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. 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
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.