M. Jayakannan et S. Ramakrishnan, Preparation of polyethers via proton acid catalyzed transetherification reactions, MACRO CH P, 201(7), 2000, pp. 759-767
An approach for the preparation of polyethers by a transetherification rout
e has been developed. This approach involves the melt condensation of a dio
l with a specifically designed diether in the presence of a catalyst to yie
ld polyethers with the exclusion of two moles of a low boiling alcohol, in
this case methanol. The diether monomers are designed so as to contain two
labile benzyl methyl ether linkages that can readily undergo a transetherif
ication process. These diether monomers (5a and 5b) readily undergo transet
herification polycondensation with di-, tri- and tetraethylene glycols as w
ell as with a variety of aliphatic diols to yield polymers of moderately hi
gh molecular weights. The glass transition temperatures (T-g) of the polyme
rs decrease with increasing length of the diol. Melting transitions (T-m) a
re observed only in some polymers containing aliphatic units but those with
the oligo(ethylene oxide) units are completely amorphous. Preliminary ioni
c conductivity studies indicate that the polyethers with oligo(ethylene oxi
de) units could serve as excellent candidates in solid polymer electrolyte
applications.