Polymerization of glycidyl phenyl ether was carried out with the dibut
yltin oxide-tributyl phosphate condensate as catalyst. The product was
fractionated. The yield of the acetone-insoluble faction was in the r
ange of 85% to 96%. The tacticity of the polymer fractions was studied
using C-13 NMR spectroscopy. The results indicated that the microstru
cture of PGPE was dependent on the catalyst structure and the reaction
conditions: By using the condensate of appropriate molecular weight a
s catalyst, the isotacticity of the acetone-insoluble fractions can re
ach as high as 87.4%. In some cases, however, the fractions rich in sy
ndiotactic structure were obtained in addition to the isotactic fracti
on. It was suggested that more than one kind of active sites were pres
ent in the catalyst.