Solute absorption into molten polystyrene

The equilibrium volatilities at near infinite dilution of various solutes absorbed in molten polystyrene have been determined by a gas chromatographic technique. This method is much more rapid, although, with the present apparatus, probably less accurate than conventional static techniques. The primary parameters obtained from measurements of retention volumes are the Henry's law constants, from which are derived the weight and volume fraction activity coefficients, the Flory-Huggins interaction parameters, and the heats of dilution and solution. Of the solutes investigated, 2-butanone (MEK) was the least, and benzene the most compatible (highest and lowest volume fraction activity coefficients, respectively) with molten polystyrene. A small, but definite, variation of the activity coefficients with polystyrene molecular weight was observed.     

Accurate fast neutron activation analysis for oxygen in geological materials

Sources of error in the fast neutron activation analysis determination of oxygen have been investigated and minimised. The oxygen contents of eighteen international rock standards and a sulphide ore standard have been determined, and compared with the values calculated by difference using the reported full analyses. Accuracies of 0.3% average deviation and reproducibilities of ±0.2% standard deviation have been obtained, where oxygen contents exceeded 1.0 g.     

Simple method for the preparation of 1-oxo-1-chlorophospholenes

Conclusions A new and simple method has been found for the synthesis of 1-oxo-1-chlorophospholenes by the reaction of phosphorus trichloride, a diene, and an oxygen-donor compound, the best of which is acetone.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1847–1848, August, 1972.     

Synthesis of 1,2-Divinyloxypropenes from Glycerol and Acetylene in the Superbasic System CsF-NaOH-DMSO

Russian Journal of Organic Chemistry -     

Reactions of diterpenoids on solid supports II. Behavior of di- and tricyclic diterpenoids on alumina containing oxidants

The behavior of epimanool (1), epimanool oil, larixol (2), cis-abienol (3) and methyl dehydroabietate (4) on alumina impregnated with oxidants (H₂CrO₄ and KMnO₄) has been studied. This has led to the methyl ketone (5) and norambrenolide (8) - precursors of the perfume substances 14,15,17-trinorlabdane-8,13-dione (6), 8-hydroxy-14,15-bisnorlabd-II-en-13-one (7), and methyl 7-oxodehydroabietate (14). -Levantenolide (11) has been synthesized in one stage from cis-abienol (3)for the first time.Novosibirsk Insitute of Organic Chemistry, Siberian Division of the Russian Academy of Sciences. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 229–234, March-April, 1995. Original article submitted July 25, 1994.     

Calculation of the gas hydrate HS-1 framework structure and its energy estimation

Using the Zimmennan-Pimentel potential, we have calculated the basic atomic coordinates of the unit cell of the gas hydrate HS-lframework. A minimum change in the strain energy of hydrogen bonh U_H fakes place in formation of this framework from ice Ih. The dependence of U_H on the lattice parameters is derived.Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated fromZhurnal Strukturnoi Khimii, Vol. 34, No. 5, pp. 175–178, September–October, 1993.Translated by T. Yudanova     

Methane Hydroxylation by Methane Monooxygenase: On the Problem of the Process Dynamics

Published data on the kinetic isotope effects of the hydroxylation of deuterium-substituted methane molecules (CHD₃, CH₂D₂, and CH₃D) by methane monooxygenase are examined in the framework of the two-step nonradical mechanism through the intermediate formation of a complex containing pentacoordinate carbon. The kinetic schemes with the first step involving one, two, and three hydrogen atoms of the oxidized substrate are considered. Contrary to the widely accepted oxygen rebound mechanism, the experimental results obtained for the oxidation of various substrates by methane monooxygenase and cytochrome P450 can be explained from the viewpoint of the dynamics of a general nonradical mechanism.     

Kinetics and Mechanism of Monomolecular Heterolysis of Commercial Organohalogen Compounds: XXVIII. Effect of the Nature of the Verdazyl Indicator on Salt Effects in Dehydrobromination of 3-Bromocyclohexene in Nitrobenzene

The salt effect on the rate of dehydrobromination of 3-bromocyclohexene in PhNO2 depends on the nature of the verdazyl indicator. With triphenylverdazyl and its chloro and nitro derivatives in the presence of Et₄NClO₄, a normal salt effect is observed, in the presence of bromides, a superposition of normal and special salt effects, while in the presence of chlorides, a superposition of normal and special negative salt effects. With the dimethoxy verdazyl derivative, a normal salt effect is always observed.