Über polyarylenalkenylene und polyheteroarylenaklenylene, 12. Synthesen und charakterisierung von poly(thieno[2,3‐b]thiophen‐2,5‐diylvinylenarylenvinylen)en, poly(thieno[3,2‐b]thiophen‐2,5‐diylvinylenarylenvinylen)en und einigen modellverbindungen

Abstract

Synthesen und Charakterisierung vonPoly(thieno[2,3-b] thiophen-2,5-diylvinylenarylenvinylen)en, Poly(thieno[3,2-b]thiophen-2,5-diylvinylenarylenvinylen)en und einigen Modellverbindungen SUMMARY:From Wittig-reactions of thieno[2,3-b]thiophene-2,5-dicarboxaldehyde (1) and thieno-[3,2-b]thiophene-2,5-carboxaldehyde (4) with "mono-and bis-Wittig-salts" of the benzene and thiophene series two series of isomeric poly(thienothiophene-2,5-diylvinylenearylenevinylene)s 3a-c and 5a-c, and some model compounds 7a-c and 8a-c were obtained. Wittig-reac- 10a-c. 12a-c, 13a, c, 14a, c. The structures of all compounds were confirmed by elemental analyses, IR, and electronic spectra, and those of the model compounds additionally by mass spectra, and in case of sufficient solubility by 'H NMR spectra. The electrical conductivities of all compounds and the thermooxidative degradation of the polymers were investigated. tions of thieno[2,3-b]thiophene-2-carboxaldehyde (9) and thieno[3,2-b]thiophene-2-carboxaldehyde (11) with "mono-and bis-Wittig-salts" gave two series more of model compounds

Poly(thieno[3,4-b]thiophene). A New Stable Low Band Gap Conducting Polymer

“…Several examples of conducting polymers derived from thieno[2,3- b ]thiophene and thieno[3,2- b ]thiophene − have been reported. The chemical structures of these monomers are depicted in Figure .…”