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951.
F. H. A. Abdalla G. A. El-Shobaky N. A. Hassan 《Journal of Thermal Analysis and Calorimetry》1996,47(6):1777-1785
A V2O5/Al2O3 mixed solids sample was prepared with a molar ratio of 0.41 Na2O (4 and 10 mol%) was added in the form of sodium nitrate prior to calcination in air in the temperature range 500–1000C. Solid-solid interactions between V2O5 and Al2O3 were studied using DTA and TG curves and their derivatives together with XRD techniques.The results obtained showed that Na2O interacted with V2O5 at temperatures starting from 500C to yield a sodium/vanadium compound, Na0.3V2O5 which remained stable and decomposed in part by heating at 1000C. V2O5 exists in orthorhombic and monoclinic forms in the case of pure mixed solids and those containing 4 mol% of Na2O and preheated at 500C, and in monoclinic form in the case of the mixed solid doped with 10 mol% of Na2O.Heating of pure and doped mixed oxide solids at 650C resulted in the conversion of most of the V2O5 into AlVO4. Doping with sodium oxide enhanced the solid-solid interaction between V2O5 and Al2O3 at 650C to produce AlVO4. The produced AlVO4 decomposed completely on heating at 700C to form -Al2O3 and V2O5, (orthorhombic and monoclinic forms).The presence of Na2O was found to decrease the relative intensity of the diffraction lines of -Al2O3 (corundum) produced at 750C which indicated some kind of hindrance of the crystallization process.Heating of pure and doped mixed solids at 1000C resulted in a further crystallization of acorundum together with V2O5 and sodium vanadate, Na0.3V2O5. However, the intensities of diffraction lines relative to those of the sodium vanadium compound were found to decrease markedly by heating at 1000C, indicating partial thermal decomposition into vanadium and aluminium oxides. 相似文献
952.
The geometry of the linear molecule HBO, has been investigated within the restricted Hartree-Fock LCAO-MO-SCF approximation. The calculated bond lengths for the near Hartree-Fock calculation were R(H-B)=2.1913 bohr, R(B-O)=2.2284 bohr. Several one electron properties have been calculated for the minimum energy configuration. 相似文献
953.
5-Alkyl(aryl)-3-arylidene-3H-pyrrolin-2-ones were synthesized by ammonolysis of their O-heteroanalogs or by the reactions of 5-alkyl(aryl)-3H-pyrrolin-2-ones with aromatic aldehydes. The structures of the compounds obtained were confirmed by 1H NMR spectra. 相似文献
954.
Tushar S. Basu Baul Keisham Surjit Singh Michal Hol?apek 《Journal of organometallic chemistry》2005,690(6):1581-1587
The complex, [(PhCH2)2{O2CC6H4{N(H)N(C6H3-4(O)-5-O)}-o}Sn]2 (1), is obtained as the exclusive reaction product from the reaction of sodium 2-[(E)-2-(3-formyl-4-hydroxyphenyl)-1-diazenyl]benzoate and (PhCH2)3SnCl. The reaction possibly proceeds via Dakin type rearrangements where arylazosalicylaldehyde is oxidized to arylazocatechol, followed by facile Sn-C bond cleavage. Complete assignments were achieved by 1H, 13C, 2D 1H-119Sn HMQC (119Sn chemical shift), 1D gs 1H-15N HMQC (1J(15N, 1H) coupling constant) NMR and ESI-MS. The crystal structure of compound 1 as determined by X-ray diffraction analyses shows a cyclic centrosymmetric dinuclear moiety linked into extended chains by pairs of long Sn?O contacts of approximately 3.2 Å. Two polymorphs were identified and their structures differ primarily in the packing arrangement afforded by the benzyl groups. In one polymorph, when viewed along the Sn?Sn vector, the benzyl groups at each Sn-atom are oriented to form an S-shape, while they form a U-shape in the second polymorph. 相似文献
955.
M. A. Zahran E. B. Pedersen C. Nielsen 《Monatshefte für Chemie / Chemical Monthly》1995,126(11):1271-1277
Summary 3-Aryl-7-(2-deoxy--D-erythro-pentofuranosyl)-3,7-dihydro-4H-pyrrolo[2,3-d]-pyrimidin-4-imines (4) as well as 4-arylamino-7-(2-deoxy--D-erythro-pentofuranosyl)-2-methyl-5-phenyl-7H-pyrrolo[2,3-d]pyrimidines (7) have been synthesized by glycosylation of the sodium salt of the corresponding nucleobases with 2-deoxy-3,5-di-O-p-toluyl--D-erythro-pentofuranosyl chloride (2) followed by subsequent deprotection with sodium methoxide in methanol. The deprotected nucleoside4 undergoes aDimroth rearrangement on reflux for 24 h in water to furnish the 4-arylamino nucleoside7.
