Flexible Amphiphilics

The polymers described so far have relatively flexible main chains which can result in complex confonnations. In some cases, tliey can double back and cross over tliemselves. There are also investigations on polymers which are constrained to remain in a confonnation corresponding, at least approximately, to a straight line, but which have amphiphilic properties tliat ensure tliat tliis line is parallel to tire water surface. Chiral molecules are one example and many polypeptides fall into tliis class [107]. Another example is cofacial phtlialocyanine polymers (figure C2.4.9). 

In some of these models (see Sec. Ill) the surfactants are still treated as flexible chains [24]. This allows one to study the role of the chain length and chain conformations. For example, the chain degrees of freedom are responsible for the internal phase transitions in monolayers and bilayers, in particular the hquid/gel transition. The chain length and chain architecture determine the efficiency of an amphiphile and thus influence the phase behavior. Moreover, they affect the shapes and size distributions of micelles. Chain models are usually fairly universal, in the sense that they can be used to study many different phenomena. 

The use of ordered supramolecular assemblies, such as micelles, monolayers, vesicles, inverted micelles, and lyotropic liquid crystalline systems, allows for the controlled nucleation of inorganic materials on molecular templates with well-defined structure and surface chemistry. Poly(propyleneimine) dendrimers modified with long aliphatic chains are a new class of amphiphiles which display a variety of aggregation states due to their conformational flexibility [38]. In the presence of octadecylamine, poly(propyleneimine) dendrimers modified with long alkyl chains self-assemble to form remarkably rigid and well-defined aggregates. When the aggregate dispersion was injected into a supersaturated... 

Calmodulin (CaM) undergoes drastic conformational change when it binds Ca2+ and amphiphilic peptides such as mas to po ran and endorphin, which results in the modulation of many important biochemical reactions. The N-terminal and C-terminal of rigid structured globular domains are bridged with a long flexible peptide of a-helical structure. Each domain binds two Ca2+ ions to its hydrophobic sites. 

In a very recent investigation, hydrophobic PFS (Sect. 7.1) was attached to a hydrophilic PEO block to form an amphiphilic PFSi2-[Ru]-PE07o block copolymer [331]. Rodlike micelles were observed in water for this copolymer (Fig. 24). These micelles have a constant diameter but are rather polydisperse in length, and DLS measurements indicate that they are flexible. Crystallization of the PFS in these micelles was observed and is thought to be the key behind the formation of rodlike structures. The cylindrical micelles can be cleaved into smaller rods whenever the temperature of the solution is increased or whenever they are exposed to ultrasound. 

More recently, Kunitake and Okahata (1978b) discovered that a stable bilayer structure could be formed from a series of single-chain amphiphiles which possess rigid segments and flexible hydrocarbon tails as in [6]. 

Amphiphilic systems containing an extended rigid-rod block, rather than a more flexible linear chain, have also been shown to self-assemble into well-defined structures. Stupp s group explored a series of rod-dendron and dendron-rod-dendron hybrids containing two to three biphenyl ester moieties as a rigid rod that was capped by one or two 3,4,5-tra-alkoxy benzoate dendrons (Lecommandoux et al. 2003). The... 

Jang C-J, R)ti J-H, Lee J-D, Sohn D, Lee M. Synthesis and supramolecular nanostructure of amphiphilic rigid aromatic-flexible dendritic block molecules. Chem Mater 2004 16 4226-4231. 

Thus the use amphiphilic macromonomers is another method to achieve the particle formation and their subsequent stabilization. Macromonomers can be pre-reacted to form graft copolymers, which are be introduced into the reaction medium afterwards. Macromonomers can also be copolymerized with classical monomers in situ to form graft copolymers. This is a simple and flexible method for producing monodisperse micron-sized polymer particles. Macromonomers can produce ion-free acrylic lattices with superior stability and film forming properties compared to conventional charge stabilized lattices. These non-con-... 

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