A series of poly(ether-ester)s derived from dimethyl terephthalate (DMT),
dimethyl fumarate (DMF), 1,4-butandiol (BD) and poly(tetramethylene oxide)
(PTMO,Mn = 1000 g/mol) was synthesized in a two stage process involving
transesterification and polycondensation in the melt. The mole ratio of the
starting components was selected to result in copolymers with a constant
hard:soft segment wieght ratio (56:44). The amount of DMF was 10 mol %,
referred to the total amount of the esters used. The synthesis was optimized
in terms of both the concentration of catalyst, tetra-n-butyl-titanate,
Ti(OBu)4 and thermal stabilizerN,N?-diphenyl-p-phenylenediamine, DPPD, as
well as the temperature. The composition and structure of the synthesized
poly(ether-ester)s were characterized by 1H-NMR. The number average
molecular weights of the polymers calculated from the 1H-NMR spectra were
compared with the corresponding values of the inherent viscosity (inh)
inm-cresol and the complex dynamic viscosity (