Simultaneous effects of relaxation and polarization transfer in LaF3-type crystals as sources of dynamic information

Fluorine nuclear magnetic resonance (NMR) spin-lattice relaxation dispersion has been measured for pure LaF(3) and La(1-x)Sr(x)F(3-x) for admixture concentrations x ranging from 0.01% up to 16%. The relaxation dispersion experiments have been carried out in a wide frequency range (20 kHz-40 MHz) at temperatures between 300 and 1400 K. The data have been analyzed using the recently published [J. Magn. Res. 179 (2006) 250] relaxation model for multispin systems of mutually interacting quadrupolar and dipolar nuclei. Rate constants of the fluorine ionic jumps within and among distinct fluorine sublattices have been extracted. Characteristic effects of the polarization transfer between fluorine and lanthanum spins have been observed and attributed to slow dynamics within one of the fluorine sublattices.     

Correlation between thermal diffusion and solvent self-diffusion in semidilute and concentrated polymer solutions

We have performed measurements of thermal diffusion coefficients DT and solvent self-diffusion coefficients Dss in semidilute to concentrated polymer solutions. Solutes of different glass transition temperatures and solvents of different solvent qualities have been used. The investigated systems are in detail: poly(dimethyl-siloxane) in toluene, tristyrene in toluene, polystyrene in toluene, polystyrene in tetrahydrofuran, polystyrene in benzene, and polystyrene in cyclohexane. The thermal diffusion data are compared to our data and literature data for solvent self-diffusion coefficients. In all systems the concentration dependence of DT closely parallels the one of Dss which may be viewed as a local probe for friction on a length scale of the size of one polymer segment. This identifies local friction as the dominating parameter determining the concentration dependence of DT. Solvent quality, in contrast, has no influence on DT.     

Raman Lidar Sensing of Saturated Hydrocarbon Molecules in the Atmospheric Boundary Layer. Numerical Modeling

Russian Physics Journal - The possibility of measuring the concentration of alkane molecules – methane, ethane, propane, butane, pentane, and hexane – at the maximum permissible...     

Self-adaptable catalysts: substrate-dependent ligand configuration

Pd(II) allyl and Pd(0) olefin complexes containing the configurationally labile ligand 1,2-bis-[4,5-dihydro-3H-dibenzo[c-e]azepino]ethane were studied as models for intermediates in Pd-catalyzed allylic alkylations. According to NMR and DFT studies, the ligand prefers C(s) conformation in both eta3-1,3-diphenylpropenyl and eta3-cyclohexenyl Pd(II) complexes, whereas in Pd(0) olefin complexes it adopts different conformations in complexes derived from the two types of allyl systems in both solution and, as verified by X-ray crystallography, in the solid state. These results demonstrate that the Pd complex is capable of adapting its structure to the reacting substrate. The different structural preferences also provide an explanation for the behavior of 1,3-diphenyl-2-propenyl acetate and 2-cyclohexenyl acetate in Pd-catalyzed allylic alkylations using pseudo-C2 and pseudo-C(s) symmetric ligands.     

A computational study of oxidation of ruthenium porphyrins via ORu(IV) and ORu(VI)O species

An unrestricted density functional theory (UDFT) was applied to study the oxidation of ruthenium porphyrins, [RuP], via an interaction with molecular oxygen. The important role of dimeric [RuP] complexes, i.e. [RuP]-O2-[RuP], in the oxidation mechanism and particular in the cleavage of O-O bond of molecular oxygen has been studied. Geometries and relative Gibbs free energies of the intermediate Ru-complexes, i.e. dimeric oxo-Ru-porphyrins and O2Ru(II)-(or O2- Ru(III))-, ORu(IV)- and ORu(VI)O-porphyrins, were evaluated along the proposed reaction pathway. The detailed thermodynamic data of the oxidation reaction [Ru(II)P] --> O[Ru(IV)P] --> O[Ru(VI)P]O and important aspects of the vibrational spectra of an oxo-[RuP] has been presented.