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41.
Dilatometrical indication can be employed to the neutralizing reactions of polybasic acids and is demonstrated by the following acid-base couples: H2SO4/NaOH, H3PO4/NaOH and H5JO6/NaOH. With amounts between 0.5 and 4 mMol several, frequently all, equivalence points can be determined with a deviation of less than 0.2%. The determination of the changes of molar volume of the reactions depending on the concentrations allow conclusions as to the course of the reactions. 相似文献
42.
Preparation of β-hydroxyesters from isoxazolines. A selective Nibpy-catalyzed electrochemical method
Viviane F. CaetanoF.W.Joachim Demnitz Flamarion B. DinizRonaldo M. Mariz Jr. Marcelo Navarro 《Tetrahedron letters》2003,44(45):8217-8220
An electrocatalytic method for the reductive N-O cleavage of isoxazolines is described. Ni0bpy, generated in situ, was used to promote selective ring opening of 3-methoxy-5-phenylisoxazoline (1a) and 3-methoxy-[4,5]cyclohexylisoxazoline (1b). DMF and NaI were used as solvent and supporting electrolyte, and β-hydroxyesters 2a and 2b were obtained in high yields respectively, after acid hydrolysis. β-Hydroxynitriles 3a and 3b were also identified as side products. 相似文献
43.
Friedrich J Dolg M Gansäuer A Geich-Gimbel D Lauterbach T 《Journal of the American Chemical Society》2005,127(19):7071-7077
The mechanism of titanocene mediated 3-exo cyclizations was investigated by a combined theoretical and experimental study. A gradient corrected density functional theory (DFT) method has been scaled against titanocene dichloride, the parent butenyl radical, and in bond dissociation energy (BDE) calculations. The BP86 method using density fitting, and a basis set of triple-zeta quality emerged as a highly reliable tool for studying titanocene mediated radical reactions. The computational results revealed important kinetic and thermodynamic features of cyclopropane formation. Surprisingly, the beta-titanoxy radicals, the first intermediates of our investigations, were demonstrated to possess essentially the same thermodynamic stabilization as the corresponding alkyl radicals by comparison of the calculated BDEs. In contrast to suggestions for samarium mediated reactions, the cyclization was shown to be thermodynamically favorable in agreement with earlier kinetic studies. It was established that stereoselectivity of the cyclization is governed by the stability of the intermediates and thus the trans disubstituted products are formed preferentially. The observed ratios of products are in good to excellent agreement with the DFT results. By a combination of computational and experimental results, it was also shown that for the completion of the overall cyclopropane formation the efficiency of the trapping of the cyclopropylcarbinyl radicals is decisive. 相似文献
44.
Iron-silicon thin films have been characterized by means of analytical transmission electron microscopic methods. Under certain conditions — composition and annealing temperature — these films exhibit thermoelectric behavior. In particular, the morphology and phase formation which results from annealing of these films, and doping with oxygen and nitrogen, are of interest. The thermoelectric phase -FeSi2 is formed at temperatures above 500°C. This phase is transformed into electrically conducting phases at about 1000°C. A small oxygen content does not influence this crystallization process. If the oxygen content is higher than 15 atom-% the electrically conducting phases exist even at 500°C. The presence of a small nitrogen content inhibits the formation of the -FeSi2 phase. The development of silicon and iron nitrides is possible. 相似文献
45.
Hans‐Jürgen Holdt Holger Müller Alexandra Kelling Hans‐Joachim Drexler Thomas Müller Thomas Schwarze Uwe Schilde Ines Starke 《无机化学与普通化学杂志》2006,632(1):114-122
Mercury(II) Chloride and Iodide Complexes of Dithia‐ and Tetrathiacrown Ethers The complexes [(HgCl2)2((ch)230S4O6)] ( 1 ), [HgCl2(mn21S2O5)] ( 2 ), [HgCl2(ch18S2O4)] ( 3 ) and [HgI(meb12S2O2)]2[Hg2I6] ( 4 ) have been synthesized, characterized and their crystal structures were determined. In [(HgCl2)2((ch)230S4O6)] two HgCl2 units are discretely bonded within the ligand cavity of the 30‐membered dichinoxaline‐tetrathia‐30‐crown‐10 ((ch)230S4O6) forming a binuclear complex. HgCl2 forms 1 : 1 “in‐cavity” complexes with the 21‐membered maleonitrile‐dithia‐21‐crown‐7 (mn21S2O5) ligand and the 18‐membered chinoxaline‐dithia‐18‐crown‐6 (ch18S2O4) ligand, respectively. The 12‐membered 4‐methyl‐benzo‐dithia‐12‐crown‐4 (meb12S2O2) ligand gave with two equivalents HgI2 the compound [HgI(meb12S2O2)]2[Hg2I6]. In the cation [HgI(meb12S2O2)]+ meb12S2O2 forms with the cation HgI+ a half‐sandwich complex. 相似文献
46.
