Reaction of silylphosphites with secondary amines

The reaction of dialkylsilylphosphites with linear and cyclic secondary amines leads to the formation of acid alkoxydialkylamidophosphites and dialkyl phosphites. Aminolysis of pyrocatecholsilylphosphite was accomplished with retention of the phosphorus atom and formation of the corresponding amidophosphites.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 235–237, January, 1991.     

Effect of the medium on the decomposition rate of di-t-butyl trioxide

Using the chemiluminescence method, the effect of the medium on the overall rate constant of the thermal decomposition of di-tert-butyl trioxide has been studied. In all solvents investigated the decomposition occurs in accordance with a first order rate law. The effect of solvent on the rate constant (0°C) is analyzed.     

An empirical force field. II. Crystalline alkanes

The EFF'93 force field is used to study crystalline alkanes. In addition to detailed molecular geometries, the sublimation enthalpy, heat capacity, and lattice vibrations for a number of saturated hydrocarbons are reported and compared with experiment. © 1995 by John Wiley & Sons, Inc.     

Comparison of theory and experiment for excited singlet states of the H2 molecule

This paper presents a survey of published and unpublished ab initio calculations of the vibrational structures of the ten lowest electronic singlet states of the hydrogen molecule up to the H(n = 1) + H(n = 2) dissociation limit. The data are based on adiabatic potential functions (clamped-nuclei electronic energies and nuclear-mass-dependent diagonal corrections). Nonadiabatic coupling has been treated ab initio within the five states. of ¹Λ symmetry (X,EF, GK, HH?) and ¹Σ I.¹Π_g. The accuracies of the theoretical energies are determined by comparisons with experimental data for H₂, HD, and D₂. The level shifts and predissociation probabilities of the excited ¹Σ states, generated by nonadiabatic coupling with the discrete and continuous vibrational structure of the ground state, and radiative properties have also been calculated.     

Ab initio Calculation of the Electronic Structure and Equilibrium Geometry of Cortisol and Its Derivatives

The molecular geometries of a series of steroid hormones including cortisol, 9-fluorocortisol, 6-fluorocortisol, and 9-chlorocortisol were optimized by 3-21G and 6-31G* ab initio calculations. The results of calculations on both levels are well consistent with each other and with the experiment. The conformational changes and electron density redistribution occurring in going from cortisol to its 6- and 9-halo derivatives were discussed. A conclusion was made that the O and F atoms can participate in hydrogen bonding with the corresponding structural groups of glucocorticoid receptors.     

Gas chromatographic-mass spectrometric analysis of acids and phenols in distilled alcohol beverages. Application of anion-exchange disk extraction combined with in-vial elution and silylation

A GC-MS protocol for profiling spirits, based on 19 acids and phenolic compounds, has been proposed and evaluated. The method combined a simple preconcentration procedure based on solid-phase (anion-exchange) disk extraction, and in-vial elution and silylation of the analytes. The derivatized extract was directly injected into the GC-MS system. These analytes were: C6, C8, C10, C12 acids, pyruvic acid, 2-furoic acid, succinic acid, fumaric acid, glutaric acid, lactic acid, glycolic acid, malic acid, tartaric acid, citric acid, vanillin, syringaldehyde, coniferaldehyde, vanillic acid and gallic acid. The profiles of six different spirits were found reproducible from day-to-day with <20% RSD for measurements of most of the analytes at different concentrations. Recoveries of individual analytes appear to be affected by the level of tannins in the spirits, and they varied from sample to sample. The method of standard addition was used to quantify age-related analytes. Good linearity of response with correlation coefficients in the range of 0.992-0.999 was obtained. The results of the study indicate that for spirits of the same brand but of different ages, the amounts of these analytes appear to increase with the ageing period.     

Free-electron attachment to coronene and corannulene in the gas phase

Electron attachment to the polyaromatic hydrocarbons coronene and corannulene is studied in the electron energy range of about 0-14 eV using a high-resolution crossed electron-neutral beam setup. The major anions observed are the parent anions peaking at about 0 eV with cross sections of 3.8 x 10(-20) and 1 x 10(-19) m(2), respectively. The only fragment anions formed in coronene and corannulene are the dehydrogenated coronene and corannulene anions. Other anions observed in the negative mass spectra at about 0 eV can be ascribed to impurities of the sample. High-level quantum-mechanical studies are carried out for the determination of electron affinities, hydrogen binding energies, and structures of both molecules. The behavior of coronene and corannulene upon electron attachment is compared with that of other polyaromatic hydrocarbons studied previously.