Abstract
Poly[(silanylene)thiopene]s, copolymers with alternating thiophene, 2,2′-bithiophene, or 2,2′:5′,5″-terthiophene and mono-, di-, or tetrasilanylene units, were prepared by condensation of the dilithium salts of the thiophenes or the bis(2′-thienyl)silanes with α,ω-dichlorosilanes in diethylether. The polymers were characterized with1H,13C, and29Si NMR, UV, IR, GPC, TGA, and elemental analyses. UV absorption maxima of these polymers all show a red shift with increasing length of the polymer backbone, suggesting that conjugation occurs through the combined σ-Si and π-thiophene backbone.
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Wildeman, J., Herrema, J.K., Hadziioannou, G. et al. Synthesis of poly[(silanylene)thiophene]s. J Inorg Organomet Polym 1, 567–580 (1991). https://doi.org/10.1007/BF00683517
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DOI: https://doi.org/10.1007/BF00683517