U. Geissler et al., POLYARYLENES ON THE BASIS OF ALKYLPYRROLE AND ALKYLCARBAZOLE DERIVATIVES AND THEIR OLIGOMERIC MODEL SYSTEMS, Polymers for advanced technologies, 8(2), 1997, pp. 87-92
The redox and spectroscopic properties of soluble poly(9-decylcarbazol
e) derivatives and poly(1-decylpyroole) were studied. The polymers wer
e synthesized via the Yamamoto polycondensation method. Analyzing the
electrochemical and optical properties of 3,6-linked poly(alkylcarbazo
le)s it is evident that the conjugation segment is the benzidine syste
m and the overall properties of these polymers can be compared with me
ta linked poly(phenylene)s. In opposite, 2,7-linked poly(alkylcarbazol
e)s reveal an even longer conjugation segment comparable with para lin
ked poly(phenylene)s. First observations in the case of poly(1-decylpy
rrole) suggest a higher steric hinderance compared to poly(1-methylpyr
role). Molecular modeling studies confirm this. (C) 1997 by John Wiley
& Sons, Ltd.