The interaction of monosubstituted benzenes with the stationary liquid in gas liquid chromatography

Kawaki, H

HERO ID

2892109

Reference Type

Journal Article

Year

2004

Language

English

PMID

14758007

HERO ID 2892109
In Press No
Year 2004
Title The interaction of monosubstituted benzenes with the stationary liquid in gas liquid chromatography
Authors Kawaki, H
Journal Chemical and Pharmaceutical Bulletin
Volume 52
Issue 2
Page Numbers 221-225
Abstract In gas liquid chromatography (GLC), the relative retention values log gamma was mainly expressed by van der Waals energy (the sum of the dispersion E(dis) and repulsive E(rep) energies) to the interactions between monosubstituted benzene derivatives and the nonpolar stationary liquid as squalane. The single exception was that of anilines, and it was corrected by the electrostatic energy (E(ES)) due to C-H/pi hydrogen bond. When the stationary liquid changed from the nonpolar to polar, log gamma was estimated by the inductive interaction energy (included in E(ES)) in addition to the sum of E(dis) and E(rep). In the benzene solution, the relative equilibrium values log K/K(o) introduced from the interactions between phenol and substituted benzene derivatives were estimated by E(ES). The E(ES) of COCH(3), CO(2)C(2)H(5) groups is especially originated in the excited dipole moments micro(e). The relative frequency values log nu/nu(o) derived from O-H or O-D stretching vibration of phenol or methanol-D gave the correlation to E(ES) as well as log K/K(o). That of anilines-methanol-D however had been out of a linear relation to E(ES). The cause is concluded that the aniline-methanol-D is making the proton transfer structure from the discussion about the proton affinity (PA) of the base.
Doi 10.1248/cpb.52.221
Pmid 14758007
Wosid WOS:000188654400009
Url <Go to ISI>://WOS:000188654400009
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword gas liquid chromatography; intermolecular interaction; substituted benzene; electrostatic interaction energy; van der Waals interaction energy