Unique Aggregation Behavior of a Carboxylate Gemini Surfactant with a Long Rigid Spacer in Aqueous Solution

A new gemini surfactant with a long and rigid spacer, O,O'-bis(sodium 2-dodecylcarboxylate)-p-dibenzenediol (referred to as C(12)φ(2)C(12)), has been synthesized. Its aggregation in aqueous solution has been studied using static and dynamic light scattering measurements. The homologue O,O'-bis(sodium 2-dodecylcarboxylate)-p-benzenediol (C(12)φC(12)) whose spacer only contains a single phenyl group was also examined for comparison. Dynamic light scattering (DLS) revealed the unexpected existence of large aggregates in the solution of C(12)φ(2)C(12). However, C(12)φC(12) showed rather normal aggregation behavior. Both the results of intrinsic viscosity and light scattering demonstrated a loose structure for the large aggregates of C(12)φ(2)C(12). This behavior was attributed to an extending configuration of C(12)φ(2)C(12) with the two alkyl tails stretching toward the solution due to the rigidity of the long spacer. The large network-like aggregate formation was an inevitable outcome of spontaneously reducing the energy of the system. Freeze-fracture transmission electron microscopy (FF-TEM) images and (1)H NMR measurements supported this speculation. Due to the columnar-like molecular geometry, the large network-like aggregates were directly transformed into rodlike micelles with increasing surfactant concentration. Depending on further micellar growth, the wormlike micelles were finally formed as confirmed by rheological measurements.