Poly polyions

The polyelectrolyte catalysis of chemical reactions involving ionic species has been the subject of extensive investigations since the pioneering studies of Morawetz et al. [12] and Ise et al. [13-17]. The catalytic effect or the ability of poly-electrolytes to enhance or retard reaction rates is mainly due to concentration or exclusion of either or both of the ionic reactants by the polyions added to the reaction systems. For example, the chemical reaction between ionic species carrying the same charge is enhanced in the presence of polyions carrying the opposite charge. This enhancement can be attributed to an increase in the local concentration... 

FIG. 9 Schematic illustration of adsorption of poly(styrenesulfonate) on an oppositely charged surface. For an amphiphile surface in pure water or in simple electrolyte solutions, dissociation of charged groups leads to buildup of a classical double layer, (a) In the initial stage of adsorption, the polymer forms stoichiometric ion pairs and the layer becomes electroneutral, (b) At higher polyion concentrations, a process of restructuring of the adsorbed polymer builds a new double layer by additional binding of the polymer. 

This quick glance at the acid-base properties of some (poly)azamacro-cycles already suggests which parameters will determine the p a of macrocyclic and related acids and bases. Hydrogen bonds will probably be very important and in polyions Coulomb interactions have to be taken into consideration. But the geometry of the acid-base function has to be defined. In Sections 2, 3 and 4 we shall therefore focus on compounds with intra-annular acid-base functionalities (the 1,3-xylyl trick). 

Random coil conformations can range from the spherical contracted state to the fully extended cylindrical or rod-like form. The conformation adopted depends on the charge on the polyion and the effect of the counterions. When the charge is low the conformation is that of a contracted random coil. As the charge increases the chains extend under the influence of mutually repulsive forces to a rod-like form (Jacobsen, 1962). Thus, as a weak polyelectrolyte acid is neutralized, its conformation changes from that of a compact random coil to an extended chain. For example poly(acrylic acid), degree of polymerization 1000, adopts a spherical form with a radius of 20 nm at low pH. As neutralization proceeds the polyion first extends spherically and then becomes rod-like with a maximum extension of 250 nm (Oosawa, 1971). These pH-dependent conformational changes are important to the chemistry of polyelectrolyte cements. 

This ratio is related linearly to the degree of polymerization n. In the case of a poly(acrylic acid) where n = 1000 and /> = 20 nm, this ratio works out at 35. Thus, many of the counterions must enter the region of the polyion. Even when 90 % of the counterions are within the polyion this ratio is still high with a value of 3-5. A similar calculation for the rod-like random coil gives an energy ratio of 26 and similar arguments apply. 

The behaviour in solution of the first type of polyions compared with that of uncharged molecules is more involved in that the coil expansion is affected not only by the solvent but also by the electric field formed by the polyion itself, by the counterions and by the ions of other low-molecular-weight electrolytes, if present in the solution. Infinite charge dilution cannot be achieved by diluting the poly electrolyte solution, as a local high-intensity... 

Fig. 9 Stabilization of polyion complex nanoparticles composed of poly(amino acid)s using hydrophobic interactions...

As a cationic polymer and a cationic amphiphile, poly(allyl amine hydrochloride) (PAA) and octadecylamine (ODA) shown in Fig. 6 were used, respectively. The stability of the monolayers of the anionic amphiphiles was increased by polyion-complexation with PAA added in the aqueous subphase in comparison with Ca2+ salt formation. Ion complexation (1 1) of each anionic amphiphile with ODA was also performed at the air-water interface by spreading a chloroform solution of a 1 1 surfactant mixture. 

In principle, an organic molecule can accept as many electron pairs as it has low-lying vacant orbitals. In the same way, high-lying occupied orbitals can release not a single, but several electrons. Such multielectron processes can result in the formation of polyion-polyradicals. As will be seen from this section, the main topic of interest in poly(ion-radicals) consists of their spin multiplicity. 

Harada A, Kataoka K. Formation of polyion complex micelles in an aqueous milieu from a pair of oppositely-charged block copolymers with poly(ethylene glycol) segments. Macromolecules 1995 28 5294-5299. 

Katayose S, Kataoka K. Water-soluble polyion complex associates of DNA and polyfethylene glycol)-poly(L-lysine) block copolymer. Bioconjugate Chem 1997 8 702-707. 

Nanosized cobalt, copper, gold, nickel, rhodium, and silver particles have been stabilized by polyions and polymers [514, 549-553]. Particularly significant has been the simultaneous reduction of HAuC14 and PdCl2 in the presence of poly(iV-vinyl-2-pyrrolidine) to give relatively uniform, 1.6-nm-diameter, palladium-coated gold bimetallic clusters [554]. 

LB films prepared from poly-thiophene-3-acetic acid stearylamine or sulfonated polyaniline stearylamine polyion complexes, transferred to substrates, and doped by SbCls Absorption and infrared spectra, X-ray diffraction, and conductivity measurements Lateral d.c. conductivities of doped films were moisture dependent and were as high as 2 S cm"molecular organization consisted of randomly oriented polymers lying as extended chains parallel between the substrates and sandwiched between layers of stearylamine molecules whose chains were interdigitated 772... 

The B block may consist of a water-soluble polymer, for example, poly(aspartic acid) P(Asp), that is rendered hydrophobic by the chemical conjugation of a hydrophobic drug (Yokoyama et al., 1992, 1993, 1996 Nakanishi et al., 2001), or is formed through the association of two oppositely changed polyions (polyion complex micelles) (Hatada etal., 1995,1998 Kataoka etal., 1996). Drugs used to couple the B block include cyclophosphamide, doxorubicin, cisplatin, pyrene, and iodine derivative of benzoic acid (Kwon and Kataoka, 1995 Trubetskoy et al., 1997 Yu etal., 1998). 

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