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41.
S. Patzer N.L. Arthur P. Potzinger H.Gg. Wagner 《Journal of photochemistry and photobiology. A, Chemistry》1997,110(3):2543-227
The photolysis of Me6Si2 at 206 nm results in two main decomposition processes: simple Si---Si bond breaking with a quantum yield of Φ = 0.21 ± 0.03, and Me3SiH elimination with the concomitant formation of Me2SiCH2 with Φ = 0.18 ± 0.01. There is also a minor decomposition channel with a very small quantum yield, Φ = (5.6 ± 0.2) × 10−3, which results in the formation of Me4Si and Me2Si. The main fate of the excited Me6Si2 molecule produced during photolysis is stabilization by collisional deactivation. The end products observed indicate that the reaction pathways followed by the main intermediates, Me3Si and Me2SiCH2, are the same as those found in the photolysis of Me4Si (Ahmed et al., J. Photochem. Photobiol. A: Chem. 86 (1995) 33). 相似文献
42.
43.
A. Mandelis W. Lo R. E. Wagner 《Applied Physics A: Materials Science & Processing》1987,43(2):123-130
The electrical and dielectric properties of mercuric iodide were studied at room temperature under various intensities and colours of light in the frequency range 1 Hz–10 kHz. In the high-frequency region (>40 Hz), the real part of the dielectric constant () is almost constant with frequency (f), colour and intensity of light. At lower frequencies, varies nearly as 1/f and monotonically increases with intensity (I) of the yellow (or green) light, whereas it is almost constant with red light intensity. This behaviour is discussed in the view of the different polarization contributions. The imaginary part of the dielectric constant () was found to vary as 1/f over the frequency range studied. This behaviour was observed whether the crystal was in dark or illuminated implying that the roomtemperature ac dark- or photo-conductivity () is independent of frequency. The observed variation of with intensity of yellow (or green) light was found to follow anI
1/2 dependence and a weaker dependence for the red light. the red light. The conductivity behaviour is discussed in the view of the current theories. 相似文献
44.
Wagner F Gruber O Lackner K Murmann HD Speth E Becker G Bosch HS Brocken H Cattanei G Dorst D Eberhagen A Elsner A Erckmann V Fussmann G Gehre O Gernhardt J Gierke Gv Glock E Grieger G Grigull P Haas G Hacker H Hartfuss HJ Jäckel H Jaenicke R Janeschitz G Junker J Karger F Kasparek W Keilhacker M Kick M Klüber O Kornherr M Kroiss H Kuehner M Lenoci M Lisitano G Maassberg M Mahn C Marlier S Mayer HM McCormick K Meisel D Mertens V Müller ER Müller Müller G Niedermeyer H Ohlendorf W 《Physical review letters》1986,56(20):2187-2190
45.
The tetraphosphides (tBu3Si)3P4M3 (M = Li, Na) and (tBu2PhSi)3P4Na3 have been synthesized in high yield from the reaction of 3 equivalents of the silanides tBu3SiM (M = Li, Na) and tBu2PhSiNa with P4 in benzene. (tBu3Si)3P4M3 (M = Li, Na) are transformed into the unsaturated triphosphides (tBu3Si)2P3M (M = Li, Na) and tBu3SiPM2 in tetrahydrofuran at ambient temperature. 相似文献
46.
For the assignment of the configuration at C(8) and C(15) of the natural oviposition-deterring pheromone 1 in Rhagoletis cerasi L., the four possible stereoisomers of 1 are synthesized. By condensing the C6 building blocks (5R)- 4 and (5S)- 4 with the boron enolates of the C10 building blocks (4S)- 13 and (4R)- 13 , followed by decarboxylative dehydration, all stereoisomers of 16 are available (Scheme 5). Glucosylation of 16 followed by formation of the taurin amide gives, after deprotection, the four stereoisomers (8R,15S)- 1 , (8R,15R)- 1 , (8R,15S) -1 , and (8S,15S)- 1 (Scheme 6). 相似文献
47.
Arseniyadis S Subhash PV Valleix A Wagner A Mioskowski C 《Chemical communications (Cambridge, England)》2005,(26):3310-3312
The high-yielding synthesis and application of the first polymer supported reagent for the kinetic resolution (KR) of amines through enantioselective acetylation is described; this new supported chiral reagent allows the KR of primary amines with excellent selectivities at room temperature; moreover, this supported approach is highly efficient as the Merrifield-supported chiral scaffold can be quantitatively recovered and recycled. 相似文献
48.
Abstract— Escherichia coli cells treated with sublethal doses of acridine plus near-UV light exhibit an effective split-dose recovery response that requires an incubation period of about 30–45 min. Studies of the metabolic requirements for split-dose recovery revealed the following: (a) DNA synthesis is not required for split-dose recovery; (b) inhibition of electron transport or protein synthesis reduces the efficiency of split-dose recovery by about one-half; (c) inhibition of phospholipid synthesis or cell wall synthesis completely eliminates the split-dose recovery response. These results suggest an involvement of membrane repair mechanisms in response to damage by acridine plus near-UV light. Additional evidence for such a process was provided by more direct assays for membrane recovery. It was found that cells treated with sublethal doses of acridine plus near-UV light are sensitive to low concentrations of detergents, and lose that sensitivity upon incubation. Likewise, treated cells are susceptible to lethal osmotic shock, but can recover from this susceptibility if incubated after treatment but prior to exposure to low osmotic conditions. Based on accumulating evidence, we propose that E. coli cells are capable of repairing membrane damage resulting from exposure to acridine plus near-UV light. 相似文献
49.
Substituierte 2-(Thiazol-4-yl)-phenole als Liganden und potentielle Extraktionsmittel für Kupfer(II)
Substituted 2-(Thiazol-4-yl)-phenols as Ligands and Potential Extractants for Copper (II) Substituted 2-(thiazol-4-yl)-phenols are obtained by the HANTZSCH synthesis. Their solubility in toluene is higher than in n-octane depending on the position, the chain length, and the polarity of the substituents. From alcoholic solutions complexes of the type CuL2n are precipitated. According to the substituents their structure is distorted octahedral (CuL22, CuL23) or distorted tetrahedral (CuL28, CuL29). The new complexes are nearly insoluble in toluene and aliphatic hydrocarbons, but CuL28 and CuL29 are soluble in chloroform. Therefore copper(II) may be extracted by HL8 and HL9 using chloroform as a diluent. 相似文献
50.
E. L. Wagner 《Theoretical chemistry accounts》1974,32(4):295-310
Potential surfaces for Li2O and Al2O have been calculated by an ab initio SCF-LCAO-MO method and by the semiempirical CNDO method. For both molecules the semiempirical methods incorrectly imply unreasonable structures with very acute apex angles and very long bond distances — rather more like diatomic Li2 or Al2 molecules with O-atoms attached to their bonds. Our ab initio treatment does correctly predict a symmetrical linear configuration for Li2O with bond distances in excellent agreement with experiment. This method also predicts a linear symmetrical structure for Al2O, in agreement with experimental gas phase measurements but in disagreement with matrix-isolation studies. 相似文献