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1.
It has been recently shown that computation with stochastic numbers as regard to addition and multiplication by scalars can be reduced to computation in familiar vector spaces. In this work we show how this can be used for the algebraic solution of linear systems of equations with stochastic right-hand sides. On several examples we compare the algebraic solution with the simulated solution using the CADNA package. 相似文献
2.
H. R. Eschnauer F. Alt J. Messerschmidt G. T?lg 《Fresenius' Journal of Analytical Chemistry》1989,332(8):874-879
Summary Little is known about selenium contents in alcoholic beverages, especially in wine, because no reliable determination method was available so far. A procedure for the detection of selenium in the pg- and low ng-range was developed, which uses the hydride-generation-condensation-AAS (HGC-AAS). Selenium contents in 103 German wines of the year vintages 1950 until 1985 were determined. In mean they range between 0.29 and 0.79 g/l Se and show a certain dependence from the geological soil formation and the wine species. Corresponding vineyard soils from Ingelheim (Rheinhessen, FRG) contain 0.18–0.44 mg/kg Se, mean 0.24 mg/kg Se, 10% of it is available for plants. The distribution of selenium in grape berries shows selenium-rich seeds and — with red wine species — selenium-rich skins. Higher selenium contents by contamination were observed near an industrial location. The behaviour of selenium in the vegetation cycle is pursued. The selenium depletion during fermentation may amount to 60%. All results are summarized in the so-called trace element vinogram. Selenium hence is a regular and natural constituent part of wine.
Herrn Prof. Dr. R. Neeb zum 60. Geburtstag gewidmet 相似文献
Herrn Prof. Dr. R. Neeb zum 60. Geburtstag gewidmet 相似文献
3.
The molecular structures and vibrational spectra of the three isomers of pyridinecarboxamide (picolinamide, nicotinamide, isonicotinamide) were calculated with the Density Functional Theory (DFT) method using the B3LYP function and the 6-31++G(d,p), Z2PolX, Z3PolX basis sets. The calculations were performed by using the Gaussian98W packet program set. The total energy distributions (TED) of the vibrational modes of these molecules were calculated by using the Scale 2.0 program and the vibrational modes of the molecules were determined. The Scaled Quantum Mechanical (SQM) method was used in the scaling procedure. In the experimental part of the study, the solid phase FT-IR and Micro Raman spectra of the three isomers of pyridinecarboxamide have been recorded in the range of 4000-650 and 1200-100 cm−1, respectively. The calculated wavenumbers were compared to the corresponding experimental values. As a result, the observed bands of the three isomers of pyridinecarboxamide were assigned with good accuracy. 相似文献
4.
First ever non-deformylating transdiazotization of acylacetaldehydes was achieved: the reactions of 2-azido-l-ethylpyridinium tetrafluoroborate ( 4 ) with acylacetaldehydes 3 proceeded partially without deformylation to yield 16 new α-diazo-β-oxoaldehydes 1 along with diazomethyl ketones 2 , especially in the presence of NaOAc (Scheme 1, Tables 1 and 2). The product distribution was substituent-dependent and could be correlated quantitatively. This new diazotization reaction appears as an alternative, direct, and more general method for the synthesis of these diazooxoaldehydes. α-Oxocycloalkanecarbaldehydes 5 gave only traces (if any) of α-diazocycloalkanones 7 , and rearrangement products 6 were isolated (Scheme 2). Mechanisms of the reactions are discussed (Schemes 4 and 5). 相似文献
5.
The structures of the essential metabolites which are excreted by the rat after oral application of GS 13005 (O,O-dimethyl-S-[(2-methoxy-1,3,4-thiadiazole-5(4H)-one-4-yl)-methyl] dithiophosphate) have been elucidated. The product of final oxidation, CO2, was found to be the main metabolite (up to 36% of the dose applied). Among the degradation products excreted in the urine (up to 45% of the dose applied) the two most important were isolated. They are 4-methylsulfinylmethyl and 4-methylsulfonylmethyl derivatives respectively of the intact 2-methoxy-1,3,4-thiadiazole-5-one heterocycle (metabolites III and II, in amounts of 20–25% and 5–7% of the dose applied, respectively). These metabolites originate by methylation and subsequent oxidation from the mercaptomethyl derivative liberated after hydrolysis of the P S bond of the dithiophosphoric acid ester. 相似文献
6.
Decomposition of triacetone triperoxide is an entropic explosion 总被引:1,自引:0,他引:1
Dubnikova F Kosloff R Almog J Zeiri Y Boese R Itzhaky H Alt A Keinan E 《Journal of the American Chemical Society》2005,127(4):1146-1159
Both X-ray crystallography and electronic structure calculations using the cc-pVDZ basis set at the DFT B3LYP level were employed to study the explosive properties of triacetone triperoxide (TATP) and diacetone diperoxide (DADP). The thermal decomposition pathway of TATP was investigated by a series of calculations that identified transition states, intermediates, and the final products. Counterintuitively, these calculations predict that the explosion of TATP is not a thermochemically highly favored event. It rather involves entropy burst, which is the result of formation of one ozone and three acetone molecules from every molecule of TATP in the solid state. 相似文献
7.
Helmut G. Alt 《Russian Chemical Bulletin》1995,44(1):1-8
Ansa metallocene dichloride complexes of titanium, zirconium, and hafnium can be activated by methyl aluminoxane (MAO) to give excellent catalysts for the homogeneous polymerization of ethylene and propylene. The symmetry of the corresponding metaliocene dichloride complexes is essential for the stereospecific polymerization of propylene (isotactic, syndiotactic or atactic). The application of fluorenyl groups instead of cyclopentadienyl groups greatly increases the activity of the catalysts. The first ansa bis(fluorenyl) complexes of zirconium and hafnium, (C13H8-C2H4-C13Hs)MCl2 (M = Zr, Hf), have been prepared. It was found that after the activation by MAO the zirconium derivative demonstrates a very high activity. Several model complexes are presented in order to discuss the mechanism of the polymerization.This paper was presented at the INEOS-94 Workshop The Modern Problems of Organometallic Chemistry (Moscow, May 21–27, 1994).Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 7–14, January, 1995. 相似文献
8.
The coordinative properties of the acceptor ligand CS are discussed on the basis of the new thiocarbonyl complexes CpCr(CO)(CS)(NO) (I), [CpCr(CS)(NO)2]PF6 (II), CpCr(CS)(L)(NO) (L = pyridine (III) or trimethylphosphane (IV) and related carbonyl complexes. The IR and NMR spectra (1H, 13C, 31P) of the complexes indicate ligand—ligand interactions between CS and both the nitrosyl group and the cyclopentadienyl ring. An attempt is made to compare CS with other sulphur-containing acceptor ligands such as NS (in CpCr(CO)2(NS)) and CS2 (in CpCr(CS2)(PMe3)(NO)). 相似文献
9.
10.
Marcos Costa Souza William Pires Macedo Marcelo Campos M. Silva Guilherme Costa de O. Ramos Helmut G. Alt 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):1047-1054
This article describes an attractive and one-pot synthesis of the title compound by phosphorylation of just prepared N-substituted guanidines from cyanamide and the desired amine. The method allows a variety of N-substituents to hang on the final phosphoryl guanidine as a function of the wider availability of commercial simple amines. 相似文献