// Workers AI · dad joke modeWhat did polyfuran say? "I'm fur-an-ly bonded".
(Redirected from C4H2O)
 Idealized chemical structure of polyfuran | |
| Identifiers | |
|---|---|
| Properties | |
| (C4H2O)n | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Polyfuran (PFu) is a polymer that consists of multiple furanylene rings. Such materials are of interest for their potential in molecular electronics, although much less studied than polythiophenes and polypyrroles. Polyfuran is distinct from furan resins, a class of non-conjugated polymers. Furan resins are of commercial interest, in contrast to polyfuran.
Polyfurans can be prepared by electrochemical approaches.[1] The mechanism of polymerization is proposed to involve radical cation intermediates, i.e. species with the formula C4R4O+.[2]
Polyfurans can also be produced using acid catalysts.[3] Radical polymerization has also been explored,[4] and oxidative cationic polymerization.[5]
References
[edit]- ↑ Gonzalez-Tejera, M. J.; Blanca, E. S.; Carrillo, I. (2008). "Polyfuran conducting polymers: Synthesis, properties, and applications". Synthetic Metals. 158 (5): 165–189. doi:10.1016/j.synthmet.2007.12.009.
- ↑ Diaz, A.; Bargon, F. (1986). Handbook of Conducting Polymers. New York: Marcel Dekker.
{{cite encyclopedia}}: Missing or empty|title=(help) - ↑ Armour, A; Davies, A. G.; Upadhyay, J.; Wassermann, A., J. Polym. Sci. A 1967, 5, 1527.
- ↑ Gandini, A. Adv. Polym. Sci. 1977, 25, 47.
- ↑ Yoshino, K.; Hayashi, S.; Sugimoto, R. (1984). "Preparation and Properties of Conducting Heterocyclic Polymer Films by Chemical Method". Jpn. J. Appl. Phys. 23: L899–L900. doi:10.1143/JJAP.23.L899.