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1.
R. Hildebrand 《Journal of Mathematical Sciences》2004,121(2):2178-2220
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Ohne Zusammenfassung 相似文献
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– Halobacterium halobium , strain ET-15, which does not contain detectable amounts of bacteriorhodopsin (BR) shows behavioral responses to UV and yellow-green light. Attractant stimuli. i.e. light-increases in the yellow-green range or light-decreases in the UV, suppress the spontaneous reversals of the swimming direction for a certain time. Repellent stimuli, i.e. light-decreases in the yellow-green range or light-increases in the UV, elicit an additional reversal response after a few seconds. Action spectra of both sensory photosystems, PS 370 and PS 565, were measured with attractant as well as with repellent stimuli. As in BR-containing cells, maximal sensitivity was always found at 370 nm for the UV-system and at 565 nm for the long-wavelength system. Fluence-response curves at 370 and 565 nm obtained with strain ET-15 and with a BR-containing strain show that the sensitivity of both photosystems is not reduced in the absence of BR. It is concluded that BR is required neither for PS 565 nor for PS 370. Instead retinal-containing pigments different from BR have to be assumed to mediate photosensory behavior. 相似文献
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Summary Lattice parameter values were determined for the ternary B 2-phase in the Al-Co-Ga system, and it was found that a continuous solid solution exists between -AlCo and -CoGa. Phase boundaries of the ternary phase at 1 100 K were derived from the variation of the lattice parameter with composition.
Über die ternäre B 2-Phase im System Al-Co-Ga
Zusammenfassung Im Bereich der ternären B 2-Phase im System Al-Co-Ga wurden die Werte des Gitterparameters bestimmt; es stellte sich heraus, daß eine durchgehende feste Lösung zwischen -AlCo und -CoGa besteht. Die Phasengrenzen der ternären Phase bei 1 100 K wurden aus der Änderung des Gitterparameters mit der Zusammensetzung abgeleitet.相似文献
7.
Adolf Slawisch 《无机化学与普通化学杂志》1970,374(3):291-296
The reaction of VOCl3 with sily-substituted amines results in the substitution of oxygen in VOCl3 and in compounds of type Cl3V = NR. In this way, we succeeded in isolating the pure compound Cl3V = NCH3 (I). The existence of compound (Cl3VNC6H5)x (II) was proved by direct synthesis from Cl3VO and ((CH3)3Si)2NC6H5, and by the decomposition of the new addition compounds Cl3VO · 2 OCNC6H5 (III) and Cl3VO · 2 OSNC6H5 (IV). 相似文献
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By means of EMF-measurements using the formation cell $$graphite/Ag/AgCl(l,x_{AgCl} ) - LiCl(l,x_{LiCl} ) - KCl x_{KCl} /(Cl_2 )graphite$$ the partial molar excessGibbs energies,G AgCl E , of silver chloride in the ternary system AgCl?LiCl?KCl were determined over the whole concentration range at five temperatures between 973 K and 1,123 K. The experimentally determinedG AgCl E -values were fitted using theRedlich-Kister equation. From theRedlich-Kister parameters and their temperature dependence, obtained by the fitting procedure, the integral and partial molar excessGibbs energies, heats of mixing, and excess entropies were calculated. The fitting process permits also the calculation of the thermodynamic excess function of the binary system lithium chloride—potassium chloride. 相似文献
9.
Prof. Dr. Hans Nowotny Josef Tomiska László Erdélyi Adolf Neckel 《Monatshefte für Chemie / Chemical Monthly》1977,108(1):7-19
By means of vapor pressure measurements using theTorker method (Torsion-Knudsen Effusion Recoil) as well as theKnudsen tanspiration technique in connection with a mass spectrometer, the heats of formation of the following compounds were found to be –6.5±0.7 kcal/g atom (Mn0.366Si0.634), –7.8±0.6 kcal/g atom (Mn0.50Si0.50), –7.3±0.6 kcal/g atom (Mn0.625Si0.375), and –6.6±0.6 kcal/g atom (Mn0.75Si0.25).
Mit 7 Abbildungen 相似文献
Mit 7 Abbildungen 相似文献
10.
Feth MP Bolm C Hildebrand JP Köhler M Beckmann O Bauer M Ramamonjisoa R Bertagnolli H 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(6):1348-1359
XANES and EXAFS spectroscopic studies at the Mn-K- and Br-K-edge of reaction products of (S,S)-(+)-N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride ([(salen)Mn(III)Cl], 1) and (S,S)-(+)-N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) bromide ([(salen)Mn(III)Br], 2) with 4-phenylpyridine N-oxide (4-PPNO) and 3-chloroperoxybenzoic acid (MCPBA) are reported. The reaction of the Mn(III) complexes with two equivalents of 4-PPNO leads to a hexacoordinated compound, in which the manganese atom is octahedrally coordinated by four oxygen/nitrogen atoms of the salen ligand at an average distance of approximately 1.90 A and two additional, axially bonded oxygen atoms of the 4-PPNO at 2.25 A. The oxidation state of this complex was determined as approximately +IV by a comparative study of Mn(III) and Mn(V) reference compounds. The green intermediate obtained in reactions of MCPBA and solutions of 1 or 2 in acetonitrile was investigated with XANES, EXAFS, UV/Vis, and Raman spectroscopy, and an increase of the coordination number of the manganese atoms from 4 to 5 and the complete abstraction of the halide was observed. A formal oxidation state of IV was deduced from the relative position of the pre-edge 1s-->3d feature of the X-ray absorption spectrum of the complex. The broad UV/Vis band of this complex in acetonitrile with lambda(max)=648 nm was consistent with a radical cation structure, in which a MCPBA molecule was bound to the Mn(IV) central atom. An oxomanganese(V) or a dimeric manganese(IV) species was not detected. 相似文献