Metal‐chloride‐anion‐containing polymers with expanded π‐conjugation systems derived from through‐space interactions in the piperazinium ring. Issue 5 (8th March 2019)

• Record Type: Journal Article
• Authors: Yamaguchi, Isao; Hamada, Yusei; Miyoshi, Kiyotaka; Wang, Aohan
• Is Part Of: Polymer international. Volume 68:Issue 5(2019)
• Page Start: 886
• Page End: 892
• Publication Date: 2019-03-08
• Subjects: metal chloride anion -- conjugated polymer -- Zincke salt -- ring‐opening copolymerization -- through‐space interaction; Plastics -- Periodicals; Polymers -- Periodicals; Polymerization -- Periodicals; 547.7
• DOI: 10.1002/pi.5778
• Languages: English
• ISSNs: 0959-8103

Abstract

Abstract: Reactions of N ‐(2, 4‐dinitrophenyl)pyridinium chloride (salt(Cl)) with H + MCl4 −1 (M ≡ Fe and Bi) resulted in an anion exchange between Cl − and MCl4 − to yield Zincke salts with metal chloride anions, namely salt(Fe) and salt(Bi), respectively. Reactions of the Zincke salts with piperazine resulted in ring‐opening of the pyridinium ring, yielding ionic polymers with 5‐piperazinium‐2, 4‐dienylideneammonium metal chloride units, namely polymer(Fe) and polymer(Bi). The corresponding model compounds were synthesized via reactions using salt(Bi) or salt(Cl) as starting materials. The UV–visible spectra of the polymers had absorption maxima at longer wavelengths than those of the model compounds. This indicated that the π‐conjugation system is expanded along the polymer main chain. Superconducting quantum interference device measurements indicated that polymer(Fe) was paramagnetic. Cyclic voltammetry analysis suggested that the polymers underwent electrochemical oxidation. © 2019 Society of Chemical Industry Abstract : Metal‐chloride‐anion‐containing ionic conjugated polymers were synthesized by ring‐opening polymerization of Zincke salt with piperazine.