Roothaan INDO CI spin density calculation

Spin densities have been calculated by the Roothaan INDO CI method in the parametrization of Pople and Kaufman. The dependence of the spin densities on both the type and the number of configurations in CI has been followed. Results have been compared with the UHF and spin-projected UHF methods.     

Transition probabilities of forbidden lines within the electronic configurations 6p 2 and 6p 7p of Pb I

The least squares fit of radial parameters involving radial functions of the 6p ²- and 6p 7p-configurations of Pb I has been carried out. The wave functions of the 9 lowest even levels of Pb I have been found in the basis of LSJ-states belonging to two configurations. On the base of the wave functions the transition probabilities for magnetic dipole (M1) and electric quadrupole (E2) radiation have been calculated. Comparison of experimental data and theoretical results is discussed.     

The shape of dilepton spectra in heavy ion collisions as a signature of quark-gluon plasma

The formation of quark-gluon plasma in heavy ion collisions should manifest itself by the increase of the ratio of medium to large mass dileptons, the former being produced predominantly in the QGP and the mixed phase whereas the latter are produced mostly by the Drell-Yan process. The increase of this ratio should be visible either when comparing collisions of lighter with heavier ions, e.g. O+O with Pb+Pb or when comparing low and large transverse energy events in heavy ion e.g. Pb+Pb collisions.     

Electrical conductivity of systems based on Na3AlF6-SiO2 melt

The electrical conductivity of molten binary and ternary mixtures based on the NaF-AlF₃-SiO₂ system was investigated by means of a tube-cell (composed of pyrolytic boron nitride) with stationary electrodes. An impedance/gain-phase analyser (National Instruments; a high-performance modular chassis controlled by Labview? software) was used for the cell impedance measurement. The conductivity was found to vary linearly with temperature in all the mixtures investigated. The concentration dependence of electrical conductivity (isotherms) thus obtained was divided into two parts. The first represents the concentration region of up to 10 mole % of SiO₂, the second the region with a higher concentration of SiO₂ (from 10 mole % to 40 mole %). While the conductivity decreased considerably with the concentration of SiO₂ in the second part, it increased surprisingly in the low concentration range. From these results, the influence of electrolyte composition and temperature on the electrical conductivity was examined.     

PHOTOPHYSICAL PROPERTIES OF PHYCOBILIPROTEINS FROM PHYCOBILISOMES: FLUORESCENCE LIFETIMES, QUANTUM YIELDS, AND POLARIZATION SPECTRA

Abstract— Absorption and fluorescence polarization spectra, as well as absolute fluorescence quantum yields, and lifetimes of phycobiliproteins separated from intact phycobilisomes of Porphyridium cruentum, Nostoc sp. and Fremyella diplosiphon were measured. Two different types of phycoerythrin, in addition to phycocyanin and allophycocyanin, were separated from both Porphyridium cruentum and Nostoc sp. phycobilisomes. They were distinguishable by the shape of their absorption spectra, values of fluorescence quantum yields and their limiting polarization. Phycobilisomes of Fremyella diplosiphon had a type of phycoerythrin that was different from the above kinds. By the use of fluorescence quantum yields and lifetime data, the values of natural lifetimes, the decadic molar extinction coefficients, as well as Förster's critical distances R ₀ for excitation energy transfer, between phycobiliproteins in phycobilisomes, were estimated. The values obtained of Förster's critical distances indicate that for most efficient energy transfer from phycoerythrin to allophycocyanin, the outer layers of Porphyridium cruentum and Nostoc sp. phycobilisomes should be composed of bangiophycean, phycoerythrin and cyanophytan phycoerythrin-II respectively.     

