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91.
The reactions of phenylhydrazine and hydroxylamine with (-X-ethyl)triphenylphosphonium salts (X = Ph, Ph3P+Br) (1, 2) afforded the corresponding -N-ethyl-substituted triphenylphosphonium salts (3, 4). The reaction of triphenyl(2-phenylhydrazinoethyl)phosphonium bromide 3with an aqueous solution of NaOH in benzene afforded a statistical mixture of the nisand transisomers of 2-(diphenylphosphoryl)acetaldehyde phenylhydrazone. (2-Hydroxyaminoethyl)triphenylphosphonium bromide reacted with sodium methoxide to give O-phosphobetaine.  相似文献   
92.
The crystal and molecular structures of the [PrIII(nta)(H2O)2]·H2O (nta = nitrilotriacetic acids), K3[GdIII(nta)2(H2O)]·6H2O, and K3[YbIII(nta)2]·5H2O complexes have been determined by single-crystal X-ray structure analyses. In [PrIII(nta)(H2O)2]·H2O, the PrIIINO8 part forms a nine-coordinate pseudo-monocapped square antiprismatic structure in which one N and three O atoms are from one nta ligand in the same molecule, three O atoms from another nta ligand in the neighboring molecule and two O atoms from two coordinate water molecules. In K3[GdIII(nta)2(H2O)]·6H2O, the [GdIII(nta)2(H2O)3- complex anion has a nine-coordinate pseudo-monocapped square antiprismatic structure in which each nta acts as a tetradentate ligand with one N atom of the amino group and three O atoms of the carboxylic groups. In K3[YbIII(nta)2]·5H2O, each nta also acts as a tetradentate ligand with one N atom of amino group and three O atoms of the carboxylic groups, but the [YbIII(nta)2 3- complex anion has an eight-coordinate structure with a distorted square antiprismatic prism. All the results including those for [TmIII(nta)(H2O)2]·2H2O confirm the inferences on the coordinate structures and coordination numbers of rare earth metal complexes with the nta ligand.  相似文献   
93.
By extraction with acetone and chromatography of the resin on a column of type KSK silica gel the epigeal part ofArtemisia gracilescens has yielded the new sesquiterpene lactone gracilin, for which the structure of 1-oxo-6, 7,11(H)-eudesm-4(5)-en-6,12-olide is proposed.Institute of Organic Synthesis and Coal Chemistry, Academy of Sciences of the Kazakh SSR, Karaganda. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 339–343, May–June, 1991.  相似文献   
94.
Transformations of 1,1,6,6,7,7-hexahydroxy-3,3-dimethyl-5,5-diisopropyl-2,2-dinaphthylidene-8,8-dibarbituric acid (batridene) in DMSO are studied.  相似文献   
95.
The reaction of dimethyl[2,4-dioxo(1H,3H) pynmido]tetrathiafulvalene and its N-alkyl derivatives with iodine leads to the formation of complexes with various numbers of iodine atoms. Depending on the conditions, the betaine of the cation-radical of dimethyl[2, 4-dioxo(1 H, 3H)pyrimidojtetrathiafulvalene or a complex of the latter with dimethy1[2,4-dioxo(1H,3H)pyrimidoltetrathiafulvalene is formed by the oxidation of the pyrimidotetrathiafulvalene. The cation-radical perchlorates are formed on carrying out the oxidation of dimethyl[2,4-dioxo(1H,3H)pyrimidojtetrathiafulvalene and its N-methyl derivatives in the presence of perchloric acid. The preparation of the cation-radical salts is usually linked with the reaction of the cation-radical betaine with acids.For part 2 see [1].  相似文献   
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Polarizabilities of spherical subwavelength silica glass particles are investigated having regard to material dispersion. It is shown that the ranges of the negative electric and magnetic polarizabilities almost coincide. This allows the particles in question to be used for producing media with a negative refractive index.  相似文献   
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