Thermal decomposition of copolymers of styrene and halogenated monomers

Copolymers of 1,2,2,2-tetrachloroethyl esters of unsaturated acids and halogenated N-phenyl maleimides with styrene were pyrolyzed; volatile products were analyzed with a mass spectrometer combined with a gas chromatograph. Hydrogen halide and carbon dioxide in the volatile products were determined during the thermal decomposition of copolymers in glass ampoules; the acyl chloride groups were determined in the residues. The thermal decomposition of copolymers of tetrachloroethyl esters with styrene sets in at ca. 230° by the release of chloral from the copolymer and splitting of some of the CCl bonds in the copolymer. The decomposition of copolymers of styrene with halogenated N-phenyl maleimides starts above 300° by depolymerization of the polystyrene chain sections and by splitting of some of the carbon-halogen bonds. At 310 and 500° for copolymers of tetrachloroethyl esters and at 500° for halogenated N-phenyl maleimides, there is radical dehydrohalogenation of the copolymers, with depolymerization of polystyrene blocks and splitting of carbon-carbon bonds in the main chain.     

Intramolecular metal—double bond interactions : VII. Intramolecular cyclization of alkenyl derivatives of lithium,aluminum, gallium and indium

The intramolecular cyclization reactions of tri-1-hex-5-enyl Group III derivatives and of 1-hex-5-enyllithium have been investigated and it is proposed that the reactions may be depicted as internal addition across the terminal double bonds of the alkenyl species. The cyclization reaction proceeds more readily for the 1-hex-5-enyl derivatives than for any other chain length and is dependent on temperature, concentration and solvent. ¹H NMR data and cryoscopic molecular weight data are presented for several diisobutyialkenyl- and diisobutylalkyl-aluminum derivatives. These data have been interpreted in terms of a direct intramolecular interaction between the metal center and the π-electron system of the olefinic site. The intramolecular cyclization reactions for the 1-hept-6-enyl, 1-oct-7-enyl- and 1-undec-10-enylaluminum derivatives also were investigated and it was found that cyclization occurred only for the 1-hept-6-enyl derivative.     

The crystal structure of CuVo3(II), a high-pressure ilmenite phase

The crystal structure of a second high-pressure copper vanadate phase, CuVO₃(II), has been determined and refined by full-matrix least-squares procedures using automatic diffractometer data to a residual R = 0.042 (R_w = 0.051). The space group is rhombohedral, $\text{R}\text{3}$, with hexagonal unit cell a = 4.966(2) and c = 14.084(5) Å [a_R = 5.501(2) Å and α = 53.66(3)°]. The structure is the fully ordered ilmenite-type and, on the basis of published magnetic data and the interatomic distances, the valence distribution Cu⁺V⁵⁺O₃ is proposed. This represents a unique example of Cu⁺ in an octahedral environment.     

Accurate local spin-polarized exchange potential: Reconciliation of generalized Slater and Kohn–Sham methods

Using simple physical arguments, a local spin-polarized exchange potential, V_xσ, is constructed from the single-particle Hartree–Fock (HF ) potentials (generalized Slater method) that reduces to the usual Kohn–Sham (KS ) result in the uniform gas limit. Numerical results for 10 closed subshell atoms demonstrate that the total energy calculated employing this V_xσ is closer to the exact KS results than those of other standard exchange approximations with electron densities and highest occupied orbital eigenvalues that closely approximate the HF results.     

Analysis of B6 vitamers by micellar electrokinetic capillary chromatography with laser-excited fluorescence detection

Micellar electrokinetic capillary chromatography (MECC) involves the application of a high voltage (10 to 40 kV) across a capillary column (25 to 75 microns i.d.) that is filled with a solution containing micelles. The mobile phase in this work consists of sodium dodecyl sulfate in an aqueous phosphate/borate buffer system. Pyridoxine (vitamin B6) and five of its metabolites are separated, with efficiencies as high as 60,000 theoretical plates/meter. Pyridoxic acid, a metabolite of B6, is separated and quantitated in human urine using laser-excited fluorescence detection. Limits of detection are less than a picogram injected.     

Investigations under quasi-isothermal and quasi-isobaric conditions by means of the Derivatograph

It is proved that under the conditions of dynamic thermoanalytical examinations the course of a decomposition reaction is determined primarily by the gas- and heattransfer partial processes, i.e. indirectly by the experimental conditions. This raises the question of whether it is justified to make kinetic calculations based on the shapes of similar curves. A new measuring technique is reported which uses a slightly modified Derivatograph. With this new method decomposition reactions can be examined under “quasi-isothermal” and “quasi-isobaric” conditions. The pernicious effects of the gas- and heat-transfer processes are thus eliminated, and the shapes of the curves obtained provide the possibility of studying the decomposition reactions in a new and more thorough way.     

Kinetics of cooperative conformational transitions of lineal biopolymers

Cooperative conformational transitions of proteins and nucleic acids are of decisive importance to many processes of molecular biology, and particularly to their regulation. They proceed via numerous interdependent elementary processes, and their kinetics are therefore often complicated. They are frequently also very fast. However, kinetic analyses can be carried out by chemical relaxation methods. The theoretical interpretation is comparatively simple in the case of linear biopolymers. When the linear Ising model extended for kinetics was applied to model peptides and polynucleotides, it provided an insight into the fundamental principles of cooperative transformations.     

Untersuchungen an Tetramethylantimonderivaten verschiedener phosphorhaltiger Säuren

Studies on Tetramethyl Antimony Derivatives of Various Phosphorus-containing Acids The preparation and the properties of tetramethyl antimony derivatives of HOOPF₂, HOOPCl₂, HOOPH₂, HOOP(CH₃)₂ and HOSP(CH₃)₂ are described. Infrared, Raman, ¹H-. ³¹P- and ¹⁹F-NMR studies of the difluorophosphat, the dichlorophosphat and the hypophosphite point to ionic structures with (partly distorted) tetrahedral Sb(CH₃)₄⁺ cations and F₂POO^?, Cl₂POO^? and H₂POO^? anions, respectively. The spectroscopic data of the dimethylphosphinate and the dimethylthiophosphinate prove non-ionic structures in the solid, the melt and the solutions in non-polar solvents.     

Birefringence induite dans les directions remarquables d'une suspension de particules rigides en ecoulement

A theoretical formula is derived for the flow birefringence exhibited along the streamlines and in the direction of the shear rate (G) by dilute suspensions of rigid spheroid-like macromolecules; numerical values are computed up to σ = G/D = 900 (D = rotary diffusion coefficient). These results provide two tests for identifying prolate and oblate particles; when combined with the data for observation perpendicular to the plane of flow, they confirm the connection between non-Newtonian viscosity and the Maxwell effect for monodisperse samples; for vanishing rate of shear, they allow a mixture of particles to be characterized by means of a mean rotary diffusion constant ($\text{D}$) and a mean shape coefficient ($\text{R}$).     

Are dipolar liquids ferroelectric?

VH and HV depolarized hyper-Rayleigh scattering spectra were measured for liquid solutions of dipolar CH3CN in nondipolar C2Cl4 at T=300 K. The VH spectrum contains a strong narrow peak due to a slowly relaxing longitudinal orientation mode. This peak is absent in the HV spectrum, and it disappears from the VH spectrum when the CH3CN concentration is reduced to 8%. This observation is consistent with a ferroelectric phase transition predicted to occur when rho mu0(2)=9epsilon0kT=49 D2 M.