The origin and evolution of solute descriptors for use in the solvation par
ameter model applied to the classification of stationary phases and other m
aterials by gas chromatography are described. The model system constants pr
ovide a breakdown of solute-stationary phase interactions in terms of the c
ontribution to retention of cavity formation and dispersion interactions, l
one-pair electron interactions, interactions of a dipole-type, and hydrogen
-bonding interactions. The solvation properties of additional stationary ph
ases with useful complementary selectivity to existing phases for method de
velopment in gas chromatography are identified. The influence of temperatur
e on system selectivity and stationary phase classification is discussed. T
he contribution of interfacial adsorption to the estimation of retention in
method development in gas chromatography is outlined. In addition, for mat
erials characterization, it is shown that the solvation parameter model pro
vides a conceptual mechanism for the evaluation of the sorption properties
of a wide range of materials compatible with the operation characteristics
of gas chromatography. (C) 1999 Elsevier Science B.V. All rights reserved.