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991.
G. R. Sudhakaran R. L. Bhattacharjee J. C. Sarker L. H. Johnston 《International Journal of Infrared and Millimeter Waves》1986,7(12):1903-1911
A submillimeter laser Stark spectrum has been observed for fully deuterated Methyl Chloride (CD3Cl) with the 337 m line of the HCN laser up to Stark fields of about 54000 V/cm. The spectra were taken for both Parallel and Perpendicular Polarizations and the multiplet transitions were identified as JK=42K41K in the ground vibrational state. Three families with K=12, 13 and 14 have been identified and their zero field frequencies have been given with improved accuracy over those calculated from available molecular constants. 相似文献
992.
G. Lhersonneau D. Weiler P. Kohl H. Ohm K. Sistemich R. A. Meyer 《Zeitschrift für Physik A Hadrons and Nuclei》1986,323(1):59-67
An isomeric state at 3,523 keV excitation energy in97Y with a half-life of 144(10) ms has been discovered with the fission-product separator JOSEF. This isomer is depopulated through aγ transition of 162 keV. AnE3 multipolarity for this transition is consistent with the measured conversion coefficients ofα K =0.98(20) andα T =1.00(19). Subsequent electromagnetic transitions populate several new97Y levels which have high spins. For the isomer the three-quasiparticle configuration [πg 9/2?ν(h 11/2,g 7/2)]27/2? is proposed. TheE3 transition with a strength about 2 single-particle units is supposed to be of the typeh 11 2/+1 →d 5 2/?1 . These findings provide evidence for the rapid shape transition atA?100 since they indicate shell-model character of 39 97 Y58 even at high excitation energies while the immediate neighbour 39 98 Y59 contains a rotational band based on a level at 495 keV. 相似文献
993.
H. -O. Carmesin D. W. Heermann K. Binder 《Zeitschrift für Physik B Condensed Matter》1986,65(1):89-102
Instead of the standard assumption in the theory of phase separation where an instantaneous quench from an initial equilibrium state to the final state in the two-phase region is assumed, we consider the more realistic situation that the change of the external control parameter (e.g. temperature) can only be performed with finite rates. During the initial stages of spinodal decomposition the system then has some memory of the states intermediate between the initial and the final one. This influence of the finite quench rate in continuous quenching procedures is studied within the linearized theory of spinodal decomposition, with the Langer-Baron-Miller decoupling, and with Monte Carlo simulations. Both the case of thermally activated mobilities (applicable to solid metallic alloys) and the case of nearly temperature-independent mobilities (applicable to fluid polymer mixtures) are treated, and possible experimental applications are discussed. We find drastic deviations from the standard instantaneous quench situations in all cases of experimental interest. 相似文献
994.
The detailed temperature variation of the Mössbauer spectral intensity in Sn(CH3)4 displays a pronounced drop of the Debye temperature from
D
96K below the transition temperature (T
t
43K) to
D
76K above it. The transition atT
t
is discussed in terms of recent INS and NMR results where increased motion of inequivalent CH3 groups has been observed around the temperatureT
t
.Supported by the U.S.-Israel Binational Science Foundation 相似文献
995.
996.
Dr. H. Demel Dipl.-Ing H. J. Grießer Prof. Dr. K. Hummel 《Colloid and polymer science》1977,255(11):1131-1132
Ohne ZusammenfassungMit 1 Abbildung und 1 Tabelle 相似文献
997.
Abstract— The rates of photosensitized oxidation of a number of sulphides were determined under standard conditions in 1, 1, 2,2-tetrachloroethane and in methanol. It was found that the ratio of the rates of reaction in the two solvents was not constant for different sulphides and that t -butyl sulphide does not react in methanol. It is inferred that the presence of an H atom in the α position is essential for reaction in polar solvents and an appropriate mechanism is suggested. The results indicate that reaction in chlorinated solvents may take place by a different mechanism which possibly involves H-abstraction by triplet sensitizer. 相似文献
998.
Analysis of tea components by high-performance liquid chromatography and high-performance capillary electrophoresis 总被引:3,自引:0,他引:3
Tea is one of the most popular beverages in the world. The number of reports on the analysis of tea components, especially for catechins, has recently been increasing. We review the recent reports on the analysis of tea components using the analytical methods of high-performance liquid chromatography and high-performance capillary electrophoresis. 相似文献
999.
D. Beese R. Steiner H. Scheer A. Angerhofer B. Robert M. Lutz 《Photochemistry and photobiology》1988,47(2):293-304
Abstract— Reaction centers from Rhodobacter sphaeroides have been modified by treatment with sodium borohydride similar to the original procedure [Ditson et al., Biochim. Biophys. Acta 766 , 623 (1984)], and investigated spectroscopically and by gel electrophoresis.
(1) Low temperature (1.2 K) absorption, fluorescence, absorption- and fluorescence-detected ODMR, and microwave-induced singlet-triplet absorption difference spectra (MIA) suggest that the treatment produces a spectroscopically homogeneous preparation with one of the 'additional' bacteriochlorophylls being removed. The modification does not alter the zero field splitting parameters of the primary donor triplet (T P870).
(2) From the circular dichroism and Raman resonance spectra in the1500–1800 cm-1 region, the removed pigment is assigned to BchlM , e.g. the "extra" Bchl on the "inactive" M-branch.
(3) A strong coupling among all pigment molecules is deduced from the circular dichroism spectra, because pronounced band-shifts and/or intensity changes occur in the spectral components assigned to all pigments. This is supported by distinct differences among the MIA spectra of untreated and modified reaction centers, as well as by Raman resonance.
(4) The modification is accompanied by partial proteolytic cleavage of the M-subunit. The preparation is thus spectroscopically homogeneous, but biochemically heterogenous. 相似文献
(1) Low temperature (1.2 K) absorption, fluorescence, absorption- and fluorescence-detected ODMR, and microwave-induced singlet-triplet absorption difference spectra (MIA) suggest that the treatment produces a spectroscopically homogeneous preparation with one of the 'additional' bacteriochlorophylls being removed. The modification does not alter the zero field splitting parameters of the primary donor triplet (
(2) From the circular dichroism and Raman resonance spectra in the1500–1800 cm
(3) A strong coupling among all pigment molecules is deduced from the circular dichroism spectra, because pronounced band-shifts and/or intensity changes occur in the spectral components assigned to all pigments. This is supported by distinct differences among the MIA spectra of untreated and modified reaction centers, as well as by Raman resonance.
(4) The modification is accompanied by partial proteolytic cleavage of the M-subunit. The preparation is thus spectroscopically homogeneous, but biochemically heterogenous. 相似文献
1000.
Subnanosecond transient-dichroism experiments have been performed to investigate the rotational diffusion of dyes in solution. Dyes and solvents were chosen in a way to obtain information on the influence of size, shape and hydrogen-bonding abilities either of the solute or the solvent molecules. One finds slow orientational relaxation of di-anionic xanthene dyes in alcohols, while oblate cationic dyes rotate faster in spite of their comparable size. The rotational diffusion times for alcohol solutions exceed the theoretical values predicted by the Debye-Einstein model except for prolate molecules. For a solute molecule with internal mobility the rotational diffusion exhibits a partial slip behaviour. It is shown that the deviations from the Debye-Einstein model are restricted to alcohols since for other solvents either with or without strong hydrogen-bonding abilities the experimental values agree with the hydrodynamic model including the stick-boundary condition. Experiments on erythrosine B reveal the influence of size and shape of the attached solvent molecules. 相似文献