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New aromatic‐aliphatic polyesters based on N‐alkyl carbazole groups in the main chain. Synthesis‐structure‐properties relationships
Author(s) -
Drzewinski Isabel,
Adès Dominique,
Bélorgey Georges,
Siove Alain
Publication year - 1997
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.19971220150
Subject(s) - carbazole , alkyl , polyester , diethylene glycol , condensation polymer , polymer chemistry , ether , ethylene glycol , catalysis , electron acceptor , materials science , acceptor , molecule , chemistry , organic chemistry , physics , condensed matter physics
Abstract Polyesters based on N ‐butyl or N ‐octylcarbazole units in the main chain were synthesized either by direct polycondensation between the carbazole dicarboxylic acids and ethylene glycol or from alcoholysis of the 2‐hydroxyethyl diesters in the presence of different catalytic systems. Depending on the reaction conditions together with the nature and the concentration of the catalyst, diethylene glycol (DEG) is formed as a side‐reaction product. DEG is incorporated in the polyester chain concurrently with EG and leads to the formation of ether links in the spacers. The DEG content as well as the length of the alkyl pendant group of the carbazole unit were found to have a drastical effect on the thermal properties. Furthermore, these materials form charge transfer complexes through carbazole nuclei with electron acceptor and electron donor molecules as well.