Influence of stereoregularity of the polymer chain on interactions with surfactants: binding of cetylpyridinium chloride by isotactic and atactic poly(methacrylic acid).

Association of a cationic surfactant cetylpyridinium chloride, CPC, with isotactic and atactic poly(methacrylic acid), i-PMA and a-PMA, respectively, in aqueous 0.01 M NaCl solutions was studied by pH and fluorescence measurements in conjunction with potentiometric studies using a surfactant-sensitive membrane electrode. pH measurements have demonstrated that the presence of an oppositely charged surfactant increases ionization of carboxyl groups on PMA at low degrees of neutralization. The increase is more pronounced in the case of i-PMA. The isotactic form of PMA is not soluble in water at zero degrees of neutralization but can be rendered soluble by the addition of CPC at the surfactant to a polyion molar ratio of around 0.4. In the solubilized complex, the positive charge of the CPC molecule is facing the polar solvent, whereas surfactant tails are oriented toward the i-PMA compact coil. Binding isotherms and cooperativity parameters show that chain tacticity has an important influence on the interaction of cetylpyridinium cation with polymethacrylate anion. At the onset of cooperative binding, the association is stronger with i-PMA than with the atactic form, as demonstrated by lower CAC values and higher values of the cooperativity parameters. In contrast, more surfactant is bound by a-PMA in the region where polyion becomes saturated with surfactant ions. Results are interpreted by taking into account local chain conformations as obtained from quantum mechanical semiempirical molecular orbital calculations. Greater hydrophobicity and possibly higher charge density of i-PMA on one hand and more flexibility of the a-PMA chain on the other are held responsible for these observations.