Processable electrochromic and fluorescent polymers based on N-substituted thienylpyrrole

4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials

“…58). 135 It was found that this polymer adopted 'cauliflower-like' structures in solution, indicating that polymer growth takes place after initial nucleation. Significant changes in transmittance were observed when the polymer was switched between À0.2 and 1.2 V electric fields.…”

Synthesis, electrochemical and fluorescence properties of three new dithienylpyrroles bearing aromatic amine units

“…It was reported that there were three characteristic peaks of SNS units at 679 cm À1 for a-H of thiophene rings, 770 cm À1 for b-H of pyrrole ring and 843 cm À1 for b/b 0 -H of thiophene rings in SNS derivatives [22][23][24][25][26][27]. As shown in Fig.…”

“…It was reported that the oxidation of dithienylpyrrole systems do not significantly affected by the groups substituted on the N-position of the central pyrrole ring [22,23,25]. Aromatic subunits inserted between the thiophene rings like fluorene, naphthol, benzene, pyrrole et al [22][23][24][25][26] could decrease the oxidation potential, while Fig. 1, in the first cycle, a single irreversible oxidation peak was observed for P1, P2 and P3 at 0.88 V, 0.92 V and 0.85 V, respectively.…”

“…Levent Toppare and Atilla Cihaner et al [14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33] reported a series of SNS derivatives synthesized by the Knorr-Paal condensation and their electrochemical, electro-optical properties, fluorescence properties and electrochromic behavior were studied. Based on these reports, we synthesized dithienylpyrroles bearing anthraquinone units [34] which exhibited multicolor electrochromic behavior.…”

Synthesis and characterization of fluorescent nitrobenzoyl polythiophenes

“…Therefore, the properties can be adjusted by modification of the monomer structure by attaching different functional groups, such as, electron-donating and/or electronwithdrawing, n-dopable, or fluorescent substituents [10][11][12][13]. For instance, the appendage of a nitro group on the monomer structure would make the resulting polymers amenable for use in sensors or electrochemical capacitors [14,15].…”