During the last two years, mesomorphic structures for polyelectrolytes
with ionically bound surfactants have been reported. This has now bee
n extended to the case of hydrogen bonding. For poly (4-vinyl pyridine
)-pentadecyl phenol (P4VP-(PDP)(x)), the long period L(p) of the lamel
lar structure is found to decrease as a function of x, in complete con
trast to polyelectrolyte systems. Scaling arguments predict that the x
-dependence of the long period is entirely due to the reduction in the
thickness of the polymer layer and satisfies L(p) proportional to x(-
1), as observed experimentally. Polyelectrolyte-surfactant complexes,
on the other hand, are always locally fully complexed due to cooperati
ve complexation with a corresponding x-independent long period.