Headgroup Effects on the Unusual Lamellar−Lamellar Coexistence and Vesicle-to-Micelle Transition of Salt-Free Catanionic Amphiphiles

• Published in: Langmuir Vol. 26; no. 5; pp. 3058 - 3066
• Main Authors: Silva, Bruno F. B, Marques, Eduardo F, Olsson, Ulf, Pons, Ramon
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 02-03-2010
• Subjects: Chemistry; Colloidal state and disperse state; Colloids: Surfactants and Self-Assembly, Dispersions, Emulsions, Foams; Exact sciences and technology; General and physical chemistry; Membranes; Micelles. Thin films; Surface physical chemistry; Water; Intermediate state; Vesicle; Self assembly; Swelling; Force; Chain length; Reference; Ion pair; Solubility; Micelle; Surfactant; Solubilization; Sulfates; Sulfonate; Charge density; Chemistry; Asymmetry; Packing
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la902963k

Salt-free ion-paired catanionic amphiphiles of the C m +C n − type, with a high solubility mismatch (n ≫ m or m ≫ n) display a remarkable phase behavior in water. A temperature-driven vesicle-to-micelle transition in the dilute side together with a coexistence of two lamellar phases on the concentrated side is one of the peculiar effects that have been reported for the hexadecyltrimethylammonium octylsulfonate surfactant, C16C8 or TA16So8 (extensive to C14C8 and C12C8). In this work, with TA16So8 as a reference, the cationic trimethylammonium (TA+) and pyridinium (P+) headgroups are combined with the anionic sulfate (S−) and sulfonate (So−) headgroups to yield other C16C8 compounds: hexadecyltrimethylammonium octylsulfate (TA16S8), 1-hexadecylpyridinium octylsulfonate (P16So8), and 1-hexadecylpyridinium octylsulfate (P16S8). We show that, if the asymmetry of the chain lengths is kept constant at C16C8 and the headgroup chemistry is changed, most of the unusual self-assembly properties are still observed, indicating that they are not system-specific but extensive to other combinations of headgroups and mainly dictated by the ion-pair solubility mismatch. Thus, all the compounds in water quite remarkably show a lamellar−lamellar phase coexistence and spontaneously form vesicles upon solubilization. Moreover, P16So8 undergoes a temperature-driven vesicle-to-micelle transition that involves an intermediate planar lamellar state, similar to TA16So8. Some interesting effects on the global phase behavior, however, do arise when the headgroups are changed. Geometric packing effects are shown to be important, but the differences in phase behavior seem to be mainly dictated by (i) the charge density of the headgroups, which tunes the solubility mismatch of the ion-pair, and (ii) specific interactions between headgroups, which affect the short-range repulsive force that controls the swelling of the concentrated lamellar phase.