System zones in capillary zone electrophoresis: moving boundaries caused by freely migrating hydrogen ions

We demonstrate that system zones (SZs) can be expected in background electrolytes (BGEs) with a low buffer capacity. The mobilities of this type of SZ (m(SZ)) could be determined by calculations both based on a mathematical model and by a simulation program. The values of m(SZ) are increasing for decreasing buffer capacities and lower concentrations of the BGEs. For completely unbuffered BGEs with a pH below 7, the m(SZ) reached values up to 350x10(-9) m(2)V(-1)s(-1). This value indicates that the existence of this type of SZ originates from migrating hydrogen ions. Although both the mathematical model and simulation program do not consider the influence of the pH of the sample solution, experiments have shown that the pH of the sample solution is also very important. The lower the pH of the sample solution, the larger the m(SZ) in a specific BGE for cationic SZs. Using completely unbuffered BGEs the hydrogen ions present in the original sample start to migrate freely through the capillary tube with the mobility of a single hydrogen ion and cause stepwise disturbances in the base line of the detector trace. It is remarkable that this type of SZ appears not to affect the electromigration dispersion (EMD) in a strong way and so far only dips could be obtained experimentally.     

Conversions of Nitroalkyl to Carbonyl Groups in Carbohydrates

Summary.  Since the development of the Sowden methodology in the middle of the twentieth century, several other efficient and complementary methods for the transformation of sugar nitromethyl groups to aldehyde functionalities in their free, hemiacetal, or otherwise derivatized forms have been developed. Hydrogen peroxide oxidation as well as ozonolysis of 1-deoxyalditol-1-nitronates in aqueous solution provide free aldoses, thus presenting alternatives to the well-known Nef reaction. When applied to 2,5- or 2,6-anhydro-1-deoxy-1-nitroalditols, also known also as glycosylnitromethanes, the Nef reaction fails, and the hydrogen peroxide oxidation overoxidizes the expected products to 2,5- or 2,6-anhydroaldonic acids. On the other hand, the ozonolysis of such compounds under pH-controlled conditions results in up to 85% of the interesting glycosylformaldehydes. The Nef reaction carried out in anhydrous low alcohols, however, has revealed a new conversion of glycosylnitromethanes to glycosylmethanal dialkyl acetals, even more interesting C-glycoside synthons. A similar acid-catalyzed methanolysis of 1-deoxyalditol-1-nitronates leads to methyl furanosides. Finally, a treatment of per-O-substituted glycosylnitromethanes with tributyltin hydride in boiling benzene causes their radical reduction under a nearly quantitative formation of glycosylmethanal oximes. Received November 12, 2001. Accepted November 20, 2001     

Multiple effect of surfactants used as additives in background electrolytes in capillary zone electrophoresis: cetyltrimethylammonium bromide as example of model surfactant

Surfactants are frequently used in the preparation of background electrolytes (BGEs) in capillary zone elcetrophoresis (CZE) in order to affect and to optimize both the electroosmotic flow (EOF) and the separation process. Their effects are, however, always multiple, the resulting situation may be very complex and the separation process may even be destroyed. We use the surfactant cetyltrimethylammonium bromide (CTAB) as a model example and bring experimental results and related discussion which elucidate the multiple effect of surfactants in an integrated way. It is shown that even at concentration levels lower than 10(-4) M CTAB strongly reduces the cathodic EOF in bare fused-silica capillaries and converts it into anodic EOF. The magnitude and polarity of the EOF depends not only on the concentration of CTAB but also on the composition of BGEs used. The interactions of CTA cations with the bare capillary wall reduce sorption of cationic analytes and enables their analysis. CTA cations at levels below their critical micelles concentration (CMC) already interact with anionic analytes and reduce their mobilities. This association is strong with highly charged anions and by this, the reversal of the EOF, applying BGEs with highly charged anions is less effective. These interactions are competitive and also depend on the composition of the BGE used. At levels above its CMC, CTAB forms micelles and enables the application of the micellar electrokinetic capillary chromatography (MEKC) mode and the analysis of, e.g., neutral components. Simultaneously, it is shown that the presence of CTAB may increase the number of potentially formed system zones.