Supramolecular "leeks" of a fluorinated hybrid amphiphile that self-assembles into a disordered columnar phase.

We report on the formation of unprecedented "leek"-shaped aggregates of an anionic fluoroalkyl sulfonate surfactant (FS) and the supramolecular assembly of these aggregates into a disordered columnar phase (CS). The leeks are formed by wrapping of 2-4 FS-water bilayers of thickness 26-28 Å into 10-20 nm thick and >100 nm long structures, in the concentration regime of 63-70 wt % FS. A lamellar (Lα) lyotropic liquid-crystalline (LLC) phase forms at higher concentration, between 70 and 84 wt %. In the two LLC phases, the FS molecules were organized in an interdigitated or tilted fashion, or a combination of the two. Such a unique supramolecular self-assembly of amphiphiles has not been predicted nor observed before. This self-assembly behavior could be of interest to various fields like microencapsulation, nanomedicine, and membrane protein crystallization.

Micellization behavior of aromatic moiety bearing hybrid fluorocarbon sulfonate surfactants.

Aggregation behavior and thermodynamic properties of two novel homologous aromatic moiety bearing hybrid fluorocarbon surfactants, sodium 2-(2-(4-ethylphenyl)-1,1,2,2-tetrafluoroethoxy)-1,1,2,2-tetrafluoroethanesulfonate (1) and sodium 2-(1,1,2,2-tetrafluoro-2-(4-vinylphenyl)ethoxy)-1,1,2,2-tetrafluoroethanesulfonate (2) were studied using surface tension measurements and isothermal titration calorimetry (ITC) in dilute aqueous solutions at room temperature. Because of the aromatic group in the hydrophobic tail, both surfactants are soluble at room temperature unlike their starting precursor, 5-iodooctafluoro-3-oxapentanesulfonate as well as several other fluorocarbon sulfonic acid salts. Moreover, the surfactant 2 has the ability that it can be polymerized once microemulsions are formed with it. The ionic conductivity measurements of 1 at five different temperatures from 288 to 313 K were carried out to study the effect of temperature on the micellization and its thermodynamics. The pseudophase separation model was applied to estimate thermodynamic quantities from conductivity data. The Gibbs energy of micellization versus temperature exhibited the characteristic U-shaped behavior with a minimum at 306 K. The micellization process was found to be largely entropy driven. Because of its hybrid structure, the entropy change of micellization for 1 was larger than what is common for hydrocarbon surfactants like SDS but less than for fully fluorinated surfactants like NaPFO. The micellization process was found to be following the entropy-enthalpy compensation phenomena.

Synthesis of a polymerizable fluorosurfactant for the construction of stable nanostructured proton-conducting membranes.

The synthesis of the polymerizable fluorinated surfactant sodium 1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-(4-vinylphenyl)ethoxy)ethanesulfonate (1) and a number of related fluorocarbon compounds is described. Compound 1 is synthesized using a copper-mediated cross-coupling reaction of 4-bromobenzaldehyde and sodium 5-iodooctafluoro-3-oxapentanesulfonate. The resulting benzaldehyde is converted to a styrene unit using a Wittig reaction with methyltriphenylphosphonium bromide in acetonitrile, using DBU as a base. This strategy for converting an iodo-functionalized fluorosurfactant to a styrene-containing fluorosurfactant is highly efficient because both reactions are performed in polar solvents and are compatible with the sulfonate moiety. In addition, the copper-mediated cross-coupling reaction is most efficient with electron-poor aryl bromides like 4-bromobenzaldehyde. We wish to employ 1 for the construction of nanostructured membranes by polymerization of 1 in a microemulsion or in lyotropic liquid crystalline phases.