The local motions of an aromatic copolyester made from hydroquinone, h
ydroxybenzoic acid and isophthalic acid were investigated in trifluoro
acetic acid/dichloromethane solution using C-13 n.m.r. The interpretat
ion of the C-13 spin-lattice relaxation times was based on results pre
viously obtained on arylaliphatic copolyesters obtained from ethylene
glycol and hydroxybenzoic acid or isophthalic acid. It was carried out
in terms of relatively slow segmental main-chain motions and faster i
nternal motions of the aromatic rings. The segmental main-chain motion
s were represented by the Dejean-Laupretre-Monnerie orientation autoco
rrelation function. In agreement with the poor mobility of the aromati
c copolyester, there is not any noticeable libration of the phenyl rin
gs. The internal motions of the aromatic rings were described in terms
of jumps between two equilibrium positions for the para-substituted p
henyl rings and by stochastic jump processes for the isophthalic rings
.