Polyacetylene
From Wikipedia, the free encyclopedia
Polyacetylene (IUPAC name: polyethyne) is an organic polymer with the repeat unit (C2H2)n. The high electrical conductivity discovered for these polymers in the 1970’s accelerated interest in the use of organic compounds in microelectronics. Polyacetylenes are also known where the H atoms are replaced with alkyl groups.
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[edit] Structure of polyacetylene
The polymer consists of a long chain of carbon atoms with alternating single and double bonds between them, each with one hydrogen atom. Schematically the structure of polyacetylene is shown below.
One distinguishes trans-polyacetylene, with all double bonds in the trans configuration, from cis-polyactylene, with all double bonds in the cis configuration. Each hydrogen atom could be replaced by a functional group.
[edit] Preparation
Acetylene polymerizes in a similar fashion to ethylene: the polymerization can be effected with anionic, cationic, and radical initiators. Polyacetylene is generally not prepared by polymerizing acetylene, which is a highly flammable gas that uncontrollably oligomerizes at high concentrations. The most common synthesis utilize ring-opening polymerization ("ROMP") of molecules like cyclooctatetraene and substituted derivatives thereof.[1][2][3] Depending on the method of preparation, some polyacetylenes are also called acetylene black or polyacetylene black.[citation needed]
[edit] Conductivity and the Nobel Prize
As prepared with a Ziegler-Natta catalyst, with high levels of catalyst, the polyacetylene is a silver, non-conductive film. It was shown in 1976 that oxidation of this material with iodine results in a 108-fold increase in conductivity. The conductivity of this doped material approache the conductivity of the best available conductor, silver. This was one of the first known examples of a conductive organic polymer.[4] The Nobel Prize in Chemistry in 2000 was awarded to Alan J. Heeger, Alan G MacDiarmid, and Hideki Shirakawa for this work.
[edit] Naturally occurring “polyacetylene”
Some fungal melanins have been described as polyacetylene.[citation needed]
[edit] References
- ^ Jozefiak, T. H.; Ginsburg, E. J.; Gorman, C. B.; Grubbs, R. H.; Lewis, N. S."Voltammetric Characterization of Soluble Polyacetylene Derivatives Obtained from the Ring-Opening Metathesis Polymerization (ROMP) of Substituted Cyclooctatetraenes" Journal of the American Chemical Society 1993; volume 115, pages 4705-4713. DOI: 10.1021/ja00064a035
- ^ Gorman, C. B. Ginsburg, E. J.; Grubbs, R. H. "Soluble, Highly Conjugated Derivatives of Polyacetylene from the Ring-Opening Metathesis Polymerization of Monosubstituted Cyclooctatetraenes: Synthesis and the Relationship Between Polymer Structure and Physical Properties" Journal of the American Chemical Society 1993, volume 115, pages 1397-1409. DOI: 10.1021/ja00057a024
- ^ Langsdorf, Brandi, L.; Zhou, Xin; Lonergan, Mark C., "Kinetic Study of the Ring-Opening Metathesis Polymerization of Ionically Functionalized Cyclooctatetraenes" Macromolecules, 2001, volume 34, pages 2450-2458. DOI: 10.1021/ma0020685
- ^ Chiang, C. K.; Druy, M. A.; Gau, S. C.; Heeger, A. J.; Louis, E. J.; MacDiarmid, A. G.; Park, Y. W.; Shirakawa, H., "Synthesis of Highly Conducting Films of Derivatives of Polyacetylene, (CH)x," J. Am. Chem. Soc. 1978, 100, 1013-15. 10.1021/ja00471a081
