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101.
Bernhard Krötz 《Japanese Journal of Mathematics》2007,2(2):303-311
In this paper we raise a question about the boundary of the crown domain of a Riemannian symmetric space X. In case X is of Hermitian type we give an affirmative answer. 相似文献
102.
M. G. Bettoli M. Ravanelli L. Tositti O. Tubertini L. Guzzi W. Martinotti G. Queirazza M. Tamba 《Radiation Physics and Chemistry》1998,52(1-6):327-331
Decomposition by ionizing radiations of p-chlorophenol and tetrachloroethylene in synthetic water samples at about 2 mg Cl L−1, has been studied on laboratory-scale experiments. Bicarbonate/carbonate and nitrate ions, at two concentration levels (20 and 200 mg HCO3−1 and 1 and 50 mg NO3−L−) were added to synthetic samples in order to evaluate their influence on decomposition yield. At 5 kGy γ dose level, a quantitative degradation of p-chlorophenol is obtained whereas only qualitative consideration can be drawn on tetracholoroethylene. Comparative study with respect to degradation of p-cholophenol solutions (about 2 mg Cl L−1) by γ-rays and electron beam irradiation treatment at 0.5 kGy dose level, are in progress; preliminary results indicate that irradiation with γ-rays seems to be more efficient in terms of removal efficiency respect to electron beams source. 相似文献
103.
R. B. King 《Russian Chemical Bulletin》1993,42(11):1772-1781
Reactions of disodium tetracarbonylferrate, Na2Fe(CO)4, with sterically hindered dialkylaminodichlorophosphines, R2NPCl2 (R2N=diisopropylamino, dicyclohexylamino, and 2,2, 6, 6-tetramethylpiperidino) in diethyl ether lead to the air-stable phosphorus-bridging carbonyl derivatives (R2NP)2COFe2(CO)6 as the major products. The phosphorus-bridging carbonyl group in (i-Pr2NP)2COFe2(CO)6 has been found to undergo the following types of reactions: 1)Reduction, 2)Acylation, 3)Extrusion of the carbonyl group. The mechanisms of the reactions have been considered.This work was presented at the Workshop «The Modern Problems of Heteroorganic Chemistry» held on the ship «Nikolai Bauman» during the period May 8–13, 1993.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 1858–1867, November, 1993. 相似文献
104.
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108.
Highly stereocontrolled additions to achiral acyclic (E) olefins are achieved via incorporation into an ansa macrolide with a non-racemic stilbene diol (molecular workbench approach). 相似文献
109.
110.
Chiral separations by host-guest complexation with cyclodextrin and crown ether in capillary zone electrophoresis 总被引:2,自引:0,他引:2
Summary Capillary zone electrophoresis using cyclodextrins and a chiral crown ether as buffer constituents was studied for the enantiomeric separation of drugs and amino acids. Based on results obtained from separation of racemic -amino acids both chiral selectors are compared with respect to resolution, efficiency and retention time. For (±)-Quinagolide effects of buffer composition and temperature are examined using -cyclodextrin as chiral agent. Optimum conditions were pH 2.5 at 30 mmol L–1 -cyclodextrin. A linear dependence of retention on -cyclodextrin concentration allowed calculation of formation constants of the host-guest complexes. Buffer concentration and temperature also influence resolution. The application of a chiral crown ether to the separation of optical isomers in capillary zone electrophoresis is described for the first time. Chiral recognition of solutes depends on the formation of protonated alkyl amines and separation is attributed to the formation of diastereomeric host-guest complexes with different interactions for each enantiomer. The effects of crown ether concentration on resolution are presented. 相似文献