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Synthesis and Characterization of Poly(arylene ether oxadiazole) Telechelics
Author(s) -
Gomes Dominique,
Nunes Suzana P.
Publication year - 2003
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.200350066
Subject(s) - arylene , monomer , polymer chemistry , oxadiazole , ether , copolymer , chemistry , nucleophilic substitution , reactivity (psychology) , prepolymer , organic chemistry , polymer , aryl , polyurethane , alternative medicine , medicine , alkyl , pathology
Poly(arylene ether oxadiazole) telechelics with fluorine and hydroxyl end groups were synthesized by nucleophilic substitution polymerizations of 2,5‐bis(4‐fluorophenyl)‐1,3,4‐oxadiazole monomer with bishydroxy compounds containing C(CH 3 ) 2 , C(CF 3 ) 2 and SO 2 groups. Fluorotelechelics were obtained with about 3 repeating units (molecular weight about 2 000 g · mol −1 ) using a rather excess (100 mol‐%) of bis(fluorophenyl) oxadiazole compound. On the other hand, hydroxytelechelics were synthesized with about 9 repeating units (molecular weight about 5 000 g · mol −1 ) using a small excess of bishydroxy compound (monomer molar ratio of 0.93). Sulfonated poly(arylene ether oxadiazole) hydroxytelechelics were also synthesized using sulfonated and unsulfonated bishydroxy compounds. All sulfonated hydroxytelechelics were partially water soluble, even when only 40 mol‐% of sulfonated monomers was used. The number of repeating units of hydroxytelechelics increased up to 12 (molecular weight about 9 000 g · mol −1 ) using sulfonated monomers, probably because of the higher reactivity of sulfonated phenoxide. The molecular weights estimated by 1 H NMR were in agreement to the results obtained by SEC. The telechelics can be used as precursor for the synthesis of block copolymer.Structure of the hydroxytelechelics.