Cooperative interactions of unlike macromolecules: NMR study of ionic of coupling of poly[2-(trimethylammonio)ethyl methacrylate chloride]-block-poly(N-(2-hydroxypropyl)methacrylamide) polycation with oligophosphates in D2O

Citation
J. Kriz et al., Cooperative interactions of unlike macromolecules: NMR study of ionic of coupling of poly[2-(trimethylammonio)ethyl methacrylate chloride]-block-poly(N-(2-hydroxypropyl)methacrylamide) polycation with oligophosphates in D2O, J PHYS CH A, 104(46), 2000, pp. 10972-10985
Citations number
28
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF PHYSICAL CHEMISTRY A
ISSN journal
10895639 → ACNP
Volume
104
Issue
46
Year of publication
2000
Pages
10972 - 10985
Database
ISI
SICI code
1089-5639(20001123)104:46<10972:CIOUMN>2.0.ZU;2-4
Abstract
Cooperative effects in the interactions of poly[2-(trimethylammonio)ethyl m ethacrylate chloride]-block-poly(N-(2-hydroxypropyl) methacrylamide) polyca tion with oligophosphates (phosphate glasses) leading to micellelike comple xes were studied using NMR. H-1, C-13, N-14, Na-23, (31)p,and Br-79 single and double-quantum high-resolution and MAS NMR at 7.2 and 12 T of the compl exes were studied at concentrations 0.1 and 0.02 mol/L of the ionic groups in D2O at 300-350' K. K-1, C-13, and P-31 longitudinal and transverse relax ations and Na-23, Cl-35, and(79)Br T-1(1), T-1(3) and T-2(3) time evolution s were studied to reveal the ionization states, local and semilocal mobilit ies, and ion coupling conversions in the products of the same polycation wi th polyphosphates of P-n = 15, 25, 35, 45, 65, and 75. Pulsed gradient spin -echo (PGSE) was used to measure self-diffusion coefficients and thus the s ize of both reactants and products. The results show that the ionic couplin g is almost complete with polyphosphates of P-n up to 35 but decreases stee ply with higher values of P-n. In all cases, the products are aggregates of ionic complexes, but their size:increases with higher P-n of the polyphosp hate. The cooperativity in the products of self-assembling is discussed in terms of kinetic, thermodynamic (entropy), and microphase stabilization.