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41.
R. Schaub G. Pensl M. Schulz C. Holm 《Applied Physics A: Materials Science & Processing》1984,34(4):215-222
Hall effect and conductivity measurements are performed on Te-doped silicon in the temperature range 30KT800K. A Hall equipment suited for high temperatures up to 800 K has been constructed. The temperature dependence of the free electron concentration is analyzed for Te-doped silicon including one double-donor and several monovalent donor species. A deep level with an electrical activation energy of 200 meV is determined from the saturation of the free electron concentration at temperatures above 400 K. This level represents the first ionization stage of the Te double-donor. The second ionization stage is estimated to have an activation energy of 440 meV. The maximum electrically active Te concentration obtained is 5×1016cm–3. Three different shallow donor states are resolved in the low-temperature range. The concentrations of these shallow donors are partially sensitive to a subsequent heat-treatment. 相似文献
42.
Tellurium-related defects inn-type silicon have been analysed by deep level transient spectroscopy (DLTS). The tellurium doping of the samples was performed by ion implantation or during epitaxy. In all the samples, a level having a thermal activation energy around 0.37 eV is observed. This activation energy is found to be dependent on the electric field. Taking into account the Poole-Frenkel (FP) effect and a temperature dependence proportional toT ?2 in the capture cross-section, a value ofE A=0.41eV is obtained. A second Te-related level having an activation energy ofE A=0.14eV without correction of the FP effect could only be measured in the implanted samples. The same concentration is observed for the two levels in the implanted samples thus indicating that both peaks in the DLTS spectra are caused by the identical Te-related defect. 相似文献
43.
Katja Schulz R. Klaus Mueller Werner Engewald Adelgunde Graefe Jan Dreßler 《Chromatographia》2007,66(11-12):879-886
Some aroma compounds found in alcoholic beverages are characteristic of a certain beverage (i.e. 2,4-decadienoic acid ethyl ester is characteristic of pear spirit and 5-butyltetrahydro-4-methylfuran-2-on “whiskey lactone” is characteristic of aged spirits like whiskey). These substances were detectable in beverages but not in blood samples. The aim of this investigation was to find a sensitive sampling technique for aroma compounds in whole blood samples. This technique may be used in forensic toxicology for examination of drinking claims. The method comprises dynamic headspace sampling using a purge and trap concentrator, followed by quantitative gas chromatography–mass spectrometry (dynamic HS–GC–MS). The influence of sample preparation, trap adsorbents and sample temperature as well as desorption time and purge time on the quality of the analytical results were investigated. The following optimal parameters were determined: stirred and diluted whole blood sample without salt addition, use of Carbotrap C as trap material, sample temperature at 80 °C, desorption time 20 min and purge time 30 min. These optimal parameters were used for the determination of detection limits (LOD). The LOD of aroma compounds by means of dynamic headspace sampling were compared with the results of conventional sampling: the static headspace technique. Limits of detection for the aroma compounds with conventional static headspace GC are in the range 400–10,000 μg L?1. Dynamic headspace–GC was found to be a more sensitive sampling technique for most of the aroma compounds investigated (e.g. C4–C8 ethyl esters, benzoic acid ethyl ester, linalool oxide and 4-ethylguaiacol) with detection limits between 1 and 50 μg L?1, but there were also limits to the sampling of substances with lower volatility like decanoic acid ethyl ester, 2,4-decadienoic acid ethyl ester, eugenol and whiskey lactone with detection limits of about 1,000 μg L?1. 相似文献
44.
Nuclear Overhauser Effect (NOE) methods in NMR are an important tool for 3D structural analysis of small molecules. Quantitative NOE methods conventionally rely on reference distances, known distances that have to be spectrally separated and are not always available. Here we present a new method for evaluation and 3D structure selection that does not require a reference distance, instead utilizing structures optimized by molecular mechanics, enabling NOE evaluation even on molecules without suitable reference groups.A quantitative Nuclear Overhauser Effect (NOE) analysis approach that avoids the use of and internal reference distance to perform molecular configuration selection. 相似文献
45.
