Electrochemical copolymerization of 2-substituted thiophene derivative linked by polyether bridge with thiophene

Elucidating the Davydov-coupling mechanism in hydrogen bond dimers: Experimental and theoretical investigation of the polarized IR spectra of 3-thiopheneacetic and 3-thiopheneacrylic acid crystals.

“…As a result of the fact that nerve agents are hydrogen-bond accepting species, thiophene derivatives have potential for application to the detection of CWA compounds [24]. Thiophenes are desirable due to their high stability, sensitivity and selectivity [25]. Furthermore, polythiophenes act as organo-electronic materials [26] and, as such, can be integrated into simple electronic detection devices [27].…”

Novel Electrchemical Polymerization of Aminofluorenone and its Electrochemical behavior on Glassy Carbon Electrode

“…Although the presence of such an electron-withdrawing group may increase the oxidation potential, it may also reduce the reduction potential making it a candidate for n-type conductor use. However, since the synthesis of the first polyfluorene, there have been very few reports on the polymerization of FO(fluorenone ) [8][9][10][11]. In the field of optics and electronics these materials are traditionally used in applications such as packaging, electrical insulators, and photoresists.…”

Electrochemical polymerization and characterization of polyether‐substituted aniline derivatives

“…It was also reported that a polymer obtained from this monomer exhibits complexing properties towards Ag + and Co 2+ , especially in its reduced (neutral) form 12. Recently, we have also investigated the synthesis and polymerization of 2‐ and 3‐substituted thiophene derivatives linked by polyether bridges 14–16. Although there are some reports on the synthesis of polyether‐substituted aniline derivatives,17, 18 there are very few reports on their polymerization 19, 20…”