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Last Modified:
12:00 PM, Mon Mar 29, 1999
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Amphiphilic Interfacial Chemistry - Chromatography
Characterization and Control of Chromatographic Interfaces
Synthesis and Characterization of Novel Organically Modified Sol Gels for use as
Chromatographic Stationary Phases

While reverse-phase liquid chromatography is
the most widely employed mode of liquid
chromatography, the molecular basis for its
action is not fully understood. While much
research has focused on the chromatographic
behavior of carefully chosen solute molecules in
an effort to elucidate retention mechanisms,
only a few researchers have applied
spectroscopic methods to study this question. In
this laboratory we are examining real
chromatographic stationary phases with normal
Raman spectroscopy to develop a molecular
picture of the chromatographic interface. The
behavior of monomeric and polymeric C18
stationary phases under various
chromatographic conditions have been
examined. Conditions studied so far include
single and binary solvent systems with
variations in the dielectric constant and
temperature. Each of these parameters affects
the relative conformational order of the
stationary phase, the parameter we believe is
directly correlated with retention behavior.
Characterization of Chromatographic Stationary Phases using Raman
Spectroscopy
A Systematic Investigation of
Operating Parameters on Stationary
Phase Conformation Order

Reverse-phase liquid chromatography (RPLC)
is arguably the most common mode of liquid
chromatography used. Not just unique to
academic research laboratories, RPLC is used
by government agencies to prove regulatory
compliance, medical laboratories to identify
drug metabolites, and industry to monitor
quality control. Despite the wide use of RPLC,
a fundamental mechanism of separation has yet
to be obtained through investigation of
stationary phases with chromatography, NMR,
fluorescence, and even IR. The ultimate purpose
of this research is to elucidate the molecular
basis of a mechanism of separation with Raman
spectroscopy.
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