R. Haase U. Illgen J. Scheve I. W. Schulz 《Reaction Kinetics and Catalysis Letters》1985,28(2):395-400
The formation of needle shaped crystallites of V6O13 at low V concentrations on V2O5-anatase coated catalysts explains the low selectivity for phthalic anhydride during o-xylene oxidation. The (010) plane of V-oxide, most active for selective oxidation of o-xylene, is not accessible and the contact of this plane with the anatase faces promotes the anatase-rutile transformation and the incorporation and blocking of V4+ ions.
V6O13 V , V2O5-, -. (010) , -, , - V+4.相似文献
46.
Hans-Joachim Schulz Jürgen Liebscher Peter Luger Minxie Quian Johann Mulzer 《Journal of heterocyclic chemistry》1992,29(5):1125-1132
2,4,6-Trialkyl-1,3,5-triazines 1 can selectively be mono, bis or trisiminoformylated by reaction with trismorpholinomethane 2 or chloromethylene iminium salts 3 (Vilsmeier reagents), with each alkyl substituent reacting with only one molecule of the electrophile. The resulting aminoalkenyltriazines 4, 5 and 6 are partially or fully hydrolysed to corresponding formylation products. The latter exist either in enol or in unusual acylenamine tautomeric structures 10, 12 , and 13 , depending on the number of enamine or enol units found in the molecule. Reaction of triazines 1 with chlorobenzylidene iminium salts 16 gives monoiminobenzoylation to enaminotriazines 17 . 相似文献
47.
The reaction behavior of NaN3, AgN3, and Me3SiN3 towards FNO2, CINO2, NO2SbF6, and NO2BF4 was investigated. At -30°C or below in a solvent-free system sodium azide did not react with CINO2, NO2BF4, or NO2SbF6. Below -30°C silver azide did not react either with neat C1NO2. Treatment of Me3SiN3 with pure C1NO2 led to the formation of C1N3, N2O, and Me3SiOSiMe3. A mechanism for this reaction has been proposed. Pure chlorine azide was isolated by fractional condensation and identified by its low-temperature Raman spectrum (liquid state). The reaction of Cp2Ti(N3)2 with C1NO2 also yielded C1N3 as the only azide-containing reaction product. Treatment of FNO2 with NaN3 at temperatures as low as -78°C always ended in an explosion which was probably due to the formation of FN3 as one of the reaction products. The reaction of NO2SbF6 with NaN3 in liquid CO2 (-55°C· T· -35°C) as the solvent afforded a new azide species which was stable at low temperature in solution only and was investigated by means of low-temperature Raman spectroscopy. The obtained vibrational data give strong evidence for the presence of tetranitrogen dioxide, N4O2, which can be regarded as nitryl azide (NO2N3). The structure and vibrational frequencies of N4O2 were computed ab initio at correlated level (MP2/6-31 + G*). In liquid xenon (-100°C· T· -60°C) NaN3 did not react with NO2SbF6. A previous literature report on the preparation of N4O2 could not be established. 相似文献
48.
Michael H. Abraham Angela F. Danil de Namor Ronald A. Schulz 《Journal of solution chemistry》1977,6(8):491-500
Heats of solution of 13 11 electrolytes in 1-propanol have been determined calorimetrically at various electrolyte concentrations, and extrapolated to zero concentration to give H
s
o
values for these electrolytes. Together with literature data on three additional 11 electrolytes, these measurements yield a self-consistent set of single-ion enthalpies of transfer from water to 1-propanol. Values are tabulated for 10 univalent cations and five univalent anions. It is shown that the H
t
o
(Ph
4
As+)=H
t
o
(Ph
4
B–) assumption yields chemically reasonable single-ion values. Using this assumption, it may be deduced that all the univalent ions studied have about the same enthalpy in 1-propanol as in methanol. 相似文献
49.
The magnetic susceptibility of liquid NaSb alloys was measured in a temperature range between 600°C and 1100°C. The NaSb system is supposed to exhibit, as does the CsSb system, a metal to semiconductor transition dependent upon composition. A relatively strong diamagnetic minimum of x = ?26 × 10?6 cm3/mol was found near the composition of the stoichiometric formula Na3Sb. This minimal susceptibility can be relatively well described with an ionic type binding model. 相似文献
50.
Siloxy substituted methyl cyclopropanecar?ylates are cleaved by bromine to afford α-bromo-γ-oxoester and, after treatment with triethylamine, good yields of α,β-unsaturated γ-oxoesters. 相似文献