Oxide ceramic masses react to simple shearing with hardening (peptisation: increase in the shear stress with the shear deformation).
In the present study the correlation between the increase in the shear stress and the porosity, agglomeration processes and
the type of flow are analysed. For this purpose oxide ceramic masses are tested in a shear device especially developed for
pastes and analysed by rheometric experiments, NMR methods and particle size analysis. The results support the hypothesis
that structural changes (hardening, increase in the mean porosity) of the material during the peptisation mainly depend on
the magnitude and not on the kind of the energy input and thus of the type of flow. The fraction of bound (more generally,
the immobilised) water increases with the shear displacement. Also crushing of primary particles could be observed. Both the
crushing of solid particles causing an increased solid surface and the formation of a three-dimensional gel structure are
microscopic effects capable of resulting in the binding or retaining water. On a macroscopic scale these phenomena cause hardening.
Magnetic resonance imaging visualises flow-induced agglomerates, which form owing to the shear flow and increase the porosity
averaged over the whole sample. After the shear experiment rolls of paste can be seen which indicate that the general assumption
of a plane shear flow in the shear device is not warrantable.
Received: 19 July 2001 Accepted: 25 October 2001 相似文献
47.
Joachim Meissner 《Polymer Testing》1983,3(4):291-301
Laser Doppler velocimetry (LDV) is a new tool for fluid dynamics studies. Using LDV the velocity vector field can be measured without disturbing the flow itself. However, in polymer melt fluid dynamics difficulties arise because of temperature problems, the relatively high pressure involved, and the often extremely slow flows. In this paper a LDV system is described which was set up especially for polymer melt flow investigations. 相似文献
48.
A simple semiconductor gas sensor (TGS 812) is used for the on-line measurement and control of indole during the production of l-tryptophan from indole and l-serine with immobilized E. coli cells. Indole is estimated in the reactor gas space. In combination with an automatic indole supply system, a feed-batch process became possible. The indole concentration was monitored and kept within the optimal range (300–600 mg l?1). A simple gas-sensing electrode dipped in the reaction medium provides direct measurement of organic solvents and gases in the liquid. Such a system is suitable for on-line determination of ethanol (10–70 g l?1) during continuous production of ethanol with immobilized yeast cells. 相似文献
49.
Joachim Franzke Maria-Antoaneta Bratescu Damir Veza Kay Niemax 《Mikrochimica acta》1994,113(3-6):349-355
Laser impedance spectroscopy in a miniature neon RF-discharge operating at 0.27 bar was performed. The dominant role of the metastable atoms to the size and the sign of the RF-signal was investigated. Excellent linearity of the RF-signal but poor detection sensitivity of excited metastable neon atoms were found at low laser powers. 相似文献
50.
Gintaras Pivoriunas Ccilia Maichle‐Mssmer Simon Schwarz Joachim Strhle 《无机化学与普通化学杂志》2005,631(10):1743-1745
Synthesis and Crystal Structure of [(Ph3PAu)3NPPh3][PF6]2, a Gold(I) Phosphoraneiminato Complex The photolytic reaction of Ph3PAuN3 with Cr(CO)6 in THF yields the phosphoraneiminato complex [(Ph3PAu)3NPPh3]2+ in low yield as well as the cluster cation [(Ph3PAu)8]2+ as the main product. The phosphoraneiminato complex crystallizes from CH2Cl2 with [PF6]? ions as [(Ph3PAu)3NPPh3][PF6]2·CH2Cl2 in the triclinic space group with a = 1200.8(1), b = 1495.6(2), 2053.5(5), α = 86.97(2)°, β = 82.79(1)°, γ = 81.87(2)°, and Z = 2. The phosphoraneiminato ligand bridges through its N atom three Au atoms, which itself are connected to each other by weak aurophilic interactions. 相似文献