Ln order to get a better knowledge on the influence of the introduction of
alkoxy group on the thermal and optical properties of the conducting polyth
iophene derivatives, poly(3-alkoxythiophene)s have been chemically polymeri
zed using iron (III) chloride as oxidizing agent under lower temperature an
d controlled addition of monomer. The polymers so obtained have relatively
higher molecular weight, less defects and increased crystallinity as compar
ed with those produced at room temperature. Their X-ray diffraction pattern
s support the stacking structure of polymer chain as proposed for poly(3-al
kylthiophene). Their thermal stability and transition behavior are studied
using TGA and MDSC techniques and compared with those of corresponding poly
(3-alkylthiophene). The glass transition and the onset of decomposition tem
perature of the polymer decrease with the increase of the side chain length
and the glass transition is dependent on the flexibility of the side chain
introduced. The extent of conjugation of these polymers are higher than th
at of poly(3-alkylthiophene) and the polymers exhibit interesting fluoresce
nce phenomena. Moreover, these polymers are photosensitive and the prelimin
ary results of the interaction between the polymer and the light are also r
eported. (C) 2000 Elsevier Science Ltd. All rights reserved.