Polyethers having well-defined comb-shaped architectures were prepared by u
sing poly(4-hydroxystyrene) (PHSt) as a multifunctional initiator for graft
polymerization of either ethylene oxide (EO) or a mixture of EO and propyl
ene oxide (PO). The grafting process was performed in 1,4-dioxane using NaH
as ionizer for the PHSt hydroxyl groups. The precursor PHSt was prepared b
y first polymerizing 4-tert-butoxystyrene, using butyllithium as initiator
in THF at -60 degreesC, and then deprotecting the butoxy groups. Finally, t
he terminal hydroxyl groups of the polyether grafts were end-capped with he
xadecanoyl units through esterification. The monomer addition sequence in t
he graft copolymerizations with the same EO/PO feed ratio proved to have a
great influence on the crystallization temperature and the crystallinity of
the grafts. Also, the end-capping was found to reduce the degree of crysta
llinity as compared to the corresponding uncapped polymers. Solid polymer e
lectrolytes containing lithium triflate (LiSO3-CF3) salt had ambient temper
ature ion conductivities of similar to 10(-5) S/cm at [Li]/[O] = 0.025. The
rmal analysis of the electrolytes showed that the polymers aggregated throu
gh phase separation of the hexadecanoyl chain ends.