Polyferrocenes: Difference between revisions
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[[File:Biferrocene.svg|thumb|left|122 px|[[Biferrocene]] is the smallest unit of polyferrocene.]] |
[[File:Biferrocene.svg|thumb|left|122 px|[[Biferrocene]] is the smallest unit of polyferrocene.]] |
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== Potential applications == |
== Potential applications == |
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Polyferrocenes have no commercial applications, despite being the subject of research for nearly 50 years. Poly[[vinylferrocene]] gives electroactive films that have been investigates as glucose sensors.<ref>{{cite journal|title= Ferrocene-mediated enzyme electrode for amperometric determination of glucose|authors=Cass, Anthony E. G.; Davis, Graham; Francis, Graeme D.; Hill, H. Allen O.; Aston, William J.; Higgins, I. John; Plotkin, Elliot V.; Scott, Lesley D. L.; Turner, Anthony P. F.|journal=Analytical Chemistry|year=1984|volume=56|pages=667–671|doi=10.1021/ac00268a018}}</ref> |
Polyferrocenes currently have no commercial applications, despite being the subject of research for nearly 50 years. Poly[[vinylferrocene]] gives electroactive films that have been investigates as glucose sensors.<ref>{{cite journal|title= Ferrocene-mediated enzyme electrode for amperometric determination of glucose|authors=Cass, Anthony E. G.; Davis, Graham; Francis, Graeme D.; Hill, H. Allen O.; Aston, William J.; Higgins, I. John; Plotkin, Elliot V.; Scott, Lesley D. L.; Turner, Anthony P. F.|journal=Analytical Chemistry|year=1984|volume=56|pages=667–671|doi=10.1021/ac00268a018}}</ref> |
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=== Coatings === |
=== Coatings === |
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Revision as of 01:42, 29 December 2017
Polyferrocenes are polymers containing ferrocene units. Ferrocene offers many advantages over pure hydrocarbons when used as a building block of macromolecular chemistry. The variety of possible substitutions at the ferrocene parent body results in a multitude of accessible polymers with interesting electronic and photonic properties. Many polyferrocenes are relatively easily accessible. Poly(1,1'-ferrocene-silane) can be prepared by ring-opening polymerization and has a variety of interesting properties, such as a high refractive index or semiconductor properties. Ring-opening polymerization usually leads to polymers containing ferrocene in the backbone. Besides the latter motif, ferrocene can be attached to the backbone as pendant unit as well.[1]
Potential applications
Polyferrocenes currently have no commercial applications, despite being the subject of research for nearly 50 years. Polyvinylferrocene gives electroactive films that have been investigates as glucose sensors.[2]
Coatings
Satellites charge themselves by the bombardment with charged particles of the solar wind. Charging can lead to an arc discharge which can impair the function of the satellite due to magnetic disturbances and material failure. To avoid these impairments, coatings of electrically weak or non-conductive plastic components of thin films of poly(1,1'-ferrocen-silane) were examined. These carry off the charge generated by the irradiation and thus could protect the satellite from overloads.[3]
Polymers with high refractive index
Polyferroccenes have attracted interest as high-refractive-index polymers, such as in antireflection coatings or for light-emitting diodes.[4]Poly(1,1'-ferrocene-silane)e, poly(1,1'-ferrocene-phosphane) and polyferrocenes with phenyl side chains are polymers with unusually high refractive index, with values in the refractive index of up to 1.74. These polyferrocenes show good film-forming ability.[5]
Plasma-assisted reactive ion etching
Poly(ferrocene-dimethylsilane)s (PFS) are promising as barrier materials in plasma-assisted reactive ion etching. Due to the presence of iron and silicon in the main chain, the polymer proved to be relatively stable compared to purely organic polymers. During the etching, a thin iron and silicon-containing oxide layer was formed on the surface of the poly(ferrocene-dimethylsilane).[6]
Additional reading
- Ian Manners: Polymers and the Periodic Table: Recent Developments in Inorganic Polymer Science. In: Angewandte Chemie International Edition in English. 35, 1996, p. 1602, doi:10.1002/anie.199616021.
- Jürgen Falbe, Manfred Regitz (Hrsg.): Römpp-Lexikon Chemie, 9th edition, Bd.5, PI-S, 1999, ISBN 3-13-735010-7, p. 3449-3455.
References
- ^ Rudolf Pietschnig: Polymers with pendant ferrocenes. In: Chemical Society Reviews. 45, 2016, S. 5216, doi:10.1039/c6cs00196c.
- ^ "Ferrocene-mediated enzyme electrode for amperometric determination of glucose". Analytical Chemistry. 56: 667–671. 1984. doi:10.1021/ac00268a018.
{{cite journal}}: Unknown parameter|authors=ignored (help) - ^ R. Resendes, A. Berenbaum, G. Stojevic, F. Jäkle, A. Bartole, F. Zamanian, I. Manners: Application of ring-opened poly(ferrocene)s as protective charge dissipation coatings for dielectrics. In: Advanced Materials, 12(5), (2000), S. 327-330, doi:10.1002/(SICI)1521-4095(200003)12:5<327::AID-ADMA327>3.0.CO;2-L.
- ^ Ian Manners: Polyferrocenylsilanes: metallopolymers for electronic and photonic applications. In: Journal of Optics A: Pure and Applied Optics. 4, 2002, S. S221, doi:10.1088/1464-4258/4/6/356.
- ^ Vasilios Bellas, Matthias Rehahn: Polyferrocenylsilane-Based Polymer Systems. In: Angewandte Chemie International Edition. 46, 2007, S. 5082, doi:10.1002/anie.200604420.
- ^ Rob G. H. Lammertink, Mark A. Hempenius, Vanessa Z.-H. Chan, Edwin L. Thomas, G. Julius Vancso: Poly(ferrocenyldimethylsilanes) for Reactive Ion Etch Barrier Applications. In: Chemistry of Materials. 13, 2001, S. 429, doi:10.1021/cm001052q.
External links
Media related to Polyferrocene at Wikimedia Commons
