A Consistent Determination of the Dimerization Constants of the Self‐Association of 2,2‐Dimethyl‐3‐ethyl‐3‐pentanol in Carbon Tetrachloride from its Infrared Spectral Data

Two equations of linear type (Eqs. 10 and 17 in the text) have been derived to analyze the IR data to determine the dimerization constant consistently. Equation 10 is to be used to fit the integrated absorbances of the monomer band to obtain the molar monomer absorptivity, ?_m, and dimerization constant, K; Eq. 17 is to be used to fit the integrated absorbances of the dimer bands to obtain the molar dimer absorptivity, ?_d, and dimerization constant, K. Thus the same dimerization constant can be independently determined either from the monomer band or from the dimer band. The discrepancy between the two determined values provides an assessment of the consistency of determination. The monomer‐dimer self‐association of 2,2‐dimethyl‐3‐ethyl‐3‐pentanol in the solvent of carbon tetrachloride was chosen to demonstrate the utility of these two equations.     

A combined experimental,theoretical, and Van't Hoff model study for identity methyl,proton, hydrogen atom,and hydride exchange reactions. Correlation with three‐center four‐, three‐, and two‐electron systems

We have studied carbon transfer reactions following an S_N2 reaction profile. With ab initio calculations and experimental geometries concerning the nature of the various complexes indicated as stable, intermediate, and transition state we were able to show the additional value of van't Hoff's tetrahedral configuration by changing its geometry via a trigonal pyramid into a trigonal bipyramid. The ratio of the apical bond and corresponding tetrahedral bond distances is then nearly 1.333. The relevance of this approach has also been shown for identity proton‐(hydrogen atom‐, and hydride‐) in‐line reactions. The use of this geometrical transmission will be demonstrated for the hydrogen bonding distances in e.g., DNA duplexes and other biological (supra) molecular systems. © 2008 Wiley Periodicals, Inc. Int J Quantum Chem, 2008     

Molecular model studies based on ab initio calculations of nucleophilic and electrophilic addition‐substitution reactions focused on carbon–halogen compounds

We describe with molecular model studies based on the intrinsic parameters of van't Hoff's regular tetrahedron nucleophilic and electrophilic addition‐substitution reactions via a selected reaction coordinate for the displacement of carbon. Geometries of stable, intermediate transition complexes or transition states are compared with the corresponding ab initio values. Specific attention is given on the hypervalent and nonhypervalent character of carbon supported by ab initio calculations, our model consideration and experimental evidence. © 2011 Wiley Periodicals, Inc. Int J Quantum Chem, 2011     

Chromatographic behavior of small organic compounds in low‐temperature high‐performance liquid chromatography using liquid carbon dioxide as the mobile phase

Low‐temperature high‐performance liquid chromatography, in which a loop injector, column, and detection cell were refrigerated at –35ºC, using liquid carbon dioxide as the mobile phase was developed. Small organic compounds (polyaromatic hydrocarbons, alkylbenzenes, and quinones) were separated by low‐temperature high‐performance liquid chromatography at temperatures from –35 to –5ºC. The combination of liquid carbon dioxide mobile phase with an octadecyl‐silica (C₁₈) column provided reversed phase mode separation, and a bare silica‐gel column resulted in normal phase mode separation. In both the cases, nonlinear behavior at approximately –15ºC was found in the relationship between the temperature and the retention factors of the analytes (van't Hoff plots). In contrast to general trends in high‐performance liquid chromatography, the decrease in temperature enhanced the separation efficiency of both the columns.     

Retention behavior of resorcinarene‐based cavitands on C8 and C18 stationary phases

The understanding of the retention behavior of large molecules is an area of interest in liquid chromatography. Resorcinarene‐based cavitands are cavity‐shaped cyclic oligomers that can create host–guest interactions. We have investigated the chromatographic behavior of two types of cyclic tetramers as analytes in high‐performance liquid chromatography. The experiments were performed at four different temperatures (15, 25, 35, 45°C) on two types of reversed stationary phases (C₈ and C₁₈) from two different manufacturers. We have found a huge difference between the retention of resorcinarenes and cavitands. In some cases, the retention factor of cavitands was even a hundred times larger than the retention factor of resorcinarenes. The retention of methylated derivates was two to four times larger compared to that of demethylated compounds on every column. The opposite retention behavior of the resorcinarenes and cavitands on the two types of stationary phases showed well the difference of the selectivity of the XTerra and BDS Hypersil columns. The retention mechanism was studied by the thermodynamic parameters calculated from the van't Hoff equation.     

A model investigation of ab initio geometries for identity and nonidentity substitution with three‐center four‐ and three‐electron transition states

With the van't Hoff model derived from the dynamics of a regular tetrahedron in which the interstitial carbon changes its position from tetrahedral into a trigonal (bi)pyramidal configuration, the introduction of dimensionless ratio numbers (R) can serve to localize significant points on the principal reaction coordinate. These numbers are expressed as R(d) and R(n) based on transition state geometries and the number of electrons involved in the three‐center bonding, respectively. Using this concept, we obtain a model for the evaluation of different ab initio calculations based on identity and nonidentity substitution reactions for three‐center four‐ and three‐electron bonding transition states. Similar ratio numbers have been derived for proton exchange reactions. The reactions under investigation show clearly that in spite of the differences in chemical outcome the transition steps reduced to the first principles of chemical bonding are similar. © 2010 Wiley Periodicals, Inc. Int J Quantum Chem, 2011