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Synthesis of rod-coil block copolymers via end-functionalized poly(p-phenylene)s

par Marsitzky, D.;Brand, T.;Geerts, Yves ;Klapper, M.;Mullen, K.
Référence Macromolecular rapid communications, 19, 7, page (385-389)
Publication Publié, 1998-07

Article révisé par les pairs

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Résumé :

This paper describes a new way to synthesize rod-coil block copolymers consisting of poly(p-phenylene) (PPP) as rigid rod and either polystyrene (PS) or poly(ethylene oxide) (PEO) as flexible coil. The Suzuki-coupling of the AB-type monomer 4-bromo-2,5-diheptylbenzeneboronic acid (1) under strictly proton-free conditions leads to the control of PPP endgroups and hence allows the synthesis of a variety of differently end-functionalized poly(p-phenylene)s. The poly(2,5-diheptyl-p-phenylene)-block-polystyrene (7) is then prepared via condensation via condensation of anionically polymerized living polystyrene (6) with α-(4-formylphenyl)-ω-phenyl-poly(2,5diheptyl-p-phenylene) (4). Toluenesulfonic acid catalyzed condensation of α-methyl-ω-amino-poly(oxyethylene) (8) with PPP 4 yields poly(2,5-diheptyl-p-phenylene)-block-poly(ethylene oxide) (9).