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Palladium‐catalyzed synthesis of oligo(methylthio)aniline and conversion to polyacene‐type electrolytes bearing phenothiazinium repeating units
Author(s) -
Oyaizu Kenichi,
Mitsuhashi Fumio,
Tsuchida Eishun
Publication year - 2002
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 - 10.1002/1521-3935(200207)203:10/11<1328::aid-macp1328>3.0.co;2-r
Subject(s) - chemistry , aniline , polymer chemistry , amination , polymer , polyaniline , catalysis , sulfonium , conductive polymer , ketone , ring (chemistry) , aryl , organic chemistry , polymerization , salt (chemistry) , alkyl
The synthetic routes to ladder polymers which consist of benzenetetrayl subunits with imino and methylsulfonio linkages are described. As the key intermediate, oligo‐ and polyaniline derivatives having pendant methylthio groups are prepared by the Pd‐catalyzed aryl amination from various monomers. The oxidation of the polymers with H 2 O 2 in the presence of CH 3 COOH effects the high yielding conversion of methylthio to methylsulfinyl groups without the formation of the undesired methylsulfonyl groups. The superacid‐induced condensation of the resulting polymers under dilution conditions induced the polymer‐analogous intramolecular electrophilic ring closure reaction of the hydroxy(methyl)(phenyl)sulfonium cation onto the adjacent benzene ring to yield the required ladder polymers which have proved to be semiconductors with intrinsic electric conductivities of ca. 10 −5 S · cm −1 .1 H NMR spectra of (a) 8a in CD 2 Cl 2 , (b) 9 in CD 2 Cl 2 and (c) 2 in DMSO‐d 6 . TMS was used as the internal standard. Residual proton signals in the deuterated solvents are marked with an asterisk.