in the same experiment, with results of other experiments and with quark-parton models. Interesting differences are found between ρ+,0 and ω production. 相似文献
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We formulate the super-KMS condition suggested by Connes and Kastler, in the context of entire cyclic cohomology of quantum algebras. We show that the Chern character of Jaffe, Lesniewski, and Osterwalder — associated by Kastler to a super-KMS functional — satisfies the entire growth condition. Hence, a super-KMS functional defines a cocycle for the entire cyclic cohomology of quantum algebras.Supported in part by the National Science Foundation. 相似文献
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Lithiation of 2,5-dimethylazaferrocene 1 with sec-BuLi/TMEDA in THF at −78 °C proceeds (as shown by quenching with D2O) to comparable extent on the methyl groups and the Cp ring. However, the outcome of the reaction of the lithiated 1 with an electrophile depends on the nature of this electrophile. In the reaction with 4-methoxybenzaldehyde only the product originated from the lateral lithiation is formed, whereas the reaction with 4-methoxyacetophenone and 4,4′-dimethoxybenzophenone afforded mixtures of the products resulting from lateral and ring-lithiation. Similar results were also obtained in the reaction of lithiated 1 with chlorodiphenylphosphine and diphenyl diselenide. On the other hand, the exclusive formation of the Cp-substituted product was observed in the reaction of lithiated 1 with N,N-dimethylformamide. The structures of selected products (oily compounds were transformed into the corresponding crystalline W(CO)5-complexes) were confirmed by X-ray diffraction. The presented reactions open a novel entry to specifically substituted azaferrocenes (especially those containing heteroatom substituents) with potential applications as ligands for the homogenous catalysis. 相似文献
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The energy transfer reation of He(23S) + CS was studied spectroscopically in a flowing afterglow apparatus. The CS+(B2Σ+ → A 2Πi) transition is identified via three members of the Δν = 0 sequence (406–415 nm). The spin-orbit splitting of the (0, 0) band of CS+(A 2Πi) is 301 ± 5 cm?1. A weak emitting system (280–340 nm) is tentatively identified as CS+(B2Σ+→ X2Σ+). 相似文献
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