Preparation of polyethers via proton acid catalyzed transetherification reactions

Citation
M. Jayakannan et S. Ramakrishnan, Preparation of polyethers via proton acid catalyzed transetherification reactions, MACRO CH P, 201(7), 2000, pp. 759-767
Citations number
17
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULAR CHEMISTRY AND PHYSICS
ISSN journal
10221352 → ACNP
Volume
201
Issue
7
Year of publication
2000
Pages
759 - 767
Database
ISI
SICI code
1022-1352(20000512)201:7<759:POPVPA>2.0.ZU;2-4
Abstract
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.