Synthese und Reaktionen von 2-Deoxy--D-ribofuranosylderivaten von 3-Aryl-4H-pyrrolo[2,3-d]pyrimidin-4-iminen
Zusammenfassung 3-Aryl-7-(2-deoxy--D-erythro-pentafuranosyl)-3,7-dihydro-4H-pyrrolo[2,3-d]-pyrimidin-4-imine (4) und 4-Arylamino-7-(2-deoxy--D-erythro-pentofuranosyl)-2-methyl-5-phenyl-7H-pyrrolo[2,3,-d]pyrimidine (7) wurden durch Glycosylierung der Natriumsalze der entsprechenden Nucleosidbasen mit 2-Deoxy-3,5-di-O-p-toluyl--D-erythro-pentofuranosylchlorid (2) und anschließende Entfernung der Schutzgruppe mit Natriummethoxid in Methanol hergestellt. Das entschützte Nucleosid4 ergibt bei 24-stündigem Erhitzen in Wasser unter Rückfluß über eineDimroth-Umlagerung das 4-Aminonucleosid7.相似文献
956.
Reactions of Tetraphosphorus Trichalcogenides with Alkyl Iodides Reactions of alkyl iodides RI (R = CHI2, CH2I or tert-Butyl) with P4E3 (E = S or Se) under the influence of light resulted in cleavage of the basal P3 ring. β-P4E3(I)R was formed initially, then it rearranged to the more stable α-P4E3(I)R structure. 31P NMR data of these products were measured and discussed, along with 77Se data for α- and β-P477SeSe2(I)CHI2. On reaction of P4S3 with tert-butyl iodide in CS2 or with sec-butyl iodide or iso-propyl iodide in dioxane, the new type of compounds P5S2R was observed. In this a sulfur bridge of P4S3 is replaced by a P? R group. 31P-NMR data for these compounds are reported. 相似文献
957.
Ali Taha Viktor Gutmann Wolfgang Linert 《Monatshefte für Chemie / Chemical Monthly》1991,122(5):327-339
Summary The solvatochromic and thermochromic behaviour of a series of mixed Ni(II) complexes with unsubstituted and substituted -diketones and diamines in the solvents 1,2-dichloroethane (DCE), acetonitrile (An), acetone (AC),n-butanol (n-BuOH), formamide (FA), N,N-dimethylformamide (DMF), dimethylsulfoxide (DMSO) and pyridine (PY) has been studied and characterized on the basis of electronic spectra. Spectrophotometric methods have been used to evaluate equilibrium constants and their enthalpic and entropic terms for the formation of Ni(-dik)(diam)L
+ and Ni(-dik)(diam)L
2
+
. Increasing donor strength of the donor-solvents (L) and (or) increasing electronwithdrawing parameters of the substituents at the -diketone and the diamine ligands lead to increasing formation constants, paralleled by relative increase in the stability of the five-coordinated species Ni(-dik)(diam)L
+. The results are discussed in terms of the extended donor-acceptor concept.On leave of absence from the Faculty of Education, Ain Schams University, Roxy, Cairo, Egypt 相似文献
958.
El-B. Yallaoui 《Periodica Mathematica Hungarica》1991,23(2):109-120
Let X be an abstract set and L a lattice of subsets of X. To each lattice regular measure µ, we associate two induced measures
and
on suitable lattices of the Wallman space IR(L) and another measure µ on the spaceIR(L). We will investigate the reflection of smoothness properties of p onto
,
and µ; and try to set some new criterion for repleteness and measure repleteness. 相似文献
959.
The problem of computing the dimension of spaces of splines whose elements are piecewise polynomials of degreed withr continuous derivatives globally has attracted a great deal of attention recently. We contribute to this theory by obtaining dimension formulae for certain spaces of super splines, including the case where varying amounts of additional smoothness is enforced at each vertex. We also explicitly construct minimally supported bases for the spaces. The main tool is the Bernstein-Bézier method.Communicated by Klaus Höllig. 相似文献
960.