The polymers based on isoindigo, thiophene and ProDOT were synthesized and characterized. Black to transmissive polymers were obtained by controlling the feed ratios of the units.

A series of π-conjugated polymers containing alternating benzoselenadiazole (BSe)-bi(thiophene derivative)-carbazole or benzoththiadiazole (BSe)-bi(thiophene derivative)-fluorene units were designed and synthesized. Thiophene derivatives, namely 3-hexylthiophene, 3,4-bihexyloxythiophene, and 3,4-bioctyloxythiophene, were used as the π-bridges of the polymers. The polymers were characterized in detail in terms of their thermal stabilities, cyclic voltammograms, UV-Vis absorption, spectroelectrochemistry, dynamic switching property and so forth. The alkoxy thiophene π-bridged polymers have lower onset oxidation potentials and bandgaps than that of their corresponding alkyl thiophene π-bridged polymers. The selection of the donor units between the carbazole and the fluorene units has nearly no effect on the bandgaps and colors as well as the onset oxidation potentials of the polymers. The increase in the length of the side alkyl chains on the thiophene ring caused a slight increase in the polymer bandgap, which may be caused by the space hindrance effect. The dynamic switching abilities of the polymers were obtained by the chronoabsorptometry method, and the results also suggested that the alkoxy thiophene-containing polymers (as π-bridges) have higher contrast ratios than the corresponding alkyl thiophene-containing polymers. Furthermore, the increase in the length of the side alkyl chain might have a detrimental effect on the optical contrast ratios of the polymers.

Abstract:In this study, four novel donor-acceptor systems, 4-(2,3-dihydrothieno [3,4-b]and 4-nitro-N,N-bis(4-(thiophen-2-yl)phenyl)aniline (NTTPA), were successfully synthesized by Stille coupling reaction and electropolymerized to obtain highly stable conducting polymers, PNETPA, PNMOTPA, PNMTPA and PNTTPA, respectively. The polymers were characterized using cyclic voltammetry (CV), step profiling and UV-Vis-NIR spectroscopy. The band gaps (E g values) were 1.34, 1.59, 2.26, and 2.34 eV, for PNETPA, PNMOTPA, PNMTPA and PNTTPA, respectively. In addition, electrochromic switching showed that all polymers exhibit outstanding optical contrasts, high coloration efficiencies and fast switching speeds in the near-infrared region (NIR). These properties make the polymers suitable materials for electrochromic applications in NIR region.

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