posted on 2000-11-10, 00:00authored byFredric M. Menger, Kevin L. Caran
On the basis of suggestive X-ray data, 14 aroyl l-cystine derivatives were designed, synthesized,
and examined for their ability to gelate water. Several members of this amino acid family are remarkably
effective aqueous gelators (the best being one that can rigidify aqueous solutions at 0.25 mM, ca. 0.01%, in
less than 30 s!). A few of the analogues separate from water as crystals, indicating a close relationship between
gelation and crystallization. All effective gelators self-assemble into fibrous structures that entrain the solvent
in the capillary spaces among them. Hydrogen-bonding sites on the compounds that might stabilize the fibers
were identified from specific substitutions that replace a hydrogen donor with a methyl group, enhance the
hydrogen-accepting ability of a carbonyl oxygen, or promote the hydrogen-donating ability of an amide proton.
The structural variations were characterized via minimal gelation concentrations and times, X-ray crystallography,
light and electron microscopy, rheology, and calorimetry. The multiple techniques, applied to the diverse
compounds, allowed an extensive search into the basis of gelation. It was learned, for example, that the compound
with the lowest minimum gelator concentration and time also has one of the weakest gels (i.e., it has a low
elastic modulus). This is attributed to kinetic effects that perturb the length of the fibers. It was also argued
that π/π stacking, the carboxyl carbonyl (but not the carboxyl proton), and solubility factors all contribute to
the stability of a fiber. Polymorphism also plays a role. Rheological studies at different temperatures show
that certain gels are stable to a 1-Hz, 3-Pa oscillating shear stress at temperatures as high as 90 °C. Other gels
have a “catastrophic” break at lower temperatures. Calorimetric data indicate a smooth transition from gel to
sol as the temperature is increased. These and other issues are discussed in this “anatomy” of a gel.