Polyelectrolyte surfactant assemblies

Electrostatic layer-by-layer assembly involving, for example, oppositely charged polyelectrolytes/surfactants and nanoparticles may be readily accomplished on suitably functionalized surfaces [58-61]. 

Another extremely useful method for cac determination, especially in the light of high sensitivity, is fluorescence emission spectroscopy [15]. Some aromatic water-insoluble dyes that are present in trace amounts in mixed polyelectrolyte-surfactant solutions have an ability to solubilize within the self-assembled surfactant aggregates and to change their photophysical properties because of the change of environmental polarity. Through this, they offer a very sensitive method for the determination of cac values. A typical and lately frequently used compound is pyrene, which is used as a fluorescence probe to assess various micellar properties. Pyrene exhibits a polarity dependent fluorescence spectrum with the ratio /,//3 (the ratio of the intensity... 

W.J. Macknight, E.A. Ponomarenko, and D.A. Tirrell, Self-assembled polyelectrolyte-surfactant complexes in nonaqueous solvents and in the solid state. Acc. Chem. Res. 31, 781-788 (1998). 

Functionalized polyelectrolytes are promising candidates for photoinduced ET reaction systems. In recent years, much attention has been focused on modifying the photophysical and photochemical processes by use of polyelectrolyte systems, because dramatic effects are often brought about by the interfacial electrostatic potential and/or the existence of microphase structures in such systems [10, 11], A characteristic feature of polymers as reaction media, in general, lies in the potential that they make a wider variety of molecular designs possible than the conventional organized molecular assemblies such as surfactant micelles and vesicles. From a practical point of view, polymer systems have a potential advantage in that polymers per se can form film and may be assembled into a variety of devices and systems with ease. 

Other examples of organized molecular assemblies of interest for photocatalysis are (1) PC-A, PC-D or D-PC-A molecules where PC, A and D fragments are separated by rigid bridges (2) host-guest complexes (3) micelles and microemulsions (4) surfactant monolayers or bilayers attached to solid surfaces, and (5) polyelectrolytes [19]. 

The complex formation of PECs and PE-surfs is closely linked to self-assembly processes. A major difference between PECs and PE-surfs can be found in their solid-state structures. PE-surfs show typically highly ordered mesophases in the solid state [15] which is in contrast to the ladder and scrambled-egg structures of PECs [2]. Reasons for the high ordering of PE-surfs are i) cooperative binding phenomena of the surfactant molecules onto the polyelectrolyte chains [16-18] and ii) the amphiphilicity of the surfactant molecules. A further result of the cooperative zipper mechanism between a polyelectrolyte and oppositely charged surfactant molecules is a 1 1 stoichiometry. The amphiphilicity of surfactants favors a microphase separation in PE-surfs that results in periodic nanostructures with repeat units of 1 to 10 nm. By contrast, structures of PECs normally display no such periodic nanostructures. 

The polar, ionic and even non-ionic head-group interactions of lipid membranes and other surfactants, (as indeed for many polymers and polyelectrolyte intra-molecular interactions) and the associated curvature at interfaces formed by such assemblies will be dependent on dissolved gas in quite complicated ways. Fluctuating nanometric sized cavities at such surfaces will be at extremely high pressure, (P = 2y/r, y= surface tension, and r the radius) resulting in formation of H and OH radicals. The immediate formation of Cl radicals and consequent damage to phospholipids offers em explanation of exercise-induced immunosuppression (through excess lactic acid CO2 production), perhaps a clue to the aging process. 

It is interesting to note that while the cnc for cationic polyelectrolytes is lower on glass than on mica, the opposite is true for cationic surfactants [11]. The reason for this difference is that both electrostatic forces and hydrophobic interactions between neighboring surfactant tails drive the surfactant self-assembly on the surface. Since the lattice sites are closer to each other on mica than on glass, the self-assembly of the surfactant is more favorable on the former surface. 

Excited triplet xanthone was initially employed as a probe molecule to study the dynamics of surfactant aggregated to polyelectrolytes [186]. Triplet-triplet absorption spectra were obtained 40 ns and 1 ps after the laser pulse, and a blue shift was observed. These two spectra were ascribed respectively to xanthone within the macroassembly and in the aqueous phase. Quenching experiments were carried out where the probe residing in the aqueous phase was quenched, whereas that in the self-assembly was protected. The xanthone dissociation rate constant from the aggregates was 1.1 x 10 s" [186]. 

Mesoporous carbon by soft template Carbons with mesostructures have been synthesized by using amphiphilic block copolymer as direct template, self-assembly surfactants or polyelectrolytes in the polymerization media of the carbon precursor. 

Using functional molecules as structural directors in the chemical polymerization bath can also produce polyaniline nanostructures. Such structural directors include surfactants [16-18], liquid crystals [19], polyelectrolytes (including DNA) [20,21], or complex bulky dopants [22-24]. It is believed that functional molecules can promote the formation of nanostructured soft condensed phase materials (e.g., micelles and emulsions) that can serve as soft templates for aniline polymerization (Figure 7.3). Polyelectrolytes such as polyacrylic acid, polystyrenesulfonic acid, and DNA can bind aniline monomer molecules, which can be polymerized in situ forming polyaniline nanowires along the polyelectrolyte molecules. Compared to templated syntheses, self-assembly routes are more scalable but they rely on the structural director molecules. It is also difficult to make nanostructures with small diameters (e.g., <50 nm). For example, in the dopant induced self-assembly route, very complex dopants with bulky side groups are needed to obtain nanotubes with diameters smaller than 100 nm, such as sulfonated naphthalene derivatives [23-25], fidlerenes [26], or dendrimers [27,28]. 

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