The wettabilities of fluorinated polymers were evaluated using a series of contacting probe liquids ranging in nature from nonpolar aprotic to polar aprotic to polar protic. Fully fluorinated polymers were wet less than partially fluorinated polymers, highlighting the weak dispersive interactions of fluorocarbons. For partially fluorinated polymers, the interactions between the distributed dipoles along the polymer backbone and the dipoles of the contacting liquids were evaluated using both polar and nonpolar probe liquids. The results demonstrate that the surface dipoles of the fluoropolymers generated by substituting fluorine atoms with hydrogen or chlorine atoms can strongly interact with polar contacting liquids. The wettabilities of the partially fluorinated polymers were enhanced by increasing the density of dipoles across the surfaces and by introducing differentially distributed dipoles.

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We report a new class of molecules, linactants, that partition at phase boundaries and reduce the line tension between coexisting two-dimensional phases in molecular monolayers. The line tension between hydrocarbon-rich and fluorocarbon-rich phases was determined by monitoring the relaxation kinetics of deformed domains. Two partially fluorinated linactant molecules (with one and two tails, respectively) were synthesized and tested; the more efficient single-tail variant reduced the line tension by more than 20% at a mole fraction of only 8 x 10(-4).

Surfactants exhibit characteristic phenomena, including the reduction of interfacial free energy, self-assembly into aggregates, and even the formation of lyotropic liquid crystalline phases at high concentrations. Our research has shown that a semifluorinated phosphonic acid can act as the two-dimensional analogue of a surfactant-a linactant-by reducing the line tension between hydrocarbon-rich and fluorocarbon-rich phases in a Langmuir monolayer. This linactant can also self-assemble into nanoscale clusters in a monolayer. Here, we explore the dependence of linactant behavior on molecular structure. Members of a homologous series of partially fluorinated phosphonic acids were synthesized and tested as linactants: CF(3)(CF(2))(n-1)(CH(2))(m)PO(3)H (abbreviated as FnHmPO(3)). The tests revealed that linactants with longer hydrophobic chains were most efficient in lowering line tension. For linactants with the same overall chain length, the length of the fluorocarbon block was correlated with efficiency. Thus, the linactant efficiency was ranked in the order F8H8PO(3) < F10H6PO(3) < F8H11PO(3) < F10H9PO(3). In all cases, linactant-containing Langmuir-Blodgett monolayers exhibited nanoscale molecular clusters with characteristic dimensions of 20-30 nm; enhanced linactant efficiency was systematically correlated with larger clusters.

The structure and conformation of self-assembled monolayers (SAMs) derived from the adsorption of a specifically designed double-chained partially fluorinated thiol having the formula 12,12,13,13,14,14,15,15,16,16,17,17,18,18,19,19,19-heptadecafluoro-2-tetradecylnona-decane-1-thiol (2) onto the surface of evaporated gold were examined by ellipsometry, contact angle goniometry, polarization modulation infrared reflection-absorption spectroscopy (PM-IRRAS), and X-ray photoelectron spectroscopy (XPS). The results were compared to those of SAMs generated from normal hexadecanethiol (1) and a structurally related single-chained partially fluorinated thiol having the formula 12,12,13,13,14,14,15,15,16,16,17,17,18,18,19,19,19-heptadecafluorononadecane-1-thiol ( 3). Collectively, the studies demonstrate that the double-chained adsorbate 2 forms SAMs on gold in which the alkyl chains are less densely packed and less conformationally ordered than those in the SAMs derived from each of the single-chained adsorbates. Furthermore, the fluorocarbon moieties in the SAMs derived from 2 are more tilted from the surface normal than those in the SAMs derived from 3. The low values of contact angle hysteresis suggest, however, that the double-chained adsorbate 2 generates homogeneous monolayer films on the surface of gold.

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We report observations of phenomena within two-component Langmuir monolayers that are analogous to surfactant self-assembly in 3D solutions. A partially fluorinated fatty phosphonic acid played the role of 2D surfactant (linactant), and a perfluorinated fatty acid acted as the 2D solvent. Langmuir-Blodgett monolayers were prepared from mixtures of these compounds and examined using atomic force microscopy. Above a critical linactant mole fraction of approximately 0.013, distinctive monodisperse structural features were observed with a characteristic diameter of approximately 30 nm and a relative height of 1.4 nm. As the linactant concentration was further increased, the number density of these features increased linearly with concentration, whereas the size remained approximately the same. A quantitative analysis of these observations suggested that the features corresponded to self-limiting clusters composed of approximately 2000 linactant molecules and that the dispersed clusters represented a 2D micellar phase. Above a linactant mole fraction of 0.63, the clusters organized into a local hexagonal structure with short-range positional order indicative of a 2D "lyotropic" liquid crystalline phase; the correlation length increased systematically with increasing linactant concentration.

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