Poly- N-vinylamides, complexation and conformational changes in aqueous solution

Abstract

Interaction between small molecules (iodine and 1-anilinonaphthalene-8-sulphonate) and poly- N-methylacetamide (PVMA), poly- N-vinylcaprolactam (PVCL), poly- N-vinylpyrrolidone (PVP) and copolymers of N-vinyleaprolactam with N-vinylpyrrolidone (CP VCL-VP) and with N-vinyl- N-methylacetamide (VMA) were studied. All the polymers formed complexes with the small molecules. The stability constant for the complexes with the probe increases in the series PVMA < PVP < copolymer < PVCL indicating the essential role of hydrophobic interactions in the complex formation. With increasing temperature of aqueous solution from 18 to 33°, the constant decreased for PVP, PVMA and copolymers with low VCL content and increased for PVCL. A folding of PVC coils was observed over the temperature range, demonstrating a relationship between the conformational changes of macromolecules and the polymer complex formation. Addition of PVCL, PVMA and PVP to aqueous I 3 − solution brings about a shift of λ max from 350 nm for free triiodide ions to 372, 367 and 364 nm respectively. It is explained by different dipole moments of the side substituents. The stability constant for the polymers and I 3 − was estimated as approx. 10 5 M. The ability of the polymers to form complexes depends on chainlength. The greatest loss of the ability was observed for PVCL with M n changing from 6 × 10 3 to 2 × 10 3. Interaction of the polymers with I 3 − is accompanied by a conformational shrinking of coils. In the case of the probe, forces of electrostatic repulsion between negative charges of sulphonate groups result in an unfolding of polimer coils.